• Psychedelic Medicine

AUTISM | +70 articles

mouse-3194768_960_720.jpg



Guilt by dissociation: The role of serotonin in Autism

Florida Atlantic University | Neuroscience News | 2 Sep 2020

SERT Ala56 impacts the structure of the SERT protein cells, increasing the activity of the transporter to abnormally high levels. The high-activity state results in the removal of too much serotonin from brain sites where serotonin is needed, both during development and in adults.

Neuroscientists in the laboratory of Randy D. Blakely, Ph.D., professor of biomedical science in Florida Atlantic University’s Schmidt College of Medicine and executive director of the FAU Brain Institute, are focused on serotonin, a mood-regulating molecule in the brain that regulates many brain synapses — the gaps between nerve cells where signals are sent and received. The supply of serotonin is tightly regulated by a protein called the serotonin transporter (SERT), which sweeps away serotonin from synapses to limit its action. Shifts in the transporter’s activity can significantly impact the ability of serotonin to act in the brain.

Changes in signaling by the neurotransmitter serotonin has been connected to autism for more than 50 years, dating back to findings of elevated serotonin levels in the blood of some people with the disorder, a feature termed hyperserotonemia. Since this time, multiple rare changes in the genetic code that impact SERT have been observed.

Recent studies of mice expressing the most common of these gene variants, called SERT Ala56, induces behavioral changes in animals that scientists connect to alterations in people with autism – repetitive behavior, altered communication, and atypical social interactions, as well as hyperserotonemia. Although the effects of the SERT Ala56 mutation are paralleled by other mutations in the SERT gene, none of these mutations are common enough to account for the number of individuals with autism demonstrating hyperserotonemia.

Blakely and collaborators have published a study in the journal Frontiers in Molecular Neuroscience, which now offers a possible explanation for this puzzle.

“We have known for some time that the activity and regulation of the SERT protein is critically dependent on a number of other proteins that tell the protein where to locate on nerve cells and how to act,” said Blakely, lead author.

It turns out that the SERT Ala56 mutation changes the structure of the transporter in ways that keep these partner proteins from interacting with the transporter, a protein that Blakely’s laboratory identified thirty years ago.

Last year, Blakely’s former graduate student Meagan Quinlan, Ph.D., first author and a post-doctoral fellow at the University of Washington, demonstrated that the SERT Ala56 mutation impacts the structure of the SERT protein in cells in culture, revving up the transporter into a state of abnormally high activity.

“We think that this high-activity state results in removal of too much serotonin from sites in the brain where serotonin is needed, both during development and in adults,” said Quinlan. “I suspect that the structural changes we have observed likely reflected changes in the regulatory ability of SERT-associated proteins to maintain serotonin inactivation at normal levels.”

To test this concept, Quinlan purified the mutant transporter from the brain of SERT Ala56 expressing mice, as well as from normal mice, and then determined whether proteins normally bound to SERT were still attached.

“We found that only a few proteins seemed to interact with SERT Ala56 more than they should. In contrast, many more proteins appeared no longer tethered to the transporter, including some proteins we already knew to be SERT regulators and others that have been linked to ASD,” said Quinlan.

Blakely was actually quite surprised at the findings. “It is quite amazing that one of the smallest changes you can make in SERT can alter its interactions with partners,” said Blakely.

According to Blakely, further work could reveal more extensive links between SERT and other genes known to associate with autism, broadening the impact of SERT Ala56 to other neurotransmitter systems.

“Following the scent of serotonin may well take us to molecules and medications we had no clue about just a few years ago,” said Blakely.

Blakely’s team recently reported a new small molecule that can tone down SERT activity and normalize behaviors in the SERT Ala56 mouse, a molecule that he hopes may lead to a new therapeutic.

“A goal moving forward with this drug is to see if it can reverse the changes in SERT Ala56 protein associations, tying the molecular changes we see with the mutant to how the drug may work,” said Blakely.

ASD is a serious developmental disorder with increased prevalence that impairs the ability to communicate and interact and impacts the nervous system. The range and severity of symptoms can vary widely and common symptoms can include difficulty with communication and social interactions, obsessive interests, and repetitive behaviors. No current medications treat the core features of ASD.

 
Last edited:
Sp1PostmortemExpressionArticle.jpg



Autistic people have lower levels of a protein that regulates serotonin in the brain

Karolinska Institute | Neuroscience News | 9 Sep 2020

People with autism spectrum disorder have lower levels of a protein that regulates the amount of serotonin in the brain, a paper from Karolinska Institutet in Sweden published in the journal Molecular Psychiatry reports. For their study, the researchers used a molecular brain imaging technique to compare people with and without autism; their results offer hope of finding a drug that can alleviate the symptoms.

Autism spectrum disorder (ASD) debuts in childhood and is a neuropsychiatric condition characterised by limited communication and social skills and repetitive behaviour.

“Unfortunately, knowledge of brain physiology in autism is scant and there are no drugs available able to affect the core symptoms in people with ASD who need such help,” says the paper’s first author Max Andersson, doctoral student at the Department of Clinical Neuroscience, Karolinska Institutet.

An important neurotransmitter

The serotonin system has been considered a possible clue to the differences in brain function observed in ASD. Serotonin is an important neurotransmitter that regulates widely disparate physiological, emotional and cognitive processes. It also acts as a growth factor during brain development.

Previous studies have shown that many people with ASD have elevated levels of serotonin in the blood. Smaller-scale brain imaging studies have revealed lower levels of the serotonin transporter 5-HTT, a protein that regulates the amount of serotonin in the brain, but these results have remained unconfirmed.

In this new study, the researchers used the PET (positron emission tomography) technique to study differences between 5-HTT levels in 15 individuals with ASD (11 men and 4 women) and 15 matched controls without ASD. The study shows that people with ASD have lower concentrations of the serotonin transporter in the cerebral cortex and several other areas of the brain, including the brain stem, which mediates signals between the cerebrum, the cerebellum, the spinal cord and the peripheral nervous system.

They also found a correlation between the participants’ scores in social cognitive tests of skills typically impaired in ASD, and levels of 5-HTT in certain areas of the brain.

Significant differences

“Our results show that there are significant differences and confirm that the brain’s serotonin system plays an important part in ASD,” says Andersson. “With a better understanding of the physiology of ASD, we will hopefully one day be able to alleviate the symptoms that cause suffering or functional impairment.”

Before undergoing a PET scan, tiny amounts of a radioactive tracer are injected direct into the blood of study participants. The tracer then binds to the particular protein in the brain to be examined. Using the PET system, scientists can estimate the amount and distribution of the target binding site by measuring the radiation that the tracer emits in different parts of the brain.

 
Last edited:
This shows a child and teddy bear



Study suggests connection between Autism and gastrointestinal problems

Ohio State University | Neuroscience News | 3 Dec 2020

A new study reports on a link between repetitive behaviors associated with autism and gastrointestinal problems. Researchers also found a connection between the severity of ASD symptoms and an increased risk of children experiencing more severe constipation, stomach pains, and other GI problems. However, no association was found between GI problems and social or communication difficulties associated with ASD.

The study found that increased severity of other autism symptoms was also associated with more severe constipation, stomach pain and other gut difficulties.

The research, which appears in the journal Autism, found no association between social and communication difficulties and gastrointestinal symptoms.

The study doesn’t explain the biological mechanism for the relationship between repetitive behaviors, such as rocking back and forth and hand flapping, and gut problems. But it helps establish that gastrointestinal symptoms may exacerbate repetitive behaviors, or vice versa, a finding that could one day help lead to helpful interventions, said Payal Chakraborty, a graduate student in The Ohio State University College of Public Health who led the study.

Children with autism spectrum disorder are more likely than their typically developing peers to experience a range of gastrointestinal abnormalities, including chronic diarrhea, constipation, food sensitivities and abdominal pain. These symptoms have been associated with higher levels of irritability and aggressive behavior, but less is known about their relationship with other autism spectrum disorder symptoms.

“In the general population, there’s a fair amount of evidence about the connection between mood and mental disorders and gastrointestinal difficulties. In autism, we wonder if the gut problems children experience are a core part of the disease itself or whether they’re brought on by other symptoms that children with autism experience,” Chakraborty said.

Chakraborty began the study as a student at Duke University, where she worked at the Center for Autism and Brain Development and became interested in the potential connection between the gut and other characteristics of the developmental disability.

Using data from a study designed to test the viability of cord blood transplants as an autism treatment, Chakraborty looked at detailed clinical measures and reports provided by the families of 176 children who were 2 to 7 years old to see if she could find any insights into the drivers of gastrointestinal problems. Almost all of the children, 93%, had at least one gastrointestinal symptom.

Children with autism spectrum disorder are more likely than their typically developing peers to experience a range of gastrointestinal abnormalities, including chronic diarrhea, constipation, food sensitivities and abdominal pain.

“GI problems are a significant issue for many people with autism and there’s evidence that these symptoms might exacerbate certain autism behaviors, which can lead to greater developmental challenges,” she said.

The specifics of the relationship are unclear, but it’s possible that repetitive behaviors in children with autism could be a coping mechanism that helps them manage their gastrointestinal discomfort, Chakraborty said, adding that the symptoms of autism often emerge at a time when children aren’t in a position to adequately communicate their physical suffering with words.
“Gastrointestinal problems are a major concern for many children with autism and we still have a lot to learn about the complicated gut/brain axis.”

*From the article here :
 
Last edited:
fly-d-ve1I7ylTths-unsplash.jpg



Psychedelics’ exciting potential to benefit autistic people

[This article is published in collaboration with Narcotica, a podcast about drugs and the people who use them, hosted by journalists Troy Farah, Zachary Siegel and Christopher Moraff. To learn more about the experiences of autistic people who have benefitted from psychedelics, you can listen here.]

by Troy Farah | FILTER | 24 May 2021

In the psychedelic sixties, Timothy Leary chanted “Turn on, Tune in, Dropout." By the end of the twentieth century, however, Leary adjusted his well-known catchphrase to changing times and evolving technology: “Turn On, Boot Up, Jack In,” he said, arguing that cyberdelics—the union of cyberculture with psychedelic substances—had the capacity to birth a new paradigm. Similarly, psychedelic spearhead Terence McKenna aptly said that the psychedelic substances of the future would be more like computers, and the computers of the future would be more like psychedelics.

Both luminaries foreshadowed a future where psychedelics and technology would merge, birthing a novel modality and new terrains to be explored. It seems as if that time has come, with new research highlighting the many similarities between psychedelic experiences and Virtual Reality (VR) and detailing the potential therapeutic and recreational implications.

In a recent article entitled “Psychedelics and Virtual Reality: Parallels and Applications,” published in Therapeutic Advances in Psychopharmacology, Aday, Davoli and Bloesch offer a comprehensive literature review of the topic, and speculate on a future where psychedelics and technology are one.

Altered states and awe-inducing experiences

As the study notes, psychedelic experiences and virtual reality have the common ability to alter perceptual experience, particularly visual processing. DMT is an emblematic example. As demonstrated by Alamina, et. al., participants in their study with eyes closed and under the influence of DMT showed patterns in cortical electroencephalogram (EEG) remarkably similar to those of controls with eyes open. Individuals undergoing a psychedelic experience having similar EEGs to controls at baseline speaks to DMT’s ability to “replace ongoing mental experience” as DMT researcher Rick Strassman says.

This capacity to immerse the user in a hallucinatory landscape is similar to VR technology, in which users find themselves immersed in a wholly artificial environment. The qualitative experience of transcending limitations proposed by the physical body and consensus reality is often expressed. A common motivation for using DMT is a general curiosity of and a desire to explore visual phenomena, which may likewise be true for VR enthusiasts.

Immersive doses of psychedelics and VR possess the mutual capacity to evoke awe, an emotion equal parts fear and reverence. This may be beneficial in therapeutic contexts. Experiences of awe reported in psychedelic states have been positively correlated with a sense of heightened curiosity, improvements in mental health, and enhanced performance in school or at work. Similarly, VR is a reliable tool in facilitating emotionally significant experiences. Chirico, Ferrise, Cordella, et al. found that exposure to awe-inducing virtual environments was associated with increased wellbeing and a perceived sense of “vastness and connectedness.” These outcomes are strikingly similar to the emotional and personal effects reported after psychedelic experiences.

Mapping uncharted territory

Research into psychedelic science has accelerated steadily, particularly since 2018 when psilocybin was granted breakthrough therapy status by the FDA as a potential remedy for Treatment-Resistant Depression (TRD). As this body of work is elaborated upon, VR may prove beneficial as an adjunct to the new psychedelic-assisted therapies currently in their infancy. A vast body of literature has accumulated using psychedelics to treat various ailments including depression, anxiety, end-of-life distress, and substance misuse. Evidence consistently suggests that these substances can facilitate remission in a vast array of afflictions.

While it has become increasingly established that psychedelics confer obvious benefits, how this happens exactly and how their actions are mediated is not fully understood. With the onslaught of modern literature, ideas ranging from the content of mystical experiences and that of ego dissolution have been proposed, in addition to mechanistic explanations like neurogenesis and changes in neural plasticity. Recently, a hampering in the activity of the brain’s default mode network has become a popular framework.

In addition to improving our understanding of psychedelics with regards to basic science, VR may have many purely therapeutic benefits of its own. VR has been studied as a potential treatment for many of the same ailments as psychedelics, a unique opportunity to survey the effects of utilizing both in tandem. Like psychedelics, VR has been proposed as a remedy for anxiety, depression, and substance misuse, among other disorders. It has also been used in bed-ridden individuals to simulate travel, illustrating that VR and psychedelics together may be especially helpful in the palliative care of the sick and those at the end of life.

Virtual environments also provide immersive settings in which individuals can confront fears and/or facilitate memory reconsolidation of events or prospects that may frighten them, aiding in the construction of new associations and alternate perceptions. Subjective ratings of “presence” and “immersion” in virtual settings correlate with many positive outcomes when used alongside psychotherapy, suggesting that transcending one’s typical perspective is important in VR’s therapeutic efficacy. This presents yet another unique opportunity to study its use alongside psychedelics.

Conclusion

Long after Leary and McKenna’s speculations, Aday, Davoli, and Bloesch’s research echoes a similar sentiment, but in a more modern and nuanced sense. This comprehensive review reiterates the potential of using VR technology as an adjunct to psychedelic therapies. This synergy could have far-reaching implications, both in the therapeutic and recreational use of psychedelics. VR used in tandem with psychedelic substances may be an entirely new direction for psychedelic research, medicine, and for the study of consciousness generally.​

Troy Farah

Troy is an independent journalist whose reporting on drug policy and science has appeared in Wired, the Guardian, Undark, Discover Magazine, Vice and more. He co-hosts the drug policy podcast Narcotica. He lives in Southwest California.

 
Last edited:
210420155350-01-amy-gravino-exlarge-169.jpg

Amy Gravino around 10 years old

I now know what caused my Autism, which changes everything — and nothing

by Amy Gravino | CNN | 21 Apr 2021

Life-changing news came on a Thursday just before Christmas, in an email so unexpected I nearly deleted it as spam. The subject line: "We have found a genetic cause for your autism."

In 2016, I sent a saliva sample to the Simons Foundation Powering Autism Research for Knowledge -- better known as SPARK -- for an autism research study, becoming one of its first participants. After five years of waiting, I assumed that SPARK didn't have any genetic answers about my autism. Even though a personal result would have been amazing, what mattered to me more was what this study could mean for our broader understanding of autism. My hope was that a study like this could help autistic people better find our way through a world that is often hard to navigate.

After the email, Dr. Wendy Chung, SPARK'S principal investigator, explained that a rare genetic condition called Kleefstra syndrome-2 is what caused my autism. Several studies have shown how the two are linked. Dr. Chung's words hung in the air for a few moments as I turned them around over and over in my mind. I started to cry, and I couldn't stop as moments of my life flashed through my memory with this new understanding and context.

For years, I had seen myself as two people: "Autism Amy," the girl who was bullied throughout childhood for being different, and "Amy Amy," a socially acceptable version of myself. Over time -- as I began to find my voice, and my self-confidence grew -- I realized there is only one Amy. But in the hazy aftermath of this new diagnosis, I wondered, "Am I still me?"

The social world of girls can be complex and puzzling, especially for a girl on the spectrum. Throughout my childhood, I was constantly targeted -- often mercilessly -- by bullies who sensed something was different about me. Fitting in proved nearly impossible. While some girls on the spectrum are able to "mask" their autism, I wasn't capable of being anything other than myself, which didn't align with social norms.

In the fourth grade, I came home from school one day and told my mother that I felt like killing myself. My parents quickly sought help. We shuffled from specialist to specialist, none having any definitive answers until we got to the Child Psychology department at Stony Brook University in New York. At age 11, I was finally diagnosed with a form of autism that used to be known as Asperger's syndrome.

Today, many children are diagnosed at 2 or 3 years old, but at the time, knowledge of autism — especially in girls and women — was extremely limited. Back then, autism was not a household word. For most people in 1994, autism meant the movie, "Rain Man," and no one knew how it could affect a pre-teen girl. The word autism didn't really have any meaning for me at that age, either. I only knew that I was different, and that different wasn't okay.

The bullying continued in middle and high school -- other students would push me to the ground, put gum in my hair and, in gym class, throw balls at my face. The emotional bullying was just as bad, if not worse, driving me further into loneliness and isolation. People assumed my social differences were a matter of choice. They would say, "Why can't you just be normal?" Very soon, their voices became the voice in my own head, and I would ask myself that same question over again and again.

I graduated from high school with no self-confidence or self-esteem, unable to look at myself in the mirror. I basically had to build Amy Gravino from scratch. And that's what I did. I went to college and earned a bachelor's degree in English, then a master's degree in Applied Behavior Analysis, the widely-used method for teaching people who have autism. I knew that, rather than working with young children on the spectrum, as many professionals do, I could fill a bigger need by focusing on autistic teens and adults.

In 2010, I started my own consulting organization and became a college coach and certified autism specialist. I found purpose and success helping others on the spectrum. I've spoken at the United Nations and at conferences all across the country and abroad about autism, sexuality, relationships, and self-advocacy. I've had my writing published in psychological journals, textbooks, and various media outlets, and I'm authoring my first book, a memoir of my experiences with dating as an autistic woman. I also work as a relationship coach.

My decision to participate in SPARK echoed many of the same reasons I became an autism advocate and speaker -- I wanted to play an active role in increasing understanding of autism and to make things better for people across the spectrum. As scientists study autism in the lab, autistic individuals like me must be included in that process — not only as subjects, but as co-investigators. Our triumphs and heartbreaks, our potential futures, our very lives are being put under the microscope. We have the greatest stake in this research.

Most of all, I want those of us who have felt out of place in the world, in our communities and in our families to know that we belong, and to learn that what lives in our DNA is not something that was done to us, but part of what makes us who we are.

I'm hopeful that the picture these results paint will show that autism is less of a puzzle to be solved and more of a story to be told. I want the answers and knowledge that we glean to open a discussion on how we can improve the quality of life not just for future generations, but for individuals on the spectrum living in the world right now.

Learning that there is a reason why I am autistic changes everything, but at the same time, it changes nothing. This is who I am. I'm not broken, or bad, or the failed version of normal I wasted years believing I was. This didn't happen because I didn't try hard enough, or because my parents did something wrong before I even came into being.

I am exactly the person I'm supposed to be.


 
Last edited:
baby-toys-language-public.jpg



Direct genetic link to Autism Spectrum Disorder identified

RIKEN | Neuroscience News | 16 Jul 2021

Summary: Researchers identified a novel, direct link between autism and the SUV39H2 gene.

New research from the RIKEN Center for Brain Science (CBS) in Japan shows that a deficit in histone methylation could lead to the development of autism spectrum disorders (ASD). A human variant of the SUV39H2 gene led researchers to examine its absence in mice.

Published in Molecular Psychiatry, the study found that when absent, adult mice exhibited cognitive inflexibility similar to what occurs in autism, and embryonic mice showed misregulated expression of genes related to brain development.

These findings represent the first direct link between the SUV39H2 gene and ASD.

Genes are turned on and off throughout our development. But genetic variation means that what is turned off in some people remains turned on in others. This is why, for example, some adults can digest dairy products and others are lactose intolerant; the gene for making the enzyme lactase is turned off when some people become adults, but not others. One way that genes can be turned on and off is through a process called histone methylation in which special enzymes transfer methyl groups to histone proteins that are wrapped around DNA.

Variations in genes related to methylation during brain development can lead to serious problems. One such variation occurs in a rare disorder called Kleefstra Syndrome, in which a mutation prevents methylation of H3K9–a specific location on histone H3. Because Kleefstra Syndrome resembles autism in some ways, RIKEN CBS researchers led by Takeo Yoshikawa looked for autism-specific variations in genes that can modify H3K9.

Among nine such genes, they found one variant in an H3K9 methyltransferase gene–SUV39H2–that was present in autism, and the mutated SUV39H2 prevented methylation when tested in the lab. Similar loss-of-function results were found for the mouse version of the variant.

The next step was to see what happens in mice that lack the Suv39h2 gene. Behaviorally, the researchers found that the mice could learn a simple cognitive task, but had difficultly when the task required cognitive flexibility. In the simple task, mice learned to get a reward by poking a door at alternating diagonal corners of a cage. After they could do this well, the possible reward locations switched to the other two diagonal corners. The genetically modified mice did this as well as wild-type mice.

In another task, after learning to alternate between the two diagonal corners, only the location of one reward was switched. When the mice were challenged to alternate randomly between these two tasks, wild-type mice could adapt quickly, but the Suv39h2-deficient mice took much longer.

“This serial reversal-learning task was essential,” says first author Shabeesh Balan. “Cognitive inflexibility is a core symptom of ASD, and our new task was able to address this behavioral feature in ways that previous mouse studies could not.”

When the researchers examined what happened in the mouse brain when H3K9 methylation failed to occur, they found that important genes that are usually silenced in early development were turned on in the experimental mice. “Suv39h2 is known to be expressed in early neurodevelopment and to methylate H3K9,” explains Yoshikawa.

asd-genetic-link-neurosicences.jpg


“This keeps a check on genes that should be switched-off. But without it, genes in the protocadherin β cluster were abnormally expressed at high levels in embryonic mice.” Because protocadherins are critical for the formation of neural circuits, the researchers believe they have found an important biological pathway that could be central to several neurodevelopmental disorders.

The team then verified the importance of SUV39H2 in human ASD by finding that its expression was lower in the postmortem brains of people with ASD than of controls. “What began with a loss-of-function mutation in only one person with ASD,” says Yoshikawa, “has led to a general causal landscape for ASD that culminates in brain circuit abnormality.”

Protocadherins have already been proposed to be related to a broad range of mental disorders. This study shows that activating the SUV39H2 gene is a potential therapy for mental disorders–including ASD–that should be investigated more thoroughly in future studies.

 
Last edited:

88533faa39b49df58f7b7c5fd0cce090-700.jpg



Exploring research on psychedelics and Autism

by Jennifer Lamas | Reality Sandwich | 29 Jun 2021

Autism spectrum disorder is perplexing and can affect a person for a lifetime. According to the Centers for Disease Control and Prevention, about 1% of the population suffers from ASD. That is approximately 75,000,000 people all over the world, and there is no known cure. Although there is a lot of controversy surrounding the idea of using psychedelic substances as a form of treatment for some disorders, psychedelics can have promising effects on the brains of individuals with ASD.​

What is Autism?

Autism Spectrum Disorder is a developmental disorder that affects how a person socializes, communicates and interacts with others. Some people with ASD can also have repetitive or limited patterns in the way they act. Therefore, not all people who suffer from this disorder will have the same severity of symptoms.

People that have autism do not always have physical traits that are different from people without ASD. The notable differences are in their speech, behavior, communication and the way they learn. After a lot of research, there is still no concrete answer about what causes these differences in people with autism. People with ASD can either be diagnosed as exceptionally gifted, significantly challenged or somewhere in between.

There used to be several different disorders that were diagnosed separately, such as Asperger syndrome, autistic disorder and pervasive developmental disorder. Now, these conditions all fall under the same term autism spectrum disorder. However, an individual’s severity of symptoms depends on where they will fall on the spectrum.

Children as little as eighteen months old can start to show symptoms of autism, and some can be even younger. Others won’t show any signs until they are around twenty-four months old. Either way, a proper diagnosis is required to get the help they need, which is usually around age three. With therapy and a lot of work, many symptoms can become better and easier to handle, although this condition will last a lifetime.

Research on Psychedelics and Autism

Autism is a lifelong battle, and there is no known cure. However, there is hope for people with ASD since there has now been a resurgence of research, and it shows potential benefits linked to treating autism with psychedelics. Studies conducted in the 1960s and 1970s on children ages six to ten showed that LSD could even help them. These children had more acute symptoms and could not be treated with conventional medications.

The children’s ages in the study and the organization of the experiments brought up ethical questions. Therefore researchers could not make a set conclusion about the psychedelic benefits to children with ASD. Despite the controversy, though, when the researchers treated the children with LSD, their moods, emotional responsiveness, and speech all improved.

Autistic individuals are known to have difficulties with social interactions and experiences.

The psychoactive drug MDMA (3,4-methylenedioxymethamphetamine), also known as ecstasy, has been found to help individuals develop better connections with others. People that have used MDMA can open up about the way they feel and become more sociable. In addition, MDMA may improve the social obstacles that people with ASD encounter.

It is unlikely that a person who uses MDMA will experience anxiety, fear, or other negative emotions. However, not impossible either. In most cases, MDMA can make individuals feel more empathetic and act or feel more loving towards other people by releasing norepinephrine, dopamine, oxytocin and serotonin. A small study with only twelve participants took MDMA or a placebo for a two-day session. This MDMA-assisted psychotherapy pilot study revealed substantial progress for autistic adults that suffer from social anxiety.

Another psychedelic that is being studied in association with helping individuals with ASD is psilocybin. It is one of the compounds responsible for causing hallucinogenic effects and is also known as magic mushrooms. Psilocybin is made up of many different mushroom species. It can promote prosocial behavior in people with ASD. Recent research points to the possibility of treating and reducing neuropsychiatric disorders with psychedelics.

Although magic mushrooms are not approved to treat conditions like ASD, many autistic adults are already experimenting with them. Some individuals have reported a significant change in their connections to other people when they consume magic mushrooms. Autism severely affects the ability to develop relationships, and these psychedelics are making a breakthrough for therapeutic purposes.

There is more scientific evidence that supports the idea of treating ASD with psychedelics.

The brain has an area called Default Mode Network (DMN), and for people with autism spectrum disorder, this area works differently than for those without ASD. The DMN is responsible for the way people focus and pay attention. Psychedelics can cause a disruption in the DMN which would help people to change recurring and detrimental thoughts. For this reason, psychedelics can help autistic people break out of a state of mind that can get hooked on things that are not important or helpful.

Can psychedelics offer relief for the Autistic?

It is difficult for many autistic people to understand emotions. Body language can seem cryptic to them, and they do not acknowledge sarcasm the way typical people do. Therefore with the renewed interest in psychedelic use for ASD individuals, there is now hope that these substances can be recognized as a treatment for a better way of life.

The therapy and medication available today are not very effective in treating social issues in patients with ASD. But, so far, there have been positive reports of the ease people feel when using psychedelics and connecting with others. Alicia Danforth is a scientist who performed a survey on hundreds of autistic adults that had used psychedelics. The ones who consumed MDMA all reported that their social anxiety had improved.

In the survey, one user described having social problems throughout life and living in a bubble or shell because of those issues. That user recounted constantly feeling isolated until psychedelics entered the picture. Then the user reported that life changed and all of those social barriers were broken. Finally, that participant detailed how different their ability to understand other people was afterward.

Psychedelics such as MDMA, psilocybin and LSD are closer now than ever to be FDA-approved to treat individuals with various disorders. Many researchers are now trying to figure out ways that psychedelics can help people with an autism spectrum disorder. The little available research shows promising results that can offer relief in social settings for adults with ASD. If you have been diagnosed with ASD and have experimented with psychedelics, we would like to hear your experiences.

 
Last edited:



How LSD is helping to treat Autism*

by Mareesa Stertz | LUCID

Aaron Orsini talks with Mareesa Stertz about how he used LSD to help treat his own autism, and what he’s doing to increase awareness and raise financial support for psychedelic-assisted approaches to treating autism. His book, “Autism on Acid: How LSD Helped Me Understand, Navigate, Alter & Appreciate My Autistic Perceptions,” was released this past February.​

*From the article here :
 
Last edited:
rexfeatures_2284965a.jpg


Nova Mentis reaches milestone developing psilocybin to treat Autism

by Emily Jarvie | PSYCHEDELIC SPOTLIGHT | 12 Aug 2021

Nova Mentis says that psilocybin could be a novel, first-in-class treatment for a brain disorder that leads to learning disabilities and behavioral problems.​

Nova Mentis Life Science Corp. is one step closer to finding a treatment for autism spectrum disorder (ASD) and Fragile X Syndrome (FXS).

The Canadian biotechnology company announced on Thursday that it has filed for orphan drug designation with the European Medicines Agency (EMA) for its propriety psilocybin drug to treat patients with FXS.

The company has been researching serotonin signaling in an effort to understand the neural underpinning of social dysfunctions in ASD and FXS. If granted, orphan drug designation would give Nova Mentis’ drug status as a medicine intended for use in treating the rare condition of FXS. It would also provide the company incentives to develop the medicine, including assistance with trial protocols, reduced regulatory fees, and 10 years of market exclusivity should the drug be approved for patient use.

FXS is a genetic disorder caused by changes in the FMR1 gene that result in its failure to produce a protein called FMRP that is required for normal brain development. Symptoms of the disorder include developmental delays, learning disabilities, and social behavior problems.

FXS, which affects 1 in 7,000 males and 1 in 11,000 females according to the Centers for Disease Control and Prevention, is also the leading genetic cause of symptoms related to autism. ASD is a developmental disability that can also cause significant social, communication, and behavioral challenges. It affects an estimated 2.21% of adults in the United States.

There is no known cure for ASD. And the therapies currently available for FXS, which include pharmaceutical and behavioral interventions, fail to address the emotional aspects of the disorder, with limited efficacy and high toxicity. But Nova Mentis says that psilocybin could be a novel, first-in-class treatment for FXS.

The company says psilocybin not only offers promising cognitive benefits, but it also has peripheral effects, like the capacity to curb inflammation and modulate micro-bacteria, which is important for FXS patients, given the high prevalence of glycemic index disorders in this population. In addition, psilocybin is expected to improve both molecular and behavioral underpinnings of the disorder by improving brain plasticity, which results in a reduction in anxiety and behavioral rigidity.

“Nova’s lead drug candidate psilocybin (NM1010) in a preclinical model of FXS has revealed positive improvement in cognition without apparent psychedelic side effects,” said Nova Mentis Scientific Advisory Board Chairman Dr. Marvin Hausman. “I am also excited to report that psilocybin-treated animals showed changes in inflammatory biomarkers that are potentially involved in the ASD disease process.”

Nova Mentis is currently setting up a data bank of biological markers associated with autism and FXS to be used alongside behavioral results to help identify subsets of the disease and aid in the development of patient-specific treatments. The company also plans to conduct clinical trials to evaluate the efficacy of psilocybin therapy in ASD and FXS patients, and to submit regulatory documents to the EMA and the Food and Drug Administration (FDA) in the United States supporting psilocybin’s potential in treating these disorders.​

 
Last edited:
shutterstock_713857579-scaled-e1603916523677.jpg



Can psychedelics provide relief for the autistic?

by Jasmine Virdi | Psychedelics Today | 5 May 2021

There is a growing community of neurodivergent and autistic folks using psychedelics, but how does it help them? We took a deep look at the growing body of research and anecdotes to find out.

Current estimates have it that between 1-2% of the world’s population is autistic. In addition to higher levels of social anxiety, depression, and ADHD, autistic individuals meet unique challenges as they seek effective therapeutic treatment methods available to them; psychedelic-assisted therapy is now seen as an attractive alternative for this often sidelined and marginalized population.

There are promising signs that indicate psychedelics could help autistic individuals manage social anxiety, recover from trauma, reduce depression and anxiety, as well as work through the unique hurdles on their path. However it may be the case that for people with lower-functioning capabilities, psychedelics might not have nearly the same effect. Despite innumerable anecdotal reports from individuals who have benefited from psychedelics in a multitude of ways, there is still a significant lack of research regarding how psychedelics could be useful for those with Autism Spectrum Disorder (ASD) diagnoses.

What is autism?

Before delving into how psychedelics can be helpful for autistic individuals, it is first important to understand what autism actually is. Defining it can be tricky because there is still no agreed upon mechanistic, neurological basis for the condition. Despite this, there is research to suggest that neurodivergent brains exhibit higher levels of functional connectivity, believed to contribute to the intense sensitivity to sensory input and sense of overwhelm that autistic individuals experience in certain environments.

Moving away from stereotyped definitions of ASD as a social impairment, many believe sensory processing issues to be at the core of autism. Typically, autistic individuals have hypersensitivity or hyposensitivity to sounds, touch, and lights, among other stimuli. As such, autism is characterized by unique, atypical ways of interacting with and processing information. Even so, everyone inherits their own unique neurocognitive version of autism, and although autistic individuals share basic neurological features as well as a common diagnosis, behaviors and traits can vary dramatically from person-to-person.

The Diagnostic and Statistical Manual of Mental Disorders (DSM-IV), defines autism in terms of deficits in social communication and interaction, and repetitive patterns of behavior and/or interests that are present (but not always noticed) in the early developmental period. However, such definitions of autism have led to false stereotypes. Looking at autism through this lens of pathology, scientists have long sought out a “cure.” However, pathologizing autism in this way is both harmful and damaging.

In his book, NeuroTribes: The Legacy of Autism and the Future of Neurodiversity, Steve Silberman reflects historically how the controversial roots in early psychology have led to widespread misunderstanding of what autism is, and how our societal failure to embrace neurodiversity has been inherently damaging. Further, Silberman speaks to the fact that embracing neurodiversity can benefit our existence in that neurodivergent individuals are often endowed with unique, specialized ways of seeing the world.

Within psychiatry, autism is classified as a “disorder,” however, in recent years this conception is being actively challenged by advocates of neurodiversity. When defining autism, Nick Walker, queer autistic scholar and Associate Professor of Somatic Psychology at California Institute of Integral Studies, makes a distinction between what he refers to as the “neurodiversity paradigm” and the “pathology paradigm.” Walker describes the neurodiversity paradigm as a perspective that “recognizes neurodiversity as a naturally-occurring form of human diversity.”

Comparatively, autistics are marginalized through the pathology paradigm, which rests on the assumption that there is only one “right” way to be and that if you stray from the dominant conception of normal there is something wrong with you. He adds, “In the context of a society designed around the sensory, cognitive, developmental, and social needs of non-autistic individuals, autistic individuals are almost always disabled to some degree.”

Although certain features of autism can be disabling, many of the challenges that autistics face aren’t necessarily related to their diagnosis, but rather, arise from the way in which society treats those who don’t fit the mold of “normal.” Many autistic individuals grow up feeling that their way of inhabiting the world is flawed because they do not conform to certain, socially-conditioned ways of being.

Difficulty meeting certain social expectations often ends in social rejection, stifling autistic individuals’ ability to interact with others. Accordingly, autism is often misrepresented as a social deficit by those who are ignorant of the fact that social difficulties in autistic populations are simply by-products of the heightened intensity of their sensory experience. Through the lens of neurodivergence, autism is a neurotype, and labelling it as a “disorder” reflects a value judgement more than anything else.

Looking into the research on psychedelics and autism

In the early 1960s, when LSD was beginning to be used experimentally in research and psychotherapy, a series of controversial studies were published around treating young children who were believed to have severe forms of autism and childhood-onset schizophrenia (COS) with LSD. Due to misconceptions surrounding autism, it was previously thought to be closely related to juvenile schizophrenia.

The driving justification for experimenting with a powerful psychoactive substance on children was that all other treatment methods had previously failed. Scientists gave a total of 91 children, aged between six and ten, LSD at differing dosage levels and fluctuating frequencies of administration with different treatment schedules, finding that the most effective results were produced at doses of 100 micrograms given daily or weekly for extended periods of time. Undoubtedly, such a study would be unacceptable to an ethics committee today.

Positive outcomes were reported with the use of LSD, with researchers summarizing the most consistent effects as improved speech, increased emotional responsiveness, frequent laughter, positive mood, and a decrease of compulsive behavior. In one such example, researchers observed that the children “appeared flushed, bright eyed, and unusually interested in the environment.” Despite these promising results, positive outcomes were largely dismissed due to the fact that the study designs were greatly flawed, and were not as scientifically rigorous as those of today’s standards because they lacked experimental controls.

Since this early research, there have been very few studies that have looked into the clinical uses of psychedelics for autistic populations. One of the first to do so was clinical psychologist and MDMA researcher Alicia Danforth’s 2013 doctoral dissertation, which explored how autistic adults experience the subjective effects of MDMA. Danforth looked at qualitative data collected via online surveys from 100 autistic individuals who had taken MDMA alongside a comparison group of 50 autistic individuals who were MDMA naïve.

MDMA is sometimes referred to as an “empathogen” or “entactogen” because it is a substance that has the ability to facilitate experiences of increased empathy, oneness, emotional connectivity, and emotional openness. In part, MDMA is able to do this because it encourages the release of oxytocin, sometimes referred to as “the love hormone,” which is associated with social connection and enhancing responses to positive emotions while decreasing the ability to perceive negative facial cues.

The group who had taken MDMA reported sustained benefits such as improvement in social anxiety and healing from trauma. Most notably after MDMA use, 91% of participants reported increased feelings of empathy and social connectedness, while 86% felt that communication came more easily with the effects lasting two years or longer for 15% of individuals.

Building on the positive trends identified in her dissertation, in 2016 Danforth published a paper detailing the rationale behind and protocol for a pilot study using MDMA-assisted therapy to treat social anxiety in autistic adults. In 2018, Danforth and her team conducted the first randomized, double-blind, placebo-controlled experiment with psychedelics and autistic adults.

Broadly speaking, social anxiety is characterized by a heightened fear of what others think about you, feeling an intensified fear of scrutiny alongside the avoidance of social interactions. Research has shown that social anxiety commonly co-occurs with ASD, and part of Danforth’s rationale behind the study was to explore MDMA as a treatment modality for individuals with an increased need.

One of the principal aims of the study was to explore the safety of MDMA-assisted psychotherapy for reduction of social fear and avoidance for individuals with ASD, finding no evidence of harm to participants. Although the study was small in size, recruiting only 12 participants, results were promising. Participants took part in two full-day sessions in which they were either given MDMA or a placebo. The study used the Liebowitz Social Anxiety Scale to measure changes in social anxiety. Subjects who received MDMA showed a significantly greater reduction in social anxiety than the placebo group. Reductions in social anxiety symptoms were long-lasting, still holding true at a 6-month follow-up.

In her work, Danforth is careful to emphasize the fact that MDMA and other psychedelics do not “cure” autism, rather when used in a psychotherapeutic setting, they can help to alleviate social anxiety and manage other concomitant issues prevalent in autistic populations.

Reflecting on the study, Danforth shared that there were substantial recruitment delays. As anxiety and depression are both common in autistic adults, many participants were ruled out because they were using conventional psychiatric medications such as SSRIs. In addition, many of these adults were often unemployed and living in social isolation, less likely to have access to information about the study.

Beyond this small study, Danforth also created guidelines to psychedelic practitioners working with neurodivergent individuals on how to be mindful of surroundings so as to create an “autism-friendly” treatment space, such as paying careful attention to lighting and taking extra measures to minimize noise.

Beyond the scope of autism, there is a growing body of research that has sought to examine how psychedelics affect social behaviour more generally. A 2020 study done by a team of researchers from McGill University examined the effect of LSD on social behavior in mice, whilst measuring their brain activity.

Under the influence of low doses of LSD, the mice became notably more social and friendly towards unfamiliar mice. While it was already known that LSD activates serotonin 5-HT2A receptors, this study illuminated that LSD’s activation of the 2A receptors also triggered a cascade activation of the AMPA receptor and the protein complex mTORC1, working together to encourage social interaction. This is important because dysregulation of mTORC1 has been linked to autism and social anxiety disorders more generally.

Obviously, behavior and brain function in mice cannot directly be translated to that in humans, however, understanding the foundational mechanism of LSD’s prosocial behavioral effects opens up the door for future research. It also advances the understanding of how the substance could be useful to autistic populations, as well as those that suffer from general social anxiety.

An earlier study conducted in 2013 also showed that both psilocybin and ketamine altered the way that the brain responds to fearful faces. People under the influence of these two psychedelics were less able to identify negative expressions when presented with images of people with angry or upset expressions.

In the same vein, a 2010 study done with MDMA demonstrated that the substance reduced people’s accuracy in distinguishing negative facial cues. Not only does MDMA enhance emotional openness and connectivity, it also impairs the capacity to notice negative emotions in others’ facial expressions. Similarly, LSD has been shown to have an effect on emotional processing, enhancing feelings of trust, closeness to others, and emotional empathy, while weakening the ability to detect sad and fearful facial expressions.

In addition, psilocybin, LSD, and MDMA, all work to reduce the activity of the amygdala, a brain region that is associated with emotional processing and stress response. Brain imaging studies with autistic individuals have shown that the amygdala is differentially activated when presented with anxiety-inducing stimuli compared to the general population.

Psychedelics’ ability to enhance states of social connection and empathy joined with their simultaneous capacity to diminish the detection of negative facial expressions make them a promising therapeutic modality for those that suffer with social anxiety disorders, including autistic individuals.

Even though research into psychedelics and autism is still very limited, we can still draw much insight from psychedelic research into non-autistic individuals and the body of anecdotal evidence that is growing quickly as more and more neurodivergent people share their healing stories.

The altered state produced by psychedelics helped Orsini better understand how he was prioritizing sensory input, realizing that he had been stuck in a particular mode of seeing and experiencing the world, awakening a deep sense of interoceptiveness.

Interoception is the awareness of what is going on inside one’s own body at any given moment and the ability to take action based on one’s inner experience. For example, noticing dryness in the mouth might serve as an indication that we are thirsty, encouraging us to take action by drinking water. In general, autistic folk tend to have lower interoceptive awareness when compared with average populations.

“If my body was a car, psychedelics allowed me to realize that my fuel light was low, that I needed food, rest, or felt a certain way,” Orsini says. “By being able to notice and interpret the cues coming in, I became able to navigate any situation.”

Speaking about his initial experience with psychedelics, Orsini shares, “ I felt connected to myself, nature, and other people—it was a relief from repetitive thinking, and from there it became the foundation upon which I could rebuild my relationship with myself, my physical and mental wellness, and lead a functional life.”

Orsini draws on the concepts of “monotropism” and what he calls “polytropism” to explain how psychedelics were able to modulate his consciousness. Monotropism, believed to be a key feature of autism, refers to a cognitive strategy in which one has a narrow set of interests and is only able to focus one’s attention on a limited number of inputs at a given time. On the one hand, monotropic thinking can lend itself to deep thinking and flow states, however, it is also limiting in that information which exists outside of the attention tunnel often gets filtered out, and it can be hard to disengage with a given task or activity when one is so fully absorbed in it.

Comparatively, polytropism designates the proclivity to process multiple inputs at once. Naturally, both types of cognitive processing have their pros and cons, however, when it comes to autistic individuals, polytropic processing is generally harder to access. In Orsini’s experience, LSD was able to occasion a state of polytropic awareness, which he committed himself to working with after his psychedelic experience.

By facilitating novel perceptions, psychedelics could also help autistic individuals learn to embrace their neurocognitive disposition and unique way of inhabiting the world. Many autistic people engage in a behavior referred to as “masking” in which they camouflage certain challenges by observing and mimicking neurotypical ways of acting in social situations. In some sense, masking is a survival strategy used to conceal behaviors that are felt to be socially unacceptable. Often, masking is the result of trauma, as individuals feel they need to hide their true selves in order to fit in.

“Autistic behaviors could be patterned off of early life traumas that are likely because of the sensitivity inherent to an autistic individual,” says Orsini. “I might not have been through war, but I was prone to a more intense sensory experience.”

Independent of neurotype, psychedelics allow for a reappraisal of our default modes of seeing, and a breaking free from the rigid patterns of perception that become habitual. In mental health conditions like anxiety, depression, and OCD, an interconnected group of brain regions referred to as the default mode network (DMN) linked to introspective functions such as self-reflection and self-criticism, tend to be overactive.

Psychedelics have been shown to dampen the function of the DMN, allowing for a kind of “reset” in the brain in which it becomes easier to separate ourselves from ways of thinking and seeing the world that have become ingrained. If psychedelics are beneficial to the general population in this way, why can’t they also be valuable to autistic folk for the same reason?

To date, there is no evidence to suggest that having an ASD diagnosis is a contraindication for psychedelic use. “In general, whether it is in a research or retreat setting, there is less certainty on how to navigate autism and so it is often sidelined,” says Orsini. “However, there is nothing obvious about autism that makes it a contraindication or makes it less safe to explore these toolsets.”

Unfortunately, more often than not, larger subsets of the population get attention first, and according to the World Health Organization, a whopping 264 million people worldwide suffer from depression. Comparatively, autistics make up a minority population that often gets overshadowed.

Expressing his hopes for future psychedelic research, Orsini shares, “What I’d like to see is keeping autistics in the conversation when it comes to their ongoing access, and keep them in the domain of people that are considered for early clinical trials.” Additionally, when psychedelic-assisted therapy becomes legalized throughout the US, just as it has in Oregon, Orsini hopes that medical or retreat centers don’t exclude autistic people.

A future therapeutic modality for autistics: Psychedelic-Assisted Immersion Therapy

Based on his extensive self-experimentation with LSD, Orsini proposed a model therapeutic approach for navigating neurodivergence with psychedelics called: “LSD-assisted immersion therapy.” Immersion therapy is different from conventional psychedelic-assisted psychotherapy in that it is formulated with the idea of facilitating social and interpersonal learning as opposed to a purely inwardly-directed experience. In this context, Orsini suggests that a moderate dose of the substance is preferable so as not to elicit a full blown mystical experience.

Moving beyond a therapist dyad, LSD-assisted immersion therapy, or more generally psychedelic-assisted immersion therapy, involves ingesting the substance in a group setting. “If I was to have this LSD, and simply reflect on my social challenges in isolation, I may come to an intellectual conclusion, but it is not the same as actually being involved with other people,” says Orsini.

“I envision a future setting in which individuals who are seeking to work on interpersonal issues and skills would be able to do so in the comfort of other individuals who are equally familiar with them,” says Orsini. “These issues have to do with one’s personal self inventory, but there is a natural therapeutic component to engaging with others in an enhanced state.”

Experiencing challenge around social interaction isn’t specific to autistic individuals, and psychedelic-assisted immersion therapy, or simply psychedelic group therapy, has the potential to help a wide range of people. Current clinical studies into the therapeutic potentials of psychedelics often overlook an important dimension of real-life psychedelic use, namely, the social dimension.

To some extent, psychedelic insights can be like training wheels on a bike. Once a person is able to access a specific way of thinking in the psychedelic state, it becomes much easier to cultivate the same state in day-to-day life. In the case of autism, people might feel more confident and empowered in daily life, finding comfort in the level of social connection that they were able to achieve in the psychedelic state.

Although pushing for the legalization and acceptance of psychedelics through the lens of medicalization is somewhat of a necessity, there is an inherent problem-solving dynamic that emerges in which psychedelics are viewed exclusively as tools that are effective in treating given issues. However, looking at psychedelics through the lens of neurodiversity, they need not be used to target a given concomitant issues associated with autism, rather they can simply help people understand and embrace their differences. Healing happens when we can move beyond a narrow view of how society should be and encourage people to flourish as they are, instead of attempting to make everyone conform.

 
Last edited:
20180926-PTSDLEAD-1900.jpg

At the intersection of Autism and Trauma

Autism and PTSD share many traits, but the connection between them was largely overlooked until now.

by Lauren Gravitz | SPECRUM NEWS

Having autism can sometimes mean enduring a litany of traumatic events, starting from a young age. And for many, those events may add up to severe and persistent post-traumatic stress disorder (PTSD).

Before Gabriel could even talk, his father’s girlfriend at the time told him his mother had abandoned him. At age 3, he was sexually abused by a cousin. He was mercilessly bullied once he started school, showed signs of depression by age 7 and by 11 began telling his mother he did not want to live. About three years ago, while at summer camp, he almost drowned. Shortly after that, he experienced life-threatening heatstroke when he went to get his Legos from the car trunk and accidentally locked himself in. Six months ago, just after his grandmother died, he attempted suicide.

“He’s been hurt and had so much disruption in his life that he’s having problems realizing that he has stability now,” says his mother, Kristina. (Kristina and Gabriel’s last names have been withheld to protect the family’s privacy.) “The world is chaotic and crazy for typically developed people. For him, it’s overwhelming and confusing.” Gabriel, now 13, started seeing a therapist about five years ago and last year was diagnosed with PTSD.

Gabriel’s autism was a contributing factor in most of the harrowing incidents he went through. Clinicians suspect that the condition increases the risk for certain kinds of trauma, such as bullying and other forms of abuse. Yet few studies have investigated that possibility or the psychological aftermath of such trauma, including PTSD.

“We know that about 70 percent of kids with autism will have a comorbid psychiatric disorder,” says Connor Kerns, assistant professor of psychology at the University of British Columbia in Vancouver, Canada. Depression, anxiety and obsessive-compulsive disorder are all known to be more common among autistic people than in the general population, but PTSD had largely been overlooked. Until a few years ago, only a few studies had delved into the problem, and most suggested that less than 3 percent of autistic people have PTSD, about the same rate as in typical children. If that were true, Kerns points out, PTSD would be one of the only psychiatric conditions that’s no more common in people with autism than in their typical peers.

One potential explanation, Kerns says, is that, like other psychiatric conditions, PTSD simply looks different in people with autism than it does in the general population.

“It seems possible to me that it’s not that PTSD is less common but potentially that we’re not measuring it well, or that the way traumatic stress expresses itself in people on the spectrum is different,” Kerns says. “It seemed we were ignoring a huge part of the picture.”

Kerns and a few other researchers are trying to get a better understanding of the interplay between autism and PTSD, which they hope will inform and shape treatment for young people like Gabriel. The more they dig in, the more these researchers are finding that many autistic people might have some form of PTSD. “We’re all just trying to put together the pieces and recognize that it’s an important area that requires further study,” she says. “It’s been a call to arms for the field to start looking at this.”

These researchers have their work cut out for them. In the typical population, PTSD is fairly well defined. According to the Diagnostic and Statistical Manual of Mental Disorders, or DSM-5, psychiatry’s guide to diagnoses, PTSD usually develops after someone sees or experiences a terrifying or life-threatening event. After that initial episode, any reminder of it can trigger panic, extreme startle reflexes and flashbacks. Beyond that, however, there’s a wide variety in the way PTSD manifests: It can lead to hypervigilance and anger; it can cause recurring nightmares and other sleep issues; or it can lead to depression, persistent fear, aggression, irritability or difficulty concentrating and remembering things.

“If you do the math, according to the PTSD criteria in the DSM-5, you can have 636,000 different combinations of symptoms that that describe PTSD,” says Danny Horesh, head of the Trauma and Stress Research Lab at Bar-Ilan University in Ramat Gan, Israel. Given all the traits in people with autism that may overlay these permutations, “you have a lot of reason to think that their version of PTSD might be very different,” he says.

Preliminary studies are just beginning to confirm that idea and to show that what constitutes trauma may be different in people on the spectrum. Together with Ofer Golan, an autism expert at Bar-Ilan, and others, Horesh has begun investigating where PTSD and autism converge. The group has recruited upwards of 130 participants, including students and some people diagnosed with autism, and tried to determine where they fall on the spectrum and whether they have any traditional signs of PTSD.

Abuse, sexual assault, violence, natural disasters and wartime combat are all common causes of PTSD in the general population. Among autistic people, though, less extreme experiences — fire alarms, paperwork, the loss of a family pet, even a stranger’s offhand comment — can also be destabilizing. They can also be traumatized by others’ behavior toward them.

“We know from the literature that individuals with autism are much more exposed to bullying, ostracizing, teasing, etc.,” Golan says. “And when you look in the clinic, you can see that they’re very sensitive to these kinds of events.” Among autistic students, Golan and Horesh have found, social incidents, such as ostracizing, predict PTSD more strongly than violent ones, such as war, terror or abuse, which are not uncommon in Israel. Among typical students, though, the researchers see the opposite tendency.

spectrum_PTSD_autism_BULLY_fina5x7l-692x1024.jpg


Given these differences, and the communication challenges autistic people often have, their PTSD can be particularly difficult to recognize and resolve.

“It’s so absurd that there are such excellent treatments for autism today, and such excellent treatments for PTSD today, and so much research on these interventions. But no one to date has connected both,” Horesh says. “How do you treat PTSD in people with autism? No one really knows.”

Characterizing the convergence

It can be difficult to treat autism and PTSD separately in people who have both conditions, because the boundaries between the two are often so blurry. And that may, ironically, be the key treating them. In other conditions that overlap with PTSD, as well as those that overlap with autism, researchers have found that it is most effective to develop therapies when they look at both conditions simultaneously.

PTSD and substance misuse, for instance, often co-occur, but for decades no one understood the dynamics between them. Once clinicians began to develop and study treatments for both at the same time, however, they were able to create a tailored and effective program that eases both conditions. “This is our model,” Horesh says. “Prove that something is co-morbid, determine why, and then develop interventions for this specific group — good interventions, accurate interventions.”

The researchers are uncovering some important overlaps between autism and PTSD in their studies. In a group of 103 college students, for instance, they found that students who have more autistic traits also have more signs of PTSD, such as avoiding sources of trauma and negative changes in mood. “The highest-risk group of one was also the highest risk group in the other,” Horesh says.

The researchers also found some unexpected trends: The association between PTSD symptoms and autism traits is, for as yet unknown reasons, stronger in men than in women, even though typical women are two to three times more likely to develop PTSD than are typical men; that gender bias might eventually inform treatments. And people with more autistic traits display a specific form of PTSD, one characterized by hyperarousal: They may be more easily startled, more likely to have insomnia, predisposed to anger and anxiety, or have greater difficulty concentrating than is seen in other forms of PTSD. "Recognizing this subtype could be particularly helpful for spotting and preventing it, and for developing treatments," Horesh says, especially because the same traits might otherwise be mistakenly attributed to autism and overlooked. "We know that each PTSD has a different color, a different presence in the clinic,” he says.

Given the low reported rates of PTSD in people with autism, Kerns questions whether the DSM-5’s criteria for PTSD are sensitive enough to detect its signs in this population and wonders whether clinicians need to be on the lookout for a different subset of both causes and features.

Kerns and her colleagues are interviewing autistic adults and children — as well as guardians of some less verbal autistic people — to find out more about what, for them, constitutes trauma. So far, they’ve interviewed 15 adults and 15 caregivers. What she’s learned, she says, is that it’s necessary to check any assumptions at the door. “You want to be cautious about applying neurotypical definitions — you could miss a lot,” she says.

In speaking with participants about causes of trauma, she has heard “everything from sexual abuse, emotional abuse and horrendous bullying, to much broader concepts, like what it’s like to go around your whole life in a world where you have 50 percent less input than everyone else because you have social deficits. Or feeling constantly overwhelmed by sensory experience — feeling marginalized in our society because you’re somebody with differences.” In other words, she says, “the experience of having autism and the trauma associated with that.”

One parent Kerns spoke with had moved to a shelter with her autistic son to escape intense domestic violence. Her son had witnessed the abuse but seemed more affected by the move, the change in his routine and sudden loss of the family pet, which had to be left behind, than by the violence. He began to hurt himself more than he had before, and to ask repetitively for the pet, Kerns says. “Three years later he was still asking for the pet,” she says, “because the pet was one of the few relationships and connections with another being that he had.”

In another instance, a 12-year-old boy she interviewed refused to go to school and was hospitalized for threatening self-harm; the root of his trauma turned out to be ear-piercing fire drills. For a 53-year-old woman she talked to, crippling, traumatic stress resulted from the paperwork she needs to fill out every year to qualify for housing and other types of assistance.

How PTSD manifests in autistic people can also be unexpected, and can exacerbate autistic traits, such as regression of skills or communication, as well as stereotyped behaviors and speech. Based on these observations, Kerns and her collaborators plan to create autism-specific trauma assessments to test on a larger scale.​

“The way traumatic stress expresses itself in people on the spectrum may be different.” - Connor Kerns

Treating the individual

This line of research is still in its earliest days: It is still difficult to tease apart correlation from causation. In other words, does autism predispose someone to post-traumatic stress, or are people with autism more vulnerable to experiencing traumatic events? Or both? Scientists simply don’t know the answers yet — although some studies do indicate that autistic children are more reactive to stressful events and, because they lack the coping skills that help them calm down, perhaps predisposed to PTSD.

Even when trauma is known and documented, however, treating someone on the spectrum is easier said than done. When children are nonverbal or simply view the world differently, practitioners can struggle to find the most effective way to help them work through their experiences.

“There’s some evidence that children on the spectrum tend to interpret questions differently, and in a more literal way, or that they tend to be more avoidant of questions about their trauma than typically developing children,” says Daniel Hoover, a clinical child and adolescent psychologist at the Kennedy Krieger Institute’s Center for Child and Family Traumatic Stress in Baltimore. “So they need measures that are more suited or adapted for children on the spectrum, which don’t really exist or are in development.”

One of the most effective treatments for PTSD, at least in children and adolescents, is trauma-focused cognitive behavioral therapy. This treatment takes a multi-pronged approach that involves both children and their parents or guardians in talk therapy and education: All of them learn what trauma is, how to navigate potentially tricky situations, and about communication tools and calming techniques for moments of distress. Clinicians prompt the affected children to talk through the traumatic experience in order to help them take control of the narrative, reframe it and make it less threatening. But in children with autism, who may be less verbal than typical children or simply less inclined to delve into the memories over and over again, such an approach can prove especially challenging.

“There are a number of core features of autism that make usual psychotherapies somewhat more complicated,” Hoover says. Typical children tend to be reluctant to talk about their traumatic experiences, but they generally give in because they know it’s good for them, he says. “Children on the spectrum are often less willing — because they’re exceedingly anxious, and because they’re not able to see the forest for the trees.” He notes that autistic children can be so keyed into the present, and so tied to routine, that they have a difficult time participating in treatment that intensifies their anxiety in the moment, even when they know it might help in the long run.

In working with these children, clinicians have also found it particularly tricky to separate the child’s understanding of a potentially traumatic event from that of their parents, who can walk away from an event with a completely different interpretation. To peel back these layers, Hoover and his colleagues at Krieger have developed a graphic, interactive phone app to help children — even minimally verbal children — use images to report experiences and the emotions associated with them. (The group is now in negotiations with a publisher and hopes to make the app publicly available within a couple of years.)

Children on the spectrum also usually take far longer to show improvement than their typical peers do. “It takes them longer to buy into it and feel comfortable, and takes them longer to integrate the concepts,” Hoover says.

That has certainly proven true for Gabriel. He is slowly making progress under Hoover’s care, Kristina says, but it has taken a long time for him to open up. “There were days when he’d sit in that chair at stare at Dr. Hoover and didn’t answer him,” she says.

After the death of his grandmother earlier this year, Gabriel became intensely afraid that Kristina might die too. When Hoover tried to talk with the boy about it, Gabriel shut down and wouldn’t engage. But just the other week, his mother says, Gabriel finally opened up. “He and Dr. Hoover bounced ideas off each other: How can we deal with these thoughts? How do we redirect them?” The dialogue showed Gabriel was gaining mastery over his story, transforming it from an overwhelming memory to something more manageable.

Just a few weeks ago, Gabriel told his mother that he worried he might try to kill himself again, and asked for her help. “Before, I had to dissect what was going on, but now Gabriel is using his words,” Kristina says, “It is a huge improvement from where he used to be.”

 
Last edited:
speech-pattern-autism-neurosciencneews-public.jpg



80% of autistic children treated with CBD saw improvement

by Jacqueline Havelka | 8 Aug 2018

Israeli researchers have found compelling evidence that medical cannabis is an effective therapy for children on the autism spectrum. In this soon-to-be-published study in the journal Neurology, researchers treated autistic children with high concentrations of CBD, a non-intoxicating cannabinoid found in the cannabis plant.

Conditions in 80% of the children improved. Alternatively, the children had not shown improvement with conventional drug therapies.

The study was led by the director of pediatric neurology at Jerusalem’s Shaare Zedek Hospital, Dr. Adi Aran, who treated the 60 children with a high-CBD cannabis oil (20% CBD and 1% THC). The children were treated for at least seven months with the oil.

After the treatment period, parents answered assessment questionnaires to characterize their child’s condition. Questions were asked about behavioral changes, anxiety levels and ability to communicate.

Here’s what they reported:

- 80% of parents noted a decrease in problematic behaviors, with 62% reporting significant improvements.
- Half of the children had improved communication.
- 40% reported significant decreases in anxiety. (Note: one-third of the study participants began the study with no anxiety.)

Just as Israel is a pioneer in medical cannabis research, Aran is a pioneer in cannabinoid therapy for autism. Aran originally began a 2017 project to test 120 autistic children. It was the first study of its kind worldwide, and was made possible by the Israeli government’s funding and progressive approach to cannabis research.

Aran said that when word of the study got out, his waiting lists were soon full with many families from all over Israel who wanted to participate.

Autism spectrum disorders are neurodevelopmental in nature, usually appearing in infancy or early childhood and lasting a lifetime. More severe cases have debilitating symptoms including compulsive, repetitive behaviors and impaired social skills and communication. Some children cannot speak at all. Autism affects around 1% of people worldwide.

The causes of autism are not understood and there is no cure—and the prevalence is climbing. In April 2018, the CDC updated its autism prevalence estimates to 1 in 59 children, up from 1 in 166 children in 2004. Doctors traditionally treat symptoms with antipsychotic medications, which have harmful side effects. Some children do not respond to these medications.

Aran began small autism research studies after similar cannabis studies on epilepsy, a disease that affects about 20% of autistic children. While studying epilepsy, researchers discovered that certain cannabis compounds would likely also help some autism symptoms. Less than 2% of the general population has epilepsy, but up to 33% of people with autism also suffer from epilepsy.

Neuroscientist Dr. Thomas Deuel of the Swedish Hospital in Seattle says there is definitely a connection. While scientists do not clearly understand the reasons behind the relationship, they suspect that the different brain development that occurs in autistic children is more likely to create circuits that cause epileptic seizures.

That link has caused many parents to seek out cannabis treatments for their autistic children. Parents certainly have anecdotal evidence of the effectiveness of CBD oils on their autistic children, but mainstream medicine has remained skeptical due to the lack of data. With most conditions treated with cannabis, anecdotal evidence and personal experience far outweigh actual peer-reviewed scientific research.

Now, New York University (NYU) neurologist Dr. Orrin Devinsky, the same scientist who did research on Epidiolex, is now conducting two studies on CBD effects on children aged 5 to 18 with moderate to severe autism. The only other doctor who is currently doing studies like this is Aran.

Since autism and epilepsy go hand in hand, CBD is showing promise for treating both conditions.

Perhaps as doctors begin to see the effects of Epidiolex, and review research like that of Aran’s and Devinsky’s autism studies, many more will begin to delve further into use of medical cannabis.

https://www.leafly.com/news/health/r...mising-results
 
banner-itin-CA-SF-to-LAX-via-the-coast-Big_Sur_Coast_California.jpg



Microdosing psilocybin for Autism, study*

Psilocybin Alpha | 16 Feb 2022

Nova Mentis Life Science, a biotechnology company and global leader in first-in-class psilocybin-based therapeutics and complementary diagnostics for neuroinflammatory disorders is pleased to announce that Nova Mentis successfully completed an oral microdose psilocybin preclinical study, in the laboratory of Dr. Viviana Trezza, Rome Tre University, Rome, Italy. The results exceeded all expectations with the findings that a very low dose of the Company’s proprietary psilocybin significantly modulated behavioural and cognitive defects, such as recognition memory, in a genetic model of fragile X syndrome (FXS).

“The science team led by Dr. Hausman, together with Dr. Viviana Trezza from Roma Tre University, continues to deliver promising preclinical results. The recent oral microdose data set not only confirms but exceeds our original injectable formulation results,” says Will Rascan, CEO of NOVA. “The clear positive data is critical as we prepare to submit our clinical trial application to Health Canada for a Phase 2A study evaluating psilocybin microdose therapy for fragile X syndrome.”

Autism spectrum disorder (ASD) is a complex neurodevelopmental disorder for which no treatments exist. Fragile X syndrome (FXS) is the most common form of inherited intellectual disability and the most frequent monogenic cause of ASD (1). The aim of the present study was to evaluate various oral doses of the company’s proprietary psilocybin in a rat model of FXS. A major question to be answered in this preclinical study was whether microdose therapy could be the potential treatment of choice in ASD, as compared to single dose macrodose therapy with associated hallucinogenic and other side effects.

Psilocybin efficacy was tested in FXS, in the Fmr1 knock-out (Fmr1 KO) rat. Wild type control and Fmr1 KO animals were treated with 0.1 mg/kg and 0.3 mg/kg oral psilocybin every other day for 6 treatments, over a 2-week period, and on day 18 underwent object recognition testing. We had great results! Both 0.1 and 0.3 mg/kg were effective in reversing the cognitive impairment displayed by Fmr1 KO animals. Moreover, the 0.1 mg/kg worked best, and did not have any apparent side effects. The 0.1 mg/kg dose in the rat translates into approximately 1.5 mg oral dose in a 70 kg person.

“I am elated to be able to report to the medical community that at long last we may have opened the door to treatment of ASD, an unmet medical need, that has a devastating impact on the patient, family and society,” stated Marvin S. Hausman MD, Chairman of NOVA’s Scientific Advisory Board. “The rat model that we used mimics key autistic-like features in humans and the study results strongly supports an important role for microdose therapy of FXS. Moreover, this positive response in the rat of every other day oral 0.1 mg/kg psilocybin, equivalent approximately to a 1.5 mg dose in a 70 kg person, may be the treatment of choice to modulate behavioural changes and cognitive defects, and perhaps have a longer term constructive neuroplastic response in the brain without the need for large doses of psychedelic drugs with associated detrimental hallucinogenic side effects.”

*From the article here :
 
Last edited:



My journey treating Asperger's with MDMA

@Land Rain | Bluelight | 22 April 2020

In the video above I'm finally able to share my journey and experience in using MDMA to help attenuate my Asperger’s symptoms, something that I've waited almost five years to share now because of stigma and due to the culture of the industry I work on. Through the mechanics and elevated state MDMA offers, combined with the power of our brain’s natural mechanism, neuroplasticity, I was able to begin practicing social communication activities, including the practice of putting myself in other people’s shoes to practice empathy, I was able to conquer the multitude of obstacles that I was originally buried in for most of my life due to my Asperger's. While empathy may be something that comes natural to most people, it’s still a practice that needs to be trained, which I missed out on severely when I was still growing up due to the environment I was in (horrible school, abusive online friends, no authoritative mentorship in my life that I could believe in, abusive exes, and bad diets with too much sugar).

While MDMA’s breakthrough in treating PTSD may be well documented at this point, this video aims to address other potential that I have noticed is still completely unexplored. I’m hoping this video can be the start to help point those in charge of researching MDMA that there is at least one, while anecdotal and singular, had monumental and indismissible effects in changing something as neurophysiological as Asperger’s. The amount of change I went through because of this substance from where I started is, to say the least, not normal. Many have told me my changes over these years has been unheard of for them. It was to the point that close friends and family noted the drastic difference. They said it was like seeing a completely different person. Hopefully this also opens up more ideas into MDMA's potential in other benefits outside of what it's currently being studied for. As another example, I can tell you that for one, it also drastically changed one of the most stubborn and arrogant people I’ve ever known to the point that they too are now a completely different person. It has also stopped yet another friend from their potential cocaine and weed addiction, and those sessions with that person were done through long distance video chats because they lived far away. I have also witnessed first hand MDMA, coupled with psilocybin, being able to change a sociopath into one of the most empathetic people I've ever met. There are countless examples that I've witnessed first hand but perhaps the most important one to me is that it has brought a tightly knit group of friends that did not think they could get any closer, even closer.

Studies aside, even just taking all of the understanding of MDMA’s basic mechanisms on a person and it’s method of action (via serotonin discharge, your body’s natural neurotransmitter responsible for modulating several areas of your consciousness, such as mood, empathy, social behavior, and perhaps even more importantly, memory, which can play a role in trauma recall when the right triggers and setting are set), one can begin to piece together possible scenarios of potential inherent to these specific functions. Imagine a world where dysfunctional families have the opportunity to reconcile misunderstandings and lack of communication. Imagine a world where rocky friendships or romantic relationships can find peace in knowing they can finally actually talk without the burdens of each other’s predisposed notions and insecurities of each other. And finally, imagine a world where everyone has been offered a second perspective to be aware that there is not only appreciation to be experienced everywhere in the world, but that there is an entire dimension of empathy of one another that has gone completely undetected and unaccounted for. I can’t picture a world like that to have missiles erected from the ground aimed at each other. And I definitely can’t picture that world to dismiss the damages we are incurring onto this planet’s natural wildlife and overall health.

Hell, I can even imagine that world to have far more inspired scientists, engineers, and innovative inventors as their ambitions are burning from the need to make positive and helpful advancements. It could mean seeing what we would have normally seen in a year like 2200 instead in a year like 2150.

MDMA Supplementation Proposal (as mentioned in the video): http://beyondtheparallax.com/mdma-supplementation/

If it interests anyone, I also found this study that shows repeat intermittent exposure to MDMA provided neuroprotective effects against its own neurotoxicity. There are people better suited to this field than I am but this could explain why my friends and I no longer feel the “hangover” effect after using MDMA, meanwhile we still feel the full spectrum of the experience. https://pubmed.ncbi.nlm.nih.gov/20169...

My friends and I are also really into a healthy diet and lifestyle so I’m not sure how much of it is from that as well. I wanted to share that study because no one has written an article on it that I’ve seen so this potential benefit doesn't seem to be getting any traction in popularity from what it seems. For my friends and I, "losing the magic" is not a thing that seems to exist That said, I am not here to crusade for substance use, rather, I am ecstatic to share what it has done for me and the deeply profound positive results I have witnessed it do to others that I have known in hopes that more eyes can be turned towards it's other potential uses.

Thank you all for watching my video and for taking the time to read what I have shared here. I plan on eventually opening up more about this in the future as well.

 
Last edited:
aaron_autism_psychedelic_Psychable.jpeg


Autism and psychedelics – An interview with Aaron Orsini

by Leia Friedman | Psychable

Aaron Paul Orsini is the author of Autism On Acid: How LSD Helped Me Understand, Navigate, Alter & Appreciate My Autistic Perceptions. He is also the co-founder of the Autistic Psychedelic Community, a peer support group for neurodivergent individuals interested in discussing psychedelics and building connection with others with similar experiences in terms of personal sensory processing. He has just finished editing and publishing his second book on the subject, entitled Autistic Psychedelic, a neurodiversity-minded anthology of psychedelic essays & survey responses that is now available via www.AutisticPsychedelic.com

Leia: What is your background, and how do you identify yourself?

Aaron: I grew up in the midwest of the United States and went to college pursuing a degree in multimedia arts. I am fascinated by different forms of creative expression tools, and I gravitated toward animation specifically because it encompasses all of these different layers of expression, such as music and language. I found a utility in being able to communicate and express and understand the world around me through these mediums, and that also informed my professional pursuits.

Leia: You learned that you were autistic later in life, right?

Aaron: Yeah, that’s correct. I was diagnosed at the age of 23. I had been dealing with issues surrounding depression and anxiety, and other energetic issues like not being able to simply get up and out of bed and get tasks accomplished over the course of many years. I was fortunate enough to participate in plenty of talk therapy over that period of time, and it wasn’t until the age of 23 that a psychotherapist gave me a questionnaire and concluded that autism might be a factor in some of these depressive or anxious or overwhelmed states.

But it took a couple of years, and it still will take probably more years to continue to understand how I relate to that diagnosis.

There are many different ways that autism can be self-identified. I personally choose to identify as an autistic rather than a person with autism. That’s something of a controversial subject in many spaces — across language barriers, etc. — but for simplicity’s sake, I identify as an autistic.

To provide a similar example, someone within deaf culture may feel more comfortable self-identifying as deaf as opposed to “a person with a hearing impairment”, even though there was a time in which it may have been considered offensive to define individuals by what may have then been exclusively seen as an impairment.

As time has gone on and sub-cultures have formed around certain variances in processing, however, autistics within these sub-cultures have adopted the outlook that autism could perhaps be seen as a neurotype; a particular mode of cognitive processing that can present challenges in certain contexts and remarkable advantages in other contexts. In this way, there are aspects that overlap between deaf culture and autistic culture where there is somewhat of a reclamatory pride in identifying as such. Thus, I personally make the choice to identify within autistic culture as an autistic.

Leia: What was your first impactful experience with a psychedelic like?

Aaron: The experience that I wrote about in my first book was with lysergic acid diethylamide (LSD). That day I was in a forest setting, and during the initial portion of that experience, I was on my own. I had some other people there with me in my periphery but I spent most of that first experience on my own with my own thoughts and my own reflections. And I believe that this first experience, even as an autistic, maps over the general psychedelic experiences of unity and connection — to nature, family, grander aspects of existence, etc. — that others of any neurotype might report.

But the most remarkable component of my experience was sometime after the peak when I encountered some other individuals — after leaving that more isolative space — and had what felt like what I’ve come to know to be an empathogenic drug effect; a very deep and immediate access to my inner feeling states, and perhaps a more intense mirroring of the feeling states of others as well.

And that specific empathogenic (engender empathy within) or entactogenic (engender feeling within) drug property is what has inspired my ongoing meta-analysis of preexisting research. Through ongoing collaborations, I hope to be able to help pinpoint — from a neuropsychopharmacological perspective — the mechanistic underpinnings that shape and influence these noteworthy fluctuations in autistic psychedelic processing.

Based on what I’ve learned through this ongoing deep dive into academic publications, I’ve learned that there are still many unknowns and debates happening in terms of how to define autism in a more universally agreed-upon way. Similarly, we’ve only just begun to understand what could very well be a long journey toward comprehending the massive complexity of psychedelic pharmacokinetics. And so as we await the evidence-based understandings, there’s one thing that can be done, and that’s the gathering of subjective and qualitative accounts, which is exactly what we’ve done with this next book, Autistic Psychedelic — a book that includes first-hand psychedelic stories and survey responses from more than forty neurodivergent contributors.

Leia: I look forward to reading that book, and I loved your first one, Autism on Acid. What do you think of the research on psychedelics for autistic people or people with autism?

Aaron: Well, I believe, in most recent years, the most noteworthy study was the work done by Dr. Alicia Danforth with the Multidisciplinary Association for Psychedelic
Studies (MAPS). That study investigated whether MDMA-assisted psychotherapy could help autistic individuals manage their social anxiety.

I have also had experiences with MDMA that lead me to believe that this approach would be quite effective, especially in the context that is still being worked towards — a context in which these drug experiences can take place in the presence of others, especially close loved ones or friends. That would create a scenario with “clay on the table” so to speak; other human beings that could present more immediate opportunities for that individual to overcome social challenges while in a more expansive, entactogenic, empathogenic, and fear-reduced state.

I personally didn’t get much out of talk therapy sessions because a lot of my therapeutic outcomes resulted from my ability to take interest in the person opposite me while my inner feeling state awareness was dialed up. In conventional therapeutic settings, the act of asking how the therapist is doing is somewhat of a fruitless endeavor. They’re almost disallowed from divulging such personal information. Therefore, the conventional psychotherapy model is inherently limiting in terms of how much it allows someone to “flex” the muscles related to interpersonal growth and engagement.

If you look back at the 1960s there was also the work of Dr. Fisher with autistic youths. Obviously, the field of psychiatry has evolved quite a bit in terms of understandings about both these substances and these conditions since that research. There were many ethical issues, such as lack of consent with nonverbal individuals, and that is of great concern in any context.

These are topics I generally don’t want to even really weigh in on because it’s so far removed from the work that I’m doing in terms of pursuing the discovery of the self-reported benefits and challenges experienced by adult autistics utilizing psychedelics in an intentional, consensual context. In the simplest terms, I’m not involved as a parent of an autistic. And I don’t want to make it seem as though I understand the struggles of any parent or any other autistic. I don’t. I try to just speak to my own personal experience and listen to the words of others as best as I can.

So, yes. As of now, the true focus of my work is discovery, and what outcomes can arise when risks are mitigated, and psychedelics are safely offered to consenting adults who understand the nature of what they’re undertaking in an intentional context.

Leia: Thank you for mentioning past studies of psychedelics and autistic people and for bringing up this issue of consent. I do think it’s important to keep in mind the history so we can be informed enough not to repeat it. You founded the Autistic Psychedelic Community, could you tell us more about that?

Aaron: The Autistic Psychedelic Community was created to be exactly that: a community that works together. And within our meetings and online discussion forums, we mainly rely upon the personal experiences of one another to serve to inform a majority of the wisdom exchanged. It’s also unique in that we interact across generations. We have persons in our group as old as 75 years old.

I didn’t live in a multi-generational household. And so to receive insights from someone who has lived another 50 more years of autism is also quite instructive. So yes, we go through a community-driven discovery model to reveal not only what sorts of outcomes people are experiencing through intentional psychedelic use but also what sorts of novel solutions they’ve discovered in terms of non-drug approaches to wellness as well. When enough people get together who are trying to solve the same problem in the same space, there’s a natural synergy. And it’s a model that’s maybe already happened elsewhere but I could see how the Internet could empower people to solve other issues as well.

Let’s say for example people are trying to better navigate something like endometriosis. With the interconnected nature of the Internet, there’s this new ability for persons impacted to not only leverage the intelligence of professionals and clinicians but to also come together to ask each other basic questions like “What does this or that cost?” or “What types of questions will I be asked?” or “What types of questions should I ask my clinicians?” — things like that. And the ability for those with especially rare conditions to find one another online, and interact in a more direct way, is tremendously helpful for more than just the pure information exchanged.

What I find to be quite charming is when I see people return to offer support to others as well even after they have resolved many of their own issues. Because being of service and providing support to others is quite therapeutic as well. And some of our elders hang around just to simply offer guidance and support. And sometimes there are days in which they return to once again need support from the group. So it feels much less hierarchical in this regard.

Leia: I relate. I helped to co-start a peer-led psychedelic integration circle for people with eating disorders and/or body dysmorphia, because I struggled with both of these things for a long time. I know it’s not quite the same as the Autistic Psychedelic Community, but I think there are some similarities. For me, being able to both offer as well as receive guidance from others has been huge. In integrating psychedelic experiences, it just feels different to be with people who understand what I’ve gone through versus being in a group of folks who don’t have the lived experience. Those spaces didn’t feel as welcoming to me in the past, so I couldn’t be as open or go as deep.

Aaron: Yeah, and that speaks to a constant unlearning that I think is somewhat synergistic with psychedelics as well — there is work involved in unlearning the concept of “disorder” and instead realizing that some of the more challenging aspects of autism — especially those related to hyper- or hyposensitivities — can instead be seen as very real strengths in certain contexts.

I’m reminded of the ways in which someone like Stan Grof was exploring how the container for psychedelic experiences was just as influential on the outcome as the psychological or physiological state of the person undergoing the psychedelic session. In much the same way, the cultural container in which we’re receiving diagnosis is going to impact our outcomes and perceptions of our outcomes just as strongly.

In this particular case, in a roundabout way, even though Zoom may not seem like it is, it in fact is a cultural container of sorts. As a digital interface, Zoom shapes cultural norms within our meeting space.

In our online community, for example, there are individuals who might have issues with auditory overstimulation. With something like Zoom, they can fully control the volume of the voices coming at them; they can also filter out background noise automatically, which is a technology that some people might otherwise only be able to utilize with wearable devices. Online platforms also allow for people to type thoughts if they have difficulty forming spoken words, or read typed thoughts when they would otherwise face challenges with interpreting heard speech. So these sorts of augmented reality layers are also incredibly enabling for a range of different intelligences and individuals with a range of sensory processing issues.

Many of us in the community also have a predisposition for being able to retain focus for sustained durations on specific topics. And so it’s quite fascinating to have a group of autistics focusing their intense focus, together, on solving problems that are facing autistics. This is an especially powerful experience for some of us in that many of us are acclimated to feeling as though we may be the problem in a given social space. And so to instead feel united as solvents is quite powerful.

Leia: That is powerful. What do you wish more people knew about autism and psychedelics?

Aaron: I think that there is an inherent gap in the ability to understand and imagine what it’s like to live through either of them. In other words: if someone has not had a psychedelic experience — or if someone has never experienced the world through the lens of autism — it may be quite difficult for them to be able to imagine what those experiences might be like.

Many aspects of autism specifically might be difficult to describe because there is no real point of contrast for the individual attempting to describe what may be, for them, the only lens they’ve ever known. In this way, there’s no substitute for direct experience. And I would say that the next best thing to direct experience is open, sincere, and attentive listening.

And there are examples in our upcoming book wherein neurodivergent individuals attempt to describe how their default mode of processing works. One particular individual describes how they interpret the world of stimulation through the filtration of their natural synesthesia; perceiving spoken language as colors and other visuals first, as a default mode of processing. And then there’s this incredibly complicated process that you can only maybe imagine wherein this individual is tasked with hearing speech as colors, then reverse translating those colors back into words, that can then be further translated into a spoken response.

In this particular example, the individual sharing their story is expressing how psychedelics enabled them to trust their intuition and to be able to interpret the language of color and respond and trust that information as it arrives to them in their default mode of processing. Even as I’m explaining this, I’m wondering if this even makes any sense. But to the person exploring this, it does make sense, literally. And they emerged capable of trusting their alternate mode of perception as a result.

In the same way, I think a lot of autistic people are tasked with having to come to an understanding that their interpretation of “consensus reality” is merely relative, and always will be. This lesson is also something I think that psychedelic users are greeted with very strongly: reality is relative, and the notion or faith in “consensus reality” is a bit of a cognitive shortcut that can be quite detrimental in certain contexts.

If someone has not had the lived experience of being on a psychedelic or of being a neurodivergent individual, then they are more than likely not going to fully understand the neurodivergent experience. What’s more, they might end up interpreting any explanation in a way that further obscures their understanding of the experience and the experiencer. And so perhaps if we could all just arrive to the understanding that everyone’s experience of reality diverges from everyone else’s experience of reality, then these labels and questions of “Whose perceptions diverge from who?” and “Who is typical?” and “Who is not typical?” would also quickly dissolve into that expanded awareness.

The more we become aware, the more we might similarly become aware that ambiguous inputs may be the only real foundation upon which a lot of our supposedly solid understandings are built.

Anyhow. I’m in an interesting position attempting to use words to express some of these ineffable experiences. By the time I double-back to try to make sure I didn’t miss any holes in what I said, I just discover still yet more holes.

Leia: This whole thing is a whole lot of (w)holes, isn’t it?

Aaron: Yeah, and the English language could use a software update, probably.
Leia: Absolutely! I’m thinking about the work of Robin Wall Kimerer and her book Braiding Sweetgrass; I learned that the English language is about 70% nouns while the Potawatomi language is heavy on verbs and actions. Life is in motion, and Potawatomi indicates that. English is all about persons, places, or things, and what is versus what happens.

Aaron: Yeah, and that goes back to one of your previous questions about how I identify as autistic for ease and simplicity, and what feels like something of solidarity with others who might exist in a somewhat marginalized group. At the same point, I think the more-long-winded or articulate version of my identification would be to identify as “the awareness that comes through me after passing through something that might be referred to as autistic filtering in certain social and task-oriented contexts, with certain sleep/diet/exercise patternings present, in tandem with endogenous and exogenous chemicals present in my bio-electric systems.” But instead, I just say I’m autistic. It’s simpler.

But really, I’m just another being being.

Leia: Thank you! I agree. We are all humans, being.

 
Last edited:
complexe-des-sciences-mcgill-2.jpg

McGill University Health Centre, Montreal, Canada
Evaluating the potential use of psychedelics in treating Autism*

Athanasios Markopoulos, Antonio Inserra, Danilo DeGregorio, Gabriella Gobbi

Recent clinical and preclinical evidence points towards empathogenic and prosocial effects elicited by psychedelic compounds, notably the serotonin 5-HT2A agonists LSD, psilocybin, DMT, and their derivatives. These findings suggest a therapeutic potential of psychedelic compounds for some of the behavioural traits associated with autism spectrum disorder (ASD), a neurodevelopmental condition characterized by atypical social behaviour. In this review, we highlight evidence suggesting that psychedelics may potentially ameliorate some of the behavioural atypicalities of ASD, including reduced social behaviour and highly co-occurring anxiety and depression. Next, we discuss dysregulated neurobiological systems in ASD and how they may underlie or potentially limit the therapeutic effects of psychedelics. These phenomena include: 1) synaptic function, 2) serotonergic signaling, 3) prefrontal cortex activity, and 4) thalamocortical signaling. Lastly, we discuss clinical studies from the 1960s and 70s that assessed the use of psychedelics in the treatment of children with ASD. We highlight the positive behavioural outcomes of these studies, including enhanced mood and social behaviour, as well as the adverse effects of these trials, including increases in aggressive behaviour and dissociative and psychotic states. Despite preliminary evidence, further studies are needed to determine whether the benefits of psychedelic treatment in ASD outweigh the risks associated with the use of these compounds in this population, and if the 5-HT2A receptor may represent a target for social-behavioural disorders.

Autism spectrum disorder (ASD) is a neurodevelopmental condition affecting 1–2% of the global population. ASD is often diagnosed in childhood, with individuals displaying characteristic atypicalities in social communication and interaction, as well as repetitive patterns of behaviour and restricted interests. These features are highly heterogeneous in ASD and are often accompanied with co-occurring diagnoses of depression and anxiety. At present, there is a lack of selective medications targeting the major phenotypes of ASD: impaired social behaviour and communication.

Psychedelics are currently experiencing a resurgence of scientific investigation, following in the footsteps of pioneering mid-twentieth century research. Although the term “psychedelic” encompasses a variety of compounds, the present review focuses on the serotonergic, or “classical,” psychedelics, which produce their hallucinogenic effects via the serotonin 5-HT2A receptor. These include LSD, psilocybin, DMT, and their derivatives. Other non-serotonergic psychedelics, such as the empathogen MDMA, have also been shown to increase social behaviour and empathy, and to reduce social anxiety in individuals with ASD. However, due to MDMA’s vastly different pharmacological properties from serotonergic psychedelics, it is not discussed in the present review.

Recent clinical and preclinical research demonstrates that psychedelics may hold therapeutic value in the treatment of some of ASD’s core features. Despite the emergence of compelling research, early clinical trials carried out in the 1960s and 70s revealed a variety of side effects after psychedelics were administered experimentally to children with ASD. Thus, the risks associated with the use of these compounds must be carefully examined when considering their potential use in neuroatypical individuals.​

Conclusions

Due to the limited treatment options for ASD, the development of novel therapies is warranted. Clinical and preclinical trials suggest that psychedelics may improve social behaviour and decrease the burden of co-occurring diagnoses in ASD by targeting synaptic function, serotonin signaling, PFC activity, and thalamocortical signaling. Early clinical trials in childhood ASD suggest that psychedelics might hold therapeutic potential; however, the side effects encountered represent potential limitations to this treatment. It is possible that psychedelics may alleviate a few core social-behavioural features in individuals with ASD, such as social anxiety, but carefully performing a risk-to-benefit assessment is crucial due to the severity of their potential side effects.

Individuals with ASD represent a highly heterogeneous demographic; therefore, only certain subsets of individuals with ASD may respond well to psychedelic treatment options. Clinical trials must proceed with caution because this population is also comprised of children and some individuals with intellectual disabilities, for which obtaining informed consent is a challenge. Future studies must make these considerations when determining if some of the positive findings obtained in the “first wave” of psychedelic research in ASD can be validated when employing contemporary scientific and ethical standards.

*From the article (including references) here :
 
Last edited:
untitled-530-780x549.jpg



Evaluating the potential use of serotonergic psychedelics in Autism*

Athanasios Markopoulos, Antonio Inserra, Danilo De Gregorio and Gabriella Gobbi

Recent clinical and preclinical evidence points towards empathogenic and prosocial effects elicited by psychedelic compounds, notably the serotonin 5-HT2A agonists LSD, psilocybin, DMT, and their derivatives. These findings suggest a therapeutic potential of psychedelic compounds for some of the behavioural traits associated with autism spectrum disorder (ASD), a neurodevelopmental condition characterized by atypical social behaviour. In this review, we highlight evidence suggesting that psychedelics may potentially ameliorate some of the behavioural atypicalities of ASD, including reduced social behaviour and highly co-occurring anxiety and depression. Next, we discuss dysregulated neurobiological systems in ASD and how they may underlie or potentially limit the therapeutic effects of psychedelics. These phenomena include: 1) synaptic function, 2) serotonergic signaling, 3) prefrontal cortex activity, and 4) thalamocortical signaling. Lastly, we discuss clinical studies from the 1960s and 70s that assessed the use of psychedelics in the treatment of children with ASD. We highlight the positive behavioural outcomes of these studies, including enhanced mood and social behaviour, as well as the adverse effects of these trials, including increases in aggressive behaviour and dissociative and psychotic states. Despite preliminary evidence, further studies are needed to determine whether the benefits of psychedelic treatment in ASD outweigh the risks associated with the use of these compounds in this population, and if the 5-HT2A receptor may represent a target for social-behavioural disorders.
Introduction

Autism spectrum disorder (ASD) is a neurodevelopmental condition affecting 1–2% of the global population. ASD is often diagnosed in childhood, with individuals displaying characteristic atypicalities in social communication and interaction, as well as repetitive patterns of behaviour and restricted interests. These features are highly heterogeneous in ASD and are often accompanied with co-occurring diagnoses of depression and anxiety. At present, there is a lack of selective medications targeting the major phenotypes of ASD: impaired social behaviour and communication.

Psychedelics are currently experiencing a resurgence of scientific investigation, following in the footsteps of pioneering mid-twentieth century research. Although the term “psychedelic” encompasses a variety of compounds, the present review focuses on the serotonergic, or “classical,” psychedelics, which produce their hallucinogenic effects via the serotonin 5-HT2A receptor. These include LSD, psilocybin, DMT, and their derivatives. Other non-serotonergic psychedelics, such as MDMA, have also been shown to increase social behaviour and empathy, and to reduce social anxiety in individuals with ASD. However, due to MDMA’s vastly different pharmacological properties from serotonergic psychedelics, it will not be discussed in the present review.

Recent clinical and preclinical research demonstrates that psychedelics may hold therapeutic value in the treatment of some of ASD’s core features. Despite the emergence of compelling research, early clinical trials carried out in the 1960s and 70s revealed a variety of side effects after psychedelics were administered experimentally to children with ASD. Thus, the risks associated with the use of these compounds must be carefully examined when considering their potential use in neuroatypical individuals.

Conclusion

Due to the limited treatment options for ASD, the development of novel therapies is warranted. Clinical and preclinical trials suggest that psychedelics may improve social behaviour and decrease the burden of co-occurring diagnoses in ASD by targeting synaptic function, serotonin signaling, PFC activity, and thalamocortical signaling. Early clinical trials in childhood ASD suggest that psychedelics might hold therapeutic potential; however, the side effects encountered represent potential limitations to this treatment. It is possible that psychedelics may alleviate a few core social-behavioural features in individuals with ASD, such as social anxiety, but carefully performing a risk-to-benefit assessment is crucial due to the severity of their potential side effects.

Individuals with ASD represent a highly heterogeneous demographic; therefore, only certain subsets of individuals with ASD may respond well to psychedelic treatment options. Clinical trials must proceed with caution because this population is also comprised of children and some individuals with intellectual disabilities, for which obtaining informed consent is a challenge. Future studies must make these considerations when determining if some of the positive findings obtained in the “first wave” of psychedelic research in ASD can be validated when employing contemporary scientific and ethical standards.

*From the article (including references) here :
 
Last edited:
raimond-klavins-azwRXQgJvUI-unsplash-scaled.jpg


LSD breakthrough could enable treatment for Autism*

The mechanism that enables the drug to stimulate sociability could be used to treat anxiety and autism spectrum disorders.

by Alexander Martin | Sky | 27 Jan 2021

Researchers have discovered the mechanism that contributes to the hallucinogenic drug LSD increasing social interactions, potentially unlocking new therapeutic applications.

Lysergic Acid Diethylamide (LSD) became a popular psychedelic drug during the 1960s and is again gaining in popularity, with some young professionals claiming to take micro-doses to enhance their creativity.

Despite rigorous analysis and experimentation, scientists have not been able to determine the mechanism of how LSD acts upon the brain - until now.

Researchers from McGill University in Canada have discovered that LSD activates the serotonin 5-HT2A receptors and AMPHA receptors in the brain, both of which combine to promote social interaction.

In their study, published in the journal PNAS, the scientists administered a low dose of LSD to mice over a period of seven days and discovered it resulted in an observable increase in their sociability.

Although the behaviour in mice is not directly equivalent with that in humans, with the researchers noting that it was largely analogous to empathy and social behaviour, the main outcome was identifying the underlying mechanism for the behavioural effect.

"The fact that LSD binds the 5-HT2A receptor was previously known," said Professor Nahum Sonenberg of McGill's department of biochemistry, co-author of the report.

"The novelty of this research is to have identified that the prosocial effects of LSD activate the 5-HT2 receptors, which in-turn activate the excitatory synapses of the AMPA receptor as well as the protein complex mTORC1."

These brain pathways have been demonstrated to be dysregulated in mental disorders with social deficits, such as autism spectrum disorder, according to Prof Sonenberg's previous research.

The next step for the researchers is to test LSD on mutant mice which display behavioural deficits similar to those in human pathologies, including autism spectrum disorders and social anxiety disorders.

"The hope," according to McGill University, "is to eventually explore whether micro-doses of LSD or some novel derivates might have a similar effect in humans and whether it could also be a viable and safe therapeutic option."

"Social interaction is a fundamental characteristic of human behaviour,"
added co-lead author Dr Gabriella Gobbi, professor in the Department of Psychiatry at McGill and psychiatrist at the McGill University Health Centre.

"These hallucinogenic compounds, which, at low doses, are able to increase sociability may help to better understand the pharmacology and neurobiology of social behaviour and, ultimately, to develop and discover novel and safer drugs for mental disorders."

*From the article here :
 
psilocybin-asd-neurosicnes-public.jpg


New study to evaluate psilocybin’s therapeutic potential an autistic adults

King’s College London | Neuroscience News | 4 Jun 2022

A new study will explore how psilocybin affects different networks and serotonin function in the brains of autistic adults.

The study will explore how psilocybin affects specific brain pathways in autistic adults, and is the first ever mechanistic study of psilocybin in autistic adults.

It will investigate whether there is a difference in the function of serotonin brain networks in autistic and non-autistic adults.

The researchers will use a range of imaging techniques and behavioural tasks to examine how the serotonin system is modulated by COMP360 psilocybin. It is an investigator-initiated exploratory study that will take place at the Institute of Psychiatry, Psychology & Neuroscience (IoPPN) at King’s College London.

The study is co-sponsored by King’s IoPPN and South London and Maudsley NHS Foundation Trust. It will enrol 70 adult participants, including 40 autistic people and 30 non-autistic people.

The study is led by Professor Grainne McAlonan, Professor of Translational Neuroscience at King’s IoPPN, and conducted by Tobias Whelan, PhD student at King’s and Research Scientist at COMPASS Pathways.

Tobias is also supervised by Professor Declan Murphy and Dr Nicolaas Puts from King’s IoPPN, who are investigators in the study. Professor Sir Simon Baron-Cohen and Dr Carrie Allison at the Autism Research Centre at the University of Cambridge are collaborators and external advisors.

“I am delighted that COMPASS Pathways is supporting our investigations into the brain science of neurodiversity."

“Our long-term goal is to provide more and better tailored choices for autistic people and those with related conditions. Before embarking on clinical trials, we need to really understand brain mechanisms in autistic people,”
said professor Grainne McAlonan, King’s IoPPN

Professor McAlonan has previously led other studies in autism at King’s IoPPN. Klara, a participant on an earlier study, said: “My son and I both have autism, and this can be challenging at times. I’m pleased that researchers are looking into what makes an autistic brain different from a neurotypical one.

“It gives me hope that in the future, we might uncover new ways to support people and families who may need help, and that society becomes more accepting of people who are neurodiverse.”

Dr Guy Goodwin, Chief Medical Officer, COMPASS Pathways, said: “We are pleased to fund this innovative research, the first of its kind using psilocybin in autistic adults. We hope that this study improves understanding of how the serotonin system is involved in autism."

“For autistic people who are seeking treatment for symptoms that are causing distress, this research may be the first step in finding new options.”

About this psychopharmacology and ASD research news

Author: Patrick O’Brien
Source: King’s College London

 
Top