• Psychedelic Drugs Welcome Guest
    View threads about
    Posting RulesBluelight Rules
    PD's Best Threads Index
    Social ThreadSupport Bluelight
    Psychedelic Beginner's FAQ
  • PD Moderators: Esperighanto | JackARoe |

Health DEPRESSION

mr peabody

Bluelight Crew
Joined
Aug 31, 2016
Messages
5,956
Location
Frostbite Falls, MN
wp1-02.jpg



Can psilocybin treat severe depression?

by Barbara Geller, MD | NEJM Journal | 3 Nov 2017

Neuroimaging findings predicted response with this hallucinogen at post-treatment week 5 and correlated with decreased depressive symptoms and heightened mystic feelings.

In 1970, the FDA categorized psilocybin as a Schedule 1 drug, largely because of its recreational uses, which include inducing spirituality and synesthesias (e.g., seeing music, hearing art). Recently, several trials of this serotonin 2A agonist have supported further research into its use for treatment-resistant major depressive disorder. The researchers administered psilocybin to 19 medication-free participants with MDD.

Significant decreases in depression occurred post-treatment; 47% of participants met response criteria at 5-week follow-up. On fMRI, blood flow decreased from baseline in temporal (including amygdala) and parietal areas, similar to previous reports. Decreased amygdala activity significantly correlated with improved depression scores and increased feelings of a mystic experience. On resting-state fMRI, connectivity between several cortical areas increased post-treatment, contrary to findings elsewhere. Treatment response at 5 weeks was predicted by increased connectivity post-treatment between the ventromedial prefrontal cortex and inferior parietal cortex and by decreased parahippocampal-prefrontal connectivity.

Both the increased connectivity on post-treatment resting-state fMRI and its predictive value were similar to findings for electroconvulsive therapy, supporting the current study's validity. Experimental options for treatment-resistant MDD include invasive procedures like deep brain stimulation, which requires implanting brain devices with possible long-term adverse effects. Thus, clinicians can tell patients with access to federally funded psilocybin trials that this is a reasonable, noninvasive approach. Further, patients need to know that psilocybin must be taken only in closely supervised research settings because of its capacity to induce unusual psychic experiences.​

https://www.jwatch.org/na45292/2017/...ere-depression
 
PS.jpg



I suffered severe depression since childhood until I tried psilocybin

I've tried prescription antidepressants and therapy. I'm proactive and intelligent, I have never taken recreational drugs, and I try not to abuse alcohol. A good friend told me about psilocybin mushrooms and said they might help. Although deeply skeptical, I felt like it was worth a shot, so I took them in a safe, controlled environment. The difference has been enormous. It's like having the volume turned down on part of my brain that seizes onto negativity, waking up the next day and feeling optimistic about the future for the first time.

-----

I suffer from moderate to severe depression. I recently started taking a low dose of psilocybin, which has definitely helped my depression. Mushrooms are great because they are non-addictive, have no side effects, and I have a built in anti-abuse mechanism in the form of built up tolerance.

It forces you to wait a couple of weeks before taking any more, and at a low dose that seems to be the right amount of time!

-----

Nothing helps quite so much as being fully rested, and taking the most minimal doses of psilocybin. I don’t particularly enjoy getting high, but a threshold dose, just enough to notice a slight peculiarity in the appearance of the world, shifts my mood tremendously. I find small, daily doses, for several weeks, seem much more effective than larger doses, less frequently. Low doses of psilocybin, once a day, for up to several weeks, leaves me in a fairly positive place for nearly a full quarter.

-----

I've had moderate to severe depression since 2007. I've tried therapy, all types of medicine, self medication, and everything else imaginable. Nothing has come close to helping me like psilocybin. I can 100% attest that psilocybin helps me with my depression for as long as 6 months after use.

-----

The benefits of psilocybin are amazing. Not only during trips, which can be life changing and eye opening experiences, but also in microdosing, to help me with the effects of depression and anxiety. Microdosing significantly helped me with many internal issues I was having.

-----

Being a veteran and someone who had a tough childhood I found myself very depressed and suicidal. Even when I began to sort my life out, gave up alcohol and got myself fit again I still had a pain in my heart that left me feeling like ending my life. I stumbled across information on how psychedelics had help others with these feelings. After much research I decided to try mushrooms. to cut a long story short after the first journey I can with hand on heart say that it took me to a place of love that removed these negative feelings and the pain. These feelings have never returned.

-----

I have suffered from depression plus alcoholism with two deep bouts which led to many weeks out of work. Through the use of magic mushrooms I was able to recover from both, without the use for any antidepressants or CBT. Psychedelics work!

-----

Psilocybin is the only thing that's ever helped me. Self-medicating with psilocybin has saved my life twice, given me hope, and helped me see that I am connected, not isolated. Nothing medically prescribed by my GP has helped - just made it worse, numbed out and dumbed down, merely existing. I need this medicine in a legitimate clinical setting.

-----

I have experienced the healing benefits of psilocybin first hand. Dealing with depression has been a life-long struggle for me, and since taking psilocybin, I have experienced a significant change in my way of thinking and behaving. Microdosing especially helps me to break my habits and rusty old thought patterns.​

^^
https://psychedelicsociety.org.uk/pe...ession-anxiety
 
Last edited:
tingri-everest-base-camp-trek.jpg



Microdosing LSD for Treatment-Resistant Depression

by Sherry Amatenstein LCSW | Third Age

For years Rachel found herself battling a recurrent and noxious depression. She tried Zoloft but it had little effect. Nor did regular psychotherapy. In 2010 the then 45-year-old, a life coach, yoga devotee, and single mother began contemplating hallucinogens. She’d tried an LSD tab decades before at a music festival and found the 20-hour experience “intense but scary.”

However, her research into the efficacy of microdosing LSD (between 1 and 10 micrograms, below one/tenth of a regular dose) under controlled conditions convinced her to try this unorthodox “treatment.”

“The idea is to produce subtle changes in cognitive function without having to enter that world of hallucinogens where I experienced the walls collapsing in on me. Swallowing a few drops I put on a mint didn’t seem too risky. Yes, this was crude and unscientific but the protocol is very new.”

For five years Rachel microdosed LSD every three days. Afterward she typically did yoga or meditated. “I wasn’t taking it and going to a party or kite-surfing afterward! And I always waited to dose until my daughter left for school.” She finished, “It’s not like drinking alcohol or smoking pot. LSD made me very lucid and very sharp.”

The lucidity helped her combat the “emotionally cancerous mental loops in my head and find more joy.” Three years after stopping she still feels clarity and joy. But, she cautions, “Everyone has to make her own decisions about giving LSD a try.”

Ayelet Waldman’s 2017 article How Microdosing Made a Mega Difference in My Mood, My Marriage and My Life is an eye-and-mind-opening look at this controversial drug as a tool to achieve emotional well-being. And Michael Pollan’s just-released How to Change Your Mind: What the New Science of Psychedelics Teaches Us About Consciousness, Dying, Addiction, Depression, and Transcendence is not just a story of personal experimentation, but also a deep dive into the revolution occurring in the scientific and academic communities about psychedelics as healing agents.

However, caveat emptor. What is billed as the first comprehensive study about the potential effects of LSD microdosing is in the early stages.

In the meantime, Dr. Gladys Frankel, a NYC-based clinical psychologist who has been on the faculty of Weill Cornell College of Medicine, is among the many mental health practitioners urging caution. She says flatly, “Microdosing is a horrible idea. I have had patients who have been fried after one dose. A patient would look at a door and see the wood grain flowing, moving all of the time, years later! For people who have a vulnerability to schizophrenia, this can potentiate it.”

Julie Barron LPC offers an invaluable perspective on this issue. Founder of the Michigan Psychedelic Society, Barron, who has a Masters in Transpersonal Counseling Psychology explains, “When I was much younger I was very interested in psychedelics and studied at Naropa University where I was taught how to do therapy while in an altered state of consciousness.” Years later, she was in the midst of a depression for which she was both in talk therapy and on a cocktail of drugs – sleeping meds, pills for anxiety and depression. This regimen was having a detrimental effect on her life. So she began to microdose. “It had and has a huge positive impact. I was able to stop the pharmaceuticals.”

Clients come to her for advice on microdosing. “I can’t supply the drug but I’ll do therapy with them and share education and safety advice. Over all, I’m the feedback person. They’ll report, ‘I tried this, and such was my experience. What should I try next?’” says Julie. “I am very clear, it’s a personalized process. There is no one size fits all microdose strategy.” Indeed, sometimes Julie microdoses every day for weeks on end. Other times her protocol is every other day; sometimes once a month.

“Someone who hasn’t tried psychedelics can’t really help others. We are not a society that understands this from normal experience. I help people learn how to integrate microdosing into everyday life,” Julie says.​

https://thirdage.com/considering-mic...ad-this-first/
 
image.jpg



Are magic mushrooms the answer to depression?

by Josh Jacobs | The Guardian | 10 Jun 2019

New trials have shown the drug psilocybin to be highly effective in treating depression, with Oakland the latest US city to in effect decriminalise it last week. Some researchers say it could become ‘indefensible’ to ignore the evidence – but how would it work as a reliable treatment?

Lying on a bed in London’s Hammersmith hospital ingesting capsules of psilocybin, the active ingredient of magic mushrooms, Michael had little idea what would happen next. The 56-year-old part-time website developer from County Durham in northern England had battled depression for 30 years and had tried talking therapies and many types of antidepressant with no success. His mother’s death from cancer, followed by a friend’s suicide, had left him at one of his lowest points yet. Searching online to see if mushrooms sprouting in his yard were the hallucinogenic variety, he had come across a pioneering medical trial at Imperial College London.

Listening to music and surrounded by candles and flowers in the decorated clinical room, Michael anxiously waited for the drug to kick in. After 50 minutes, he saw bright lights leading into the distance and embarked on a five-hour journey into his own mind, where he would re-live a range of childhood memories and confront his grief. For the next three months, his depressive symptoms waned. He felt upbeat and accepting, enjoying pastimes he had come to feel apathetic about, such as walking through the Yorkshire countryside and taking photographs of nature.

“I became a different person,” says Michael. “I couldn’t wait to get dressed, to get into the outside world, to see people. I was supremely confident – more like I was when I was younger, before the depression started and got to its worst.”

The trial, finished in 2016, was the first modern study to target treatment-resistant depression with psilocybin, a psychedelic drug naturally occurring in around 200 species of mushroom. To varying degrees, Michael and all 18 other participants saw their symptoms reduce a week after two treatments, including a high, 25mg dose. Five weeks later, nine out of 19 patients found that their depression was still significantly reduced (by 50% or more) – results that largely held steady for three months. They had suffered from depression for an average of 18 years and all had tried other treatments. In January this year, the trial launched its second stage: an ambitious effort to test psilocybin on a larger group and with more scientific rigour (including a control group, which Michael’s study lacked), comparing the drug’s performance with escitalopram, a common antidepressant. The team has now treated about a third of the 60 patients and say that early results are promising for psilocybin.

Imperial’s current work is among a string of new studies that a group of professors, campaigners and investors hope will lead to psilocybin’s medical approval as a transformative treatment. Others soon to begin include an 80-person study run by Usona Institute, a Wisconsin-based medical non-profit, and a trial at King’s College London, as well as a 216-person trial that is already under way around the US, Europe and Canada, managed by the London-based life sciences company Compass Pathways. Robin Carhart-Harris, head of Imperial’s Centre for Psychedelic Research and a Compass scientific adviser, believes psilocybin could be a licensed medicine within five years, or potentially even sooner. “By about that point,” he says, “it would be like an irresistible force, and indefensible to ignore the weight of the evidence.”

Psilocybin mushrooms have been part of religious rituals for thousands of years. The Aztecs of Mexico referred to the mushroom as teonanácatl, or “God’s flesh”, in homage to its believed sacred power. In 1957, Albert Hoffman, a Swiss chemist working for the pharmaceutical company Sandoz, isolated psilocybin from the mushroom. Fifteen years earlier, he had accidentally ingested LSD, left work feeling dizzy, and experienced its psychedelic effects when he got home. During the 1960s, Sandoz sold psilocybin and LSD for research in medical trials, but the substances were soon outlawed after they became associated with the 60s counterculture.

Psilocybin remains in the most restricted category today under the UN Convention on Psychotropic Substances, the US 1970 Controlled Substances Act and the 1971 UK Misuse of Drugs Act, among others. David Nutt, a professor of neuropsychoparmacology at Imperial, who is overseeing the current trials, disputes the evidence for this, saying that heavily restricting the drug (and other psychedelics) has hindered research and propelled “lies” about its risks and medical potential. For him, the decision is “one of the most atrocious examples of the censorship of science and medicine in the history of the world”.

If successful, the new wave of research may continue to change psilocybin’s reputation after decades of prohibition. Carhart-Harris believes the drug offers a better and more comprehensive treatment than current antidepressants, and that it could well be a powerful new therapy for a host of other mental illnesses, including anxiety and food disorders. A 2016 Johns Hopkins University study of 51 patients with life-threatening cancer showed high doses of psilocybin significantly reduced end-of-life depression and anxiety for six months in 80% of cases, and helped patients accept death; a New York University study that year showed similar results. Current trials are looking further at psilocybin’s potential for reducing smoking addiction and alcohol dependency, after initial pilots yielded powerful results. (Johns Hopkins researchers showed in a small study, for example, that 80% of heavy smokers had not smoked for a least a week, six months after psilocybin treatment.)

Carhart-Harris thinks part of the reason the drug has been effective in treating depression in trials so far is that it can help people see their lives more clearly. When watching patients tripping, he often feels as if they see a truer version of reality than the sober therapists guiding them: “It is almost like being in the presence of someone particularly wise, in terms of what comes out of their mouth.” It is unclear how much of the depression alleviation comes from the psychiatric support surrounding the treatment. Either way, several patients have sourced top-ups independently since the first trial, as their depression has returned.

Much about the neuroscience of psychedelics remains unknown, but fMRI scans of patients’ brains after taking psilocybin showed reduced blood flow and resting activity in the amygdala, which is often overactive in depression and anxiety. They also show looser connections between brain networks, which then reintegrate in what the Imperial team suggests is part of the brain “resetting” itself on psilocybin. This may explain why the drug drives some patients to rethink entrenched beliefs and break compulsive thought patterns and behaviours. Imperial researchers believe that psilocybin operates differently from most current treatments. If common antidepressants dull emotions to help people cope, they theorise, psilocybin works on our serotonin system to heighten emotional responses and encourage people to actively confront their depression, which can prompt enduring shifts in mind-set.

For 48-year-old university design technician Kirk Rutter, this is why psilocybin seems to work – and why he hopes it will become medically available. He sees the drug not as a silver bullet but as a medicine that shows patients deep truths and requires them to apply teachings of this kind. Some other treatments, such as cognitive behavioural therapy, also seek to reshape thinking patterns, often in conjunction with antidepressants, but for many the current options fail to work. More than 300 million people suffer from depression globally, according to the World Health Organization, but researchers say that many of the most serious cases do not respond to antidepressants.

Rutter was in this group, having tried counseling and two prescription medicines in the five years before the Imperial trial, as his depression worsened following his mother’s death. After psilocybin, he began to break cycles of catastrophic thinking and had the confidence to make profound life changes, such as selling his house and moving away from abusive neighbours, reorganising his finances and traveling for enjoyment after years of not leaving the country. He says of psilocybin: “It removes any barriers and allows you to process what you need to in an almost seductive way. You are inevitably and irresistibly drawn into it.” One week after the treatment, he noticed a feeling of optimism come back to his life. “Hell,” he thought, “I haven’t had this for a long time.”

Even psilocybin’s fiercest proponents agree that it will take more evidence of its effectiveness on larger groups in controlled settings, and investigation into potential adverse effects, before it can be unleashed as a medicine. Current trials exclude people with a family history of psychosis for fear that the drug could trigger latent schizophrenia. And there are questions about psilocybin’s impact. Some patients say they hardly experienced the psychedelic effects, while others such as Michael had strong reactions to lower doses but less to higher ones. James Rucker, who worked on the first Imperial study and now directs psilocybin trials at King’s College London, remains agnostic about the drug as a reliable treatment.

“It’s an illusion that we know so much about psilocybin,” says Ekaterina Malievskaia, co-founder of Compass, which hopes to sell the drug as part of an approved treatment. “We really don’t. We know it can cause profound personal experiences; it can also cause all sorts of complications.”

But Malievskaia hopes that the Compass trials will provide the evidence needed to get the drug medically approved for treatment-resistant depression. She founded the company with her husband, George Goldsmith, three years ago, after her son’s severe depression and OCD got progressively worse while he was being treated with traditional antidepressants in a top US hospital. He later recovered with the help of psilocybin therapy, and the company says it has now attracted around £28m in funding, including from the venture capitalist Peter Thiel, and has applied to patent a process to make psilocybin at scale. Some former Compass associates fear the company seeks to monopolise the psilocybin market and control medical access, criticisms that were aired last year by the US business website Quartz, although Malievskaia denies this.

There are already signs that authorities may be beginning to shift. In October, US regulators gave Compass’s treatment breakthrough therapy status, a designation given to new medicines that might improve treatments for serious conditions, which means authorities will expedite their review of evidence. That decision was followed this May with Denver’s vote to in effect decriminalise magic mushrooms, making it the first US city to do so, followed last week by a similar measure for several psychedelic plants in Oakland, California. Activists are pushing for a state-wide vote in Oregon next year on whether to legalise psilocybin for medical use. Meanwhile, Compass hopes to request marketing authorisation for the drug within three years, if its trials are successful. It is proceeding slowly, though, having treated around six people since trials began in January, and Malievskaia says the process could take a decade until approval. She aims to accelerate progress, with new treatment sites recently opened at Columbia University, as well as in New Orleans and the Netherlands, among others.

Licensing is not the only obstacle to the drug becoming a common medicine. Taken over multiple hours in clinical settings with expert guides, psilocybin therapy does not come cheap. The new Imperial treatments cost more than £2,000 each, including doctors and therapists, and many patients could need multiple treatments each year for continued benefits. Malievskaia would not comment on how much Compass would plan to charge, but says she wants to maximise how many people can access the drug. Carhart-Harris says psilocybin therapy would be significantly more expensive than antidepressants and potentially more than counselling. “There is a cold reality as to why selective serotonin reuptake inhibitors [antidepressants] dominate mental healthcare and that is that they are cheap,” he says.

The scientific, legal and commercial challenges may take years to be settled. But for many of the patients who have already been treated, and for some of the therapists guiding them, there is little doubt: it is only a matter of time before psilocybin and similar psychedelics reshape how we treat suffering – and understand our minds.

Forty-year-old operations manager Melissa Elwin is among them. After an unpleasant first treatment, in which she felt trapped, during her second psychedelic trip inside Hammersmith Hospital, she felt as though she had left her body and was seeing her problems objectively. Psilocybin helped her confront her depression, fueled by a difficult relationship and fraught breakup, and anxiety she had had since childhood. Under the drug, she started to find a resilience that has since helped her face her father’s death from dementia and a protracted legal battle with her ex-partner. Her descriptions of the trip are similar to the awe and unity Hoffman at times experienced on psychedelics while testing them: he saw in them a powerful ability to put our self and troubles in perspective.

“I was literally everywhere during my trip,” says Elwin. “In the most amazing nature scenes, like the orb of light twinkling through trees, in the ocean, in waterfalls. I had no recollection of time and I just wanted it to last for ever. For so long, I felt my depression was part of me, there was nothing I could do to change it. The antidepressants only made me feel drowsy and stopped me caring about things. This made me completely break my mental shackles. I returned to work and I was euphoric. I felt: 'I can do this, I can change my situation.'
 
Last edited:
SHARPEN.jpg



Ketamine hailed as 'a miracle for treating severe depression'

by Sara Solovitch | Washington Post

It was November 2012 when Dennis Hartman, a Seattle business executive, managed to pull himself out of bed, force himself to shower for the first time in days and board a plane that would carry him across the country to a clinical trial at the National Institute of Mental Health (NIMH) in Bethesda.

After a lifetime of profound depression, 25 years of therapy and cycling through 18 antidepressants and mood stabilizers, Hartman, then 46, had settled on a date and a plan to end it all. The clinical trial would be his last attempt at salvation.

For 40 minutes, he sat in a hospital room as an IV drip delivered ketamine through his system. Several more hours passed before it occurred to him that all his thoughts of suicide had evaporated.

"My life will always be divided into the time before that first infusion and the time after," Hartman says today. "That sense of suffering and pain draining away. I was bewildered by the absence of pain."

Ketamine has been around since the early 1960s. It is a staple anesthetic in emergency rooms, regularly used for children when they come in with broken bones and dislocated shoulders. Its an important tool in burn centers and veterinary medicine, as well as a notorious date-rape drug, known for its power to quickly numb and render someone immobile.

Since 2006, dozens of studies have reported that it can also reverse the kind of severe depression that traditional antidepressants often don't touch. The momentum behind the drug has now reached the American Psychiatric Association, which, according to members of a ketamine task force, seems headed toward a tacit endorsement of the drug for treatment-resistant depression.

Experts are calling it the most significant advance in mental health in more than half a century. They point to studies showing ketamine not only produces a rapid and robust antidepressant effect; it also puts a quick end to suicidal thinking.

Traditional antidepressants and mood stabilizers, by comparison, can take weeks or months to work. In 2010, a major study published in JAMA, the journal of the American Medical Association, reported that drugs in a leading class of antidepressants were no better than placebos for most depression.

A growing number of academic medical centers, including Yale University, the University of California at San Diego, the Mayo Clinic and the Cleveland Clinic, have begun offering ketamine treatments off-label for severe depression, as has Kaiser Permanente in Northern California.

The next big thing?

"This is the next big thing in psychiatry," says L. Alison McInnes, a San Francisco psychiatrist who has enrolled 58 severely depressed patients at Kaiser's San Francisco clinic. She says her long-term success rate of 60 percent for people with treatment-resistant depression who try the drug has persuaded Kaiser to expand treatment to two other clinics in the Bay Area. The excitement stems from the fact that its working for patients who have spent years cycling through antidepressants, mood stabilizers and various therapies.

"Psychiatry has run out of gas," she says. "There are a significant number of depressed people who don't respond to antidepressants, and we've had nothing to offer them other than cognitive behavior therapy, electroshock therapy and transcranial stimulation."

McInnes is a member of the APAs ketamine task force, assigned to codify the protocol for how and when the drug will be given. She says she expects the APA to support the use of ketamine treatment early this year.

The guidelines, which follow the protocol used in the NIMH clinical trial involving Hartman, call for six IV drips over a two-week period. The dosage is very low, about 1/10 of the amount used in anesthesia. And when it works, it does so within minutes or hours.

"It's not subtle," says Enrique Abreu, a Portland, Ore., anesthesiologist who began treating depressed patients with it in 2012. "It's really obvious if it's going to be effective. And the response rate is unbelievable. This drug is 75 percent effective, which means that three-quarters of my patients do well. Nothing in medicine has those kind of numbers."

So far, there is no evidence of addiction at the low dose in which infusions are delivered. Ketamine does have one major limitation: Its relief is temporary. Clinical trials have found that relapse usually occurs about a week after a single infusion.

Ketamine works differently from traditional antidepressants, which target the brains serotonin and noradrenalin systems. It blocks N-methyl-D-aspartate (NMDA), a receptor in the brain that is activated by glutamate, a neurotransmitter.

In excessive quantities, glutamate becomes an excitotoxin, meaning that it overstimulates brain cells.

"Ketamine almost certainly modifies the function of synapses and circuits, turning certain circuits on and off," explains Carlos Zarate, NIMH chief of neurobiology and treatment of mood disorders, who has led the research on ketamine. "The result is a rapid antidepressant effect."

Rapid effect

A study published in the journal Science in 2010 suggested that ketamine restores brain function through a process called synaptogenesis. Scientists at Yale University found that ketamine not only improved depression-like behavior in rats but also promoted the growth of new synaptic connections between neurons in the brain.

Even a low-dose infusion can cause intense hallucinations. Patients often describe a kind of lucid dreaming or dissociative state in which they lose track of time and feel separated from their bodies. Many enjoy it; some dont. But studies at NIMH and elsewhere suggest that the psychedelic experience may play a small but significant role in the drugs efficacy.

"It's one of the things that's really striking," says Steven Levine, a Princeton, N.J., psychiatrist who estimates that he has treated 500 patients with ketamine since 2011. "With depression, people often feel very isolated and disconnected. Ketamine seems to leave something indelible behind. People use remarkably similar language to describe their experience: a sense of connection to other people, a greater sense of connection to the universe."

Although bladder problems and cognitive deficits have been reported among long-term ketamine abusers, none of these effects have been observed in low-dose clinical trials. In addition to depression, the drug is being studied for its effectiveness in treating obsessive-compulsive disorder, post-traumatic stress disorder, extreme anxiety and Rett syndrome, a rare developmental disorder on the autism spectrum.

Booster treatments

The drugs fleeting remission effect has led many patients to seek booster infusions. Hartman, for one, began his search before he even left his hospital room in Bethesda.

4 years ago, he couldn't find a doctor in the Pacific Northwest willing to administer ketamine. "At the time, psychiatrists hovered between willful ignorance and outright opposition to it," says Hartman, whose depression began creeping back a few weeks after his return to Seattle.

It took nine months before he found an anesthesiologist in New York who was treating patients with ketamine. Soon, he was flying back and forth across the country for bimonthly infusions.

Upon his request, he received the same dosage and routine he received in Bethesda: six infusions over two weeks. And with each return to New York, his relief seemed to last a little longer. These days, he says that his periods of remission between infusions often stretch to six months. He says he no longer takes any medication for depression besides ketamine.

"I don't consider myself permanently cured, but now its something I can manage," Hartman says, "like diabetes or arthritis. Before, it was unmanageable, it dominated my life
and prevented me from functioning."


In 2012 he helped found the Ketamine Advocacy Network, a group that vets ketamine clinics, advocates for insurance coverage and spreads the word about the drug.

And word has indeed spread. Ketamine clinics, typically operated by psychiatrists or anesthesiologists, are popping up in major cities around the country.

Levine, for one, is about to expand from New Jersey to Denver and Baltimore. Portland's Abreu recently opened a second clinic in Seattle.

Depression is big business. An estimated 15.7 million adults in the United States experienced at least one major depressive episode in 2014, according to the NIMH.

"There's a great unmet need in depression," says Gerard Sanacora, director of the Yale Depression Research Program. "We think this is an extremely important treatment. The concern comes if people start using ketamine before CBT [cognitive behavioral therapy] or Prozac. Maybe someday it will be a first-line treatment. But we are not there yet."

https://www.washingtonpost.com/nati...e73862-b490-11e5-a76a-0b5145e8679a_story.html
 
Last edited:
SP.jpg

Sgt. Pepper

Microdosing for Depression

Is microdosing helpful for treating depression? Join Dr. Erica Zelfand as we explore healing depression through psychedelic medicine.

by Erica Zelfand, ND | Psychedelic.Support

Matias’s appointment fell on Valentine’s Day that year. During the visit, he stared at the wall behind my head and admitted he had been having “those thoughts” again. That is to say, our code for suicidal ideation.

Matias had tried many things to get relief from his major depressive disorder (MDD). This included too many pharmaceutical antidepressants to list here, a couple of anti-psychotic medications, a beta blocker, an intensive outpatient program (IOP) at the local hospital, and weekly therapy. The medications made him feel “foggy” more than calm. Nor did they do much to change his PHQ-9 depression scores. Meanwhile, it didn’t help that today was a holiday that celebrated romantic, partnered love. Thus highlighting Matias’ single status. Matias felt at the end of his rope.

Just a few days later, however, Matias sent me this message: “This is the best I have felt in months. Could one drop really have such an effect?” He went on to explain that at the suggestion of a friend, he had taken a microdose of LSD. A 10 microgram dose to be precise.

So, Matias isn’t the only person who has turned to microdosing in the hope of getting relief from a mood disorder. A 2018 study of 1,102 people who had microdosed found that 40% of them did it specifically to try and improve their mental health. A 2020 survey found that 44% of those microdosing psilocybin or LSD for mental health reasons reported their mental health was much better. (21% of these individuals started microdosing to help their depression, and 7% were doing it for anxiety).

Microdosing for depression, self-reported success

Most of the studies on microdosing are based on surveys completed online by individuals who have tried microdosing themselves. While this method of research is by no means the scientific gold standard of the double blind, controlled randomized trial we like to see in drug research, it still allows us to understand people’s motivations for trying microdosing and their perceived results.

Nonetheless, based on these self-report studies, many people who try microdosing say they notice significant improvements in their mood with reports of less perceived depression, lower stress levels, decreased trauma triggering, and improved energy and focus.

While we cannot say for certain that microdosing helps with depression, the data currently available certainly implies that low doses of psilocybin and LSD may indeed help in some cases.

Does microdosing work better than conventional prescription antidepressants?

But is microdosing as effective as conventional pharmaceutical antidepressant drugs like fluoxetine (Prozac) in the treatment of mental health disorders? Yes – according to one small 2019 study. In this study, individuals age 18 and up completed an online questionnaire focusing on mental health and answered questions about the various treatments they’d tried in the past and how well (or poorly) they worked.

Of the people who completed the questionnaire, 7 percent (or 410 individuals) had a diagnosis or one or more mental health and/or physiological disorders. (*A physiological disorder is an illness that interferes with the normal, healthy functions of the body. Examples of physiological conditions include diabetes, asthma, Parkinson’s, cancer, and rheumatoid arthritis.) Their responses showed a clear pattern: these people felt that microdosing had worked significantly better than conventional prescription medications for a variety of health conditions, including depression, ADD/ADHD, and anxiety disorders.

In the case of Matias, a number of his friends had told him that they didn’t think his prescription medications were helping. They gently told him that he didn’t seem any happier or functional. He seemed “flat and spacey” on the other hand and suggested he mention it to his prescriber. After two weeks of microdosing, however, Matias felt energetic enough to meet up with these same friends for a picnic. During the meal, his best friend commented that Matias seemed better that day. “I’ve been trying microdosing,” Matias confessed. “It’s working, bro, keep going,” his friend replied, “I feel like I’m catching a glimpse of the Matias I used to know, of the guy you were before.”

An unexpected microdosing perk

Another perk of microdosing is that it seems to combine safely with most other psychiatric medications – meaning that individuals do not have to stop their antidepressant or anxiolytic medications before they give microdosing a try (the one possible exception being lithium) [8]. Furthermore, people often report that after a few months of microdosing they are able to easily taper down to lower doses of their pharmaceutical antidepressant and anxiolytic medications – or wean off them entirely.

That’s exactly what happened with Matias. He gradually weaned off of all psychiatric prescription medications within a few months of starting microdosing (with the support of his prescriber). So now he’s grateful to be free of those pesky side effects and the plastic pill organizer that used to sit on his kitchen counter.

Does microdosing work better than larger psychedelic doses?

How does microdosing psychedelics measure up against taking higher, trip-inducing macrodoses of psilocybin or LSD? Again, the answer is not yet clear, but according to the reports of 410 people analyzed in a 2019 survey,[9] it depends on the condition. Microdosing and macrodosing seem to work about as well in treating physiological disorders (physical ailments).

When it comes to psychological conditions, however, people reported that macrodosing helped them more significantly than microdosing. Most importantly, this may be on account of the mystical experience element seen with psychedelic trips that is absent in the microdosing experience. In controlled clinical trials of depression, the degree of the mystical experience was related to depression symptom improvement.

After microdosing for a few months, Matias took a break. Then he noticed that after about 10 days he started “slipping” back into some of his old, dark ways of thinking – and his PHQ-9 depression scores reflected this. He joined his friends for a day on the beach, during which time the group ate psilocybin-containing mushrooms. Matias tells me that his trip on 3 grams of dried fungus that day was both challenging and beautiful. Moreover, he described the experience as “spiritual.” Whereas Matias used to constantly think about suicide, he reports that since his trip, “I think about it sometimes, but then I’m like, ‘Nah, no way am I actually gonna do that.’”

Microdosing for depression, in summary

There is a lot we do not know about microdosing psychedelics. The little we do know comes mainly from people’s reports about their subjective experiences. Based on that limited information, it seems that microdoses of psilocybin and LSD:​
  • Can likely be taken concurrently with conventional pharmaceutical antidepressants (with the potential exception of lithium);​
  • May help people gradually taper down their use of conventional medications;​
  • Maybe more effective than conventional pharmaceuticals in the treatment of depression, anxiety, ADD/ADHD, and other conditions;​
  • May work just as well as psychedelic macrodoses in the treatment of physiological conditions; and​
  • Might not be quite as effective as macrodoses (psychedelic trips with mystical experiences) in the treatment of psychological conditions like depression.​
As always, it’s important to weigh the risks and benefits of any new medical intervention – especially one that has yet to undergo rigorous controlled studies. But based on these initial findings, we are seeing an upsurge in studies being planned to evaluate microdosing for mood disorders.​
 
IMAGE.jpg



Powerful psychedelic improves depression in one hour

Psychedelic found to treat mental health conditions more efficiently than psilocybin, study.

by Molly Hanson | BIG THINK​
  • A survey study found that around 80 percent of people using the psychedelic 5-MeO-DMT in a ceremonial setting said that their depression or anxiety improved following its use.​
  • The "mystical" experience of drug trip might allow people to gain unique insight into themselves or their relationships and make positive life changes.​
  • While the substance is found in the poison of the Sonoran Desert Toad, researchers say there is no reason to disturb the toad because the synthetic version of 5-MeO-DMT is identical in its effect.​
A new, powerful — yet still relatively rare — hallucinogen called 5-MeO-DMT has made its way into United States psychedelic circles, and research is backing its use as an effective treatment for certain mental health conditions.

Said to be up to six-times more intense than its sensationalized cousin DMT, researchers have found strong evidence to suggest that 5-MeO-DMT could be used to treat anxiety, depression, and addiction more efficiently than psilocybin.

What is 5-MeO-DMT?

5-MeO-DMT, is an extremely potent natural psychedelic found in certain plants and the poisonous secretions of the Sonoran Desert Toad, also known as the Colorado River Toad. It can also be made synthetically in a lab.

Typically, the experience a person has after ingesting 5-MeO-DMT, a schedule 1 classified substance, is described as feeling unified with the universe or some holy, transcendent “other.” The perception of bright colors and recursive patterns are often associated with the experience. It can also lead to extreme nausea and confusion days after ingesting it.

Assistant Professor at Ohio State University Alan Davis, who is also affiliated with the Department of Psychiatry and Behavioral Sciences at John Hopkins University, has conducted two large-scale survey studies examining the use of 5-MeO-DMT in the general population and in a specific ceremonial group in the United States.

Despite reports dubbing it the “hottest new psychedelic” among trend setters in the United States, Davis’s research has found that the drug is still rare, and most people are using it for psycho-spiritual endeavors rather than for recreation. Typically, he says, it is used in a ritualistic setting with a specific process similar to what might be done during an ayahuasca ritual.

And, he emphasizes, it definitely isn’t a party drug.

“This is a very potent and powerful psychedelic substance that usually has an onset within seconds and a person is completely incapacitated,” he says. “They are in a whole different realm of consciousness for 20 to 60 minutes.”

Research in treating anxiety and depression

In a survey study of 362 adults, Davis found that when administered in a ceremonial group setting with a knowledgeable facilitator, approximately 80 percent of people said that their depression or anxiety is improved following the use of 5-MeO-DMT.

According to Davis, this is likely because of the type of “mystical” experience one has on the drug trip, which allows the person to gain new, novel insight into themselves or their relationships through a shift in consciousness.

“This information, these experiences, seem to be really powerful and profound and they seem to help people to change, and to make different choices in their life,” says Davis.

Interestingly, this fits in with research on other psychedelic substances such as psilocybin, which has also been found to have significant anti-depression and anti-anxiety effects. One of the major downsides to the potential use of psilocybin in a clinical setting is that the psychedelic experience lasts four to six hours. Tacking on an extra hour before to get ready and after to ensure the patient is ready to be discharged, psilocybin would mean a whole day of treatment. That will add up to a very expensive session if it is eventually approved for public use, according to Davis.

Enter 5-Meo-DMT


“One of the interesting things about 5-Meo-DMT is that the duration of effect is anywhere from 20 to 60 minutes,” says Davis. “You can start to imagine a world where if this was a medication, you could actually have someone there for more of a standard psychotherapy time frame and have an entire psychedelic healing experience.”

Because this treatment could more easily be scaled into our current mental health care, it would likely be more accessible to people who might benefit from the treatment. Currently, Davis is working with a larger team on creating a clinical trial with the aim to eventually look at the administration of the drug in a laboratory setting.

Although Davis’s team has heard of potential risks involved with use of the drug, in part because of instances of it being mis-administered, he says that the data indicates that in the right setting where facilitators pay proper attention to people’s well-being, users are having mostly positive experiences.

As far as researchers know, the only animal on Earth that produces the chemical compound is the Sonoran Desert Toad, although it is also found in some plant species.

But the mystical psychedelic association with the toad has facilitated an ecologically harmful market for the amphibian’s poisonous secretions. This has led researchers to strongly condemn the practice of harvesting the toads for the compound.

According to local Tucson naturalist Robert Villa, the toad produces is milky white poison as a defense mechanism, so there is no humane way to obtain it. People in the Sonoran Desert region, where the toad is native, have noticed a decline in the amphibians’ numbers likely due to the psychedelic community’s demand for 5-MeO-DMT.

“Traumatizing an animal (or plant) for personal benefit is fraught with ethical dilemmas,” Villa wrote in an email.

Faced with other threats to its habitat, the psychedelic blackmarket is one more problem the Sonoran Desert Toad doesn’t need. Davis stresses that there is no need to disturb the toads or their environments at all.

“What we’ve been able to show is that the synthetic version is no different in terms of the intensity or the positive effects of taking it compared to the toad,” says Davis. In fact, he found that most of the people he surveyed in his study were using the synthetic version of the drug.​
 
SHARPEN.jpg



Depression and grief wrecked a man's life—until he took psilocybin

by Aristos Georgiou | Newsweek

We are in a psychedelic renaissance, in which long-stigmatized drugs such as psilocybin—the psychoactive compound in magic mushrooms—and MDMA are being assessed in clinical trials and showing promise for the treatment of a host of mental health problems, ranging from depression to PTSD.

Last month, mental health care company Compass Pathways announced the results of a Phase IIb study—the largest psilocybin therapy trial ever conducted—that found the drug appears to be effective as a therapy for treatment-resistant depression.

Five years earlier in 2016, researchers at Imperial College London completed a small study that was the first trial to assess psilocybin as a treatment for this condition.

Imperial's pioneering study formed the basis for the U.S. Food and Drug Administration's designation of psilocybin as a "breakthrough therapy"—an action intended to expedite the development and review of drugs designed to treat serious or life-threatening conditions—and much of the subsequent research on this issue.

Among the participants in the 2016 study, published in The Lancet Psychiatry, was Kirk Rutter.

Five years later, Rutter, now 51, spoke to Newsweek about his experiences of the trial and its impact on his mental health. The conversation below has been edited for length and clarity.

How was your mental health in 2016?

I was suffering from very bad depression that was basically kicked off by the death of my mother. She was ill for some time. It was a terminal illness. My mother told me she had started to come to terms with dying and felt it might be some relief from the pain she was experiencing. And so I thought, foolishly, that I was quite prepared and it wouldn't impact me in a normal way, because I'd already done some grieving through dealing with her illness and supporting my dad, who was a full-time carer for her. I really thought that it would take some of the sting out of the grief.

But when it finally came, it was the opposite—it was like being hit by a truck. I got stuck in the grief. At the same time, I was living with really terrible neighbors who were above me. They would fight, they were alcoholics, they would smash things up. I had this oppressive presence and noise above me all the time. So, I didn't really have any peace at home. And then I'd go to work and, well—work is work. Then around a year after the anniversary of my mother's death, I ended both the relationship with my partner and a friendship. That was another big loss. I found it very difficult to be positive.

The treatment-resistant depression trial involves people who are depressed and have tried a few treatments that haven't worked. I tried some antidepressants and didn't really like the way they made me feel. I knew anyway that it wouldn't cure anything or sort anything out, it was just chemically altering how you felt. Deep down I didn't have a lot of faith in it because I knew it wasn't really working on the problem itself. And then I did a year of talk therapy. I think it helped in some ways, but I was still feeling kind of terrible. I was still being hit by the grief. And then the opportunity came to do the psilocybin trial.

So, I had a telephone screening with Imperial. They checked my notes to make sure I had had treatment and accepted me into the trial based on the screening. That was where the journey started.

Had you tried psychedelics before?

I was new to psilocybin and had never tried psychedelics before.

What was your view of psychedelic substances at the time?

I was worried about it. I remember walking through Camden [an area of London] and seeing the magic mushrooms there when they used to be on sale. I would think, 'Dangerous, stay away from that,' because of all the stuff that was in the media. You know, the kind of bulls*** stories about people jumping out of windows and stuff like that. So, I didn't have a positive view of it, really.

How many times did you receive the psilocybin during the trial?

Twice. There was a 10 milligram session, which was fairly psychedelic, and then there was a 25 milligram session, which was the more potent dose.

Before that there was a telephone screening, then a meeting in person that lasted about two or three hours. We talked about everything—what I could expect, what the issues would be, what could potentially come up, etcetera. I was very nervous. During the sessions I had a therapist either side of me and it was all underpinned by music.

The 10 milligram session was quite pleasant. It was nice, being relaxed and listening to the music. You're in a hospital, so I felt safe eventually, even though I was very anxious about it. It came on quite slow. I started seeing almost like an orange glow, just kind of flickering slowly and then it would get more and more intense. And then it was like going down a psychedelic tunnel on a toboggan. Nothing major really came up in the first session, although I was really blown away by hearing Indian instruments like the sitar. It just sounded absolutely amazing. So, that was that.

And then a week later, it was the 25 milligram dose. I was very nervous about that because I'd had the 10 milligram and that was quite potent. I thought, 'This is gonna blow my socks off.' But even with the 10 milligrams I thought this could be really dialled up—I knew that the colors are quite muted, for example, so, I was looking forward to it in a way.

In the end, it was very potent. It really penetrated me emotionally in a way that the 10 milligram dose didn't. The music kind of seeps into you, it gets into your pores. So, particularly sad music was quite moving, for example. And then I reflected a lot on situations with my mother and I started to see that the way I was hanging on to the grief … I was afraid to let go. I had a realization that you can let go of the grief and it doesn't mean you're letting go of the person. And that you can still have that connection without the grief poisoning you and keeping you in that place. Previously, I was worried that detaching from the grief or letting it go would almost be a betrayal or something like that. So, that was a good insight.

There were a few other things as well. I realized that I needed to make a connection with one or two people. I did that and it worked out quite well. I also told [the therapist] about these thoughts I had that go round and round. This rumination that was almost like a fixed record—this negative playlist. And that was broken.

It was quite a startling experience. It knocked me out of that hole and allowed me to start picking things up again. I needed to make some infrastructure changes though. As I said, my neighbors were kind of toxic, alcoholic criminals. So I realized I needed to get out of that situation. Mentally, I wasn't in a place where I could have done that beforehand. After the trial, I sold my flat and I bought a house because I didn't want to live underneath anyone. That was one big change that really was very helpful. I also moved in a more creative direction work-wise, which was very good.

I just think, generally, I started taking care of things I needed to. I still have the grief—not as bad as I did, it's still there—but I'm not feeling it all the time. So for me, it was really beneficial. It was overall a positive experience.

So would you say you experienced lasting changes from those two doses?

Yes, very much so. You have these insights and awareness of stuff. I think psychedelics are the difference between knowing something and then really absorbing it and feeling it.

What's your view on growing interest in psychedelic therapy?

I think it should be available. The efficacy of it looks good. It's been used for thousands of years. It's a very humane intervention.​
 
Top