Ham-milton
Bluelighter
- Joined
- Jul 20, 2007
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Does anyone know more about the recreational potential of something like this?
WIKI FAAH inhibitor AD?
WIKI FAAH inhibitor AD?
N&PD Moderators: Skorpio | someguyontheinternet
"The results were similar to the effect we might expect from the use of commonly prescribed antidepressants, which are effective on only around 30 percent of the population," said Gobbi. "Our discovery strengthens the case for URB597 as a safer, non-addictive, non-psychotropic alternative to cannabis for the treatment of pain and depression."
I have yet to see any human tests of FAAH inhibitors, though they do appear to be antinociceptive in rats.
I'd rather try 2-octyl-gamma-bromoacetoacetone simply for the fact that it is endogenous.
I thought the efficacy of almost all (coincidentally) anti-depressants was usually put around 70%
Here is a quote about URB597.
"For me after first researchers it works perfectly as relax and sleep enhacer at the evening. After oral 1-2mg for my rat he was sleeping after 30min with nice morning , good funny moodalso his apetite went up! SO IT CAN BE GREAT FOR ANY KIND OF DEPRESIONS or "AFTER E" for fast recovery, +APETITE UP AFTER ANY STIMULATION !
After 5mg rat was sleeping really hard! Almost impossible to move and turn off light and tv in middle of night...really sleppy and lazy....at morning he was also lazy for 2-3hours after clock alarm. "
also, this person does have some incentive to be biased about it. FYI
I'm sure more reports will come in the next few weeks.
Stahl, for example says 67% of patients respond to any given AD, so that is about 70 percent. I can see the definition of respond and effective being quite different. This means, you can basically make up any definition and make outragious claims without actually lying.
First time I read about the depressing effects of chronic thc-use - mind you, in teen ladyrats. I've been told so by medics before and common sense pointed this negative effects out to me and others, but generally this waseasily dismissed by most weedsmokers as not applying to their holy sacrament. Drugs lead to all kinds of denial IMHO, I tend to be biased towards positive effects as well.We have recently shown that chronic THC administration in adolescent female rats induces subtle but lasting alterations in the emotional circuit ending in depressive-like behaviour at adulthood. Here we describe other relevant depressive-like symptoms present in these animals. Adult female rats pretreated with THC display passive coping strategy towards acute stressful situations as demonstrated by their behaviours in the first session of the forced swim test, develop a profound anhedonic state as demonstrated by the reduced consumption of palatable food and present a decrease in social functioning. Besides the emotional symptoms, adolescent exposure to THC induced a significant deficit in object recognition memory. Since it has been reported that deficits in adult hippocampal neurogenesis may underlie the cognitive dysfunction seen in depression, we then survey cell proliferation in the dentate gyrus of the hippocampus. Adolescent THC exposure significantly reduced the number of BrdU-positive cells in THC-treated rats as well as hippocampal volume. We suggest that this complex depressive-like phenotype is triggered by a long-lasting decrease in CB1 receptor functionality in specific brain regions. To test whether an increase in the endocannabinoid signalling could ameliorate the depressive phenotype, adult female rats pre-exposed to THC were injected with URB597 (0.3mg/kg ip) and then tested in behavioural assays. URB597 was able to reverse most depressive-like symptoms induced by adolescent THC exposure such as the passive coping strategy observed in THC exposed animals in the forced swim test as well as anhedonia and the reduced social activity. These results support a role for the endocannabinoid system in the neurobiology of depression and suggest the use of URB597 as a new therapeutic tool with antidepressant properties.
I'd rather try 2-octyl-gamma-bromoacetoacetone simply for the fact that it is endogenous.
I'd rather try 2-octyl-gamma-bromoacetoacetone simply for the fact that it is endogenous.