SUBJECTIVE STUDIES SHOW
THE GLOW OF PALLIATIVES IS
REAL
(to those who believe in
palliatives)
ORGANIC food may be
mislabeled
There may be salmonella in
sprouts
Bacteria in farm raised
fish
And food studies are only analogies
to the application of drugs in our
system
We accept hemp for rope,caffeine in
coffee
We take pills as prescribed via
doctors
Multi-vitamins as New Age
remedies
Mushrooms have been used in
ceremonies
older than all official
histories."Supervised studies"now find
they may not harm our bodies.In
fact,they may alleviate depression.
Much as "marijuana refugees"say for the effect of hydroponics
Much as "marijuana refugees"say for the effect of hydroponics
upon the humble weed that is
used,abused,misused and sold medicinally.
Nothing new here.Fear subsides when no
casualties arise
More die by car and alcohol than ever
via peyote,mushrooms,marijuana.
Selectivity and more "supervised
studies"might validate subjective research
Weeds may not kill you,and mushrooms
may heal emotional damage.
Nothing here deserves penal
servitude.Tell that to your local police force...
Even in Colorado..
‘Magic’ Mushrooms Show Promise Against Depression In First-Ever Trial
There’s more to these little fungi than a trippy concert experience.
05/17/2016 01:15 pm ET | Updated 17 hours ago
2.6 K
- Anna Almendrala Senior Healthy Living Editor
Aeriform
& Maria Teijeiro via Getty Images
“Magic mushrooms,” the
recreational hallucinogen long associated with music festivals and hippies, may
also one day prove to have a powerful pharmaceutical effect for people with
treatment-resistant depression.
In a small pilot
study at the Center for Neuropsychopharmacology at Imperial College London,
more than half of participants who took psilocybin, the active compound in
psychedelic mushrooms, showed a marked improvement in their depression symptoms
while also demonstrating the compound’s safety in a supervised setting.
This is the first clinical trial
to use the active chemical compound in so-called “magic mushrooms” to treat
major depression. If the findings are confirmed in larger studies, it could mean
a change in the way we treat depression symptoms in those who don’t respond to
therapy and traditional medications, like selective serotonin reuptake
inhibitors.
What we knew before:
Mushrooms from the genus Psilocybe
contain psilocybin, which the human body breaks down into a substance called
psilocin. This psychedelic substance then crosses the blood-brain barrier and
binds to a specific serotonin receptor known as 5-HT2A, creating a profound
alteration of consciousness that has been described as a mystical event, a
spiritual journey or simply a “trip.” Psychedelic compounds in LSD, ayahuasca
and mescaline bind to this same receptor.
Human beings have been consuming
psychedelic mushrooms for
thousands of years because of this effect, but it wasn’t until the 1950s
that scientists began examining psilocybin’s
therapeutic properties in earnest.
Previous pilot studies have shown
that psilocybin could be a promising new way to treat mental health symptoms
like anxiety,
obsessive-compulsive
behavior and addiction.
Those worried about the compound’s effects on mental health needn’t
worry: Research shows that lifetime use of psychedelics like psilocybin is not an
independent risk factor for mental health problems.
Beyond binding with the 5-HT2A
receptor, scientists don’t really understand the chemical process that leads to
this psychedelic experience. It’s even less clear how having a mystical
experience might produce long-term mental health benefits, but there are at
least two theories, according to Dr. Stephen Ross, director of the Psychedelic
Research Group at NYU Langone Medical Center. He was not involved in the study,
but reviewed it.
In the first theory, the memory of
the “trip” — which can be a profound and extremely meaningful experience — could
have a strong psychological effect on people, lifting their moods for months at
a time. Alternatively, there may be a biological explanation: It’s possible the
binding of psilocin to the serotonin receptor sets off a cascade of yet-unknown
chemical reactions that persist for weeks or months.
The study details:
Six men and six women with
chronic, treatment-resistant, moderate to severe major depression consented to
take two different doses of psilocybin (10 mg and 25 mg), separated by one week.
There was no control group, and the participants and in what’s called an “open
label trial,” the investigators all knew that they were either taking or
administering psilocybin.
During the dosing sessions,
participants relaxed on a bed in a room with dim lighting and listened to music
through earphones. Supervisors monitored their blood pressure, heart rate and
the psychoactive effects of the compound intermittently for up to six hours
after they took the pills, while psychiatrists offered support but mostly let
patients have their own “inner journey,” as the study put it, without
interruptions.
None of the participants
experienced serious or unexpected negative side effects that required medical
intervention from the dosing, though some reported mild anxiety, confusion,
nausea or headache. The psychedelic effects peaked about two to three hours
after dosing and then became negligible after about six hours.
Most significantly, eight of the
12 patients responded extremely well to the psilocybin, meeting the criteria for
remission from depression one week after the two treatments. After three months,
five of them remained in remission, while another two continued to show
improvement in their depression symptoms compared to baseline. Overall, all 12
patients showed at least some improvement in their symptoms for up to three
weeks after the dose.
The results seem promising, but
there are some caveats. The overall positive response to the dosing treatment
could in part be chalked up to the fact that the participants actively sought
out the psilocybin trial and were probably expecting the medicine to work on
some level, creating a bias in favor of the intervention. Indeed, five of the
participants had already tried psilocybin at least once — one just six months
before the experiment, others ranging from 14 to 48 years prior.
This past experience with a drug
and its presumed positive effects could increase suggestibility and expectancy
in people, which could affect the results. Double-blind trials in which neither
patient nor therapist knows which intervention they received or administered, as
well as the inclusion of a control group, could address these issues in future
experiments.
What experts say:
These findings offer hope for the
estimated 10 to 30
percent of people with depressive symptoms that what’s known as
treatment-resistant depression — a condition that doesn’t respond to traditional
antidepressant medication and therapy. Indeed, before the experiment, the
participants reported that they had tried at least two unsuccessful courses of
traditional antidepressant medication. Eleven had received some kind of
psychotherapy in the past, and on average, the participants had experienced
depression for about 18 years.
The chronic, relentless nature of
this kind of depression is what makes the possibility of psilocybin so exciting,
and if the findings are confirmed in randomized, controlled trials down the
road, it would be a “historic, huge shift” in psychopharmacological treatment
for depression because of how fast it worked and how long the effect endured,
said Ross.
However, because the pilot was so
small and did not have a control group, there’s no way to tell if the impressive
and immediate improvement in depression symptoms was due to other factors in the
experiment.
“You cannot conclude from this
trial that psilocybin is a treatment for depression because there could be other
reasons people responded, including the psychotherapy treatment [that
accompanied the experimental treatment] and expectancy biases which can be part
of this placebo effect,” said Ross, who is conducting his own clinical trials on
psilocybin’s effects on cancer-related depression.
Still, the researchers deserve
praise for creating a safe framework for psilocybin research that protects
against anxiety, paranoia and long-term negative consequences, wrote Phil Cowen,
a depression researcher with the University of Oxford, in an accompanying
commentary in the medical journal Lancet. He also pointed out that psychedelic
experiences in general are “exquisitely sensitive to individual disposition” and
could vary vastly depending on who took the dose. In other words, the trips can
sometimes be negative and extremely scary for some people.
“The author Edna O’Brien describes
a petrifying LSD psychotherapy session with RD Laing, during which the famous
anti-psychiatrist metamorphosed into a rat,” Cowen wrote. “Patients with
treatment-resistant depression seeking psychological insight with a less
exciting trajectory might consider the slow route offered by traditional dynamic
psychotherapy.”
How this could affect you:
Psilocybin remains a
controlled substance in the U.S., which means it’s illegal to buy it for
personal use and very difficult to obtain for research purposes. But if the
preliminary findings from this pilot study are confirmed, it suggests that
patients who are screened thoroughly and properly prepared for the experience
can safely take doses of psilocybin alongside psychological support in the hopes
of a positive, safe experience that might decrease the symptoms
treatment-resistant depression — at least temporarily.
However, a lot more research needs
to be carried out before this treatment becomes a reality for the approximately
15.7
million Americans with depression. Ross estimates that it might be about 10
years before psilocybin becomes an FDA-approved mainstream treatment for
depression.
The next step, the researchers
write, would be to conduct a larger experiment with a control group that
received just contact with a therapist and/or a placebo.
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