Clinical Uses for Psychedelic Drugs
Missouri S&T’s Peer to Peer
Volume 1 | Issue 2
Article 1
May 2017
Clinical Uses for Psychedelic Drugs
Matthew Clarkson
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Clarkson, Matthew. 2017. "Clinical Uses for Psychedelic Drugs." Missouri S&T’s Peer to Peer 1, (2). https://scholarsmine.mst.edu/
peer2peer/vol1/iss2/1
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Clarkson: Clinical Uses for Psychedelic Drugs
CLINICAL USES FOR PSYCHEDELIC DRUGS
Clarkson 1
Matthew Clarkson
Psychology at Missouri University of Science and Technology
CLINICAL USES FOR PSYCHEDELIC DRUGS
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CLINICAL USES FOR PSYCHEDELIC DRUGS
Clarkson 2
Abstract
Throughout the last forty years, psychedelic drugs have been illegal in the United States.
Stigmatized due to the potential for abuse, the use of these drugs has been relegated to simple
criminal activity and research stagnated for those 40 years. Slowly, research has begun to pick up
as the restrictions begin to lift incrementally. However, the current restrictions are intense,
further limiting the amount of research conducted that can reveal the medical benefits of these
drugs. Through multiple studies, both open-label and double-blinded to show both feasibility and
efficacy, as well as the biological impact of the drugs, significant anxiolytic, antidepressant, and
anti-addictive effects of hallucinogens have been demonstrated. The medical use of these drugs
could have a lasting effect regarding substance abuse addictions, severe cases of anxiety, and
treatment resistant depression providing alternatives to current methods of treatment.
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Clarkson: Clinical Uses for Psychedelic Drugs
CLINICAL USES FOR PSYCHEDELIC DRUGS
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Clinical Uses for Psychedelic Drugs
Since the late 1960s, psychedelic drugs have been outlawed in the United States. Prior to
their ban, psychedelic drugs were thought to have significant medical uses, showing promise in
treating a broad array of psychological disorders. Because of their proposed medical uses,
psychedelic drugs were often studied prior to the ban. However, in the late 1960s, a large part of
the population began to abuse psychedelic drugs and because of this, scientific research
regarding psychedelics had been slowed. Although some of the barriers to the research and
medical use of psychedelic drugs have been lifted, they remain heavily stigmatized and
restricted, limiting the amount and the extensiveness of the research that can be conducted. As
the restrictions slowly start to lift, research on psychedelics has started to proceed. This research
has been conducted on lysergic acid diethylamide (LSD), psilocybin, and ayahuasca, a
hallucinogen originating from the Amazon region of South America. Throughout this paper,
hallucinogenic and psychedelic drugs will be used interchangeably to refer to drugs that have the
potential to induce hallucinations or an altered sense of reality. Typically, the hallucinations or
altered sense of reality are the goals of abuse of these drugs and cause the stigmatization of these
drugs. However, despite the ban on hallucinogens, the abuse of these drugs has not significantly
diminished and only serves to majorly limit the research allowed for these drugs. Current
research indicates that hallucinogens have medical benefits as shown through studies and
biological processes. The purported uses of psychedelics are as antidepressants, anxiolytics,
meaning antianxiety, and as anti-addictive drugs.
Biology
Outside of clinical trials, hallucinogens demonstrate potential efficacy in the treatment of mood
disorders. Using functional magnetic resonance imaging (fMRI) to scan the brain, psychedelic
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drugs exhibited effects correlated to a decrease in mood disorders. Hyperactivity in the medial
prefrontal cortex of the brain is associated with depression. With administration of psilocybin as
well as non-hallucinogenic-based treatments for depression, the medial prefrontal cortex
displays lessened activity and eventually leading to normalization. fMRIs also revealed that
amygdala activation resulting from threat related stimuli decreased with the use of psilocybin.
The amygdala plays a significant role in the creation of emotions and the hyperactivity of this
section of the brain due to negative stimuli has regularly been associated with negative mood
states in depressed patients. (Mahaptra, 2017, p. 55) The use of the fMRI to link the activity of
hallucinogenic drugs with a decrease in brain activity related to depression shows a biological
basis for clinical use of these drugs. Additionally, since both psychedelic drugs and traditional
methods of depression treatment created similar responses in the brain, the medical use of these
drugs is further supported.
In addition to the changes in brain activity, other biological factors also contribute to the
use of hallucinogens as medication. Mahapatra (2017) writes, “Downregulation of 5-HT 2A
receptors is purported to mediate antidepressant and antianxiety effects of antidepressants and
atypical antipsychotics…Because of the high binding affinity of psilocybin to the 5-HT 2A
receptor, its effects are thought to be mediated.” (p. 54) These receptors are responsible for
regulation of serotonin, a neurotransmitter. A deficit of this neurotransmitter can often lead to
depression. Furthermore, the 5-HT 2A receptors correspond to additional factors related to
depression. Idell (2017) explains that expression of 5-HT 2A receptors link to neuroinflammation.
(pg. 50) Heightened levels of neuroinflammation can lead to depression as well and is widely
regarded as a risk factor for depression. Psilocybin has the potential to regulate the expression of
5-HT 2A receptors and decrease inflammation in the brain. (Idell, 2017, p. 50) The potential for
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hallucinogens to reduce depression in patients further supports the proposal for the clinical uses
of these drugs.
Antidepressant/Anxiolytic
The proposed clinical use of psychedelic drugs revolves primarily around their use as
antidepressants. In a study consisting of 22 patients with depression were treated with LSD
weekly for 5-6 we (...truncated)