American journal of therapeutics
Burton J Tabaac, Kenneth Shinozuka, Alejandro Arenas et al.
14 citations
Psilocybin, the primary psychoactive compound in magic mushrooms, alters consciousness through the 5-HT2A receptor. This review consolidates findings on its pharmacology, safety, and clinical uses. Psilocybin is generally safe in controlled settings, with transient nausea and headache as common adverse effects. In the largest clinical trial, 7 cases of suicidal ideation occurred up to 12 weeks after a single 25 mg dose, and none of those cases responded to treatment. Selective serotonin reuptake inhibitors may blunt psilocybin's hallucinogenic effects but could enhance its antidepressant effects.
American journal of therapeutics
Kenneth Shinozuka, Burton J Tabaac, Alejandro Arenas et al.
12 citations
DMT, a serotonergic psychedelic and the main psychoactive component of ayahuasca, has been used by indigenous peoples for centuries. A double-blind, randomized controlled trial found that ayahuasca led to remission in 36% of patients with treatment-resistant depression within one week. Top-line results from a recent phase IIa trial showed that 57% of patients with major depressive disorder experienced remission 12 weeks after a single intravenous dose of DMT. DMT and ayahuasca appear physiologically and psychiatrically safe, though ayahuasca can cause transient vomiting. All clinical trials have had small sample sizes (≤34 participants). The hypothesis that endogenous DMT is released during dying remains debated.
American journal of therapeutics
Burton J Tabaac, Kenneth Shinozuka, Alejandro Arenas et al.
12 citations
Psychedelic drugs show promise for treating depression, anxiety, and other neuropsychiatric conditions, including treatment-resistant cases. Despite a mental health crisis affecting nearly one billion people worldwide, large double-blind randomized controlled trials remain scarce due to the long-standing Schedule I status of many psychedelics. Esketamine was approved for major depressive disorder in 2019. Two Phase III trials of MDMA indicate it is superior to existing treatments for post-traumatic stress disorder. However, larger trials of psilocybin (100+ participants) suggest its remission rate is 25%-29%, similar to the roughly 30% remission rate of antidepressants from the STAR*D trial. Clinicians should learn to integrate psychedelic therapy into care.
American journal of therapeutics
Bryce D Beutler, Kenneth Shinozuka, Burton J Tabaac et al.
11 citations
LSD, a hallucinogenic agent once used to augment psychoanalysis and treat alcohol use disorder, was banned in 1970 partly due to concerns it could cause or worsen mental illness. Adverse events in clinical trials are almost always mild and transient, with serious events like psychosis or suicidal ideation reported in very few or no participants. In trials for anxiety and depression linked to life-threatening illnesses, 77% of participants experience durable relief one year after treatment. A phase IIb trial (n=198) found 50% of participants remitted from generalized anxiety disorder after a single 100 μg dose. A meta-analysis of mid-20th century RCTs indicates single-dose LSD significantly improves alcohol use disorder.
American journal of therapeutics
Viviana D Evans, Alejandro Arenas, Kenneth Shinozuka et al.
10 citations
Ketamine, originally a dissociative anesthetic, is now used for treatment-resistant depression, major depressive disorder with suicidal ideation, and PTSD. A single intravenous infusion shows antidepressant effects within hours, with a weighted effect size of d = 0.96 at 24 hours (N = 518). It reduces PTSD symptom severity (Clinician-Administered PTSD Scale scores: -11.88 points) and suicidal ideation in emergency settings (Scale for Suicidal Ideation scores: -4.96 points) compared to midazolam. However, effects may subside within weeks, requiring repeated administrations. Risks include temporary cognitive impairment, cardiovascular instability, liver toxicity with prolonged use, and ketamine cystitis. Ketamine also reduces postoperative pain and opioid consumption.
American journal of therapeutics
Owen S Muir, Kenneth Shinozuka, Bryce D Beutler et al.
5 citations
This article reviews seven psychedelic compounds and their potential roles in medicine, using a SWOT (strengths, weaknesses, opportunities, threats) format to assess how they fit into the broader healthcare landscape. Historically, psychiatric conditions have been treated with small-molecule drugs that have limited effectiveness and many side effects. Psychedelic medicines may offer more potent and faster-acting treatments. However, the field is emerging: only esketamine is FDA-approved for depression, and the other compounds remain investigational, making the discussion prospective and imaginative.
American journal of therapeutics
Kenneth Shinozuka, Burton J Tabaac, Alejandro Arenas et al.
MDMA, once notorious as a party drug, has shown strong promise as a treatment for PTSD. Animal studies that suggested neurotoxicity used doses far above human levels, and human samples often included recreational users taking multiple substances. Phase III clinical trials found MDMA-assisted psychotherapy has an effect size of d = 0.7–0.91, two to three times larger than existing antidepressants, with 67%–71% of patients no longer meeting PTSD diagnostic criteria within 18 weeks. Other potential applications include alcohol use disorder and social anxiety. Most trials have been sponsored by MAPS, and more research is needed comparing it to nonpharmacological treatments. FDA approval could come as soon as 2024.