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Open AccessJournal ArticleDOI

Psychedelic medicines for mood disorders: current evidence and clinical considerations.

TLDR
For example, the authors found Serotonergic psychedelics have been found to modulate brain networks underlying various psychiatric disorders, as well promoting neurogenesis and neuroplasticity.
Abstract
Purpose of review Despite advances in treatment modalities for mood disorders over recent decades, further therapeutic options are still required. Increased research is occurring, with the pursuit of psychedelic-based pharmacotherapies for a range of mood disorders and other conditions. Recent findings Serotonergic psychedelics have been found to modulate brain networks underlying various psychiatric disorders, as well promoting neurogenesis and neuroplasticity. Randomized placebo-controlled trials have found psilocybin with psychological support effective at treating depression, including treatment-resistant depression; with emergent research also signalling N,N-dimethyltryptamine/ayahuasca also as a potential option for the treatment of depression. Lysergic acid diethylamide has been found to have anxiolytic effects, whereas 3,4-methylenedioxymethamphetamine (MDMA) has been used effectively to treat post-traumatic stress disorder (PTSD), with Phase III clinical trial evidence. Microdosing of psychedelics is a growing phenomenon that has shown benefits in some preclinical data; however, a recent self-directed controlled trial reported no evidence of improved mood. Summary Current research with medicinal psychedelics, usually as an adjunct to psychotherapy, has shown encouraging results in treating mood disorders. However, there are challenges regarding blinding and sample sizes remain small, and there have been no definitive Phase III studies (aside from MDMA for PTSD). Further work exploring novel formulations, interface with pharmacogenomics and the microbiome, and inflammatory pathways can be advised.

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Where do we go next in antidepressant drug discovery? A new generation of antidepressants: a pivotal role of AMPA receptor potentiation and mGlu2/3 receptor antagonism

TL;DR: The mechanism of action of these compounds suggests a strong glutamatergic component that involves the facilitation of AMPA receptor function, which appears to be relevant to the antidepressant pharmacology of this new class of drugs.
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Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity

TL;DR: Both high dose psilocybin and metformin decreased consumption of the high calorie diet, and exhibited decreased central adiposity, which demonstrated modest but significant effects on weight gain.
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Returning Wholeness to Health

TL;DR: A remarkable scope of articles from scientists and clinician scientists in diverse fields, representing the multifaceted dimensions of what it takes to create Whole Health are gathered together, including medicine, behavioral medicine, consciousness studies, education, finance, and political advocacy.
Journal ArticleDOI

Moderators of ayahuasca’s biological antidepressant action

TL;DR: In this paper , a set of acute parameters, namely emotional (depressive symptoms), cognitive (psychedelic experience), and physiological (salivary cortisol), recorded during an ayahuasca dosing session, modulated serum brain-derived neurotrophic factor (BDNF), serum cortisol (SC), serum interleukin 6 (IL-6), plasma C-reactive protein (CRP), and salivary Cortisol awakening response (CAR).
References
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Journal ArticleDOI

Interpreting scores on the Kessler Psychological Distress Scale (K10).

TL;DR: The aim is to provide normative data on the Kessler Psychological Distress Scale (K10), a scale that is being increasingly used for clinical and epidemiological purposes.
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TL;DR: Improved scoring and weighting approach of MCDA increases the differentiation between the most and least harmful drugs, however, the findings correlate poorly with present UK drug classification, which is not based simply on considerations of harm.
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Human hallucinogen research: guidelines for safety.

TL;DR: The unique history of human hallucinogens research is discussed, the risks of hallucinogen administration and safeguards for minimizing these risks are reviewed, and carefully conducted research may inform the treatment of psychiatric disorders, and may lead to advances in basic science.
Journal ArticleDOI

Psilocybin with psychological support for treatment-resistant depression: six-month follow-up.

TL;DR: Although limited conclusions can be drawn about treatment efficacy from open-label trials, tolerability was good, effect sizes large and symptom improvements appeared rapidly after just two psilocybin treatment sessions and remained significant 6 months post-treatment in a treatment-resistant cohort.