Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity.

adiposity animal model obesity psilocybin psychedelic weight gain

Journal

Frontiers in psychiatry
ISSN: 1664-0640
Titre abrégé: Front Psychiatry
Pays: Switzerland
ID NLM: 101545006

Informations de publication

Date de publication:
2022
Historique:
received: 07 03 2022
accepted: 27 04 2022
entrez: 6 6 2022
pubmed: 7 6 2022
medline: 7 6 2022
Statut: epublish

Résumé

There are currently relatively few effective pharmacological treatments for obesity, and existing ones may be associated with limiting side-effects. In the search for novel anti-obesity agents, drugs that modify central serotonergic systems have historically proven to be effective in promoting weight loss. Psilocin, which is rapidly metabolized from psilocybin, is an agonist at multiple serotonin receptors. In the present study we assessed the effects of psilocybin and a positive control (metformin) on changes in body weight in a rat model of obesity. Five groups of adult male rats were pre-conditioned with a cafeteria diet until obese (>600 g) and then treated with either psilocybin (0.1, 1, or 5 mg/kg, i.p.), metformin (300 mg/kg, p.o.) or vehicle control. Treatments were for 27 consecutive weekdays, and body weights and high calorie food intake were recorded daily. Fasting glucose levels were recorded after 11 days of treatment. At the end of treatment rats completed a glucose tolerance test, and multiple fat pads were dissected out to assess adiposity. The medium dose psilocybin group had to be terminated from the study prematurely. Both the low and high dose psilocybin groups caused a significant decrease in changes in body weight compared to controls. The metformin group produced a greater decrease in change in body weight than either psilocybin groups or controls. Both high dose psilocybin and metformin decreased consumption of the high calorie diet, and exhibited decreased central adiposity. Psilocybin demonstrated modest but significant effects on weight gain. Further study is recommended.

Sections du résumé

Background UNASSIGNED
There are currently relatively few effective pharmacological treatments for obesity, and existing ones may be associated with limiting side-effects. In the search for novel anti-obesity agents, drugs that modify central serotonergic systems have historically proven to be effective in promoting weight loss. Psilocin, which is rapidly metabolized from psilocybin, is an agonist at multiple serotonin receptors. In the present study we assessed the effects of psilocybin and a positive control (metformin) on changes in body weight in a rat model of obesity.
Methods UNASSIGNED
Five groups of adult male rats were pre-conditioned with a cafeteria diet until obese (>600 g) and then treated with either psilocybin (0.1, 1, or 5 mg/kg, i.p.), metformin (300 mg/kg, p.o.) or vehicle control. Treatments were for 27 consecutive weekdays, and body weights and high calorie food intake were recorded daily. Fasting glucose levels were recorded after 11 days of treatment. At the end of treatment rats completed a glucose tolerance test, and multiple fat pads were dissected out to assess adiposity.
Results UNASSIGNED
The medium dose psilocybin group had to be terminated from the study prematurely. Both the low and high dose psilocybin groups caused a significant decrease in changes in body weight compared to controls. The metformin group produced a greater decrease in change in body weight than either psilocybin groups or controls. Both high dose psilocybin and metformin decreased consumption of the high calorie diet, and exhibited decreased central adiposity.
Conclusion UNASSIGNED
Psilocybin demonstrated modest but significant effects on weight gain. Further study is recommended.

Identifiants

pubmed: 35664477
doi: 10.3389/fpsyt.2022.891512
pmc: PMC9157591
doi:

Types de publication

Journal Article

Langues

eng

Pagination

891512

Informations de copyright

Copyright © 2022 Huang, Pham, Panenka, Honer and Barr.

Déclaration de conflit d'intérêts

WH has received consulting fees or sat on paid advisory boards for the Canadian Agency for Drugs and Technology in Health, AlphaSights, Guiepoint, in silico, Translational Life Sciences, Otsuka, Lundbeck, and Newron. WP was the founder and CEO of Translational Life Sciences, an early stage science company focused on psychedelic-based therapeutics. AB served as a consultant to Translational Life Sciences. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

Joyce Huang (J)

Department of Anesthesiology, Pharmacology and Therapeutics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.

Michelle Pham (M)

Department of Anesthesiology, Pharmacology and Therapeutics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.

William J Panenka (WJ)

Department of Psychiatry, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
British Columbia Mental Health & Substance Use Services Research Institute, Vancouver, BC, Canada.

William G Honer (WG)

Department of Psychiatry, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
British Columbia Mental Health & Substance Use Services Research Institute, Vancouver, BC, Canada.

Alasdair M Barr (AM)

Department of Anesthesiology, Pharmacology and Therapeutics, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada.
British Columbia Mental Health & Substance Use Services Research Institute, Vancouver, BC, Canada.

Classifications MeSH