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

BACKGROUND: 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 pro...

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Autores principales: Huang, Joyce, Pham, Michelle, Panenka, William J., Honer, William G., Barr, Alasdair M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157591/
https://www.ncbi.nlm.nih.gov/pubmed/35664477
http://dx.doi.org/10.3389/fpsyt.2022.891512
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author Huang, Joyce
Pham, Michelle
Panenka, William J.
Honer, William G.
Barr, Alasdair M.
author_facet Huang, Joyce
Pham, Michelle
Panenka, William J.
Honer, William G.
Barr, Alasdair M.
author_sort Huang, Joyce
collection PubMed
description BACKGROUND: 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: 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: 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: Psilocybin demonstrated modest but significant effects on weight gain. Further study is recommended.
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spelling pubmed-91575912022-06-02 Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity Huang, Joyce Pham, Michelle Panenka, William J. Honer, William G. Barr, Alasdair M. Front Psychiatry Psychiatry BACKGROUND: 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: 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: 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: Psilocybin demonstrated modest but significant effects on weight gain. Further study is recommended. Frontiers Media S.A. 2022-05-18 /pmc/articles/PMC9157591/ /pubmed/35664477 http://dx.doi.org/10.3389/fpsyt.2022.891512 Text en Copyright © 2022 Huang, Pham, Panenka, Honer and Barr. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Psychiatry
Huang, Joyce
Pham, Michelle
Panenka, William J.
Honer, William G.
Barr, Alasdair M.
Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity
title Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity
title_full Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity
title_fullStr Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity
title_full_unstemmed Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity
title_short Chronic Treatment With Psilocybin Decreases Changes in Body Weight in a Rodent Model of Obesity
title_sort chronic treatment with psilocybin decreases changes in body weight in a rodent model of obesity
topic Psychiatry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9157591/
https://www.ncbi.nlm.nih.gov/pubmed/35664477
http://dx.doi.org/10.3389/fpsyt.2022.891512
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