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Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats

OBJECTIVE(S): As olanzapine has side effects such as weight gain and metabolic disorders, and alpha-mangostin has been shown to control metabolic disorders, the effects of alpha-mangostin on metabolic disorders induced by olanzapine were investigated in this study. MATERIALS AND METHODS: Obesity was...

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Autores principales: Ardakanian, Alireza, Ghasemzadeh Rahbardar, Mahboobeh, Omidkhoda, Farzaneh, Razavi, Bibi Marjan, Hosseinzadeh, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124543/
https://www.ncbi.nlm.nih.gov/pubmed/35655598
http://dx.doi.org/10.22038/IJBMS.2022.58734.13047
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author Ardakanian, Alireza
Ghasemzadeh Rahbardar, Mahboobeh
Omidkhoda, Farzaneh
Razavi, Bibi Marjan
Hosseinzadeh, Hossein
author_facet Ardakanian, Alireza
Ghasemzadeh Rahbardar, Mahboobeh
Omidkhoda, Farzaneh
Razavi, Bibi Marjan
Hosseinzadeh, Hossein
author_sort Ardakanian, Alireza
collection PubMed
description OBJECTIVE(S): As olanzapine has side effects such as weight gain and metabolic disorders, and alpha-mangostin has been shown to control metabolic disorders, the effects of alpha-mangostin on metabolic disorders induced by olanzapine were investigated in this study. MATERIALS AND METHODS: Obesity was induced in female Wistar rats by daily administration of olanzapine (5 mg/kg/day, IP, 14 days). Rats were divided into 6 groups:1) vehicle (control); 2) olanzapine (5 mg/kg/day); 3,4,5) olanzapine+ alpha-mangostin (10, 20, 40 mg/kg/day, IP); 6) alpha-mangostin (40 mg/kg/day). Weight changes were measured every 3 days and food intake was assessed every day. Systolic blood pressure, plasma levels of blood sugar, triglycerides, total cholesterol, HDL, LDL, leptin, oxidative stress markers (MDA, GSH), AMPK, and P-AMPK protein levels in liver tissue were assessed on the last day of the study. RESULTS: Administration of olanzapine significantly increased weight gain, food intake, blood pressure, triglycerides, LDL, blood sugar, leptin, and MDA in rat liver tissue and also decreased GSH, AMPK, and P-AMPK in liver tissue compared with the control group. Different doses of alpha-mangostin significantly reduced weight gain, food intake, systolic blood pressure, triglycerides, LDL, blood sugar, leptin, and MDA. Also, they significantly increased GSH, AMPK, and P-AMPK in liver tissue compared with the olanzapine group. CONCLUSION: Olanzapine increases leptin levels, food intake, and weight, induces oxidative stress, decreases the levels of AMPK and P-AMPK proteins in liver tissue, and causes metabolic disorders. But, alpha-mangostin reduces the negative effects of olanzapine by activation of AMPK.
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spelling pubmed-91245432022-06-01 Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats Ardakanian, Alireza Ghasemzadeh Rahbardar, Mahboobeh Omidkhoda, Farzaneh Razavi, Bibi Marjan Hosseinzadeh, Hossein Iran J Basic Med Sci Original Article OBJECTIVE(S): As olanzapine has side effects such as weight gain and metabolic disorders, and alpha-mangostin has been shown to control metabolic disorders, the effects of alpha-mangostin on metabolic disorders induced by olanzapine were investigated in this study. MATERIALS AND METHODS: Obesity was induced in female Wistar rats by daily administration of olanzapine (5 mg/kg/day, IP, 14 days). Rats were divided into 6 groups:1) vehicle (control); 2) olanzapine (5 mg/kg/day); 3,4,5) olanzapine+ alpha-mangostin (10, 20, 40 mg/kg/day, IP); 6) alpha-mangostin (40 mg/kg/day). Weight changes were measured every 3 days and food intake was assessed every day. Systolic blood pressure, plasma levels of blood sugar, triglycerides, total cholesterol, HDL, LDL, leptin, oxidative stress markers (MDA, GSH), AMPK, and P-AMPK protein levels in liver tissue were assessed on the last day of the study. RESULTS: Administration of olanzapine significantly increased weight gain, food intake, blood pressure, triglycerides, LDL, blood sugar, leptin, and MDA in rat liver tissue and also decreased GSH, AMPK, and P-AMPK in liver tissue compared with the control group. Different doses of alpha-mangostin significantly reduced weight gain, food intake, systolic blood pressure, triglycerides, LDL, blood sugar, leptin, and MDA. Also, they significantly increased GSH, AMPK, and P-AMPK in liver tissue compared with the olanzapine group. CONCLUSION: Olanzapine increases leptin levels, food intake, and weight, induces oxidative stress, decreases the levels of AMPK and P-AMPK proteins in liver tissue, and causes metabolic disorders. But, alpha-mangostin reduces the negative effects of olanzapine by activation of AMPK. Mashhad University of Medical Sciences 2022-02 /pmc/articles/PMC9124543/ /pubmed/35655598 http://dx.doi.org/10.22038/IJBMS.2022.58734.13047 Text en https://creativecommons.org/licenses/by/3.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License, (http://creativecommons.org/licenses/by/3.0/ (https://creativecommons.org/licenses/by/3.0/) ) which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Ardakanian, Alireza
Ghasemzadeh Rahbardar, Mahboobeh
Omidkhoda, Farzaneh
Razavi, Bibi Marjan
Hosseinzadeh, Hossein
Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats
title Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats
title_full Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats
title_fullStr Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats
title_full_unstemmed Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats
title_short Effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats
title_sort effect of alpha-mangostin on olanzapine-induced metabolic disorders in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9124543/
https://www.ncbi.nlm.nih.gov/pubmed/35655598
http://dx.doi.org/10.22038/IJBMS.2022.58734.13047
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