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Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin
BACKGROUND: Prescription of second-generation antipsychotic drugs (SGAs) to childhood/adolescent has exponentially increased in recent years, which was associated with the greater risk of significant weight gain and dyslipidemia. Statin is considered a potential preventive and treatment approach for...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325271/ https://www.ncbi.nlm.nih.gov/pubmed/32605639 http://dx.doi.org/10.1186/s40360-020-00427-0 |
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author | Liu, Xuemei Feng, Xiyu Deng, Chao Liu, Lu Zeng, Yanping Hu, Chang-Hua |
author_facet | Liu, Xuemei Feng, Xiyu Deng, Chao Liu, Lu Zeng, Yanping Hu, Chang-Hua |
author_sort | Liu, Xuemei |
collection | PubMed |
description | BACKGROUND: Prescription of second-generation antipsychotic drugs (SGAs) to childhood/adolescent has exponentially increased in recent years, which was associated with the greater risk of significant weight gain and dyslipidemia. Statin is considered a potential preventive and treatment approach for reducing SGA-induced weight gain and dyslipidemia in schizophrenia patients. However, the effect of statin treatment in children and adolescents with SGA-induced dyslipidemia is not clearly demonstrated. METHODS: To investigate the efficacy of statin interventions for reversing SGA-induced dyslipidemia, young Sprague Dawley rats were treated orally with either olanzapine (1.0 mg/kg, t.i.d.), simvastatin (3.0 mg/kg, t.i.d.), olanzapine plus simvastatin (O + S), or vehicle (control) for 5 weeks. RESULTS: Olanzapine treatment increased weight gain, food intake and feeding efficiency compared to the control, while O + S co-treatment significantly reversed body weight gain but without significant effects on food intake. Moreover, olanzapine treatment induced a slight but significant reduction in body temperature, with a decrease in locomotor activity. Fasting plasma glucose, triglycerides (TG), and total cholesterol (TC) levels were markedly elevated in the olanzapine-only group, whereas O + S co-treatment significantly ameliorated these changes. Pronounced activation of lipogenic gene expression in the liver and down-regulated expression of uncoupling protein-1 (UCP1) and peroxisome-proliferator-activated receptor-γ co-activator-1α (PGC-1α) in brown adipose tissue (BAT) was observed in the olanzapine-only group. Interestingly, these protein changes could be reversed by co-treatment with O + B. CONCLUSIONS: Simvastatin is effective in ameliorating TC and TG elevated by olanzapine. Modulation of BAT activity by statins could be a partial mechanism in reducing metabolic side effects caused by SGAs in child and adolescent patients. GRAPHICAL ABSTRACT: [Image: see text] |
format | Online Article Text |
id | pubmed-7325271 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-73252712020-06-30 Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin Liu, Xuemei Feng, Xiyu Deng, Chao Liu, Lu Zeng, Yanping Hu, Chang-Hua BMC Pharmacol Toxicol Research Article BACKGROUND: Prescription of second-generation antipsychotic drugs (SGAs) to childhood/adolescent has exponentially increased in recent years, which was associated with the greater risk of significant weight gain and dyslipidemia. Statin is considered a potential preventive and treatment approach for reducing SGA-induced weight gain and dyslipidemia in schizophrenia patients. However, the effect of statin treatment in children and adolescents with SGA-induced dyslipidemia is not clearly demonstrated. METHODS: To investigate the efficacy of statin interventions for reversing SGA-induced dyslipidemia, young Sprague Dawley rats were treated orally with either olanzapine (1.0 mg/kg, t.i.d.), simvastatin (3.0 mg/kg, t.i.d.), olanzapine plus simvastatin (O + S), or vehicle (control) for 5 weeks. RESULTS: Olanzapine treatment increased weight gain, food intake and feeding efficiency compared to the control, while O + S co-treatment significantly reversed body weight gain but without significant effects on food intake. Moreover, olanzapine treatment induced a slight but significant reduction in body temperature, with a decrease in locomotor activity. Fasting plasma glucose, triglycerides (TG), and total cholesterol (TC) levels were markedly elevated in the olanzapine-only group, whereas O + S co-treatment significantly ameliorated these changes. Pronounced activation of lipogenic gene expression in the liver and down-regulated expression of uncoupling protein-1 (UCP1) and peroxisome-proliferator-activated receptor-γ co-activator-1α (PGC-1α) in brown adipose tissue (BAT) was observed in the olanzapine-only group. Interestingly, these protein changes could be reversed by co-treatment with O + B. CONCLUSIONS: Simvastatin is effective in ameliorating TC and TG elevated by olanzapine. Modulation of BAT activity by statins could be a partial mechanism in reducing metabolic side effects caused by SGAs in child and adolescent patients. GRAPHICAL ABSTRACT: [Image: see text] BioMed Central 2020-06-30 /pmc/articles/PMC7325271/ /pubmed/32605639 http://dx.doi.org/10.1186/s40360-020-00427-0 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Liu, Xuemei Feng, Xiyu Deng, Chao Liu, Lu Zeng, Yanping Hu, Chang-Hua Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin |
title | Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin |
title_full | Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin |
title_fullStr | Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin |
title_full_unstemmed | Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin |
title_short | Brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin |
title_sort | brown adipose tissue activity is modulated in olanzapine-treated young rats by simvastatin |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7325271/ https://www.ncbi.nlm.nih.gov/pubmed/32605639 http://dx.doi.org/10.1186/s40360-020-00427-0 |
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