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Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats

BACKGROUND: Obesity has become one of the most serious issues threatening the health of humankind, and we conducted this study to examine whether and how celastrol protects against obesity. METHODS: We fed male Sprague-Dawley rats a high-fat diet and administered celastrol to obese rats for 3 weeks....

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Autores principales: Hu, Weiyue, Wang, Lingling, Du, Guizhen, Guan, Quanquan, Dong, Tianyu, Song, Ling, Xia, Yankai, Wang, Xinru
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Diabetes Association 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643605/
https://www.ncbi.nlm.nih.gov/pubmed/32431112
http://dx.doi.org/10.4093/dmj.2019.0124
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author Hu, Weiyue
Wang, Lingling
Du, Guizhen
Guan, Quanquan
Dong, Tianyu
Song, Ling
Xia, Yankai
Wang, Xinru
author_facet Hu, Weiyue
Wang, Lingling
Du, Guizhen
Guan, Quanquan
Dong, Tianyu
Song, Ling
Xia, Yankai
Wang, Xinru
author_sort Hu, Weiyue
collection PubMed
description BACKGROUND: Obesity has become one of the most serious issues threatening the health of humankind, and we conducted this study to examine whether and how celastrol protects against obesity. METHODS: We fed male Sprague-Dawley rats a high-fat diet and administered celastrol to obese rats for 3 weeks. By recording body weight (BW) and other measures, we identified the effective dose of celastrol for obesity treatment. Feces were collected to perform 16S rRNA sequencing, and hypothalami were extracted for transcriptome sequencing. We then treated leptin knockout rats with celastrol and explored the changes in energy metabolism. Male Institute of Cancer Research (ICR) mice were used to test the acute toxicity of celastrol. RESULTS: We observed that celastrol reduced BW and promoted energy expenditure at a dose of 500 µg/kg BW but that food intake was not changed after administration. The diversity of the gut microbiota was improved, with an increased ratio of Bacteroidetes to Firmicutes, and the gut microbiota played an important role in the anti-obesity effects of celastrol. Hypothalamic transcriptome analysis showed a significant enrichment of the leptin signaling pathway, and we found that celastrol significantly enhanced energy expenditure, which was mediated by the leptin signaling pathway. Acute lethal toxicity of celastrol was not observed at doses ranging from 0 to 62.5 mg/kg BW. CONCLUSION: Our study revealed that celastrol decreased the BW of obese rats by enhancing energy expenditure but not by suppressing food intake and that this effect was mediated by the improvement of the gut microbiota and the activation of the hypothalamic leptin signaling pathway.
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spelling pubmed-76436052020-11-13 Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats Hu, Weiyue Wang, Lingling Du, Guizhen Guan, Quanquan Dong, Tianyu Song, Ling Xia, Yankai Wang, Xinru Diabetes Metab J Original Article BACKGROUND: Obesity has become one of the most serious issues threatening the health of humankind, and we conducted this study to examine whether and how celastrol protects against obesity. METHODS: We fed male Sprague-Dawley rats a high-fat diet and administered celastrol to obese rats for 3 weeks. By recording body weight (BW) and other measures, we identified the effective dose of celastrol for obesity treatment. Feces were collected to perform 16S rRNA sequencing, and hypothalami were extracted for transcriptome sequencing. We then treated leptin knockout rats with celastrol and explored the changes in energy metabolism. Male Institute of Cancer Research (ICR) mice were used to test the acute toxicity of celastrol. RESULTS: We observed that celastrol reduced BW and promoted energy expenditure at a dose of 500 µg/kg BW but that food intake was not changed after administration. The diversity of the gut microbiota was improved, with an increased ratio of Bacteroidetes to Firmicutes, and the gut microbiota played an important role in the anti-obesity effects of celastrol. Hypothalamic transcriptome analysis showed a significant enrichment of the leptin signaling pathway, and we found that celastrol significantly enhanced energy expenditure, which was mediated by the leptin signaling pathway. Acute lethal toxicity of celastrol was not observed at doses ranging from 0 to 62.5 mg/kg BW. CONCLUSION: Our study revealed that celastrol decreased the BW of obese rats by enhancing energy expenditure but not by suppressing food intake and that this effect was mediated by the improvement of the gut microbiota and the activation of the hypothalamic leptin signaling pathway. Korean Diabetes Association 2020-10 2020-05-11 /pmc/articles/PMC7643605/ /pubmed/32431112 http://dx.doi.org/10.4093/dmj.2019.0124 Text en Copyright © 2020 Korean Diabetes Association http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Hu, Weiyue
Wang, Lingling
Du, Guizhen
Guan, Quanquan
Dong, Tianyu
Song, Ling
Xia, Yankai
Wang, Xinru
Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats
title Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats
title_full Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats
title_fullStr Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats
title_full_unstemmed Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats
title_short Effects of Microbiota on the Treatment of Obesity with the Natural Product Celastrol in Rats
title_sort effects of microbiota on the treatment of obesity with the natural product celastrol in rats
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7643605/
https://www.ncbi.nlm.nih.gov/pubmed/32431112
http://dx.doi.org/10.4093/dmj.2019.0124
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