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

• Published in: Diabetes & metabolism journal Vol. 44; no. 5; pp. 747 - 763
• Main Authors: Hu, Weiyue, Wang, Lingling, Du, Guizhen, Guan, Quanquan, Dong, Tianyu, Song, Ling, Xia, Yankai, Wang, Xinru
• Format: Journal Article
• Language: English
• Published: Korea (South) Korean Diabetes Association 01-10-2020; 대한당뇨병학회
• Subjects: Animals; Biological Products; energy metabolism; gastrointestinal microbiome; leptin; Male; Mice; Microbiota; Obesity; Original; Pentacyclic Triterpenes; Rats; Rats, Sprague-Dawley; RNA, Ribosomal, 16S; tripterine; 내과학; Energy metabolism; Tripterine; Gastrointestinal microbiome; Leptin
• ISSN: 2233-6079; 2233-6087
• DOI: 10.4093/dmj.2019.0124

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.
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.
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.
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.