Celastrol inhibits intestinal lipid absorption by reprofiling the gut microbiota to attenuate high-fat diet-induced obesity.
Celastrol inhibits intestinal lipid absorption by reprofiling the gut microbiota to attenuate high-fat diet-induced obesity.
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南蛇藤酚通过重组肠道微生物群来抑制肠道脂质吸收,以减轻高脂饮食引起的肥胖。
DOI:
10.1016/j.isci.2021.102077
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发表时间:
2021-02-19
期刊:
影响因子:
5.8
通讯作者:
Jia Z
中科院分区:
文献类型:
--
作者:
Hua H;Zhang Y;Zhao F;Chen K;Wu T;Liu Q;Huang S;Zhang A;Jia Z
Celastrol, a compound extracted from traditional Chinese medicine, has been reported as a potent anti-obesity agent with controversial mechanisms. Here both C57BL/6J and leptin-deficient (ob/ob) mice fed a high-fat diet (HFD) displayed body weight loss after celastrol therapy, opposing the previous viewpoint that celastrol improves obesity by sensitizing leptin signaling. More importantly, celastrol downregulated lipid transporters in the intestine, increased lipid excretion in feces, and reduced body weight gain in HFD mice. Meanwhile, analysis of gut microbiota revealed that celastrol altered the gut microbiota composition in HFD-fed mice, and modulating gut microbiota by antibiotics or fecal microbiota transplantation blocked the celastrol effect on intestinal lipid transport and body weight gain, suggesting a critical role of the gut microbiota composition in mediating the anti-obesity role of celastrol under HFD. Together, the findings revealed that celastrol reduces intestinal lipid absorption to antagonize obesity by resetting the gut microbiota profile under HFD feeding. Celastrol reduced intestinal lipid transporters and lipids absorption Celastrol reset gut microbiota profile to modulate intestinal lipid transport Celastrol attenuated obesity in leptin-deficient (ob/ob) mice fed high fat diet Biological Sciences; Endocrinology; Microbiology; Microbiome Physiology
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影响因子:
4.4
作者:
de Vogel-van den Bosch HM;Bünger M;de Groot PJ;Bosch-Vermeulen H;Hooiveld GJ;Müller M
通讯作者:
Müller M
影响因子:
16
作者:
Hu M;Luo Q;Alitongbieke G;Chong S;Xu C;Xie L;Chen X;Zhang D;Zhou Y;Wang Z;Ye X;Cai L;Zhang F;Chen H;Jiang F;Fang H;Yang S;Liu J;Diaz-Meco MT;Su Y;Zhou H;Moscat J;Lin X;Zhang XK
通讯作者:
Zhang XK
影响因子:
12.2
作者:
Chang, Eugene B.;Martinez-Guryn, Kristina
通讯作者:
Martinez-Guryn, Kristina
DOI:
10.1016/j.bbadis.2019.02.002
发表时间:
2019-06-01
影响因子:
6.2
作者:
Fang, Penghua;He, Biao;Bo, Ping
通讯作者:
Bo, Ping
影响因子:
4.6
作者:
Bunger, Meike;van den Bosch, Heleen M.;Muller, Michael
通讯作者:
Muller, Michael