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IL1R1 是白藜芦醇增敏瘦素和抗肥胖作用所必需的。

IL1R1 is required for celastrol's leptin-sensitization and antiobesity effects.

机构信息

Division of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.

Department of Mathematics and Statistics, Boston University, Boston, MA, USA.

出版信息

Nat Med. 2019 Apr;25(4):575-582. doi: 10.1038/s41591-019-0358-x. Epub 2019 Mar 4.

Abstract

Celastrol, a pentacyclic triterpene, is the most potent antiobesity agent that has been reported thus far. The mechanism of celastrol's leptin-sensitizing and antiobesity effects has not yet been elucidated. In this study, we identified interleukin-1 receptor 1 (IL1R1) as a mediator of celastrol's action by using temporally resolved analysis of the hypothalamic transcriptome in celastrol-treated DIO, lean, and db/db mice. We demonstrate that IL1R1-deficient mice are completely resistant to the effects of celastrol in leptin sensitization and treatment of obesity, diabetes, and nonalcoholic steatohepatitis. Thus, we conclude that IL1R1 is a gatekeeper for celastrol's metabolic actions.

摘要

藜芦醇是一种五环三萜,是迄今为止报道的最强的抗肥胖剂。藜芦醇的瘦素敏化和抗肥胖作用的机制尚未阐明。在这项研究中,我们通过对藜芦醇处理的 DIO、瘦鼠和 db/db 小鼠下丘脑转录组的时间分辨分析,鉴定出白细胞介素 1 受体 1(IL1R1)是藜芦醇作用的介体。我们证明,IL1R1 缺陷小鼠对藜芦醇在瘦素敏化和肥胖、糖尿病和非酒精性脂肪性肝炎治疗中的作用完全有抗性。因此,我们得出结论,IL1R1 是藜芦醇代谢作用的守门员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/00d7/7158951/67126bacbedc/nihms-1518860-f0005.jpg

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