Division of Endocrinology, Boston Children's Hospital, Harvard Medical School, Boston, MA, USA.
Department of Mathematics and Statistics, Boston University, Boston, MA, USA.
Nat Med. 2019 Apr;25(4):575-582. doi: 10.1038/s41591-019-0358-x. Epub 2019 Mar 4.
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.
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。