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首个雷帕霉素(mTOR调节相关蛋白)抑制剂作为新型抗脂肪生成剂的发现。

Discovery of the First Raptor (Regulatory-Associated Protein of mTOR) Inhibitor as a New Type of Antiadipogenic Agent.

作者信息

Yan Xue-Long, Pan Yue-Hua, Fan Run-Zhu, Song Qin-Qin, Li Shen, Huang Jia-Luo, Li Wei, Huang Dong, Yuan Fang-Yu, Tang Gui-Hua, Rao Yong, Huang Zhi-Shu, Yin Sheng

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, Guangzhou, Guangdong 510006, China.

School of Pharmacy, Guizhou Medical University, Guian New District, Guizhou 550025, China.

出版信息

J Med Chem. 2023 Apr 27;66(8):5839-5858. doi: 10.1021/acs.jmedchem.3c00067. Epub 2023 Apr 4.

Abstract

Raptor, a regulatory-associated protein of mTOR, has been genetically proved to be an important regulator in lipogenesis. However, its druggable potential is rarely investigated, largely due to the lack of an inhibitor. In this study, the antiadipogenic screening of a daphnane diterpenoid library followed by target fishing led to the identification of a Raptor inhibitor, (5/7/6 carbon ring with orthoester and chlorine functionalities). Pharmacodynamic studies verified that is a potent and tolerable antiadipogenic agent in vitro and in vivo. Mechanistic studies revealed that the targeting of Raptor by could block the formation of mTORC1 and then downregulate the downstream S6K1- and 4E-BP1-mediated C/EBPs/PPARγ signaling, eventually retarding adipocyte cell differentiation at the early stage. These findings suggest that Raptor can be explored as a novel therapeutic target for obesity and its related complications, and as the first Raptor inhibitor may provide a new therapeutic option for these conditions.

摘要

雷帕霉素靶蛋白调节相关蛋白(Raptor)已通过遗传学证明是脂肪生成中的重要调节因子。然而,其可成药潜力很少被研究,这主要是由于缺乏抑制剂。在本研究中,对瑞香烷二萜类化合物库进行抗脂肪生成筛选并随后进行靶点钓取,从而鉴定出一种Raptor抑制剂(具有原酸酯和氯官能团的5/7/6碳环)。药效学研究证实,该抑制剂在体外和体内都是一种有效且耐受性良好的抗脂肪生成剂。机制研究表明,该抑制剂靶向Raptor可阻断mTORC1的形成,进而下调下游S6K1和4E-BP1介导的C/EBPs/PPARγ信号传导,最终在早期阶段延缓脂肪细胞分化。这些发现表明,Raptor可作为肥胖及其相关并发症的新型治疗靶点进行探索,而该抑制剂作为首个Raptor抑制剂可能为这些病症提供新的治疗选择。

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