阿托伐他汀
血脂异常
药理学
耐受性
体内
高脂血症
他汀类
胆固醇
临床试验
医学
化学
生物信息学
计算生物学
内科学
生物
内分泌学
糖尿病
不利影响
生物技术
作者
Jiang Wang,Jing Zhao,Cong Yan,Cong Xi,Chenglin Wu,Jingxiang Zhao,Fengwei Li,Yanhua Ding,Rui Zhang,Shankang Qi,Xingjun Li,Chao Liu,Wanting Hou,Hong Chen,Yi‐Ping Wang,Dalei Wu,Kaixian Chen,Hualiang Jiang,He Huang,Hong Liu
出处
期刊:Cell Metabolism
[Cell Press]
日期:2022-04-14
卷期号:34 (5): 667-680.e6
被引量:26
标识
DOI:10.1016/j.cmet.2022.03.006
摘要
Developing non-statin-based small compounds to battle the global epidemic of hyperlipidemia remains challenging. Here, we report the discovery of DC371739, an indole-containing tetrahydroisoquinoline compound with promising lipid-lowering effects, both in vitro and in vivo, and with good tolerability in a Phase I clinical trial (NCT04927221). DC371739 significantly reduced the plasma levels of total cholesterol, low-density lipoprotein cholesterol, and triglycerides simultaneously in several animal models and showed preliminary positive results in the Phase I trial. Mechanistically, DC371739 acts in a distinct manner from other known lipid-lowering reagents. We show that it physically binds HNF-1α, impeding the transcription of both PCSK9 and ANGPTL3, two genes that are known to contribute to hypercholesterolemia and dyslipidemia. Moreover, the distinct mechanism of action of DC371739 allows its combination with atorvastatin treatment to additively improve dyslipidemia, while providing a potential alternative therapeutic strategy for individuals with statin intolerance.
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