G蛋白偶联胆汁酸受体
胆汁酸
法尼甾体X受体
葡萄糖稳态
新视野
医学
糖尿病
生物信息学
生物
核受体
胰岛素抵抗
内科学
内分泌学
生物化学
转录因子
基因
工程类
航空航天工程
航天器
作者
Wangrui Jin,Mingyue Zheng,Yihua Chen,Hai Xiong
标识
DOI:10.1016/j.ejmech.2024.116462
摘要
The G protein-coupled bile acid receptor 1 (GPBAR1) or TGR5 is widely distributed across organs, including the small intestine, stomach, liver, spleen, and gallbladder. Many studies have established strong correlations between TGR5 and glucose homeostasis, energy metabolism, immune-inflammatory responses, and gastrointestinal functions. These results indicate that TGR5 has a significant impact on the progression of tumor development and metabolic disorders such as diabetes mellitus and obesity. Targeting TGR5 represents an encouraging therapeutic approach for treating associated human ailments. Notably, the GLP-1 receptor has shown exceptional efficacy in clinical settings for diabetes management and weight loss promotion. Currently, numerous TGR5 agonists have been identified through natural product-based approaches and virtual screening methods, with some successfully progressing to clinical trials. This review summarizes the intricate relationships between TGR5 and various diseases emphasizing recent advancements in research on TGR5 agonists, including their structural characteristics, design tactics, and biological activities. We anticipate that this meticulous review could facilitate the expedited discovery and optimization of novel TGR5 agonists.
科研通智能强力驱动
Strongly Powered by AbleSci AI