胆汁酸
G蛋白偶联胆汁酸受体
法尼甾体X受体
医学
胰岛素抵抗
2型糖尿病
碳水化合物代谢
内质网
受体
糖尿病
内分泌学
内科学
生物化学
核受体
生物
基因
转录因子
作者
Yisen Hou,Xinzhe Zhai,Xiaotao Wang,Yi Wu,Heyue Wang,Yaxin Qin,Jianli Han,Yong Meng
标识
DOI:10.1186/s13098-023-01207-6
摘要
Abstract Bile acids, which are steroid molecules originating from cholesterol and synthesized in the liver, play a pivotal role in regulating glucose metabolism and maintaining energy balance. Upon release into the intestine alongside bile, they activate various nuclear and membrane receptors, influencing crucial processes. These bile acids have emerged as significant contributors to managing type 2 diabetes mellitus, a complex clinical syndrome primarily driven by insulin resistance. Bile acids substantially lower blood glucose levels through multiple pathways: BA-FXR-SHP, BA-FXR-FGFR15/19, BA-TGR5-GLP-1, and BA-TGR5-cAMP. They also impact blood glucose regulation by influencing intestinal flora, endoplasmic reticulum stress, and bitter taste receptors. Collectively, these regulatory mechanisms enhance insulin sensitivity, stimulate insulin secretion, and boost energy expenditure. This review aims to comprehensively explore the interplay between bile acid metabolism and T2DM, focusing on primary regulatory pathways. By examining the latest advancements in our understanding of these interactions, we aim to illuminate potential therapeutic strategies and identify areas for future research. Additionally, this review critically assesses current research limitations to contribute to the effective management of T2DM.
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