Taoka Hiroki, Yokoyama Yoko, Morimoto Kohkichi, Kitamura Naho, Tanigaki Tatsuya, Takashina Yoko, Tsubota Kazuo, Watanabe Mitsuhiro
Hiroki Taoka, Tatsuya Tanigaki, Department of Environmental Information, Keio University, Fujisawa, Kanagawa 252-0882, Japan.
World J Diabetes. 2016 Jul 10;7(13):260-70. doi: 10.4239/wjd.v7.i13.260.
Recent studies have revealed that bile acids (BAs) are not only facilitators of dietary lipid absorption but also important signaling molecules exerting multiple physiological functions. Some major signaling pathways involving the nuclear BAs receptor farnesoid X receptor and the G protein-coupled BAs receptor TGR5/M-BAR have been identified to be the targets of BAs. BAs regulate their own homeostasis via signaling pathways. BAs also affect diverse metabolic pathways including glucose metabolism, lipid metabolism and energy expenditure. This paper suggests the mechanism of controlling metabolism via BA signaling and demonstrates that BA signaling is an attractive therapeutic target of the metabolic syndrome.
最近的研究表明,胆汁酸(BAs)不仅是膳食脂质吸收的促进剂,也是发挥多种生理功能的重要信号分子。一些涉及核胆汁酸受体法尼醇X受体和G蛋白偶联胆汁酸受体TGR5/M-BAR的主要信号通路已被确定为胆汁酸的作用靶点。胆汁酸通过信号通路调节自身的稳态。胆汁酸还影响多种代谢途径,包括葡萄糖代谢、脂质代谢和能量消耗。本文提出了通过胆汁酸信号控制代谢的机制,并证明胆汁酸信号是代谢综合征一个有吸引力的治疗靶点。