| Literature DB >> 27433295 |
Hiroki Taoka1, Yoko Yokoyama1, Kohkichi Morimoto1, Naho Kitamura1, Tatsuya Tanigaki1, Yoko Takashina1, Kazuo Tsubota1, Mitsuhiro Watanabe1.
Abstract
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.Entities:
Keywords: Bariatric surgery; Bile acid binding resin; Bile acids; Energy metabolism; Farnesoid X receptor; Glucose metabolism; Incretin; Lipid metabolism; Microbiota; TGR5/M-BAR
Year: 2016 PMID: 27433295 PMCID: PMC4937164 DOI: 10.4239/wjd.v7.i13.260
Source DB: PubMed Journal: World J Diabetes ISSN: 1948-9358