Bile acids promote glucagon-like peptide-1 secretion through TGR5 in a murine enteroendocrine cell line STC-1.
By S. Katsuma, A. Hirasawa, G. Tsujimoto. Biochemical and Biophysical Research Communications - BBRC, 2005
765 citations recorded by the source corpus.
Subfields: Endocrinology, Diabetes and Metabolism, Oncology, Pediatrics, Perinatology and Child Health
View Paper: https://www.semanticscholar.org/paper/95eb24e569b462bfba021909300bb095e9ca1545
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In Endocrinology, Diabetes and Metabolism
In Oncology
In Pediatrics, Perinatology and Child Health
Citations in the corpus
- Bile Acid Signaling in Metabolic Disease and Drug Therapy (2014, neutral): “Katsuma et al. (2005) first”
- Role of bile acids and bile acid receptors in metabolic regulation. (2009, background): “In addition, in vitro studies demonstrated that BAs promote GLP-1 secretion through the activation of TGR5 in the murine enteroendocrine STC-1 cell line (143).”
- Gut microbiota functions: metabolism of nutrients and other food components (2017, background): “Through binding to these receptors, bile acids can regulate genes critical to their synthesis, conjugation, transport, and detoxification [75–77] as well as lipid [78, 79] and glucose metabolism [80, 81] and energy homeostasis [82].”
- TGR5-mediated bile acid sensing controls glucose homeostasis. (2009, background): “, 2006), and inspired by the fact that TGR5 is expressed in enteroendocrine cells (Katsuma et al., 2005; Reimann et al., 2008), we explored in this study whether TGR5 activation could alter glucose homeostasis.”
- Bile acids: regulation of synthesis (2009, background): “stimulates glucagon-like peptide 1 (GLP-1) (39), which has anti-diabetic activity.”
- Bile Acid Metabolism and Signaling (2013, neutral): “Knockdown of TGR5 mRNA expression by siRNA GLP-1 secretion suggesting that bile acids induce GLP-1 secretion by TGR5-dependent cAMP production (95).”
- Pleiotropic Roles of Bile Acids in Metabolism (2013, background): “It is hypothesized that GLP-1 then binds to the GLP-1 receptor in the liver, leading to the improved insulin sensitivity (Katsuma et al., 2005; Keitel and Häussinger, 2012; Thomas et al., 2009).”