Results 1 to 10 of about 1,660 (124)

The degradation of TGR5 mediated by Smurf1 contributes to diabetic nephropathy

open access: yesCell Reports, 2023
Summary: The multiple roles of TGR5 in the regulation of glucose metabolism, inflammation, and oxidative stress have drawn attention as therapeutic candidates for diabetes-related kidney disease.
Zhongqiu Liu, Heqing Huang, Zeyuan Lin
exaly   +4 more sources

TGR5 expression in normal kidney and renal neoplasms

open access: yesDiagnostic Pathology, 2018
Background The G protein-coupled bile acid receptor (TGR5) is a cell surface receptor which induces the production of intracellular cAMP and promotes epithelial-mesenchymal transition in gastric cancer cell lines.
Chaohui Lisa Zhao   +4 more
doaj   +2 more sources

Mechanism of action of the bile acid receptor TGR5 in obesity

open access: yesActa Pharmaceutica Sinica B
G protein-coupled receptors (GPCRs) are a large family of membrane protein receptors, and Takeda G protein-coupled receptor 5 (TGR5) is a member of this family.
Zhengquan Su, Hua Cao, Jiao Guo
exaly   +3 more sources

Identification of key amino acid residues in the hTGR5-nomilin interaction and construction of its binding model. [PDF]

open access: yesPLoS ONE, 2017
TGR5, a member of the G protein-coupled receptor (GPCR) family, is activated by bile acids. Because TGR5 promotes energy expenditure and improves glucose homeostasis, it is recognized as a key target in treating metabolic diseases.
Takashi Sasaki   +9 more
doaj   +1 more source

Bile acid-receptor TGR5 deficiency worsens liver injury in alcohol-fed mice by inducing intestinal microbiota dysbiosis

open access: yesJHEP Reports, 2021
Background & Aims: Bile-acid metabolism and the intestinal microbiota are impaired in alcohol-related liver disease. Activation of the bile-acid receptor TGR5 (or GPBAR1) controls both biliary homeostasis and inflammatory processes.
Madeleine Spatz   +15 more
doaj   +1 more source

Bile Acid–Mediated Activation of Brown Fat Protects From Alcohol-Induced Steatosis and Liver Injury in MiceSummary

open access: yesCellular and Molecular Gastroenterology and Hepatology, 2022
Background & Aims: Alcohol-associated liver disease (AALD) is one of the most common causes of liver injury and failure. Limited knowledge of the mechanisms underlying AALD impedes the development of efficacious therapies.
Mingjie Fan   +15 more
doaj   +1 more source

TGR5 deficiency activates antitumor immunity in non-small cell lung cancer via restraining M2 macrophage polarization

open access: yesActa Pharmaceutica Sinica B, 2022
The bile acid-responsive G-protein-coupled receptor TGR5 is expressed in monocytes and macrophages, and plays a critical role in regulating inflammatory response.
Lifang Zhao   +6 more
doaj   +1 more source

Investigation of the potential role of TGR5 in pancreatic cancer by a comprehensive molecular experiments and the liquid chromatography mass spectrometry (LC–MS) based metabolomics

open access: yesDiscover Oncology, 2022
Background Takeda G protein receptor 5 (TGR5) is widely recognized as a potential drug target for the treatment of metabolic diseases. TGR5 is not only a metabolic regulator, but also has a potential role that participating in developing and progressing ...
Yangyang Lei   +9 more
doaj   +1 more source

Taurochenodeoxycholic Acid Increases cAMP Content via Specially Interacting with Bile Acid Receptor TGR5

open access: yesMolecules, 2021
Taurochenodeoxycholic acid (TCDCA) is one of the main components of bile acids (BAs). TCDCA has been reported as a signaling molecule, exerting anti-inflammatory and immunomodulatory functions.
Youchao Qi   +4 more
doaj   +1 more source

TGR5 Regulates Macrophage Inflammation in Nonalcoholic Steatohepatitis by Modulating NLRP3 Inflammasome Activation

open access: yesFrontiers in Immunology, 2021
Nonalcoholic steatohepatitis (NASH) is a chronic liver disease associated with dysregulation of liver metabolism and inflammation. G-protein coupled bile acid receptor 1 (TGR5) is a cell surface receptor that is involved in multiple metabolic pathways ...
Yong Shi   +67 more
doaj   +1 more source

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