Literature DB >> 26818602

Therapeutic potential of Takeda-G-protein-receptor-5 (TGR5) agonists. Hope or hype?

R J Hodge1, D J Nunez1.   

Abstract

The gastrointestinal tract regulates glucose and energy metabolism, and there is increasing recognition that bile acids function as key signalling molecules in these processes. For example, bile acid changes that occur after bariatric surgery have been implicated in the effects on satiety, lipid and cholesterol regulation, glucose and energy metabolism, and the gut microbiome. In recent years, Takeda-G-protein-receptor-5 (TGR5), a bile acid receptor found in widely dispersed tissues, has been the target of significant drug discovery efforts in the hope of identifying effective treatments for metabolic diseases including type 2 diabetes, obesity, atherosclerosis, fatty liver disease and cancer. Although the benefits of targeting the TGR5 receptor are potentially great, drug development work to date has identified risks that include histopathological changes, tumorigenesis, gender differences, and questions about the translation of animal data to humans. The present article reviews the noteworthy challenges that must be addressed along the path of development of a safe and effective TGR5 agonist therapy.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  antidiabetic drug; antiobesity drug; drug development; experimental pharmacology

Mesh:

Substances:

Year:  2016        PMID: 26818602     DOI: 10.1111/dom.12636

Source DB:  PubMed          Journal:  Diabetes Obes Metab        ISSN: 1462-8902            Impact factor:   6.577


  22 in total

Review 1.  Obesity: Current and potential pharmacotherapeutics and targets.

Authors:  Vidya Narayanaswami; Linda P Dwoskin
Journal:  Pharmacol Ther       Date:  2016-10-20       Impact factor: 12.310

2.  TGR5 contributes to hepatic cystogenesis in rodents with polycystic liver diseases through cyclic adenosine monophosphate/Gαs signaling.

Authors:  Tatyana V Masyuk; Anatoliy I Masyuk; Maria Lorenzo Pisarello; Brynn N Howard; Bing Q Huang; Pui-Yuen Lee; Xavier Fung; Eduard Sergienko; Robert J Ardecky; Thomas D Y Chung; Anthony B Pinkerton; Nicholas F LaRusso
Journal:  Hepatology       Date:  2017-08-26       Impact factor: 17.425

3.  Intestinal Co-culture System to Study TGR5 Agonism and Gut Restriction.

Authors:  Snehal N Chaudhari; A Sloan Devlin
Journal:  Bio Protoc       Date:  2021-03-20

Review 4.  Bile acids and nonalcoholic fatty liver disease: Molecular insights and therapeutic perspectives.

Authors:  Juan P Arab; Saul J Karpen; Paul A Dawson; Marco Arrese; Michael Trauner
Journal:  Hepatology       Date:  2016-08-04       Impact factor: 17.425

Review 5.  Bile Acids in Neurodegenerative Disorders.

Authors:  Hayley D Ackerman; Glenn S Gerhard
Journal:  Front Aging Neurosci       Date:  2016-11-22       Impact factor: 5.750

6.  Targeting Bile Acid Receptors: Discovery of a Potent and Selective Farnesoid X Receptor Agonist as a New Lead in the Pharmacological Approach to Liver Diseases.

Authors:  Carmen Festa; Simona De Marino; Adriana Carino; Valentina Sepe; Silvia Marchianò; Sabrina Cipriani; Francesco S Di Leva; Vittorio Limongelli; Maria C Monti; Angela Capolupo; Eleonora Distrutti; Stefano Fiorucci; Angela Zampella
Journal:  Front Pharmacol       Date:  2017-03-30       Impact factor: 5.810

7.  Intestinally-targeted TGR5 agonists equipped with quaternary ammonium have an improved hypoglycemic effect and reduced gallbladder filling effect.

Authors:  Hua Cao; Zhi-Xiang Chen; Kai Wang; Meng-Meng Ning; Qing-An Zou; Ying Feng; Yang-Liang Ye; Ying Leng; Jian-Hua Shen
Journal:  Sci Rep       Date:  2016-06-24       Impact factor: 4.379

Review 8.  Bile acids in glucose metabolism in health and disease.

Authors:  Hagit Shapiro; Aleksandra A Kolodziejczyk; Daniel Halstuch; Eran Elinav
Journal:  J Exp Med       Date:  2018-01-16       Impact factor: 14.307

9.  In Silico Workflow for the Discovery of Natural Products Activating the G Protein-Coupled Bile Acid Receptor 1.

Authors:  Benjamin Kirchweger; Jadel M Kratz; Angela Ladurner; Ulrike Grienke; Thierry Langer; Verena M Dirsch; Judith M Rollinger
Journal:  Front Chem       Date:  2018-07-02       Impact factor: 5.221

10.  Inhibition of Hepatic Bile Acid Uptake by Myrcludex B Promotes Glucagon-Like Peptide-1 Release and Reduces Obesity.

Authors:  Joanne M Donkers; Reinout L P Roscam Abbing; Michel van Weeghel; Johannes H M Levels; Anita Boelen; Alfred H Schinkel; Ronald P J Oude Elferink; Stan F J van de Graaf
Journal:  Cell Mol Gastroenterol Hepatol       Date:  2020-04-21
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