Literature DB >> 28880474

β-Cell signalling and insulin secretagogues: A path for improved diabetes therapy.

Susumu Seino1, Kenji Sugawara1,2, Norihide Yokoi1, Harumi Takahashi1.   

Abstract

Insulin secretagogues including sulfonylureas, glinides and incretin-related drugs such as dipeptidyl peptidase 4 (DPP-4) inhibitors and glucagon-like peptide-1 receptor agonists are widely used for treatment of type 2 diabetes. In addition, glucokinase activators and G-protein-coupled receptor 40 (GPR40) agonists also have been developed, although the drugs are not clinically usable. These different drugs exert their effects on insulin secretion by different mechanisms. Recent advances in β-cell signalling studies have not only deepened our understanding of insulin secretion but also revealed novel mechanisms of insulin secretagogues. Clarification of the signalling mechanisms of the insulin secretagogues will contribute to improved drug therapy for diabetes.
© 2017 John Wiley & Sons Ltd.

Entities:  

Keywords:  Epac2A; KATP channel; glutamate; in silico similarity search; incretin; sulfonylurea; β-cell

Mesh:

Substances:

Year:  2017        PMID: 28880474     DOI: 10.1111/dom.12995

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


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