Obesity-induced changes in human islet G protein-coupled receptor expression: Implications for metabolic regulation

被引:21
作者
Atanes, Patricio [1 ]
Ashik, Tanyel [1 ]
Persaud, Shanta J. [1 ]
机构
[1] Kings Coll London, Dept Diabet, Guys Campus, London SE1 1UL, England
关键词
Obesity; Diabetes; GPCRs; Adipose; Human islets; Insulin secretion; STIMULATED INSULIN-SECRETION; PROLACTIN-RELEASING PEPTIDE; BETA-CELL FUNCTION; ADIPOSE-TISSUE; GLUCOSE-TOLERANCE; NEUROPEPTIDE-Y; PANCREATIC-ISLETS; SPHINGOSINE; 1-PHOSPHATE; PARATHYROID-HORMONE; ENERGY-EXPENDITURE;
D O I
10.1016/j.pharmthera.2021.107928
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
G protein-coupled receptors (GPCRs) are a large family of cell surface receptors that are the targets for many different classes of pharmacotherapy. The islets of Langerhans are central to appropriate glucose homeostasis through their secretion of insulin, and islet function can be modified by ligands acting at the large number of GPCRs that islets express. The human islet GPCRome is not a static entity, but one that is altered under pathophysiological conditions and, in this review, we have compared expression of GPCR mRNAs in human islets obtained from normal weight range donors, and those with a weight range classified as obese. We have also considered the likely outcomes on islet function that the altered GPCR expression status confers and the possible impact that adipokines, secreted from expanded fat depots, could have at those GPCRs showing altered expression in obesity. (c) 2021 The Author(s). Published by Elsevier Inc. This is an open access article under the CC BY license (http:// creativecommons.org/licenses/by/4.0/).
引用
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页数:26
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