Simple jQuery Dropdowns
Please use this identifier to cite or link to this item: http://repository.li.mahidol.ac.th/dspace/handle/123456789/45020
Title: Prolonged stimulation of β<inf>2</inf>-adrenergic receptor with β<inf>2</inf>-agonists impairs insulin actions in H9c2 cells
Authors: Warisara Parichatikanond
Akiyuki Nishimura
Motohiro Nishida
Supachoke Mangmool
National Institutes of Natural Sciences - Exploratory Research Center on Life and Living Systems
The Graduate University for Advanced Studies
Mahidol University
Kyushu University
Keywords: Biochemistry, Genetics and Molecular Biology;Pharmacology, Toxicology and Pharmaceutics
Issue Date: 1-Nov-2018
Citation: Journal of Pharmacological Sciences. Vol.138, No.3 (2018), 184-191
Abstract: © 2018 The Authors Insulin resistance is a condition in which there is a defect in insulin actions to induce glucose uptake into the cells. Overstimulation of β2-adrenergic receptors (β2ARs) is associated with the pathogenesis of insulin resistance in the heart. However, the mechanisms by which β2-agonists affect insulin resistance in the heart are incompletely understood. The β2-agonists are used for treatment of asthma due to bronchodilating effects. We also investigated the effects of β2-agonists in human bronchial smooth muscle (HBSM) cells. In this study, we demonstrate that chronic treatment with salbutamol, salmeterol, and formoterol inhibited insulin-induced glucose uptake and GLUT4 synthesis in H9c2 myoblast cells. Sustained β2AR stimulation also attenuated GLUT4 translocation to the plasma membrane, whereas short-term stimulation had no effect. In HBSM cells, prolonged treatment with β2-agonists had no effect on insulin-induced glucose uptake and did not alter insulin-induced expressions of GLUT1, GLUT4, and GLUT10. In addition, genetic polymorphisms at amino acid positions 16 and 27 of β2AR are linked to insulin resistance by significant suppression of GLUT4 translocation compared to wild-type. Thus, prolonged β2AR stimulation by β2-agonists impairs insulin actions through suppression of GLUT synthesis and translocation only in H9c2 cells.
URI: https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85054701355&origin=inward
http://repository.li.mahidol.ac.th/dspace/handle/123456789/45020
ISSN: 13478648
13478613
Appears in Collections:Scopus 2018

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.