Cross-Talk Between Insulin Signaling and G Protein-Coupled Receptors

被引:16
|
作者
Fu, Qin [1 ,2 ]
Shi, Qian [3 ]
West, Toni M. [3 ]
Xiang, Yang K. [3 ,4 ]
机构
[1] Huazhong Univ Sci & Technol, Tongji Med Coll, Dept Pharmacol, Sch Basic Med, Wuhan, Hubei, Peoples R China
[2] Key Lab Drug Target Res & Pharmacodynam Evaluat H, Wuhan, Hubei, Peoples R China
[3] Univ Calif Davis, Dept Pharmacol, Davis, CA 95616 USA
[4] VA Northern Calif Healthcare Syst, Mather, CA USA
关键词
diabetes; insulin receptor; adrenergic receptor; contractility; BETA-ADRENERGIC-RECEPTOR; GLUCAGON-LIKE PEPTIDE-1; SMOOTH-MUSCLE-CELLS; BETA(2)-ADRENERGIC RECEPTOR; ANGIOTENSIN-II; THERAPEUTIC TARGET; KINASE-A; BETA-2-ADRENERGIC RECEPTOR; TYROSINE KINASE; HEART-FAILURE;
D O I
10.1097/FJC.0000000000000481
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diabetes is a major risk factor for the development of heart failure. One of the hallmarks of diabetes is insulin resistance associated with hyperinsulinemia. The literature shows that insulin and adrenergic signaling is intimately linked to each other; however, whether and how insulin may modulate cardiac adrenergic signaling and cardiac function remains unknown. Notably, recent studies have revealed that insulin receptor and beta(2) adrenergic receptor (beta(2)AR) forms a membrane complex in animal hearts, bringing together the direct contact between 2 receptor signaling systems, and forming an integrated and dynamic network. Moreover, insulin can drive cardiac adrenergic desensitization via protein kinase A and G protein-receptor kinases phosphorylation of the beta 2AR, which compromises adrenergic regulation of cardiac contractile function. In this review, we will explore the current state of knowledge linking insulin and G protein-coupled receptor signaling, especially beta-adrenergic receptor signaling in the heart, with emphasis on molecular insights regarding its role in diabetic cardiomyopathy.
引用
收藏
页码:74 / 86
页数:13
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