| Literature DB >> 34687394 |
Nian-Hua Deng1, Wen Luo1, Dan-Dan Gui1, Bin-Jie Yan1, Kun Zhou1, Kai-Jiang Tian1, Zhong Ren1, Wen-Hao Xiong1, Zhi-Sheng Jiang2.
Abstract
Diabetic cardiomyopathy (DCM) is a cardiovascular complication that tends to occur in patients with diabetes, obesity, or insulin resistance, with a higher late mortality rate. Sustained hyperglycemia, increased free fatty acids, or insulin resistance induces metabolic disorders in cardiac tissues and cells, leading to myocardial fibrosis, left ventricular hypertrophy, diastolic and/or systolic dysfunction, and finally develop into congestive heart failure. The close connection between all signaling pathways and the complex pathogenesis of DCM cause difficulties in finding effective targets for the treatment of DCM. It reported that hydrogen sulfide (H2S) could regulate cell energy substrate metabolism, reduce insulin resistance, protect cardiomyocytes, and improve myocardial function by acting on related key proteins such as differentiation cluster 36 (CD36) and glucose transporter 4 (GLUT4). In this article, the relative mechanisms of H2S in alleviating metabolic disorders of DCM were reviewed, and how H2S can better prevent and treat DCM in clinical practice will be discussed.Entities:
Keywords: Diabetic cardiomyopathy; Exosome; Hydrogen sulfide; Myocardial function; Myocardial metabolism
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Year: 2021 PMID: 34687394 DOI: 10.1007/s11010-021-04278-z
Source DB: PubMed Journal: Mol Cell Biochem ISSN: 0300-8177 Impact factor: 3.396