糖尿病性心肌病
糖原
糖尿病
心肌病
自噬
内科学
医学
糖酵解
内分泌学
焊剂(冶金)
平衡
糖原贮积病
心脏病
心脏病学
心力衰竭
生物
化学
新陈代谢
生物化学
细胞凋亡
有机化学
作者
Kimberley M. Mellor,Upasna Varma,Parisa Koutsifeli,Lorna J. Daniels,V.L. Benson,Marco Annandale,Xun Li,Yohanes Nursalim,Johannes V. Janssens,Kate L. Weeks,Kim L. Powell,Terence J. O’Brien,Rajesh Katare,Rebecca H. Ritchie,James R. Bell,Roberta A. Gottlieb,Lea M.D. Delbridge
标识
DOI:10.1016/j.yjmcc.2024.02.009
摘要
Diabetic heart disease morbidity and mortality is escalating. No specific therapeutics exist and mechanistic understanding of diabetic cardiomyopathy etiology is lacking. While lipid accumulation is a recognized cardiomyocyte phenotype of diabetes, less is known about glycolytic fuel handling and storage. Based on in vitro studies, we postulated the operation of an autophagy pathway in the myocardium specific for glycogen homeostasis - glycophagy. Here we visualize occurrence of cardiac glycophagy and show that the diabetic myocardium is characterized by marked glycogen elevation and altered cardiomyocyte glycogen localization. We establish that cardiac glycophagy flux is disturbed in diabetes. Glycophagy may represent a potential therapeutic target for alleviating the myocardial impacts of metabolic disruption in diabetic heart disease.
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