A Ca^(2+) cycling defect connects insulin resistance and heart failure
作者机构:Division of Cardiovascular MedicineDepartment of Internal MedicineAbboud Cardiovascular Research CenterCarver College of MedicineUniversity of IowaIowa CityIA 52242USA
出 版 物:《Life Metabolism》 (生命(代谢(英文))
年 卷 期:2022年第1卷第1期
页 面:2-3页
学科分类:1002[医学-临床医学] 100201[医学-内科学(含:心血管病、血液病、呼吸系病、消化系病、内分泌与代谢病、肾病、风湿病、传染病)] 10[医学]
主 题:metabolism cardiac al.
摘 要:In a recent study published in Life Metabolism,Quan et *** that intracellular Ca^(2+)dysregulation in cardiomyocyte can be both a cause and an effect of cardiac insulin resistance that ultimately leads to diabetic *** epidemiologic studies across several decades indicate that insulin-resistant states such as diabetes and obesity are risk factors for congestive heart failure independent of common cardiovascular disease factors such as hypertension and coronary artery diseases[1,2].On the other hand,there is evidence that heart failure itself causes the onset and development of insulin resistance[3].Restoring normal cardiac output in advanced heart failure patients with left ventricular assistance devices improves insulin sensitivity and cardiac metabolism[4].