Remodeling of Calcium Handling in Human Heart Failure

被引:89
作者
Lou, Qing [1 ]
Janardhan, Ajit [2 ]
Efimov, Igor R. [1 ]
机构
[1] Washington Univ, Dept Biomed Engn, St Louis, MO 63130 USA
[2] Washington Univ, Sch Med, Dept Med, Div Cardiol, St Louis, MO 63110 USA
来源
CALCIUM SIGNALING | 2012年 / 740卷
关键词
Calcium; Remodeling; Heart failure; Human; Clinical treatment; CHANNEL RYANODINE RECEPTOR; CA2+/CALMODULIN-DEPENDENT PROTEIN-KINASE; SARCOPLASMIC-RETICULUM CA2+-ATPASE; HUMAN VENTRICULAR MYOCYTES; MYOCARDIAL GENE-EXPRESSION; FORCE-FREQUENCY RELATION; T-WAVE ALTERNANS; FAILING HUMAN; RELEASE CHANNEL; DILATED CARDIOMYOPATHY;
D O I
10.1007/978-94-007-2888-2_52
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Heart failure (HF) is an increasing public health problem accelerated by a rapidly aging global population. Despite considerable progress in managing the disease, the development of new therapies for effective treatment of HF remains a challenge. To identify targets for early diagnosis and therapeutic intervention, it is essential to understand the molecular and cellular basis of calcium handling and the signaling pathways governing the functional remodeling associated with HF in humans. Calcium (Ca2+) cycling is an essential mediator of cardiac contractile function, and remodeling of calcium handling is thought to be one of the major factors contributing to the mechanical and electrical dysfunction observed in HF. Active research in this field aims to bridge the gap between basic research and effective clinical treatments of HF. This chapter reviews the most relevant studies of calcium remodeling in failing human hearts and discusses their connections to current and emerging clinical therapies for HF patients
引用
收藏
页码:1145 / 1174
页数:30
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