钙
内科学
心力衰竭
肌肉肥大
内质网
收缩(语法)
化学
内分泌学
兴奋-收缩耦合
心肌细胞
联轴节(管道)
心脏病学
生物物理学
医学
生物
材料科学
生物化学
冶金
作者
Ana M. Gómez,H. H. Valdivia,Heping Cheng,Miriam R. Lederer,Luis Fernando Santana,Mark B. Cannell,Sylvia A. McCune,Ruth A. Altschuld,W. Jonathan Lederer
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:1997-05-02
卷期号:276 (5313): 800-806
被引量:720
标识
DOI:10.1126/science.276.5313.800
摘要
Cardiac hypertrophy and heart failure caused by high blood pressure were studied in single myocytes taken from hypertensive rats (Dahl SS/Jr) and SH-HF rats in heart failure. Confocal microscopy and patch-clamp methods were used to examine excitation-contraction (EC) coupling, and the relation between the plasma membrane calcium current (ICa) and evoked calcium release from the sarcoplasmic reticulum (SR), which was visualized as "calcium sparks." The ability of ICa to trigger calcium release from the SR in both hypertrophied and failing hearts was reduced. Because ICa density and SR calcium-release channels were normal, the defect appears to reside in a change in the relation between SR calcium-release channels and sarcolemmal calcium channels. beta-Adrenergic stimulation largely overcame the defect in hypertrophic but not failing heart cells. Thus, the same defect in EC coupling that develops during hypertrophy may contribute to heart failure when compensatory mechanisms fail.
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