Determination of rate constants for turnover of myosin isoforms in rat myocardium: implications for in vivo contractile kinetics

被引:33
作者
Locher, Matthew R. [1 ]
Razumova, Maria V. [2 ]
Stelzer, Julian E. [1 ]
Norman, Holly S. [1 ]
Patel, Jitandrakumar R. [1 ]
Moss, Richard L. [1 ]
机构
[1] Univ Wisconsin, Sch Med & Publ Hlth, Dept Physiol, Madison, WI 53711 USA
[2] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
来源
AMERICAN JOURNAL OF PHYSIOLOGY-HEART AND CIRCULATORY PHYSIOLOGY | 2009年 / 297卷 / 01期
关键词
alpha-myosin heavy chain; rate constants of cross-bridge attachment and detachment; rate of rise of force; HEAVY-CHAIN COMPOSITION; RABBIT PSOAS FIBERS; CARDIAC MYOSIN; ALPHA-MYOSIN; HUMAN-HEART; VENTRICULAR MYOCARDIUM; THYROID-HORMONE; MUSCLE-FIBERS; POWER OUTPUT; FUNCTIONAL-SIGNIFICANCE;
D O I
10.1152/ajpheart.00922.2008
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Locher MR, Razumova MV, Stelzer JE, Norman HS, Patel JR, Moss RL. Determination of rate constants for turnover of myosin isoforms in rat myocardium: implications for in vivo contractile kinetics. Am J Physiol Heart Circ Physiol 297: H247-H256, 2009. First published April 24, 2009; doi: 10.1152/ajpheart.00922.2008.-The ventricles of small mammals express mostly alpha-myosin heavy chain (alpha-MHC), a fast isoform, whereas the ventricles of large mammals, including humans, express similar to 10% alpha-MHC on a predominately beta-MHC (slow isoform) background. In failing human ventricles, the amount of alpha-MHC is dramatically reduced, leading to the hypothesis that even small amounts of alpha-MHC on a predominately beta-MHC background confer significantly higher rates of force development in healthy ventricles. To test this hypothesis, it is necessary to determine the fundamental rate constants of cross-bridge attachment (f(app)) and detachment (g(app)) for myosins composed of 100% alpha-MHC or beta-MHC, which can then be used to calculate twitch time courses for muscles expressing variable ratios of MHC isoforms. In the present study, rat skinned trabeculae expressing either 100% alpha-MHC or 100% beta-MHC were used to measure ATPase activity, isometric force, and the rate constant of force redevelopment (k(tr)) in solutions of varying Ca2+ concentrations. The rate of ATP utilization was similar to 2.5-fold higher in preparations expressing 100% alpha-MHC compared with those expressing only beta-MHC, whereas k(tr) was 2-fold faster in the alpha-MHC myocardium. From these variables, we calculated f(app) to be approximately threefold higher for alpha-MHC than beta-MHC and g(app) to be twofold higher in alpha-MHC. Mathematical modeling of isometric twitches predicted that small increases in alpha-MHC significantly increased the rate of force development. These results suggest that low-level expression of alpha-MHC has significant effects on contraction kinetics.
引用
收藏
页码:H247 / H256
页数:10
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