Sarcoplasmic reticulum Ca2+ release declines in muscle fibers from aging mice

被引:57
作者
Jimenez-Moreno, Ramon [1 ]
Wang, Zhong-Min [1 ]
Gerring, Robert C. [1 ]
Delbono, Osvaldo [1 ,2 ,3 ]
机构
[1] Wake Forest Univ, Bowman Gray Sch Med, Dept Physiol & Pharmacol, Winston Salem, NC 27157 USA
[2] Wake Forest Univ, Bowman Gray Sch Med, Dept Internal Med, Sect Gerontol, Winston Salem, NC 27157 USA
[3] Wake Forest Univ, Bowman Gray Sch Med, Neurosci Program, Winston Salem, NC 27157 USA
关键词
D O I
10.1529/biophysj.107.118786
中图分类号
Q6 [生物物理学];
学科分类号
071011 [生物物理学];
摘要
This study hypothesized that decline in sarcoplasmic reticulum (SR) Ca2+ release and maximal SR-releasable Ca2+ contributes to decreased specific force with aging. To test it, we recorded electrically evoked maximal isometric specific force followed by 4-chloro-m-cresol (4-CmC)-evoked maximal contracture force in single intact fibers from the mouse flexor digitorum brevis muscle. Significant differences in tetanic, but not in 4-CmC-evoked, contracture forces were recorded in fibers from aging mice as compared to younger mice. Peak intracellular Ca2+ in response to 4-CmC did not differ significantly. SR Ca2+ release was recorded in whole-cell patch-clamped fibers in the linescan mode of confocal microscopy using a low-affinity Ca2+ indicator (Oregon green bapta-5N) with high-intracellular ethylene glycol-bis(alpha-aminoethyl ether)-N,N,N',N'-tetraacetic acid (20 mM). Maximal SR Ca2+ release, but not voltage dependence, was significantly changed in fibers from old compared to young mice. Increasing the duration of fiber depolarization did not increase the maximal rate of SR Ca2+ release in fibers from old compared to young mice. Voltage-dependent inactivation of SR Ca2+ release did not differ significantly between fibers from young and old mice. These findings indicate that alterations in excitation-contraction coupling, but not in maximal SR-releasable Ca2+, account for the age-dependent decline in intracellular Ca2+ mobilization and specific force.
引用
收藏
页码:3178 / 3188
页数:11
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