Jiménez-Moreno Ramón, Wang Zhong-Min, Gerring Robert C, Delbono Osvaldo
Department of Physiology and Pharmacology, Wake Forest University School of Medicine, Winston-Salem, North Carolina 27157, USA.
Biophys J. 2008 Apr 15;94(8):3178-88. doi: 10.1529/biophysj.107.118786. Epub 2008 Jan 4.
This study hypothesized that decline in sarcoplasmic reticulum (SR) Ca(2+) release and maximal SR-releasable Ca(2+) 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 Ca(2+) in response to 4-CmC did not differ significantly. SR Ca(2+) release was recorded in whole-cell patch-clamped fibers in the linescan mode of confocal microscopy using a low-affinity Ca(2+) indicator (Oregon green bapta-5N) with high-intracellular ethylene glycol-bis(alpha-aminoethyl ether)-N,N,N'N'-tetraacetic acid (20 mM). Maximal SR Ca(2+) 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 Ca(2+) release in fibers from old compared to young mice. Voltage-dependent inactivation of SR Ca(2+) 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 Ca(2+), account for the age-dependent decline in intracellular Ca(2+) mobilization and specific force.
本研究假设,肌浆网(SR)钙(Ca2+)释放量的下降以及SR可释放的最大钙量导致了随着衰老比肌力的降低。为了验证这一假设,我们记录了电诱发的最大等长比肌力,随后记录了来自小鼠趾短屈肌的单根完整纤维中4-氯间甲酚(4-CmC)诱发的最大收缩力。与年轻小鼠相比,衰老小鼠纤维中记录到强直收缩力存在显著差异,但4-CmC诱发的收缩力无显著差异。对4-CmC反应的细胞内钙(Ca2+)峰值无显著差异。使用低亲和力钙(Ca2+)指示剂(俄勒冈绿巴普塔-5N)和高细胞内乙二醇双(α-氨基乙醚)-N,N,N',N'-四乙酸(20 mM),以共聚焦显微镜的线扫描模式在全细胞膜片钳记录的纤维中记录SR钙(Ca2+)释放。与年轻小鼠相比,老年小鼠纤维中最大SR钙(Ca2+)释放量显著改变,但电压依赖性无显著变化。与年轻小鼠相比,增加老年小鼠纤维去极化的持续时间并未增加SR钙(Ca2+)释放的最大速率。年轻和老年小鼠纤维之间SR钙(Ca2+)释放的电压依赖性失活无显著差异。这些发现表明,兴奋-收缩偶联的改变而非最大SR可释放钙(Ca2+)的改变,是细胞内钙(Ca2+)动员和比肌力随年龄下降的原因。