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细胞内酸中毒对青蛙骨骼肌钙离子激活、收缩及舒张的影响。

Effects of intracellular acidosis on Ca2+ activation, contraction, and relaxation of frog skeletal muscle.

作者信息

Baker A J, Brandes R, Weiner M W

机构信息

Magnetic Resonance Unit, Department of Veteran Affairs Medical Center, San Francisco, California.

出版信息

Am J Physiol. 1995 Jan;268(1 Pt 1):C55-63. doi: 10.1152/ajpcell.1995.268.1.C55.

DOI:10.1152/ajpcell.1995.268.1.C55
PMID:7840160
Abstract

The goal of this study was to determine the effects of intracellular acidosis (pH approximately 6.3) of frog skeletal muscle on force and on intracellular Ca2+ concentration ([Ca2+]i; measured at 20 degrees C using indo 1 fluorescence). Acidosis reduced tetanic force by only 11 +/- 2% (mean +/- SE, n = 8) but increased tetanic [Ca2+]i by 33 +/- 6%, suggesting that acidosis reduced the maximum Ca(2+)-activated force. During relaxation, the [Ca2+]i at half-maximal force was doubled with acidosis, suggesting that acidosis altered the Ca(2+)-force relationship. Acidosis markedly slowed force relaxation and [Ca2+]i decline (time constants fitted to force and [Ca2+]i during relaxation increased by 133 +/- 20 and 68 +/- 13%, respectively, with acidosis), suggesting that slowed force relaxation with acidosis may arise from slowed Ca2+ clearance from the cytosol. Late in relaxation, at approximately 30% of initial force, there was a transient phase of [Ca2+]i increase that was delayed with acidosis in proportion to the slowing of force relaxation. This is consistent with previous suggestions that dissociation of cross-bridges from the thin filament during relaxation promotes Ca2+ release to the cytosol from troponin. This study concludes that in skeletal muscle acidosis has little effect on tetanic force and that the major effects are decreased Ca2+ sensitivity and slower relaxation.

摘要

本研究的目的是确定青蛙骨骼肌细胞内酸中毒(pH约为6.3)对肌力和细胞内钙离子浓度([Ca2+]i;20℃下使用indo 1荧光法测量)的影响。酸中毒使强直收缩力仅降低11±2%(平均值±标准误,n = 8),但使强直收缩时的[Ca2+]i增加33±6%,这表明酸中毒降低了最大钙激活力。在松弛过程中,酸中毒使达到最大力一半时的[Ca2+]i增加了一倍,这表明酸中毒改变了钙-力关系。酸中毒显著减慢了力的松弛和[Ca2+]i的下降(松弛过程中拟合力和[Ca2+]i的时间常数分别因酸中毒增加了133±20%和68±13%),这表明酸中毒时力松弛减慢可能是由于胞质溶胶中Ca2+清除减慢所致。在松弛后期,当力约为初始力的30%时,出现了一个[Ca2+]i增加的瞬态阶段,酸中毒使其延迟,延迟程度与力松弛减慢成比例。这与之前的观点一致,即松弛过程中横桥从细肌丝上解离会促进Ca2+从肌钙蛋白释放到胞质溶胶中。本研究得出结论,在骨骼肌中,酸中毒对强直收缩力影响很小,主要影响是降低了Ca2+敏感性和减慢了松弛。

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