Langer G A
Fed Proc. 1976 May 1;35(6):1274-8.
At present there is a controversy about the appropriate model for excitation-contraction (E-C) coupling in mammalian heart muscle. There is an apparent conflict between the data derived from voltage clamp experiments and data derived from isotopic exchange studies. The maximum transsarcolemmal Ca influx as derived from voltage clamp studies is not more than 10 mumoles/kg wet weight heart per beat. This is barely enough to achieve 10% activation of contractile force. It has been proposed, therefore, that the remainder of the required Ca is derived from intracellular sites. However, ionic exchange studies, using specific E-C uncouplers such as lanthanum, indicate that the major source of coupling Ca is external to the sarcolemma. Its movement, during E-C coupling, would then have to be nonelectrogenic since influx of this quantity of Ca is not discerned with voltage clamp experiments. It is proposed that on excitation, Ca moves across the cardiac sarcolemma by two routes: 1) a small amount through a pore or channel and 2) a much larger amount via an electroneutral carrier. Movement through the pore would be electrogenic and therefore measurable with the voltage clamp whereas movement via the carrier would not be evident with the clamp. The model is consistent with the proposal that the immediate source of contractile-dependent Ca in mammalian heart is derived from sites external to the sarcolemmal (and T tubular) membrane.
目前,关于哺乳动物心肌兴奋 - 收缩(E - C)偶联的合适模型存在争议。电压钳实验数据与同位素交换研究数据之间存在明显冲突。电压钳研究得出的每次心跳跨肌膜最大钙内流不超过10微摩尔/千克湿重心脏。这仅足以使收缩力达到10%的激活程度。因此,有人提出所需的其余钙来自细胞内位点。然而,使用镧等特定E - C解偶联剂的离子交换研究表明,偶联钙的主要来源在肌膜外部。在E - C偶联过程中,其移动必定是非电生的,因为通过电压钳实验无法检测到如此大量钙的内流。有人提出,兴奋时钙通过两条途径穿过心肌肌膜:1)少量通过孔道或通道;2)大量通过电中性载体。通过孔道的移动是电生的,因此可用电压钳测量,而通过载体的移动用钳法则不明显。该模型与哺乳动物心脏中收缩依赖性钙的直接来源来自肌膜(和T小管)膜外部位点的提议一致。