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肌膜内小叶钙离子结合:其在心脏钠钙交换中的作用

Inner sarcolemmal leaflet Ca(2+) binding: its role in cardiac Na/Ca exchange.

作者信息

Wang S Y, Peskoff A, Langer G A

机构信息

Department of Physiology, UCLA School of Medicine, Los Angeles, California 90095-1760, USA.

出版信息

Biophys J. 1996 May;70(5):2266-74. doi: 10.1016/S0006-3495(96)79792-8.

Abstract

A recently completed model of Ca concentration and movements in the cardiac cell diadic cleft space predicts that removal or neutralization of inner sarcolemmal (SL) leaflet anionic Ca-binding sites at the sarcolemmal border of this space will greatly diminish Na/Ca exchange-mediated Ca efflux. The present study tests this prediction using the local anesthetic dibucaine as a probe. It is shown, in isolated SL, that dibucaine competitively displaces Ca specifically from anionic phospholipid headgroups. Dibucaine also displaces Ca from the SL when applied to intact cells. It does not affect the content or release of Ca from sarcoplasmic reticulum (SR) in these cells. This eliminates a primary effect on SR Ca as a contributing factor to dibucaine's effect on Na/Ca exchange-mediated Ca efflux. Measurement of this efflux from whole cells shows a highly significant reduction of 58% (p < 0.001) by 0.5 mM dibucaine. The inhibiting effect of dibucaine on Na/Ca exchange-mediated Ca efflux can be significantly reversed by augmentation of Ca release from SR by caffeine at the time of activation of Na/Ca exchange. This supports the contention that the dibucaine-SL interaction is a competitive one vis-a-vis Ca. The results are supportive of the model in which inner SL leaflet Ca-binding sites account for the delay of Ca diffusion from the diadic cleft, thereby prolonging the time for which [Ca] remains elevated in the cleft. The prolonged increased [Ca] significantly enhances the ability of Na/Ca exchange to remove Ca from the cell during the excitation-contraction cycle.

摘要

最近完成的一个关于心肌细胞二联体裂隙空间中钙浓度和移动的模型预测,去除或中和该空间肌膜边界处肌膜(SL)内小叶的阴离子钙结合位点,将大大减少钠钙交换介导的钙外流。本研究使用局部麻醉药丁卡因作为探针来验证这一预测。结果表明,在分离的肌膜中,丁卡因能竞争性地将钙从阴离子磷脂头部特异性置换出来。将丁卡因应用于完整细胞时,它也能从肌膜中置换出钙。它不影响这些细胞中肌浆网(SR)的钙含量或释放。这就排除了对肌浆网钙的主要影响作为丁卡因对钠钙交换介导的钙外流作用的一个促成因素。对全细胞钙外流的测量显示,0.5 mM丁卡因使其显著降低了58%(p < 0.001)。在激活钠钙交换时,通过咖啡因增强肌浆网的钙释放,可显著逆转丁卡因对钠钙交换介导的钙外流的抑制作用。这支持了丁卡因与肌膜的相互作用相对于钙是竞争性的这一论点。这些结果支持了这样一个模型,即肌膜内小叶的钙结合位点导致了钙从二联体裂隙扩散的延迟,从而延长了裂隙中钙浓度升高的时间。裂隙中钙浓度长时间升高显著增强了钠钙交换在兴奋 - 收缩周期中从细胞中去除钙的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e835/1225201/4a8f849809a9/biophysj00047-0230-a.jpg

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