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培养的大鼠骨骼肌管中钠通道与电活动之间关系的表征:调节方面。

Characterization of the relation between sodium channels and electrical activity in cultured rat skeletal myotubes: regulatory aspects.

作者信息

Brodie C, Brody M, Sampson S R

机构信息

Department of Life Sciences, Bar-Ilan University, Ramat-Gan, Israel.

出版信息

Brain Res. 1989 May 29;488(1-2):186-94. doi: 10.1016/0006-8993(89)90708-7.

Abstract

The relation among sodium channel density, frequency of electrical activity and maximal rate of rise of the action potential was studied in developing and mature rat skeletal myotubes in culture. The number of tetrodotoxin (TTX)-sensitive Na-channels was determined by measurements of the amount of [3H]saxitoxin (STX) bound to the cultures, and electrical properties were recorded with intracellular microelectrodes. The EC50 for TTX-induced decreases in maximal STX-binding, frequency and rate of rise of action potentials was in the range 8-20 nM. The 3 variables increased in parallel with age in culture to reach peak values at age 7-8 days, and then decreased in parallel until 10-12 days in culture. The age-related increase in Na-channel density was decreased, but not abolished, by prevention of myoblast fusion. Treatment with the Ca2+ ionophore, A23187, down-regulated, and blockade of Ca-channels with verapamil up-regulated the number of Na-channels. Na-channel density was also increased by chronic treatment with TTX and elevated external [K+], which eliminated spontaneous electrical and contractile activity. Parallel effects were observed on frequency and rate of rise of action potentials. Up-regulation of Na-channels was prevented by simultaneous treatment of myotubes with inhibitors of protein synthesis. We conclude that electrical and mechanical activity of cultured myotubes regulate de novo synthesis of Na-channels through alterations in the level of cytosolic Ca2+.

摘要

在培养的发育中和成熟的大鼠骨骼肌肌管中,研究了钠通道密度、电活动频率与动作电位最大上升速率之间的关系。通过测量与培养物结合的[3H]石房蛤毒素(STX)的量来确定河豚毒素(TTX)敏感钠通道的数量,并用细胞内微电极记录电特性。TTX诱导的最大STX结合、动作电位频率和上升速率降低的EC50在8-20 nM范围内。这三个变量在培养过程中随年龄平行增加,在7-8天时达到峰值,然后平行下降,直到培养10-12天。通过阻止成肌细胞融合,与年龄相关的钠通道密度增加有所降低,但并未消除。用Ca2+离子载体A23187处理可下调钠通道数量,而用维拉帕米阻断钙通道则可上调钠通道数量。长期用TTX处理和提高细胞外[K+]浓度也可增加钠通道密度,这消除了自发的电活动和收缩活动。在动作电位频率和上升速率方面也观察到了平行效应。同时用蛋白质合成抑制剂处理肌管可阻止钠通道的上调。我们得出结论,培养的肌管的电活动和机械活动通过改变胞质Ca2+水平来调节钠通道的从头合成。

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