氟烷对豚鼠心室肌单细胞膜正电位收缩的影响。

D A Terrar, J G Victory
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引用次数: 6

摘要

在电压箝位条件下,研究了氟烷对豚鼠心室肌单细胞的作用。步进退极化至0 mV引起的收缩(用光学方法测量)被氟烷持续地降低。在正膜电位(+60 mV)下,2%的氟烷没有引起收缩峰的持续抑制,在大多数细胞中收缩增强。2%的氟化烷增加了在+60毫伏时达到峰值的收缩时间。然而,当通过l通道对无活性钙电流施加0 mV预脉冲时,2%氟烷对收缩峰值时间的任何影响都被减少或消除。在动作电位平台(+20和+40 mV)范围内,也观察到氟烷引起的膜电位峰缩时间增加。在双脉冲实验中,在“条件”退极化至0 mV后,测量了“测试”退极化至+60时的收缩。在“调理”去极化至0 mV后,+60 mV的收缩在短脉冲间隔(小于400 ms)内略有减少,并随着间隔的延长而恢复;暴露于+60 mV氟烷收缩的细胞不再受脉冲间隔的影响。异氟烷(3.2%)在质量上与氟烷相似,但在+60毫伏时的收缩效果不如氟烷。这些观察结果与钙的进入机制可能随膜电位的变化而变化的建议一致:在0 mV时,钙的主要进入途径可能是通过对卤代烷敏感的l型钙通道,而在+60 mV时,可能通过相对耐卤代烷的其他途径进入。氟烷对收缩峰值时间的作用可能是由于它对肌浆网的影响,减少了钙的净吸收和释放。氟烷的这些作用在动作电位平台期可能是重要的。
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Influence of halothane on contraction at positive membrane potentials in single cells isolated from guinea-pig ventricular muscle.

Actions of halothane were investigated under voltage-clamp conditions in single cells from guinea-pig ventricular muscle. Contraction (measured by an optical method) evoked by step depolarization to 0 mV was consistently reduced by halothane. At positive membrane potentials (+60 mV) 2% halothane did not cause a consistent depression of peak contraction, and in the majority of cells contraction was enhanced. Two per cent halothane increased the time-to-peak contraction at +60 mV. However, when a pre-pulse to 0 mV was applied to inactive calcium current through L-channels, any effect of 2% halothane on the time-to-peak of contraction was reduced or abolished. A halothane-induced increase in time-to-peak contraction was also observed at membrane potentials in the range of the action potential plateau (+20 and +40 mV). In double-pulse experiments contraction during a 'test' depolarization to +60 was measured following a 'conditioning' depolarization to 0 mV. Contraction at +60 mV was slightly reduced at brief interpulse intervals (less than 400 ms) following the 'conditioning' depolarization to 0 mV, and recovered as the interval was prolonged; in cells exposed to halothane contraction at +60 mV was no longer influenced by the interval between the pulses. Isoflurane (3.2%) had qualitatively similar but less potent effects than halothane on contraction at +60 mV. These observations are consistent with the suggestion that mechanisms for calcium entry may vary with the membrane potential: at 0 mV, the major pathway for calcium entry may be through halothane-sensitive L-type calcium channels, while at +60 mV entry may be through additional pathways which are relatively resistant to halothane. Actions of halothane on the time-to-peak of contraction may be accounted for by its influence on the sarcoplasmic reticulum to decrease net uptake and release of calcium. These actions of halothane might be of importance during the action potential plateau.

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