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巯基抑制剂对蛙骨骼肌纤维去极化-收缩偶联的影响。

Effects of sulfhydryl inhibitors on depolarizations-contraction coupling in frog skeletal muscle fibers.

作者信息

Caputo C, Bolaños P, Gonzalez A

机构信息

Centro de Biofisica y Bioquimica, Instituto Venezolano de Investigaciones Cientificas, Caracas, Venezuela.

出版信息

J Gen Physiol. 1993 Mar;101(3):411-24. doi: 10.1085/jgp.101.3.411.

Abstract

We have studied the effects of the sulfhydryl reagents on contractile responses, using either electrically stimulated single muscle fibers or short muscle fibers that were voltage-clamped with a two-microelectrode voltage-clamp technique that allows the fiber tension in response to membrane depolarization to be recorded. The sulfhydryl inhibitors para-chloromercuribenzoic acid (PCMB) and parahydroximercuriphenyl sulfonic acid (PHMPS), at concentrations from 0.5 to 2 mM, cause loss of the contractile ability; however, before this effect is completed, they change the fiber contractile behavior in a complex way. After relatively short exposure to the compounds, < 20 min, before the fibers lose their contractile capacity, secondary tension responses may appear after electrically elicited twitches or tetani. After losing their ability to contract in response to electrical stimulation, the fibers maintain their capacity to develop caffeine contractures, even after prolonged periods (120 min) of exposure to PHMPS. In fibers under voltage-clamp conditions, contractility is also lost; however, before this happens, long-lasting (i.e., minutes) episodes of spontaneous contractile activity may occur with the membrane polarized at -100 mV. After more prolonged exposure (> 30 min), the responses to membrane depolarization are reduced and eventually disappear. The agent DTT at a concentration of 2 mM appears to protect the fibers from the effects of PCMB and PHMPS. Furthermore, after loss of the contractile responses by the action of PCMB or PHMPS, addition of 2 mM DTT causes recovery of tension development capacity.

摘要

我们使用电刺激的单根肌纤维或采用双微电极电压钳技术进行电压钳制的短肌纤维(该技术可记录纤维在膜去极化时的张力响应),研究了巯基试剂对收缩反应的影响。巯基抑制剂对氯汞苯甲酸(PCMB)和对羟基汞苯磺酸(PHMPS),浓度在0.5至2 mM时,会导致收缩能力丧失;然而,在这种效应完全显现之前,它们会以复杂的方式改变纤维的收缩行为。在相对较短时间(<20分钟)接触这些化合物后,在纤维失去收缩能力之前,电诱发的抽搐或强直收缩后可能会出现继发性张力反应。在失去对电刺激的收缩能力后,即使在长时间(120分钟)暴露于PHMPS后,纤维仍保持产生咖啡因挛缩的能力。在电压钳制条件下的纤维中,收缩性也会丧失;然而,在此之前,当膜极化至-100 mV时,可能会出现持续较长时间(即数分钟)的自发收缩活动。在更长时间(>30分钟)暴露后,对膜去极化的反应会减弱并最终消失。浓度为2 mM的二硫苏糖醇(DTT)似乎能保护纤维免受PCMB和PHMPS的影响。此外,在PCMB或PHMPS作用导致收缩反应丧失后,添加2 mM DTT可使张力产生能力恢复。

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