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对青蛙神经和肌肉膜的温度实验。相变的迹象。

Temperature experiments on nerve and muscle membranes of frogs. Indications for a phase transition.

作者信息

Schwarz W

出版信息

Pflugers Arch. 1979 Oct;382(1):27-34. doi: 10.1007/BF00585900.

Abstract

The influence of temperature changes in the range of 25 degrees C to -6 degrees C on the time constants of Na activation (tau m) and inactivation (tau h) was studied in twitch muscle fibers and the node of Ranvier under voltage-clamp conditions. Arrhenius plots of tau m and tau h exhibit a change in activation enthalpy at temperatures below 10 degrees C. Cooling and subsequent heating induce a hysteresis in the temperature dependence of tau m and tau h; Ni2+ and UO22+ increase the hysteresis width. With fast temperature changes the gating kinetics relax to their new values more slowly than the temperature change. Hence, temperature must be changed more slowly than 5 degrees C/min if an additional apparent hysteresis due simply to this relaxation is to be avoided. The data are explained by the hypothesis of a phase transition in the membrane lipids. This conception is favoured over a temperature-induced change in protein conformation, since the neutral local anaesthetic benzocaine shows use-dependent block as if low temperature restricted the access of the drug through the lipid phase to its receptor.

摘要

在电压钳制条件下,研究了25℃至-6℃温度范围内温度变化对抽搐肌纤维和郎飞结处钠激活时间常数(τm)和失活时间常数(τh)的影响。τm和τh的阿累尼乌斯图显示,在温度低于10℃时,激活焓发生变化。冷却及随后的加热在τm和τh的温度依赖性上诱导出滞后现象;Ni2+和UO22+会增加滞后宽度。在快速温度变化时,门控动力学向其新值的松弛比温度变化更慢。因此,如果要避免仅仅由于这种松弛而产生的额外明显滞后现象,温度变化必须比5℃/分钟更慢。这些数据由膜脂质中相变的假设来解释。这种概念比蛋白质构象的温度诱导变化更受青睐,因为中性局部麻醉药苯佐卡因表现出使用依赖性阻滞,就好像低温限制了药物通过脂质相到达其受体的通道。

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