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两例遗传性发作性肌无力:肌肉细胞膜及收缩参数的体外研究

Two cases of adynamia episodica hereditaria: in vitro investigation of muscle cell membrane and contraction parameters.

作者信息

Lehmann-Horn F, Rüdel R, Ricker K, Lorković H, Dengler R, Hopf H C

出版信息

Muscle Nerve. 1983 Feb;6(2):113-21. doi: 10.1002/mus.880060206.

Abstract

Membrane potentials, current-voltage relationships, and contractile parameters were studied in intact muscle cell bundles obtained from two patients with adynamia episodica hereditaria. In a normal extracellular medium, the cell membranes had resting potentials of about -80 mV and their current-voltage relationships were not significantly different from control curves. In contrast to normal muscles the afflicted cells were paralyzed in a medium having 6-10 mmol/liter potassium. The mechanisms of paralysis in the two specimens were different from each other. Many fibers from one patient were spontaneously active even in normal solution. In high potassium solution spontaneous activity was increased and the cells gradually depolarized to values at which excitatory sodium current is normally inactivated. This depolarization was connected with an increased sodium conductance and was reversed by the application of tetrodotoxin (TTX). The fibers from the other patient were not spontaneously active. In high potassium solution they were paralyzed at membrane potential values at which normal fibers would still contract. The reason for this paralysis was a reduced excitability.

摘要

对两名遗传性发作性肌无力患者的完整肌细胞束进行了膜电位、电流-电压关系和收缩参数的研究。在正常细胞外介质中,细胞膜的静息电位约为-80 mV,其电流-电压关系与对照曲线无显著差异。与正常肌肉不同的是,患病细胞在含有6-10 mmol/升钾的介质中会发生麻痹。两个标本中的麻痹机制彼此不同。一名患者的许多纤维即使在正常溶液中也会自发活动。在高钾溶液中,自发活动增加,细胞逐渐去极化至正常情况下兴奋性钠电流失活的值。这种去极化与钠电导增加有关,并可通过应用河豚毒素(TTX)逆转。另一名患者的纤维不会自发活动。在高钾溶液中,它们在正常纤维仍会收缩的膜电位值时发生麻痹。这种麻痹的原因是兴奋性降低。

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