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去极化诱导的锰离子在豚鼠心肌细胞膜上的移动。

Depolarization-induced movement of Mn 2 cations across the cell membrane in the guinea pig myocardium.

作者信息

Delahayes J F

出版信息

Circ Res. 1975 Jun;36(6):713-8. doi: 10.1161/01.res.36.6.713.

Abstract

The effects of Mn-2+-containing solutions on the mechanical and electrical responses of myocardial tissue were studied on guinea pig ventricular strips. At a concentration of 10 mM, Mn-2+ abolished the twitch responses and caused the development of a contracture in stimulated preparations but not in resting or in Ca-2+-depleted preparations. The duration of action potentials was shortened, and dV/dt-max was decreased. In Ca-2+-depleted (0.1 mM), Mg-2+-free medium, Mn-2+ also increased the amplitude of the overshoot; the increase was due to a slow phase of depolarization. Measurement of the Mn-2+ uptake showed an increased influx of these ions in stimulated preparations compared with that in quiescent preparations. These results suggest that Mn-2+ (1) generates a transmembrane current in guinea pig myocardial cells and (2) interferes with the excitation-contraction coupling process at two levels: the cell membrane and an intracellular site.

摘要

在豚鼠心室肌条上研究了含Mn²⁺溶液对心肌组织机械和电反应的影响。在浓度为10 mM时,Mn²⁺消除了抽搐反应,并在受刺激的标本中引起挛缩,但在静息或Ca²⁺耗尽的标本中未出现。动作电位的持续时间缩短,最大dV/dt降低。在Ca²⁺耗尽(0.1 mM)、无Mg²⁺的培养基中,Mn²⁺也增加了超射幅度;这种增加归因于缓慢的去极化阶段。Mn²⁺摄取量的测量表明,与静止标本相比,受刺激标本中这些离子的流入增加。这些结果表明,Mn²⁺(1)在豚鼠心肌细胞中产生跨膜电流,(2)在两个水平上干扰兴奋-收缩偶联过程:细胞膜和细胞内位点。

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