Sieks B, Hochstrate P, Schlue W R
Institut für Neurobiologie, Heinrich-Heine-Universität Düsseldorf, Germany.
Comp Biochem Physiol C Toxicol Pharmacol. 2000 Dec;127(3):273-9. doi: 10.1016/s0742-8413(00)00151-1.
In leech P neurones caffeine activates unselective ion channels in the plasma membrane and induces intracellular Ca2+ release (Schoppe, J., Hochstrate, P., Schlue, W.-R., 1997. Caffeine mediates cation influx and intracellular Ca2+ release in leech P neurones. Cell Calcium 22, 385-397). These effects are prominent only upon the first caffeine exposure, while subsequent applications are largely ineffective; i.e. both plasma membrane channels and intracellular Ca2+ release mechanism desensitize irreversibly. In order to examine whether this desensitization is paralleled by irreversible changes in the electrophysiological parameters of the cells, we investigated the action of caffeine on changes in membrane potential and the cytosolic free Ca2+ concentration, which were induced by varying the ionic composition of the extracellular fluid or by application of 5-hydroxytryptamine. Neither the resting values nor any of the experimentally induced shifts in membrane potential or cytosolic Ca2+ concentration were affected by caffeine, which suggests strongly that activation and/or desensitization of the caffeine-sensitive ion channels and Ca2+ stores have no long-lasting effect on the relevant electrochemical gradients, membrane conductances, or transport mechanisms.
在水蛭的P神经元中,咖啡因可激活质膜中的非选择性离子通道,并诱导细胞内Ca2+释放(朔普,J.,霍施特拉特,P.,施吕,W.-R.,1997年。咖啡因介导水蛭P神经元中的阳离子内流和细胞内Ca2+释放。《细胞钙》22卷,385 - 397页)。这些效应仅在首次接触咖啡因时显著,而后续应用大多无效;也就是说,质膜通道和细胞内Ca2+释放机制都会发生不可逆的脱敏。为了研究这种脱敏是否与细胞电生理参数的不可逆变化同时发生,我们研究了咖啡因对膜电位变化和胞质游离Ca2+浓度的作用,这些变化是通过改变细胞外液的离子组成或应用5-羟色胺诱导产生的。咖啡因对静息值以及实验诱导的膜电位或胞质Ca2+浓度的任何变化均无影响,这强烈表明咖啡因敏感离子通道和Ca2+储存的激活和/或脱敏对相关的电化学梯度、膜电导或转运机制没有持久影响。