首页> 外文期刊>Comparative biochemistry and physiology. Toxicology & pharmacology: CBP >Activation and desensitization of the caffeine-sensitive cationc channels and calcium stores have no persistent effect on the electrophysiological properties of leech P neurones
【24h】

Activation and desensitization of the caffeine-sensitive cationc channels and calcium stores have no persistent effect on the electrophysiological properties of leech P neurones

机译:咖啡因敏感阳离子通道和钙存储的激活和脱敏对水le P神经元的电生理特性没有持久影响

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

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-Iasting effect on the relevant electrochemical gradients, membrane conductances, or transport mechanisms.
机译:在水ech P神经元中,咖啡因激活质膜中的非选择性离子通道并诱导细胞内Ca2 +释放(Schoppe,J.,Hochstrate,P.,Schlue,W.-R.,1997。咖啡因介导水in中的阳离子流入和细胞内Ca2 +释放。 P神经元,细胞钙22,385-397)。这些影响仅在第一次咖啡因暴露时才显着,而随后的应用在很大程度上无效。即质膜通道和细胞内Ca2 +释放机制均不可逆转地脱敏。为了检查这种脱敏是否与细胞的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和胞浆游离Ca 2 +浓度变化的作用,这是通过改变细胞外离子组成而引起的。液体或使用5-羟色胺。咖啡因既不影响静止值,也不影响膜电位或胞浆中Ca2 +浓度的任何实验诱导变化,这强烈表明咖啡因敏感性离子通道和Ca2 +储存的激活和/或脱敏没有长期的影响。有关的电化学梯度,膜电导或传输机制。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号