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细胞内钙与神经元起搏器活动的调控

Intracellular calcium and the control of neuronal pacemaker activity.

作者信息

Gorman A L, Hermann A, Thomas M V

出版信息

Fed Proc. 1981 Jun;40(8):2233-9.

PMID:6786922
Abstract

Pacemaker activity of the Aplysia bursting pacemaker neuron R-15 was analyzed. It was shown that the free intracellular Ca2+ concentration, as measured by arsenazo III, increases during the depolarizing phase of the pacemaker cycle and declines throughout the hyperpolarizing phase that follows. This increase in Ca2+ results from the activation of voltage-dependent Ca2+ channels that open during the depolarizing phase of the cycle. The extracellular K+ concentration also increases during the depolarizing phase of the cycle and is correlated with an outward K+ current that opposes the inward current carried by Ca2+ ions. The increase in internal Ca2+ is sufficient to activate a K+ conductance that depends on the magnitude of the change in internal Ca2+ and on membrane potential, which is responsible for the hyperpolarizing phase of the cycle. It is proposed that the membrane oscillation depends on three separate but linked systems, which include a voltage-dependent Ca2+ channel, the internal Ca2+ concentration, and a Ca2+-activated K+ channel.

摘要

对海兔爆发性起搏神经元R-15的起搏活动进行了分析。结果表明,用偶氮胂III测量的细胞内游离Ca2+浓度在起搏周期的去极化阶段升高,并在随后的超极化阶段持续下降。Ca2+的这种升高是由于在周期的去极化阶段开放的电压依赖性Ca2+通道的激活。细胞外K+浓度在周期的去极化阶段也会升高,并且与一种外向K+电流相关,该电流与Ca2+离子携带的内向电流相反。内部Ca2+的增加足以激活一种K+电导,该电导取决于内部Ca2+变化的幅度和膜电位,这负责周期的超极化阶段。有人提出,膜振荡依赖于三个独立但相互关联的系统,其中包括一个电压依赖性Ca2+通道、内部Ca2+浓度和一个Ca2+激活的K+通道。

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