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钙调神经磷酸酶调节交感神经元中的M通道模式门控。

Calcineurin regulates M channel modal gating in sympathetic neurons.

作者信息

Marrion N V

机构信息

Vollum Institute, Oregon Health Sciences University, Portland 97201-3098, USA.

出版信息

Neuron. 1996 Jan;16(1):163-73. doi: 10.1016/s0896-6273(00)80033-1.

Abstract

The M current regulates neuronal excitability, with its amplitude resulting from high open probability modal M channel behavior. The M current is affected by changing intracellular calcium levels. It is proposed that internal calcium acts by regulating M channel modal gating. Intracellular application of a preactivated form of the calcium-dependent phosphatase calcineurin (CaN420) inhibited the macroscopic M current, while its application to excised inside-out patches reduced high open probability M channel activity. Addition of ATP reversed the action of CaN420 on excised patches. The change in M channel gating induced by CaN420 was different from the effect of muscarine. A kinetic model supports the proposition that shifts in channel gating induced by calcium-dependent phosphorylation and dephosphorylation control M current amplitude.

摘要

M电流调节神经元兴奋性,其幅度源于高开放概率模式的M通道行为。M电流受细胞内钙水平变化的影响。有人提出,细胞内钙通过调节M通道模式门控起作用。细胞内应用钙依赖性磷酸酶钙调神经磷酸酶(CaN420)的预激活形式可抑制宏观M电流,而将其应用于切除的内向外膜片则降低了高开放概率M通道活性。添加ATP可逆转CaN420对切除膜片的作用。CaN420诱导的M通道门控变化不同于毒蕈碱的作用。一个动力学模型支持这样的观点,即钙依赖性磷酸化和去磷酸化诱导的通道门控变化控制M电流幅度。

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