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哺乳动物双孔结构域钾离子通道的特性与调控

Properties and modulation of mammalian 2P domain K+ channels.

作者信息

Patel A J, Honoré E

机构信息

Institut de Pharmacologie Moléculaire et Cellulaire, CNRS-UMR6097, 660 route des Lucioles, Sophia Antipolis, 06560, Valbonne, France.

出版信息

Trends Neurosci. 2001 Jun;24(6):339-46. doi: 10.1016/s0166-2236(00)01810-5.

Abstract

Mammalian 2P domain K(+) channels are responsible for background or 'leak' K(+) currents. These channels are regulated by various physical and chemical stimuli, including membrane stretch, temperature, acidosis, lipids and inhalational anaesthetics. Furthermore, channel activity is tightly controlled by membrane receptor stimulation and second messenger phosphorylation pathways. Several members of this novel family of K(+) channels are highly expressed in the central and peripheral nervous systems in which they are proposed to play an important physiological role. The pharmacological modulation of this novel class of ion channels could be of interest for both general anaesthesia and ischaemic neuroprotection.

摘要

哺乳动物的2P结构域钾离子通道负责背景或“渗漏”钾离子电流。这些通道受多种物理和化学刺激的调节,包括膜拉伸、温度、酸中毒、脂质和吸入性麻醉剂。此外,通道活性受膜受体刺激和第二信使磷酸化途径的严格控制。这个新的钾离子通道家族的几个成员在中枢和外周神经系统中高度表达,据推测它们在其中发挥重要的生理作用。这类新型离子通道的药理学调节可能对全身麻醉和缺血性神经保护都具有重要意义。

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