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细胞内钾离子和氯离子通道:特性、药理学及功能(综述)

The intracellular potassium and chloride channels: properties, pharmacology and function (review).

作者信息

Szewczyk A

机构信息

Nencki Institute of Experimental Biology, Warsaw, Poland.

出版信息

Mol Membr Biol. 1998 Apr-Jun;15(2):49-58. doi: 10.3109/09687689809027518.

Abstract

Channels selective for potassium or chloride ions are present in membranes of intracellular organelles such as sarcoplasmic (endoplasmic) reticulum, mitochondria, nucleus, synaptic vesicles, and chromaffin, and zymogen granules. They probably play an important role in cellular events such as compensation of electrical charges during transport of Ca2+, delta pH formation in mitochondria or V-ATPase containing membrane granules, and regulation of volume changes, due to potassium and chloride transport into intracellular organelles. Intracellular potassium and chloride channels could also be the target for pharmacologically active compounds. This mini-review describes the basic properties, pharmacology, and current hypotheses concerning the functional role of intracellular potassium and chloride channels.

摘要

对钾离子或氯离子具有选择性的通道存在于细胞内细胞器的膜中,如肌浆网(内质网)、线粒体、细胞核、突触小泡以及嗜铬颗粒和酶原颗粒。它们可能在细胞活动中发挥重要作用,例如在Ca2+转运过程中的电荷补偿、线粒体或含V-ATP酶的膜颗粒中ΔpH的形成,以及由于钾离子和氯离子转运到细胞内细胞器而导致的体积变化调节。细胞内的钾离子和氯离子通道也可能是药理活性化合物的作用靶点。这篇小型综述描述了关于细胞内钾离子和氯离子通道功能作用的基本特性、药理学及当前假说。

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