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线粒体钾通道的药理学:该领域的阴暗面。

Pharmacology of mitochondrial potassium channels: dark side of the field.

机构信息

Laboratory of Intracellular Ion Channels, Nencki Institute of Experimental Biology, 3 Pasteur St., 02-093 Warsaw, Poland.

出版信息

FEBS Lett. 2010 May 17;584(10):2063-9. doi: 10.1016/j.febslet.2010.02.048. Epub 2010 Feb 20.

Abstract

Mitochondrial potassium channels play an important role in cytoprotection. Potassium channels in the inner mitochondrial membrane are modulated by inhibitors and activators (potassium channel openers) previously described for plasma membrane potassium channels. The majority of mitochondrial potassium channel modulators exhibit a broad spectrum of off-target effects. These include uncoupling properties, inhibition of the respiratory chain and effects on cellular calcium homeostasis. Therefore, the rational application of channel inhibitors or activators is crucial to understanding the cellular consequences of mitochondrial channel inhibition or activation. Moreover, understanding their side-effects should facilitate the design of a specific mitochondrial channel opener with cytoprotective properties. In this review, we discuss the complex interactions of potassium channel inhibitors and activators with cellular structures.

摘要

线粒体钾通道在细胞保护中发挥着重要作用。先前已经描述了质膜钾通道的抑制剂和激活剂(钾通道开放剂)来调节线粒体内膜中的钾通道。大多数线粒体钾通道调节剂具有广泛的非靶标作用。这些作用包括解偶联特性、抑制呼吸链以及对细胞内钙稳态的影响。因此,合理应用通道抑制剂或激活剂对于理解线粒体通道抑制或激活的细胞后果至关重要。此外,了解其副作用应该有助于设计具有细胞保护特性的特定线粒体通道开放剂。在这篇综述中,我们讨论了钾通道抑制剂和激活剂与细胞结构的复杂相互作用。

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