4.7 Review

K+ channels as therapeutic drug targets

期刊

PHARMACOLOGY & THERAPEUTICS
卷 94, 期 1-2, 页码 157-182

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/S0163-7258(02)00201-2

关键词

K+ channels; immunosuppression; arrhythmia; epilepsy; dementia; secretion

向作者/读者索取更多资源

K+ channels play critical roles in a wide variety of physiological processes, including the regulation of heart rate, muscle contraction, neurotransmitter release, neuronal excitability, insulin secretion, epithelial electrolyte transport, cell volume regulation, and cell proliferation. As such, K+ channels have been recognized as potential therapeutic drug targets for many years. Unfortunately, progress toward identifying selective K+ channel modulators has been severely hampered by the need to use native currents and primary cells in the drug-screening process. Today, however, more than 80 K+ channel and K+ channel-related genes have been identified, and an understanding of the molecular composition of many important native K+ currents has begun to emerge. The identification of these molecular K+ channel drug targets should lead to the discovery of novel drug candidates. A summary of progress is presented. (C) 2002 Elsevier Science Inc. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据