Molecular pharmacology of T-type Ca2+ channels

被引:70
作者
Heady, TN
Gomora, JC
Macdonald, TL
Perez-Reyes, E [1 ]
机构
[1] Univ Virginia, Dept Pharmacol, Charlottesville, VA 22908 USA
[2] Univ Virginia, Dept Chem, Charlottesville, VA 22904 USA
关键词
T-type calcium channel; antihypertensive; mibefradil; antiepileptic; anesthetic; antipsychotic; amiloride;
D O I
10.1254/jjp.85.339
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Over the past few years increasing attention has been focused on T-type calcium channels and their possible physiological and pathophysiological roles. Efforts toward elucidating the exact role(s) of these calcium channels have been hampered by the lack of T-type specific antagonists, resulting in the subsequent use of less selective calcium channel antagonists. In addition, the activity of these blockers often varies with cell or tissue type, as well as recording conditions. This review summarizes a variety of compounds that exhibit varying degrees of blocking activity towards T-type Ca2+ channels. It is designed as an aid for researchers in need of antagonists to study the biophysical and pathological nature of T-type channels, as well as a starting point for those attempting to develop potent and selective antagonists of the channel.
引用
收藏
页码:339 / 350
页数:12
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