Heart rate reduction via selective 'funny' channel blockers

被引:55
作者
Bucchi, Annalisa
Barbuti, Andrea
Baruscotti, Mirko
DiFrancesco, Dario
机构
[1] Univ Milan, Dept Biomol Sci & Biotechnol, Lab Mol Physiol & Neurobiol, I-20133 Milan, Italy
[2] Columbia Univ, Dept Pharmacol, New York, NY 10032 USA
[3] Ctr Mol Therapeut, New York, NY 10032 USA
关键词
D O I
10.1016/j.coph.2006.09.005
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The 'funny' current, first described in cardiac pacemaker cells almost 30 years ago, is a key player in the generation of pacemaker activity and the autonomic modulation of heart rate. Because of these specific functions, a search for molecules able to interfere selectively with the 'funny' current was undertaken soon after its discovery, with the aim of developing tools for the pharmacological control of heart rate. This search has succeeded in generating a new class of drugs, the heart rate-reducing agents, which act through specific blockade of f-channels; one of these drugs, ivabradine, is presently marketed against stable angina. Because of their many functions in heart and other tissues, pharmacological utilization of "funny" channel properties is an exciting new frontier open to further developments.
引用
收藏
页码:208 / 213
页数:6
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