Ca2+ channel α2δ ligands:: novel modulators of neurotransmission

被引:291
作者
Dooley, David J. [1 ]
Taylor, Charles P.
Donevan, Sean
Feltner, Douglas
机构
[1] Pfizer Global Res & Dev, Dept CNS Pharmacol, Ann Arbor, MI 48105 USA
[2] Pfizer Global Res & Dev, Dept Expt Med, Ann Arbor, MI 48105 USA
关键词
D O I
10.1016/j.tips.2006.12.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
The term 'Ca2+, channel alpha(2)delta ligands' has recently been applied to an evolving drug class that includes gabapentin (Neurontin (R)) and pregalbalin (Lyrica (R)), and reflects significant progress over the past decade in elucidating the mechanism of action of these drugs: a novel, specific action at one of the subunits constituting voltage-sensitive Ca2+, channels. Binding of these ligands to the alpha(2)delta subunit is considered to explain their usefulness in treating several clinical disorders, including epilepsy, pain from diabetic neuropathy, postherpetic neuralgia and fibromyalgia, and generalized anxiety disorder. The evidence indicates a relationship between alpha(2)delta subunit binding and the modulation of processes that subserve neurotransmission. This modulation is characterized by a reduction of the excessive neurotransmitter release that is observed in certain neurological and psychiatric disorders.
引用
收藏
页码:75 / 82
页数:8
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