Molecular pharmacodynamics, clinical therapeutics, and pharmacokinetics of topiramate

被引:116
作者
Shank, Richard P. [1 ]
Maryanoff, Bruce E. [1 ]
机构
[1] Johnson & Johnson Pharmaceut Res & Dev, Res & Early Dev, Spring House, PA 19477 USA
关键词
antiepileptic drug; aquaporin; carbonic anhydrase; epilepsy; GABA receptor; glutamate receptor; migraine; ion channel; protein phosphorylation; topiramate;
D O I
10.1111/j.1527-3458.2008.00041.x
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Topiramate (TPM; TOPAMAX(R)) is a broad-spectrum antiepileptic drug (AED) that is approved in many world markets for preventing or reducing the frequency of epileptic seizures (as monotherapy or adjunctive therapy), and for the prophylaxis of migraine. TPM, a sulfamate derivative of the naturally occurring sugar D-fructose, possesses several pharmacodynamic properties that may contribute to its clinically useful attributes, and to its observed adverse effects. The sulfamate moiety is essential, but not sufficient, for its pharmacodynamic properties. In this review, we discuss the known pharmacodynamic and pharmacokinetic properties of TPM, as well as its various clinically beneficial and adverse effects.
引用
收藏
页码:120 / 142
页数:23
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