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新型抗癫痫药物唑尼沙胺的神经药理学

Neuropharmacology of zonisamide, a new antiepileptic drug.

作者信息

Hammond E J, Perchalski R J, Wilder B J, McLean J R

出版信息

Gen Pharmacol. 1987;18(3):303-7. doi: 10.1016/0306-3623(87)90016-4.

Abstract

Zonisamide readily crosses the blood-brain barrier and is readily absorbed after oral administration with a Tmax of about 3 hr. The half-life of ZNA in epileptic patients is about 28 hr. Zonisamide has a broader therapeutic range than other antiepileptic drugs. Neurotoxic, hemapoietic, renal, and liver effects have been minimal in patients participating in controlled clinical studies. It is effective in several experimental models of epilepsy and in initial clinical trials has been shown to be effective in generalized tonic-clonic, simple, and complex partial seizures.

摘要

唑尼沙胺易于穿过血脑屏障,口服给药后易于吸收,达峰时间约为3小时。癫痫患者中唑尼沙胺的半衰期约为28小时。唑尼沙胺的治疗范围比其他抗癫痫药物更广。参与对照临床研究的患者中,其神经毒性、血液系统、肾脏和肝脏方面的影响极小。它在几种癫痫实验模型中有效,在初步临床试验中已显示对全身强直阵挛性发作、简单和复杂部分性发作有效。

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