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[抗帕金森病药物唑尼沙胺的发现]

[The discovery of an antiparkinsonian drug, zonisamide].

作者信息

Murata Miho

机构信息

Department of Neurology, National Center Hospital of Neurology & Psychiatry.

出版信息

Rinsho Shinkeigaku. 2010 Feb;50(2):67-73. doi: 10.5692/clinicalneurol.50.67.

Abstract

We serendipitously found that zonisamide (ZNS), an antiepileptic agent, has beneficial effects on Parkinson disease. A 25 mg once a day of ZNS (200-600 mg/day for epilepsy), significantly improves motor function of advanced patients with Parkinson disease. Its effects maintained at least one year even in patients with advanced stage. It was finally approved as an anti parkinsonian agent in Japan on January 2009. As the mechanism of antiparkinsonian effects of ZNS, we showed that ZNS increases dopamine contents in the striatum by activating dopamine synthesis through increasing the levels of tyrosine hydroxylase (TH) mRNA and TH protein. It moderately inhibits monoamine oxydase (MAO) activity. ZNS shows significant inhibition on T-type Ca++ channel. It may also affect the beneficial effects of ZNS on Parkinson disease. ZNS also showed neuroprotective effects on several parkinsonian models. It markedly inhibited quinoprotein formation and increased the level of glutathione by enhancing the astroglial cystine transport system and/or astroglial proliferation through S100beta. We will verify the neuroprotective effects of ZNS on patients with Parkinson disease and study the factors responsible for the individual difference of the effects of ZNS by using genome wide association study (GWAS) in the near feature.

摘要

我们偶然发现,抗癫痫药物唑尼沙胺(ZNS)对帕金森病有有益作用。每天一次服用25毫克的ZNS(用于癫痫的剂量为200 - 600毫克/天),可显著改善晚期帕金森病患者的运动功能。即使在晚期患者中,其效果也能维持至少一年。最终,它于2009年1月在日本被批准为抗帕金森病药物。关于ZNS抗帕金森病作用的机制,我们发现ZNS通过增加酪氨酸羟化酶(TH)mRNA和TH蛋白水平来激活多巴胺合成,从而增加纹状体中的多巴胺含量。它适度抑制单胺氧化酶(MAO)活性。ZNS对T型Ca++通道有显著抑制作用。这也可能影响ZNS对帕金森病的有益作用。ZNS在几种帕金森病模型中也显示出神经保护作用。它通过增强星形胶质细胞胱氨酸转运系统和/或通过S100β促进星形胶质细胞增殖,显著抑制醌蛋白形成并增加谷胱甘肽水平。在不久的将来,我们将通过全基因组关联研究(GWAS)验证ZNS对帕金森病患者的神经保护作用,并研究导致ZNS作用个体差异的因素。

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