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自由基清除剂依达拉奉对匹罗卡品诱导的癫痫持续状态大鼠海马的神经保护作用。

Neuroprotective effects of edaravone, a free radical scavenger, on the rat hippocampus after pilocarpine-induced status epilepticus.

作者信息

Kamida T, Fujiki M, Ooba H, Anan M, Abe T, Kobayashi H

机构信息

Department of Neurosurgery, Oita University, Faculty of Medicine, 1-1 Idaigaoka, Hasama-machi, Oita 879-5593, Japan.

出版信息

Seizure. 2009 Jan;18(1):71-5. doi: 10.1016/j.seizure.2008.06.012. Epub 2008 Jul 30.

Abstract

PURPOSE

Edaravone (MCI-186) is a newly developed antioxidative radical scavenger for the treatment of acute cerebral infarction, exerting neuroprotective effects against ischemic insult. The neuroprotective effects of edaravone on pilocarpine-induced seizures in rats were investigated.

METHODS

Rats were treated intraperitoneally with saline or edaravone (1-30 mg/kg), applied 30 min before pilocarpine hydrochloride (330 mg/kg). The onset of status epilepticus (SE) and mortality were recorded for a period of at least 3 days. The cell loss and immunoreactivities of nitric oxide synthase (NOS) in the hippocampus from control and the day 3 rats after SE, treated with saline or edaravone, were evaluated.

RESULTS

Edaravone (1mg/kg) significantly prevented cell loss in the hippocampus after SE while easier inducing SE. The higher dose of drug could not induce SE significantly but tended to increase the rate of mortality. Inducible NOS (iNOS) expression was significantly decreased in the hippocampus from day 3 rats treated with 1mg/kg edaravone, compared with saline group, while neuronal NOS (nNOS) and iNOS significantly increased in the hippocampus treated with saline, compared with control group. Significant alteration of endothelial NOS (eNOS) expression in the hippocampus among control group, saline group, and edaravone group was not shown.

CONCLUSIONS

Edaravone may act as a neuroprotector for the hippocampus after SE by reducing at least iNOS although the low dose of drug easier induces SE because of preventing an endogenous antiepileptic effect of NO.

摘要

目的

依达拉奉(MCI - 186)是一种新开发的用于治疗急性脑梗死的抗氧化自由基清除剂,对缺血性损伤具有神经保护作用。本研究旨在探讨依达拉奉对匹鲁卡品诱导的大鼠癫痫发作的神经保护作用。

方法

大鼠腹腔注射生理盐水或依达拉奉(1 - 30mg/kg),于盐酸匹鲁卡品(330mg/kg)注射前30分钟给药。记录癫痫持续状态(SE)的发作情况和死亡率,观察至少3天。评估对照组以及SE后第3天经生理盐水或依达拉奉处理的大鼠海马区的细胞损失和一氧化氮合酶(NOS)的免疫反应性。

结果

依达拉奉(1mg/kg)能显著预防SE后海马区的细胞损失,但更容易诱发SE。较高剂量的药物虽不能显著诱发SE,但有增加死亡率的趋势。与生理盐水组相比,1mg/kg依达拉奉处理的第3天大鼠海马区诱导型NOS(iNOS)表达显著降低;与对照组相比,生理盐水处理的大鼠海马区神经元型NOS(nNOS)和iNOS显著增加。对照组、生理盐水组和依达拉奉组海马区内皮型NOS(eNOS)表达未显示出显著变化。

结论

依达拉奉可能通过至少降低iNOS的表达而对SE后的海马起到神经保护作用,尽管低剂量药物因阻止NO的内源性抗癫痫作用而更容易诱发SE。

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