Laboratory of Neurophysiology, Zoology Department, Faculty of Science, Cairo University, Giza, Egypt.
Neurochem Res. 2011 Nov;36(11):2195-204. doi: 10.1007/s11064-011-0544-9. Epub 2011 Jul 13.
Oxidative stress has been implicated to play a role in epileptogenesis and pilocarpine-induced seizures. The present study aims to evaluate the antioxidant effects of curcumin, Nigella sativa oil (NSO) and valproate on the levels of malondialdehyde, nitric oxide, reduced glutathione and the activities of catalase, Na⁺, K⁺-ATPase and acetylcholinesterase in the hippocampus of pilocarpine-treated rats. The animal model of epilepsy was induced by pilocarpine and left for 22 days to establish the chronic phase of epilepsy. These animals were then treated with curcumin, NSO or valproate for 21 days. The data revealed evidence of oxidative stress in the hippocampus of pilocarpinized rats as indicated by the increased nitric oxide levels and the decreased glutathione levels and catalase activity. Moreover, a decrease in Na⁺, K⁺-ATPase activity and an increase in acetylcholinesterase activity occurred in the hippocampus after pilocarpine. Treatment with curcumin, NSO or valproate ameliorated most of the changes induced by pilocarpine and restored Na⁺, K⁺-ATPase activity in the hippocampus to control levels. This study reflects the promising anticonvulsant and potent antioxidant effects of curcumin and NSO in reducing oxidative stress, excitability and the induction of seizures in epileptic animals and improving some of the adverse effects of antiepileptic drugs.
氧化应激被认为在癫痫发生和匹鲁卡品诱导的癫痫发作中起作用。本研究旨在评估姜黄素、黑种草籽油(NSO)和丙戊酸钠对匹鲁卡品处理大鼠海马中海马酸水平、一氧化氮、还原型谷胱甘肽、过氧化氢酶、Na ⁺ 、K ⁺ -ATP 酶和乙酰胆碱酯酶活性的抗氧化作用。癫痫动物模型通过匹鲁卡品诱导,并持续 22 天以建立癫痫慢性期。然后,这些动物用姜黄素、NSO 或丙戊酸钠治疗 21 天。数据显示,匹鲁卡品化大鼠海马中存在氧化应激证据,表现为一氧化氮水平升高、谷胱甘肽水平降低和过氧化氢酶活性降低。此外,匹鲁卡品后海马中 Na ⁺ 、K ⁺ -ATP 酶活性降低,乙酰胆碱酯酶活性升高。用姜黄素、NSO 或丙戊酸钠治疗可改善匹鲁卡品诱导的大多数变化,并将海马中的 Na ⁺ 、K ⁺ -ATP 酶活性恢复到对照水平。本研究反映了姜黄素和 NSO 在减少癫痫动物氧化应激、兴奋性和癫痫发作诱导方面的有希望的抗惊厥和有效的抗氧化作用,并改善了抗癫痫药物的一些不良反应。