香芹酚对戊四唑(PTZ)诱发的雄性小鼠癫痫发作的抗惊厥作用的评价:n -甲基- d -天冬氨酸受体的作用

H. Amini-khoei, Shakiba Nasiri Boroujeni, Z. Lorigooini, Sepideh Yadollahi, Seyyed Kamal Solati Dehkordi, Mahmoud Rafieian Koopai
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引用次数: 0

摘要

背景。癫痫是中风后最常见的神经系统疾病之一。由于常规抗惊厥药物的副作用和不良反应,研究人员已将注意力转向寻找新的药物。香芹酚是一种酚类化合物,具有神经保护、抗炎、抗氧化和抗惊厥作用。本研究旨在探讨香芹酚对ptz诱导的雄性小鼠癫痫发作的抗惊厥作用,并探讨n -甲基- d -天冬氨酸(NMDA)受体的作用。方法。在本实验研究中,90只小鼠随机分为9组(n=10)。药物于PTZ注射前30分钟腹腔注射。然后检测癫痫发作时间、血清和脑抗氧化能力(TAC)、海马丙二醛(MDA)和NMDA受体基因表达。结果。卡伐克罗(20、40 mg/kg)组癫痫发作时间明显长于PTZ组(P<0.05)。与PTZ组(剂量为5、10、20和40 mg/kg)相比,carvacrol(20和40 mg/kg)显著提高了血清和脑抗氧化能力,降低了血清和脑MDA。carvacrol组小鼠海马NMDA受体NR2A、NR2B亚基表达量显著低于PTZ组(P<0.05)。结论。香芹酚具有抗惊厥作用,可能是通过抑制氧化应激和减少NMDA受体亚基的表达。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Evaluation of the anticonvulsant effect of carvacrol in Pentylenetetrazole (PTZ)-induced seizures in male mice: N-Methyl-D-Aspartic Acid receptor role
Background. Epilepsy is one of the most common neurological disorders after stroke. Due to the side effects and poor response of conventional anticonvulsant drugs, researchers have turned their attention to find new drugs. Carvacrol is a phenolic compound with neuroprotective, anti-inflammatory, antioxidant and anticonvulsant effects. The aim of the study was to investigate the anticonvulsant effects of carvacrol in PTZ-induced seizures in male mice and to investigate the role of N-Methyl-D-Aspartic Acid (NMDA) receptor. Methods. In the present experimental study, 90 mice were randomly divided into 9 groups (n=10). Drugs were injected intraperitoneally 30 minutes before PTZ injection. Then, seizure onset time, serum and brain antioxidant capacity (TAC) and malondialdehyde (MDA) and NMDA receptor gene expression in the hippocampus were examined. Results. Seizure onset time in the group received carvacrol (20 and 40 mg/kg) was significantly longer than the PTZ group (P<0.05). Treatment with carvacrol (20 and 40 mg/kg) significantly increased serum and brain antioxidant capacity and reduced serum and brain MDA in compared to the PTZ group (at doses of 5, 10, 20 and 40 mg/kg). The expression of NR2A and NR2B subunits of hippocampal NMDA receptors in carvacrol-received mice was significantly lower than the PTZ group (P<0.05). Conclusion. Carvacrol has anticonvulsant effects, possibly by inhibiting oxidative stress and reducing the expression of subunits of NMDA receptors.
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