香柏树抗惊厥和抗氧化性能的评价。在不同类型的实验性大鼠癫痫中

T. Sudha
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引用次数: 3

摘要

目的:采用最大电击发作(MES)、戊四唑(PTZ)和硝酸士的宁(STN)诱导大鼠癫痫发作的动物模型,研究香柏乙醇提取物的抗惊厥和抗氧化作用。方法:在MES、PTZ和STN三种动物模型中,每种模型分为四组,每组取白化大鼠(n = 6)。第1组为对照组,第2组为标准组,给予地西泮4 mg/kg,第3组和第4组为试验组,分别给予马尾草乙醇提取物200和400 mg/kg。3种实验动物模型,各组均治疗14 d。3种动物模型共12组大鼠,在给药结束后的最后一天,即第14天,分别用惊厥仪耳电极对大鼠施加150 mA的电击2 s (MES模型)、75 mg/kg PTZ模型和2 mg/kg士的宁(STN)模型)诱导大鼠在30-40 min内发生癫痫发作。只有在MES模型中取消后肢强直伸展(HLTE),以及在PTZ和STN实验模型中测量癫痫发作持续时间和潜伏期诱发癫痫阈值后,抗惊厥活性才能得到更好的评价。结果:在MES模型中,400 mg/kg剂量的EECE消除了大鼠的完全HLTE,同样在PTZ和STN实验动物模型中,相同剂量的EECE也观察到癫痫发作潜伏期延长。结论:EECE在这些动物模型中显示出有效的抗惊厥活性,其消除了MES模型中的HLTE,延迟了PTZ和STN模型中的癫痫发作阈值潜伏期。
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 anticonvulsant and antioxidant properties of Cyperus esculentus Linn. in various types of experimentally induced seizures in rats
Purpose: The purpose of the study was to evaluate the anticonvulsant and antioxidant properties of ethanolic extract of Cyperus esculentus using three animal models maximal electroshock seizure (MES), pentylenetetrazole (PTZ), and strychnine nitrate (STN) for inducing seizures in rats. Methods: In the entire three animal models, MES, PTZ, and STN, each model was included four groups, in which albino rats (n = 6) were used in each group. The first group was considered as control, the 2nd group as standard where diazepam 4 mg/kg is administered, and the 3rd and 4th served as test groups which were treated with ethanolic extract of C. esculentus (EECE) 200 and 400 mg/kg, respectively. In all the three experimental animal models, all the groups were treated for 14 days. On the last day, that is, 14th day after completion of all drugs administration in all three animal models which is total 12 groups of rats, within 30–40 min seizures were induced by exposing them to a shock of 150 mA with convulsiometer using ear electrodes for 2 s in MES model, 75 mg/kg of intraperitoneal injection of PTZ model and 2 mg/kg of strychnine (STN) model. Anticonvulsant activity was appreciated better only after abolition of hindlimb tonic extension (HLTE) in MES model and by measuring the duration of seizures and latency-induced seizure threshold in the PTZ and STN experimental rat models. Results: In MES model, EECE at a dose of 400 mg/kg abolishes complete HLTE in the rats, similarly at the same dose observed prolonged latency in the onset of seizures in both PTZ and STN experimental animal models. Conclusion: It is concluded that EECE has shown effective anticonvulsant activity in these animal models as it abolishes HLTE in MES model and delayed the latency of seizure threshold in PTZ and STN models.
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