含羞草(豆科)乙醇根皮提取物在实验动物中的植物化学和抗惊厥活性

O. Aiyelero, K.O. Olatunde, M. K. Salawu, O. I. Eniayewu, F. I. Ojuade, L. Akinpelu, M. G. Magaji
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摘要

背景和目的:含羞草(MPG)的各种部分在传统医学中被用于治疗惊厥性疾病。本研究旨在调查含羞草乙醇根提取物(EREM)的抗惊厥特性:方法:采用 2002 年 OECD 423 协议对提取物的急性毒性进行了研究。采用最大电击试验(MEST)评价了 200、400 和 800 mg/kg 剂量的含羞草乙醇根提取物对小鸡的抗惊厥特性;评价了马钱子碱(SCN)和戊四唑(PTZ)诱导的小鼠癫痫发作:在马钱子碱诱导的小鼠惊厥模型中,400 毫克/千克和 800 毫克/千克的提取物能明显(p<0.05)延长阵挛性和强直性惊厥的平均发作时间。在 PTZ 诱导的惊厥中,与对照组相比,400 毫克/千克的提取物能明显(p<0.05)增加阵挛性惊厥的平均发作时间,而 800 毫克/千克的提取物能明显(p<0.05)延长阵挛性和强直性惊厥的平均发作时间。在 200、400 和 800 毫克/千克的剂量下,提取物不能保护小鸡免受 MEST 的伤害,但能显著缩短平均恢复时间(p < 0.05)。在 SCN 诱导的癫痫发作中,400 和 800 毫克/千克的提取物分别能提供 60% 和 100% 的保护。同样,在 PTZ 诱导的癫痫发作中,EREM 在 400 毫克/千克和 800 毫克/千克的剂量下分别提供了 20% 和 40% 的保护。参考药物地西泮(10 毫克/千克)可明显(p<0.05)延长阵挛-强直发作的开始时间,并对 SCN 和 PTZ 诱导的小鼠惊厥具有保护作用:这些研究结果表明,EREM 对 SCN 和 PTZ 诱导的小鼠惊厥具有抗惊厥活性。因此,EREM 在民族医药中的抗惊厥作用具有科学可信性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phytochemical and Anticonvulsant Activity of the Ethanol Root Bark Extract of Mimosa pigra L. (Fabaceae) in Laboratory Animals
Background and objectives: Various parts of Mimosa pigra (MPG) are used in traditional medicines to treat convulsive disorders. The objective of this study was to investigate the anticonvulsant properties of Mimosa pigra ethanol root extract (EREM).Methods: The acute toxicity of the extract was investigated using OECD 423 protocol of 2002. The anticonvulsant properties of EREM at  200,400 and 800 mg/kg were evaluated using Maximal Electroshock Test (MEST) in chicks; strychnine (SCN-) and pentylenetetrazole (PTZ)-induced seizures in mice.Results: The extract at 400 and 800 mg/kg significantly (p<0.05) prolonged the mean onset of clonic and tonic convulsions in mouse  model of SCN-induced seizure. In PTZ-induced seizure, the extract at 400 mg/kg significantly (p<0.05) increased the mean onset of clonic seizure, while at 800 mg/kg, there was significant (p<0.05) prolongation in the mean onset of clonic and tonic seizure compared to  control. The extract did not protect the chick against MEST but significantly (p < 0.05) reduced the mean recovery time at the of 200, 400 and 800 mg/kg. The extract offered 60 and 100% protection at 400 and 800 mg/kg respectively in SCN-induced seizure. Similarly, EREM  offered 20 and 40% protection at 400 and 800 mg/kg respectively in PTZ-induced seizure. Diazepam (10 mg/kg), a reference drug significantly (p<0.05) prolonged the onset of clonic-tonic seizure and protected against SCN-, and PTZ-induced convulsion in mice.Conclusion: These findings indicated that EREM may possess anticonvulsant activity in SCN-, and PTZ-induced seizure in mice. Thus, lend scientific credence to the anticonvulsant claim of EREM in ethnomedicine.
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