Effects of different extracts of Eugenia caryophyllata on pentylenetetrazole-induced seizures in mice.

Mahmoud Hosseini, Taha Jafarianheris, Navid Seddighi, Mohammad Parvaneh, Ahmad Ghorbani, Hamid Reza Sadeghnia, Hassan Rakhshandeh
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引用次数: 7

Abstract

Objective: To investigate the possible anticonvulsant effect of different extracts of Eugenia caryophyllata (clove) on pentylenetetrazole (PTZ)-induced seizures in mice.

Methods: The animals were divided into saline, 50, 100, 250 and 500 mg/kg of aqueous extract, 50, 100, 250 and 500 mg/kg of ethanolic extract, and 50, 100, 250 and 500 mg/kg of chloroformic extract of clove groups. The extracts or saline were injected 60 min before each PTZ injection. Latency to the first minimal clonic seizure (MCS) and generalized tonic-clonic seizure (GTCS) and the percent of mortality were recorded.

Results: Aqueous extract of clove at doses of 50, 100, 250 and 500 mg/kg significantly extended the MCS and GTCS latency (P<0.05). The MCS latency in mice treated with 50, 100 and 250 mg/kg of the ethanolic extract was significantly increased (P<0.05). The GTCS latency in mice treated with 50, 100, 250 and 500 mg/kg of ethanolic extract was significantly higher than that of the saline-treated group (P<0.05). There were no significant differences in MCS and GTCS latency between mice treated with different chloroformic extract of clove or saline.

Conclusion: The aqueous and ethanolic extracts of clove could inhibit the PTZ-induced convulsion, and this plant has the potential to be used as a new therapeutic agent for control of seizures. The exact mechanisms and the active compounds that are responsible for the anticonvulsive effect need to be clarified in future studies.

丁香不同提取物对戊四唑致小鼠癫痫发作的影响。
目的:探讨丁香不同提取物对戊四唑(PTZ)致小鼠癫痫发作的可能抗惊厥作用。方法:将动物分为盐水组、50、100、250、500 mg/kg水提物组、50、100、250、500 mg/kg乙醇提物组和50、100、250、500 mg/kg氯甲酸提物组。每次注射PTZ前60分钟注射提取物或生理盐水。记录首次最小阵挛性发作(MCS)和全身性强直阵挛性发作(GTCS)的潜伏期和死亡率百分比。结果:50、100、250和500 mg/kg剂量丁香水提物均能显著延长大鼠MCS和GTCS潜伏期(p)。结论:丁香水提物和乙醇提物均能抑制ptz诱导的惊厥,具有作为控制癫痫发作新药物的潜力。确切的机制和抗惊厥作用的活性化合物需要在未来的研究中澄清。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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