首页> 外文期刊>Pharmacology & Pharmacy >Anticonvulsant, Anxiolytic and Neurotoxicity Profile of Aqarqarha (Anacyclus pyrethrum) DC (Compositae) Root Ethanolic Extract
【24h】

Anticonvulsant, Anxiolytic and Neurotoxicity Profile of Aqarqarha (Anacyclus pyrethrum) DC (Compositae) Root Ethanolic Extract

机译:Aqarqarha(拟除虫菊酯)DC(菊科)根乙醇提取物的抗惊厥,抗焦虑和神经毒性作用

获取原文
       

摘要

Ethnopharmacological relevance: Aqarqarha (Anacyclus pyrethrum) DC root has long been used as a traditional an-tiepileptic remedy in Unani system of medicine over centuries. Aim of the Study: To rationalize the ethnomedical claim and screen for anxiolytic and neurotoxicity profile of ethanolic extract of Aqarqarha (Anacyclus pyrethrum) root (APE). Materials and Methods: The anticonvulsant and anxiolytic potential of APE (100-800 mg/kg) was evaluated against Pentylenetetrazole (PTZ), Bicuculline (BCL), Increasing current electroshock (ICES) and Elevated plus maze(EPM) models. Rotarod test was employed as neurotoxicity model including an additional higher dose (1600 mg/kg). Results: The APE showed significant anticonvulsant activity (p i.p.) in a dose-dependent manner but against BCL (30 mg/kg, i.p.) at the dose 800 mg/kg only (p 0.05). The extract also showed anxiolytic behaviour in EPM (p Conclusions: The results suggested significant anticonvulsant activity of APE against PTZ and BCL but failure against ICES. Moreover, APE also exhibited anxiolytic potential without any evidence of neurotoxicity at the effective dose level. We concluded that anticonvulsant effect of APE is probably mediated by enhancing GABAergic neurotransmission.
机译:民族药理学相关性:几个世纪以来,Aqarqarha(除虫菊酯)DC根一直被用作Unani医学体系中的传统抗癫痫药。研究的目的:为了合理化人类学上的主张,并筛选Aqarqarha(除虫菊除草菊)根(APE)乙醇提取物的抗焦虑和神经毒性特征。材料和方法:针对Pentylenetetrazole(PTZ),Bicuculline(BCL),加大电击(ICES)和Elevated plus Maze(EPM)模型评估了APE(100-800 mg / kg)的抗惊厥和抗焦虑能力。使用Rotarod试验作为神经毒性模型,包括更高的剂量(1600 mg / kg)。结果:APE表现出显着的剂量依赖性抗惊厥活性(p i.p.),但仅以800 mg / kg的剂量对BCL(30 mg / kg,i.p.)有抑制作用(p 0.05)。该提取物在EPM中也表现出抗焦虑行为(p结论:结果表明APE对PTZ和BCL具有明显的抗惊厥活性,但对ICES无效。此外,APE在有效剂量下也具有抗焦虑潜力,而没有任何神经毒性的证据。 APE的抗惊厥作用可能是通过增强GABA能神经传递介导的。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号