首页> 外文期刊>European Journal of Medicinal Plants >Antiepileptogenic and Anticonvulsant Actionsof Dalbergia saxatilis (Hook, F.) in Sub-toxicChemical Kindling and Toxic ConvulsantModels
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Antiepileptogenic and Anticonvulsant Actionsof Dalbergia saxatilis (Hook, F.) in Sub-toxicChemical Kindling and Toxic ConvulsantModels

机译:黄檀(Hook,F.)在亚毒性化学点燃和毒性惊厥模型中的抗癫痫发生和抗惊厥作用

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Aims: The aqueous root extract of Dalbergia saxatilis (DS) is used in traditional African medicine to manage convulsions and epilepsies. This study aimed at investigating DS action against models that mimic seizure development in the neurons of epileptics, the sub-toxic dose kindling models.Study Design: Sub-toxic doses of strychnine and picrotoxin chemical kindling models; as well as single-dose toxic bicuculline convulsive models in mice.Place and Duration of Study: Neuropharmacology Unit Laboratory, Department of Pharmacology, College of Medicine, University of Lagos, Lagos, Nigeria, between July 2006 and March 2008.Methodology: Strychnine kindling was produced by a 48h interval, i.m administration of 1.5mg/kg strychnine for 9 trials. The mice were treated with 200mg/kg, p.o. DS, before strychnine thus: Group I: throughout the 1st - 9th kindling; group II: During the 1st - 5th kindling; and group III: during the 6th - 9th kindling trials. Control group received distilled water instead of DS throughout the 1st - 9th kindling trials. For picrotoxin study, a subconvulsant dose of 1.5mg/kg picrotoxin was injected i.p. 3 times a week for 10 weeks, 200mg/kg of DS was administered orally before picrotoxin thus: Group I: throughout the 1st - 30th kindling trials; group II: during the 1st - 12th kindling trials; group III: during the 13th - 30th kindling trials; control group received distilled water instead of DS throughout the 30 trials. Behavioural seizures were classified for seizure stages. In another study, DS (50-200 mg/kg, p.o.) was administered to mice, 30 min. before 10mg/kg, s.c. bicuculline and onset to seizures and time to death noted.Results: DS significantly (P=.05) retarded the development and progression of strychnine kindling, but did not reverse already reached kindled state. Moreover, DS significantly (P=.05) retarded the development of picrotoxin kindling, decreased the scoring from kindling progression and prevented convulsion in fully picrotoxin-kindled mice. A significant delay of seizure onset, with complete protection at 200mg/kg DS was produced against bicuculline seizures in mice.Conclusion: DS may attenuate development of seizures in both GABAergic and glycinergic mechanisms and be useful in the prevention of seizures as well as neuroprotection in epileptics, justifying its use in the folkloric management of epilepsies.
机译:目的:非洲黄檀(DS)的水性根提取物用于传统的非洲医学中以治疗惊厥和癫痫病。这项研究旨在研究DS对模拟癫痫神经元癫痫发作模型的作用,即亚毒性剂量点燃模型。研究设计:士的宁和次毒素化学点燃模型的亚毒性剂量;研究地点和持续时间:2006年7月至2008年3月,尼日利亚拉各斯大学医学院药理学系神经药理学部实验室,药理学方法。每隔48小时生产一次,每次9项试验均以1.5mg / kg的士的宁施用。小鼠口服200mg / kg。 DS,在士的宁之前是这样的:第一组:整个第1-第9点燃;第二组:在第一至第五次点燃期间;第三组:在第六至第九次点燃试验中。在第1至第9次点燃试验中,对照组接受蒸馏水代替DS。对于微毒素研究,腹膜内注射亚抽搐剂量为1.5mg / kg的微毒素。每周3次,共10周,在次甲基毒素之前口服200mg / kg的DS,因此:第一组:在第1次至第30次点燃试验中;第二组:在第1-12次点燃试验中;第三组:在第13-30次点燃试验中;在整个30个试验中,对照组均接受蒸馏水代替DS。将行为性癫痫发作分为癫痫发作阶段。在另一项研究中,将DS(50-200 mg / kg,p.o.)给予小鼠30分钟。在10mg / kg之前,s.c.结果:DS显着(P = .05)阻碍了士的宁点燃的发生和发展,但并未逆转已经达到点燃状态。此外,DS显着(P = .05)抑制了微毒素点燃过程的发展,降低了点燃过程的得分,并防止了完全由微毒素点燃的小鼠惊厥。癫痫发作的显着延迟,以200mg / kg的剂量完全保护了DS,可以抵抗小鼠的双小分子性癫痫。癫痫病患者,证明其在癫痫病的民间治疗中的应用是合理的。

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