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首页> 外文期刊>International Journal of Basic & Clinical Pharmacology >Anticonvulsant effect of nifedipine, dizepam and in combination on pentylenetetrazol induced experimental models of epilepsy on albino rats
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Anticonvulsant effect of nifedipine, dizepam and in combination on pentylenetetrazol induced experimental models of epilepsy on albino rats

机译:硝苯地平,地西p及其组合对戊四氮诱发的白化病大鼠癫痫实验模型的抗惊厥作用

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Background: In many patients, the presently available antiepileptic drugs such as phenobarbital, phenytoin, benzodiazepines, sodium valproate, etc., are unable to control seizures efficiently and the problem of adverse effects has also not been circumvented completely and approximately 30% of the patients continue to have seizures with current antiepileptic drugs therapy. Hence, search should continue to develop newer, more effective, and safer neuro-protective agents for treatment of epilepsy. Aim of the study was to investigate the activity of nifedipine, the dihydropyridine calcium channel blocker, diazepam, the benzodiazepine anti- convulsant of established efficacy and their combinations against rat models of pentylenetetrazol (PTZ) induced convulsions. Method: Wister albino rats of either sex, weighing between 150-220gm were used. Rats were divided into 10 groups, in each group n=6 total N=60. Methods: PTZ was administration 30 min after test drug administration. Intraperitoneal injection of PTZ at the dose of 80mg/Kg body weight were administered to the rats to produce chemically-induced seizure. The effect of nifedipine and diazepam were assessed on such seizure model. The onset and duration of clonic convulsion were recorded. Results: The onset time of PTZ-induced clonic convulsion was significantly prolonged with the Nifedipine in the doses of 4mg and 8mg per Kg. in comparison to nifedipine in dose of 2mg per Kg. The interesting observation was that while Diazepam in 1mg/Kg. dose significantly (P<0.05) prolonged the onset time, there was significant decrease (P <0.001) in the onset time of PTZ-induced clonic convulsion with diazepam in doses of 2 and 4mg per Kg. in comparison to Diazepam 1mg per Kg. But the combination of diazepam 2.5 mg and Nifedipine 2.6mg and 5.3mg exhibited significant prolongation of the onset time. Diazepam 1 and 2mg per Kg was found to be equally effective in reduction of convulsion time, while 4mg dose showed more reduction of convulsion time. The combination of diazepam and nifedipine showed no better reduction in the convulsion time and also valproic acid in doses of 135mg. Kg. Conclusions: Nifedipine (3-5mg/Kg) and diazepam (2.5mg/Kg.) combination delayed the onset of convulsion. Diazepam 2mg / Kg. alone was effective in reduction of duration of convulsion. The combination dose having 2.6mg of nifedipine showed comparable protection with valproic acid 135mg per Kg. while the combination having 5.3mg of nifedipine showed significantly better protection.
机译:背景:在许多患者中,目前可用的抗癫痫药(如苯巴比妥,苯妥英,苯二氮卓类,丙戊酸钠等)无法有效控制癫痫发作,并且尚未完全规避不良反应问题,约有30%的患者当前的抗癫痫药疗法仍会导致癫痫发作。因此,研究应继续开发更新,更有效,更安全的神经保护剂来治疗癫痫。该研究的目的是研究硝苯地平,二氢吡啶钙通道阻滞剂,地西epa,已确立效力的苯二氮卓类抗惊厥药及其组合对戊四氮(PTZ)诱发的大鼠惊厥模型的活性。方法:使用体重在150-220gm之间的两性性白化大鼠。大鼠分为10组,每组n = 6,总N = 60。方法:在试验药物给药后30分钟给药PTZ。给大鼠腹腔注射PTZ,剂量为80mg / Kg,以产生化学诱导的癫痫发作。在这种癫痫发作模型中评估了硝苯地平和地西epa的作用。记录阵挛性抽搐的发作和持续时间。结果:硝苯地平分别以每千克4mg和8mg的剂量显着延长了PTZ引起的阵挛性抽搐的发作时间。与硝苯地平相比,每公斤2mg的剂量。有趣的观察是,地西p的含量为1mg / Kg。剂量显着(P <0.05)延长了发作时间,剂量为2和4mg / Kg的PTZ引起的地西epa引起的阵挛性惊厥的发作时间显着减少(P <0.001)。与地西p每公斤1mg相比。但是地西epa 2.5 mg,硝苯地平2.6mg和5.3mg的组合显示起效时间明显延长。发现地西p 1和2mg / Kg对减少惊厥时间同样有效,而4mg剂量显示更多的惊厥时间减少。地西epa和硝苯地平的组合显示惊厥时间没有更好的减少,丙戊酸在135mg剂量下也没有更好的减少。公斤。结论:硝苯地平(3-5mg / Kg)和地西epa(2.5mg / Kg。)合用可延迟惊厥发作。地西p 2mg / Kg。单独使用可有效减少惊厥持续时间。具有2.6mg硝苯地平的联合剂量显示出与丙戊酸135mg / Kg相当的保护作用。而含有5.3mg硝苯地平的组合显示出明显更好的保护作用。

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