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首页> 外文期刊>Journal of Pharmacy and Pharmacology >Influence of etoricoxib on anticonvulsant activity of phenytoin and diazepam in experimental seizure models in mice
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Influence of etoricoxib on anticonvulsant activity of phenytoin and diazepam in experimental seizure models in mice

机译:依托考昔对小鼠实验性癫痫模型中苯妥英和地西epa的抗惊厥活性的影响

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Objectives Our aim was to investigate the effect of etoricoxib on the anticonvulsant activity of phenytoin and diazepam against seizure models in mice. In addition the acute adverse effect of etoricoxib was assessed with a chimney test. Methods The maximal seizure pattern was induced in mice by giving an alternating current of 50 mA for 0.2 s, while chemical seizures were induced by intraperitoneal injection of pentylenetetrazole at its CD97 dose (97% convulsive dose for the clonic phase). Test drug was administered 45 min before the electrical or chemical induction of seizures in combination with conventional antiepileptics. The ability of the test drag to reduce or abolish the extensor phase of maximal electroshock and clonk-type seizures in the chemical induction method was selected as anti-seizure criteria. Key findings Concurrent treatment with etoricoxib at an oral dose of 10 mg/kg reduced the anticonvulsant potency of phenytoin. The protective effects of diazepam against pentylenetetrazole-induced convulsions was significantly increased and the mortality rate was reduced by concurrent treatment with etoricoxib (10 mg/kg p.o.) when compared with diazepam groups. No neurotoxic effect was observed with etoricoxib (10 mg/kg p.o.) and it had no impact on motor coordination in the chimney test in mice. Etoricoxib applied at its highest dose (10 mg/kg) significantly enhanced the free plasma levels of diazepam whereas the free plasma levels of phenytoin were significantly reduced. Conclusions The obtained results suggest that the preferential cyclooxygenase-2 inhibitor etoricoxib significantly reduced the anticonvulsant action of phenytoin and significantly increased the beneficial action of diazepam against maximal electroshock and pentylenetetrazole-induced convulsions in a mouse model.
机译:目的我们的目的是研究依托考昔对苯妥英钠和地西epa对小鼠癫痫发作模型的抗惊厥作用。另外,通过烟囱试验评估了依托昔布的急性不良反应。方法给予50 mA交流电流0.2 s,在小鼠中诱发最大癫痫发作模式,而腹膜内注射CD97剂量的戊烯四唑(抽搐期为惊厥剂量的97%)则诱发化学性癫痫发作。在与常规抗癫痫药联合用电或化学诱发癫痫发作之前45分钟给予测试药物。选择在化学诱导法中减少或消除最大电击和血栓型癫痫发作的伸肌相的能力作为抗癫痫发作的标准。主要发现口服10 mg / kg的依托昔布同时治疗可降低苯妥英钠的抗惊厥作用。与地西epa组相比,通过同时用依托昔布(10 mg / kg p.o.)治疗,地西m对戊烯四唑诱发的惊厥的保护作用显着提高,死亡率降低。依托昔布(10 mg / kg p.o.)没有观察到神经毒性作用,并且在小鼠的烟囱试验中对运动协调性没有影响。以最高剂量(10 mg / kg)施用的Etoricoxib显着提高了地西epa的游离血浆水平,而苯妥英的游离血浆水平则明显降低。结论获得的结果表明,优先的环氧合酶-2抑制剂依托考昔显着降低了苯妥英的抗惊厥作用,并显着增强了地西mouse对小鼠模型中最大的电击和戊四唑诱发的惊厥的有益作用。

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