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首页> 外文期刊>Indian Journal of Experimental Biology >Effect of cyclooxygenase-2 (COX-2) inhibitors in various animal models (bicuculline, picrotoxin, maximal electroshock-induced convulsions) of epilepsy with possible mechanism of action
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Effect of cyclooxygenase-2 (COX-2) inhibitors in various animal models (bicuculline, picrotoxin, maximal electroshock-induced convulsions) of epilepsy with possible mechanism of action

机译:环氧合酶-2(COX-2)抑制剂在癫痫的各种动物模型(比库林,微毒素,最大电击诱发的惊厥)中的作用及其可能的作用机制

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摘要

Enzyme cyclooxygenase (COX) is reported to play a significant role in neurodegeneration and may play a significant role in the pathogenesis of epilepsy. Bicuculline (4 mg/kg; ip), picrotoxin (8 mg/kg; ip) and electroshock (60 mA for 0.2 sec) significantly induced convulsions in male Laka mice. COX-inhibitors viz. nimesulide (2.5 mg/kg; ip) and rofecoxib (2 mg/kg, ip) administered 45 minutes prior to an epileptic challenge prolonged mean onset time of convulsions, decreased duration of clonus and decreased % mortality rate against bicuculline- and picrotoxin-induced convulsions in mice. COX-2 inhibitors were ineffective towards maximal electroshock-induced convulsions. Nimesulide (1 mg/kg) and rofecoxib (1 mg/kg) also enhanced the effect of subprotective dose of muscimol against picrotoxin-induced convulsions. The result of the present study strongly suggests for a possible role of cyclooxygenase isoenzymes particularly, COX-2 in the pathophysiology of epilepsy and its GABAergic modulation.
机译:据报道,酶环氧合酶(COX)在神经退行性疾病中起重要作用,并且可能在癫痫的发病机理中起重要作用。 Bicuculline(4 mg / kg; ip),pictotoxin(8 mg / kg; ip)和电击(60 mA,持续0.2 sec)在雄性Laka小鼠中引起惊厥。 COX抑制剂在癫痫发作前45分钟服用尼美舒利(2.5 mg / kg; ip)和罗非考昔(2 mg / kg,ip)延长了惊厥的平均发作时间,缩短了凝结持续时间,降低了因双小分子和苦参毒素诱发的死亡率小鼠惊厥。 COX-2抑制剂对最大程度的电击诱发的抽搐无效。尼美舒利(1 mg / kg)和罗非考昔(1 mg / kg)还增强了亚保护剂量的muscimol对次毒素引起的惊厥的保护作用。本研究的结果强烈暗示了环氧合酶同工酶,特别是COX-2在癫痫的病理生理及其GABA能调节中的可能作用。

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