Kulkarni S K, Ticku M K
Department of Pharmacology, University of Texas Health Science Center, San Antonio 78284-7764.
Life Sci. 1989;44(18):1317-23. doi: 10.1016/0024-3205(89)90370-6.
The interaction between GABAergic (barbiturates, diazepam, ethanol) and other (phenytoin) anticonvulsants and the N-methyl-D-aspartate (NMDA) receptor antagonist MK 801 in protecting rats against maximal electroshock (MES)- and picrotoxin-induced (10 mg/kg) convulsions was studied. MK 801 (0.1 to 5 mg/kg) showed anticonvulsant responses against MES-induced convulsions in a dose dependent manner, higher doses showing severe muscle relaxation, motor incoordination, and anticonvulsant action. It also produced stereotypic head movement, circling behavior, and affected locomotion. When subanticonvulsant dose (1 mg/kg) of MK 801 was simultaneously administered with subprotective doses of GABAergic anticonvulsants, it significantly potentiated the effects of barbiturates, as compared to other agents. At 1 mg/kg, MK 801 did not offer protection against tonic convulsions though protected (100%) the animals from mortality due to picrotoxin-induced convulsions. It potentiated the effect of a subprotective dose (5 mg/kg) of pentobarbital, but not of diazepam, against tonic convulsions. However, no mortality was observed in either group. The antiglutamate action of barbiturates, particularly that of pentobarbital, may contribute to the observed potentiating response between pentobarbital and MK 801.
研究了γ-氨基丁酸能药物(巴比妥类、地西泮、乙醇)和其他抗惊厥药物(苯妥英)与N-甲基-D-天冬氨酸(NMDA)受体拮抗剂MK 801在保护大鼠对抗最大电休克(MES)和匹鲁卡品诱导(10毫克/千克)惊厥方面的相互作用。MK 801(0.1至5毫克/千克)对MES诱导的惊厥呈现剂量依赖性的抗惊厥反应,较高剂量表现出严重的肌肉松弛、运动不协调和抗惊厥作用。它还会产生刻板的头部运动、转圈行为,并影响运动。当MK 801的亚抗惊厥剂量(1毫克/千克)与亚保护剂量的γ-氨基丁酸能抗惊厥药物同时给药时,与其他药物相比,它显著增强了巴比妥类药物的效果。在1毫克/千克时,MK 801虽能使动物免于匹鲁卡品诱导惊厥导致的死亡(100%),但对强直性惊厥无保护作用。它增强了戊巴比妥亚保护剂量(5毫克/千克)对强直性惊厥的作用,但未增强地西泮的作用。然而,两组均未观察到死亡情况。巴比妥类药物,尤其是戊巴比妥的抗谷氨酸作用,可能是观察到的戊巴比妥与MK 801之间增强反应的原因。