首页> 外文期刊>Pharmacology, Biochemistry and Behavior >The effect of N-nitro-L-arginine methyl ester posttreatment on the anticonvulsant effect of phenobarbitone and diazepam on picrotoxin-induced convulsions in rats.
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The effect of N-nitro-L-arginine methyl ester posttreatment on the anticonvulsant effect of phenobarbitone and diazepam on picrotoxin-induced convulsions in rats.

机译:N-硝基-L-精氨酸甲酯后处理对苯巴比妥和地西epa对微毒素诱导的大鼠惊厥的抗惊厥作用的影响。

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摘要

The present study has investigated the effect of posttreatment of the nonspecific inhibitor of nitric oxide (NO) synthase (NOS), N-nitro-L-arginine methyl ester (L-NAME), on the anticonvulsant effect of phenobarbitone and diazepam on picrotoxin-induced convulsions in rats. Phenobarbitone, which is known to inhibit convulsions by potentiating gamma-aminobutyric acid (GABA) activity in the brain, did not inhibit the convulsive action of picrotoxin in L-NAME-posttreated animals. L-NAME produced no such interaction with diazepam, which inhibits convulsions through GABA potentiation as well as by a GABA-independent mechanism. L-arginine, the precursor of NO, increased the protective effect of both phenobarbitone and diazepam. These results suggest that a decreased synthesis of NO in the brain by the nonspecific inhibitors of NOS is likely to result in an impairment of the anticonvulsant effect of antiepileptics that inhibit convulsions solely by potentiating GABA activity in the brain.
机译:本研究研究了一氧化氮(NO)合酶(NOS)的非特异性抑制剂N-硝基-L-精氨酸甲酯(L-NAME)的后处理对苯巴比妥和地西epa对微毒素的抗惊厥作用的影响诱发大鼠惊厥。苯巴比妥已知通过增强脑中的γ-氨基丁酸(GABA)活性来抑制惊厥,但在L-NAME后处理的动物中并未抑制微毒素的惊厥作用。 L-NAME与地西epa没有产生这种相互作用,后者通过GABA增强作用以及通过GABA独立机制抑制惊厥。 NO的前体L-精氨酸增强了苯巴比妥和地西epa的保护作用。这些结果表明,NOS的非特异性抑制剂在大脑中减少的NO合成很可能会导致抗癫痫药的抗惊厥作用受损,这些止痛药仅通过增强脑中的GABA活性来抑制惊厥。

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