Przegaliñski E, Baran L, Siwanowicz J
Institute of Pharmacology, Polish Academy of Sciences, Kraków, Poland.
Neurosci Lett. 1996 Oct 18;217(2-3):145-8.
The effect of the nitric oxide synthase (NOS) inhibitors N-nitro-L-arginine methyl ester (L-NAME) and 7-nitroindazole (7-NI) on seizures induced by N-methyl-D-aspartate (NMDA), pilocarpine (PIL) and pentylenetetrazol (PTZ), as well as on the electroconvulsive threshold was studied in mice. It was found that L-NAME and 7-NI decreased the dose of NMDA necessary to produce clonic convulsions in 50% of animals (CD50). Such a proconvulsant effect was not observed in mice pretreated with N-nitro-D-arginine methyl ester (D-NAME), an inactive isomer of L-NAME. Neither L-NAME nor 7-NI affected the convulsions induced by PIL (clonic seizures) or PTZ (clonic and tonic seizures), having no effect on their CD50 values. Similarly, neither NOS inhibitor affected the electroshock threshold. These results, together with some literature data, indicate that nitric oxide (NO) may be regarded as an anticonvulsant substance in relation to seizures induced by NMDA and other excitatory amino acids, but not by other agents, in mice.
在小鼠中研究了一氧化氮合酶(NOS)抑制剂N-硝基-L-精氨酸甲酯(L-NAME)和7-硝基吲唑(7-NI)对由N-甲基-D-天冬氨酸(NMDA)、毛果芸香碱(PIL)和戊四氮(PTZ)诱导的癫痫发作以及对电惊厥阈值的影响。发现L-NAME和7-NI降低了在50%的动物中产生阵挛性惊厥所需的NMDA剂量(CD50)。在用L-NAME的无活性异构体N-硝基-D-精氨酸甲酯(D-NAME)预处理的小鼠中未观察到这种促惊厥作用。L-NAME和7-NI均未影响由PIL(阵挛性发作)或PTZ(阵挛性和强直性发作)诱导的惊厥,对它们的CD50值没有影响。同样,两种NOS抑制剂均未影响电休克阈值。这些结果与一些文献数据一起表明,在小鼠中,一氧化氮(NO)对于由NMDA和其他兴奋性氨基酸诱导的癫痫发作可被视为一种抗惊厥物质,但对于由其他药剂诱导的癫痫发作则不然。