
pmid: 9588756
NG-Nitro-L-arginine methyl ester (L-NAME, an unspecific nitric oxide synthase inhibitor), applied at 1 and 40 mg/kg, did not influence the electroconvulsive threshold, but impaired the anticonvulsant activity of valproate (at 40 mg/kg) and phenobarbital (at 1 and 40 mg/kg). No effect was observed in the case of carbamazepine and diphenylhydantoin. The effect of L-NAME upon the protective activity of phenobarbital was not reversed by L-arginine (500 mg/kg), a source of endogenous nitric oxide. Moreover, this nitric oxide synthase inhibitor did not alter the plasma levels of antiepileptic drugs studied, so a pharmacokinetic interaction is not probable. L-NAME per se (40 mg/kg) caused a moderate motor impairment but did not affect long-term memory. The combined treatment of L-NAME and antiepileptic drugs (providing a 50% protection against maximal electroshock) resulted in motor disturbances. On the other hand, mice performed the memory task better upon combined treatment of antiepileptic drugs with L-NAME compared to antiepileptic drugs alone. A 4-day administration of L-NAME, similarly to acute injections, decreased the protective action of phenobarbital but not that of diphenylhydantoin. The results indicate that L-NAME is able to reduce the protective activity of some conventional antiepileptics and this effect may be not associated with impaired synthesis of nitric oxide.
Electroshock, Valproic Acid, Motor Activity, Mice, Carbamazepine, NG-Nitroarginine Methyl Ester, Memory, Seizures, Phenobarbital, Phenytoin, Avoidance Learning, Animals, Anticonvulsants, Female, Enzyme Inhibitors, Nitric Oxide Synthase, Drug Antagonism
Electroshock, Valproic Acid, Motor Activity, Mice, Carbamazepine, NG-Nitroarginine Methyl Ester, Memory, Seizures, Phenobarbital, Phenytoin, Avoidance Learning, Animals, Anticonvulsants, Female, Enzyme Inhibitors, Nitric Oxide Synthase, Drug Antagonism
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