The role of nitric oxide in the anticonvulsant effects of pyridoxine on penicillin-induced epileptiform activity in rats.

摘要

The present study was conducted to identify the role of nitric oxide (NO) in the anticonvulsant effects of pyridoxine hydrochloride on penicillin-induced epileptiform activity in rats. A single microinjection of penicillin (500units) into the left sensorimotor cortex induced epileptiform activity within 2-4min, progressing to full seizure activity lasting about 3-5h. Thirty minutes after penicillin injection, 20, 40, 80, and 160mg/kg of pyridoxine hydrochloride was administered intraperitoneally (i.p.). Pyridoxine significantly reduced the frequency of penicillin-induced epileptiform activity. A low dose of pyridoxine (40mg/kg) was the most effective in reducing both the frequency and amplitude of epileptiform activity. The effect of systemic administration of nitric oxide synthase (NOS) inhibitors, non-selective N(G)-nitro-l-arginine methyl ester (l-NAME), selective neuronal NOS inhibitor, 7-nitroindazole (7-NI) and NO substrate, l-arginine on anticonvulsive effects of pyridoxine was investigated. Theadministration of l-arginine (500mg/kg, i.p.) and 7-NI (25 and 50mg/kg, i.p.) significantly decreased the frequency of epileptiform electrocorticographical (ECoG) activity while administration of l-NAME (60mg/kg, i.p.) and the inactive form of arginine (d-arginine) did not influence it. The administration of l-NAME (60mg/kg, i.p.) 15min before pyridoxine (40mg/kg i.p.) application reversed the anticonvulsant effects of pyridoxine whereas 7-NI (25 and 50mg/kg, i.p.) did not influence it. The same dose of its inactive enantiomer N(G)-nitro-d-arginine methyl ester (d-NAME) failed to reverse the anticonvulsant effects of pyridoxine. The administration of l-arginine (500mg/kg, i.p.) did not affect the frequency of epileptiform ECoG activity in the pyridoxine administered group. l-Arginine did not reverse the anticonvulsant effect of 7-NI in the penicillin and pyridoxine administered groups. The results of present study indicate that the inhibitory effect on the anticonvulsant activity of pyridoxine against penicillin-induced epileptiform activity was produced by l-NAME, not by 7-NI, and is probably not related to the decrease of NOS activity in the brain.