NITRIC-OXIDE SYNTHASE INHIBITORS L-NAME AND 7-NITROINDAZOLE PROTECT RAT HIPPOCAMPUS AGAINST KAINATE-INDUCED EXCITOTOXICITY

The role of nitric oxide in cerebral insults remains controversial. Wh ile numerous studies have used models of ischaemia and hypoxia, few ha ve examined nitric oxide in the kainate model of excitotoxicity. Kaina te (10 mg/kg) was administered to rats via the intraperitoneal (i,p.) route to induce submaximal damage to the CA1, CA2 and CA3a regions of the hippocampus after 7 days. Systemic injections of the nitric oxide synthase (NOS) inhibitors N-G-nitro-L-argjnine methyl ester (L-NAME) a nd 7-nitroindazole (7-NI), both at a dose of 5 mg/kg, reduced cell dea th in all three regions. As 7-NI selectively inhibits the neuronal for m of NOS, this study suggests that nitric oxide produced from a neuron al and not epithelial source may contribute to neuronal damage in this model. (C) 1998 Elsevier Science Ireland Ltd. All rights reserved.