The hippocampus has been shown to exhibit particular vulnerability to
ischemia, suggesting the existence of inherent processes leading to ne
uronal death. Nitric oxide (NO) has been implicated in neurotoxicity d
ue to ischemia. The relationship between regional distribution of NO s
ynthesis induced by ischemia and the areas vulnerable to ischemia rema
ins elusive. In the present study, we explored regional variation in N
O synthesis by determining the concentrations of nitrite (NO2-), a maj
or metabolite of NO, in the brain in vivo microdialysis samples obtain
ed from the hippocampus and the striatum subjected to ischemia. Spragu
e-Dawley rats were anesthetized with pentobarbital (40 mg/kg, i.p.). A
n in vivo microdialysis probe was implanted into the hippocampus or th
e striatum. Subsequently, the animals were subjected to forebrain isch
emia for 20 min by occlusion of both common carotid arteries and induc
ed hypotension. Forebrain ischemia gave rise to a significant change i
n NO2- level only in the hippocampus, resulting in an increase to 111.
2 +/- 5.4 (mean +/- SEM) % of the preischemia level. This finding sugg
ests the presence of a regional difference in NO production during isc
hemia, which may be concerned with the underlying mechanism of ischemi
c vulnerability. (C) 1997 Academic Press.