Nitric oxide (NO) is a free radical synthesized by nitric oxide synthase (N
OS) during the conversion of L-arginine to citrulline. Lead (Pb) affects ne
uronal functioning in the rat brain. Nitric oxide, a neuronal messenger has
a short half life and converts immediately into nitrite and nitrate. The p
resent study is designed to determine lead-induced alterations in NO produc
tion by measuring nitrite and nitrate in the cerebellum, the hippocampus, t
he frontal cortex and the brain stem of the rat brain. Male Sprague-Dawley
rats were treated with lead acetate (5 and 15 mg/kg body wt.) by intraperit
oneal injection. The control and experimental rats were sacrificed at the e
nd of 7 and 14 days after treatment and different regions of the brain were
isolated. Nitrite and nitrate (NOx) levels were estimated by the chemilumi
nescent method using the NOA 280 (Sievers). The data suggested dose-depende
nt and region-specific responses to lead. Both treatments of lead reduced N
Ox levels in the cerebellum and the hippocampus. However, the frontal corte
x and the brain stem responded differently to Pb exposure. NOx levels in th
e frontal cortex were significantly increased in rats treated with low and
high doses of Pb for 7 days but not in rats treated for 14 days, whereas in
the brain stem, NOx levels were increased in a dose- and time-dependent ma
nner. Although, the response was time-dependent, the variation between 7- a
nd 14-day treatment was not clearly delineated. These results provide addit
ional evidence that Pb exposure alters NO-production in rat brain leading t
o neuronal dysfunction. (C) 2000 Elsevier Science Inc. All rights reserved.