THE role played by nitric oxide (NO) in modulating seizure activity an
d cerebral blood flow (CBF) during seizures was investigated in rats.
Seizures were induced with bicuculline (a GABA antagonist, 1.2 mg kg(-
1), i.v.). Each animal was subjected to an initial bicuculline-induced
seizure followed by treatment with either L-nitroarginine (L-NA, a NO
synthase inhibitor) or its less active enantiomer D-NA as a 50 mg kg(
-1) bolus followed by an infusion of 1 mg kg(-1) min(-1). The animals
then received a second bicuculline treatment. Seizure duration was mon
itored using EEG and CBF was measured with laser-Doppler. There was no
difference in seizure duration before or after D-NA administration. S
eizure duration doubled from (6 +/- 1 to 12 +/- 2 min p < 0.05) follow
ing inhibition of NO synthase with L-NA. The increase in CBF that acco
mpanied the seizure activity paralleled the seizure duration. Our data
support the concept that (1) NO acts as an endogenous anticonvulsant,
with seizure duration doubling when NO synthase is acutely inhibited,
and (2) that NO is not the messenger that couples CBF to metabolism d
uring bicuculline-induced seizures.