Central administration of neuropeptide Y (NPY) in low concentrations h
as been shown to produce anxiolysis and suppression of locomotor activ
ity, a behavioral profile not dissimilar to that of ethanol. The prese
nt study was conducted to ascertain whether NPY and ethanol have simil
ar electrophysiological profiles and to evaluate the combined actions
of NPY and ethanol. Eighty-five Wistar rats were stereotaxically impla
nted with electrodes aimed at dorsal hippocampus, amygdala, and fronta
l cortex. Rats were administered NPY [or saline (SAL)] intracerebroven
tricularly (ICV) whereas the doses of alcohol (or SAL) were given intr
aperitoneally (IP). Two doses of alcohol (0.75, 1.5 g/kg) and two dose
s of NPY (1, 3 nmol) were given alone and in combination. Drug effects
were assessed using event related potentials (ERP) recorded in respon
se to an auditory ''odd-ball'' plus noise paradigm between 30 and 40 m
in postdrug. Multivariate analyses of variance (MANOVA) revealed that:
NPY produced a significant decrease in the amplitude and increase in
the latency of the N1 component in cortex and a decrease in the amplit
ude of the P3 component in amygdala, but no overall effects in hippoca
mpus. Ethanol produced identical effects to NPY on the N1 and P3 compo
nents of the ERP in cortex and amygdala. Combined administration of Et
OH and NPY (1 nmol) produced effects equivalent to those seen followin
g the higher doses of NPY (3 nmol) or EtOH (1.5 g/kg). These studies d
emonstrate that NPY and ethanol have a similar electrophysiological pr
ofile. In addition, the combined administration of NPY and ethanol pro
duced additive effects.