Neuropeptide Y-like immunoreactivity (NPY-LI) was investigated in naive Spr
ague-Dawley rats subjected to acute, subchronic (7 days) or chronic (21 day
s) intraperitoneal treatment with diazepam (1 or 3 mg/kg once daily) or bus
pirone (1.5 or 5 mg/kg twice daily). NPY-LI was determined by radioimmunoas
say in the amygdala, nucleus accumbens, hypothalamus and frontal cortex 24
h after the last dose of the drugs. Amygdala NPY-LI decreased after acute d
iazepam (3 mg/kg) or buspirone (1.5 mg/kg) and increased after subchronic t
reatment with both doses of diazepam and after chronic buspirone (1.5 mg/kg
) treatment. Both diazepam and buspirone given in subchronic and chronic do
ses decreased NPY-LI levels in the nucleus accumbens. Hypothalamic NPY-LI c
hanged only after chronic treatment: it decreased after diazepam and increa
sed after buspirone (5 mg/kg). NPY-LI content in the frontal cortex decreas
ed after subchronic diazepam (3 mg/kg) treatment and slightly increased aft
er buspirone. The study has shown that both diazepam and buspirone affect N
PY-LI levels in rats. These results suggest that the NPY system in the amyg
dala and nucleus accumbens is implicated in the anxiolytic effects of the d
rugs studied. (C) 1999 Harcourt Publishers Ltd.