The mechanisms through which leptin, the protein product of the ob gene, af
fects food intake remain to be determined. To assess whether the actions of
leptin depend on modulation of within-meal satiety signals, we measured th
e effect of third ventricular leptin administration on the satiety actions
of CCK. Leptin (10 mu g) administered 1 h before 30-min access to a liquid
diet had no effect on intake when administered alone, but doses of 3.5 or 1
0 mu g dose dependently increased the suppression of intake produced by 1 n
mol/kg CCK. Examination of patterns of c-Fos activation induced by 3.5 mu g
leptin and 1 nmol/kg CCK revealed that the combination produced significan
t c-Fos activation within the area postrema and the caudal and medial nucle
us of the solitary tract (NST) compared with either leptin or CCK treatment
s alone. The leptin-CCK combination also resulted in increased c-Fos activa
tion within the paraventricular nucleus of the hypothalamus above that prod
uced by leptin alone. These data suggest that the actions of leptin in food
intake are mediated through its ability to modulate responsivity to within
-meal satiety signals.