The modulation of alpha(2)-adrenoceptor-induced food intake by oxytocin has
been evaluated in studies on food intake and by quantitative receptor auto
radiography in the hypothalamus and the amygdala of the rat. The effects of
lateral intracerebroventricular administration of clonidine and oxytocin w
ere evaluated on food intake in satiated animals, Food consumption was meas
ured at 30, 90, 240 min and 22 h (1,320 min) after injection. The coinjecti
on of oxytocin and clonidine was found to counteract the increase in food i
ntake produced by clonidine (p < 0.001) in satiated rats. Receptor autoradi
ographic experiments showed that oxytocin significantly increased the K-d v
alues of [H-3]p-aminoclonidine alpha(2)-agonist-binding sites in the hypoth
alamus. Effective oxytocin concentrations ranged between 0.3 and 1 nM (p <
0.05) with a maximal action of 250% at 1 nM. The B-max value was significan
tly increased (p < 0.05) for all concentrations of oxytocin. In the amygdal
a, oxytocin also increased both the K-d of [H-3]p-aminoclonidine-binding si
tes by about 190% at 1 nM and the B-max values at 1 and 3 nM (p < 0.05). Ox
ytocin (1 nM) also significantly and substantially(p < 0.01) increased the
K-d and B-max values of the [H-3]UK 14.304 alpha(2)-agonist-binding sites i
n the hypothalamus and amygdala in agreement with the results obtained with
the other agonist of the alpha(2)-adrenoceptor [H-3]p-aminoclonidine. This
effect was partially blocked by the presence of the specific oxytocin rece
ptor antagonist, CAP. These findings suggest the existence of an antagonist
ic oxytocin/alpha(2)-receptor interaction in the hypothalamus and amygdala
that may be of relevance for the demonstrated modulation of alpha(2)-adreno
ceptor-induced feeding responses by oxytocin. Copyright (C) 2000 S. Karger
AG, Basel.