The effects of acidic fibroblast growth factor (aFGF), basic FGF (bFGF
), and related peptides, such as aFGF fragments, on food and water int
ake were investigated. Infusion of aFGF and bFGF into the third cerebr
al ventricle significantly suppressed food intake. The potency of aFGF
was 1.5 that of bFGF in food intake inhibition. Both FGFs also suppre
ssed water intake. Infusion of a carboxyl-terminal fragment of aFGF, a
FGF-(114-140), did not affect food intake, whereas an amino-terminal f
ragment of aFGF, aFGF-(1-5), was significantly inhibitory. Other amino
-terminal fragments, aFGF-(1-20) and aFGF-(1-29), did not affect food
intake. However, [Ala(16)]aFGF-(1-29), in which the cysteine residue a
t position 16 was replaced with alanine, significantly suppressed food
intake. Infusions of functional antagonists for FGFs, anti-aFGF, anti
-bFGF, and anti-aFGF-(1-15) IgGs, into the lateral hypothalamus signif
icantly increased food intake. The results suggest that: aFGF, bFGF, a
nd some amino-terminal peptides of aFGF participate in the central reg
ulation of food intake; the lateral hypothalamus is involved in their
feeding suppression actions; and these peptides may function as physio
logically relevant substances in the adult central nervous system, oth
er than as neurotrophic factors.