We evaluated the effects of systemic delivery of amphibian bombesin an
d its mammalian homologues on the length of the postprandial intermeal
interval. Adult male rats, feeding ad libitum, were injected intraper
itoneally (i.p.) 5 min after the end of the first nocturnal meal with
0 (vehicle), 2.5, 5, or 10 nM/kg of tetradecapeptide bombesin (BN), ga
strin-releasing peptide(1-27) (GRP(1-27)), the C-terminal decapeptide
of GRP(1-27) (GRP(18-27)), the C-terminal decapeptide of neuromedin B
(NMB23-32), or combinations of equimolar doses of GRP(1-27) and NMB23-
32. BN produced a potent, dose-related extension (maximum of 177%) of
the first postprandial intermeal interval; GRP(1-27) produced a lesser
but significant prolongation (maximum of 47%); the combination of GRP
(1-27) and NMB23-32 produced an intermediate prolongation (maximum of
70%); GRP(18-27) alone and NMB23-32 alone failed to produce any signif
icant change. Peptide effects were limited to the first postprandial i
ntermeal interval. The results demonstrate that systemic, postprandial
injection of BN, GRP(1-27), or the combination of GRP(1-27) and NMB23
-32 extends the duration of the postprandial intermeal interval. The r
esults suggest that the endogenous peptides, released in the gastroint
estinal tract by ingested food, have a potent satiety action, selectiv
ely lengthening the inter-meal interval. (C) 1998 Elsevier Science Inc
.