L. Trigazis et al., CCK-A receptor antagonists have selective effects on nutrient-induced foodintake suppression in rats, AM J P-REG, 45(2), 1999, pp. R323-R330
Citations number
28
Categorie Soggetti
Physiology
Journal title
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY
To provide additional support to the hypothesis that only dietary protein (
Pro; chicken egg albumin) and not amino acids (AA; patterned after albumin)
, carbohydrates (CHO; cornstarch), or fats (Fat; corn oil) produces a satia
ting effect via CCK receptors, two CCK-A receptor antagonists (PD-140,548 a
nd devazepide) were coadministered with each nutrient. Given alone [4 ml in
tragastrically (ig)] Pro (1.0 g), AA (1.0 g), CHO (1.4 g), and Fat (2.4 g)
suppressed (P < 0.05) food intake on average during the first 2 h of feedin
g by 1.4 (36%), 1.5 (48%), 1.0 (33%), and 1.2 g (41%), respectively. Devaze
pide (0.5 mg/kg) and PD-140,548 (1.0 mg/kg) given alone increased food inta
ke during 0-2 h by 0.7 g (18%) and during 0-1 h by 0.5 g (15%), respectivel
y. When coadministered with PD-140,548 (1.0 mg/kg ip), the suppression of f
ood intake caused by Pro was modulated during 0-2 h by 57% (Pro X drug inte
raction, P < 0.05), but AA-, CHO-, and Fat-induced suppression of feeding w
as not affected (nutrient x drug interaction, P > 0.05). Devazepide (0.5 mg
/kg ip) did not modulate AA-, CHO-, and Fat-induced food intake suppression
during any time period (nutrient x drug interaction, P > 0.05). These stud
ies provide additional evidence that CCK-A receptors play a role in Pro (al
bumin) but not AA-, CHO (cornstarch)-, or Fat (corn oil)-induced food intak
e suppression in rats.