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Am J Physiol Regul Integr Comp Physiol 274: R618-R625, 1998;
0363-6119/98 $5.00
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Vol. 274, Issue 3, R618-R625, March 1998

Disordered food intake and obesity in rats lacking cholecystokinin A receptors

Timothy H. Moran1, Laura F. Katz1, Carlos R. Plata-Salaman2, and Gary J. Schwartz1

1 Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, Maryland 21205; and 2 School of Life and Health Sciences, University of Delaware, Newark, Delaware 19716-2590

Otsuka Long-Evans Tokushima Fatty (OLETF) rats develop obesity, hyperglycemia, and non-insulin-dependent diabetes mellitus and do not express cholecystokinin A (CCK-A) receptors, the receptor subtype mediating the satiety actions of CCK. In short-term feeding tests, male OLETF rats were completely resistant to exogenous CCK, and their response to bombesin was attenuated. Comparisons of liquid meal consumption in OLETF and control Long-Evans Tokushima (LETO) rats demonstrated that 1) OLETF rats had greater intakes during 30-min scheduled daytime meals and significantly larger and fewer spontaneous nighttime meals and 2) although the initial rates of licking were the same, OLETF rats maintained the initial rate longer and the rate at which their licking declined was slower. In 24-h solid food access tests, OLETF rats consumed significantly more pellets than LETO controls, and this increase was attributable to significant increases in meal size. Together, these data are consistent with the interpretation that the lack of CCK-A receptors in OLETF rats results in a satiety deficit leading to increases in meal size, overall hyperphagia, and obesity.

satiety; peptides; hyperphagia; bombesin


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