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Clinical Trial
. 1999 Dec;277(6):R1718-24.
doi: 10.1152/ajpregu.1999.277.6.R1718.

Inhibition of food intake in response to intestinal lipid is mediated by cholecystokinin in humans

Affiliations
Clinical Trial

Inhibition of food intake in response to intestinal lipid is mediated by cholecystokinin in humans

D Matzinger et al. Am J Physiol. 1999 Dec.

Abstract

Intraduodenal fat inhibits gastric emptying and exerts early satiation in animals and humans, but it is not clear whether the effects are mediated by cholecystokinin (CCK) in humans. Here, we tested whether CCK-A receptors mediate the inhibition of fat on food intake. Two sequential, double-blind, crossover studies were performed in 24 male subjects. First, subjects received either intraduodenal fat or saline together with a preload of either water or banana shake. Second, 12 subjects received either intraduodenal fat or saline perfusion plus a concomitant infusion of saline or loxiglumide, a specific CCK-A receptor antagonist, together with a preload of banana shake. In both studies, subjects were free to eat and drink as much as they wished. Fat induced a reduction in calorie intake (P < 0.05) compared with controls. Furthermore, a decrease in hunger feelings was observed. Infusion of loxiglumide abolished the effects of fat. Duodenal fat interacts with an appetizer to modulate energy intake in humans. This effect is mediated by CCK-A receptors.

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