Loxiglumide, a CCK-A receptor antagonist, stimulates calorie intake and hunger feelings in humans

Am J Physiol Regul Integr Comp Physiol. 2001 Apr;280(4):R1149-54. doi: 10.1152/ajpregu.2001.280.4.R1149.

Abstract

Exogenous cholecystokinin (CCK) induces early satiety when infused into humans. Whether alimentary CCK (CCK-A) receptor blockade stimulates food intake in humans is, however, uncertain. The aim of the present investigation was, therefore, to establish the effect of CCK-A receptor blockade on satiety and eating behavior in healthy volunteers. To further explore the role of endogenous CCK, the effects of the specific CCK-A receptor antagonist loxiglumide (Lox; 22 micromol. kg(-1). h(-1)) on satiety and eating behavior were investigated in healthy men and compared with saline infusions (as placebo) in a series of randomized, double-blind, placebo-controlled, crossover studies. Lox produced a slight (7%), but not significant (P = 0.104), increase in food intake that was accompanied by a modest (10%), but significant (P < 0.004), increase in calorie intake. Fluid ingestion was not affected by Lox. Subjects experienced more hunger and delayed fullness during Lox infusion than during saline infusion (P < 0.05). This study provides further evidence that CCK is an endogenous physiological satiety signal acting through CCK-A receptor-mediated mechanisms. Repeated-dose studies comparing hunger and satiety responses after CCK-A receptor blockade in healthy subjects and patients with eating disorders may help clarify the possible involvement of endogenous CCK in these conditions.

MeSH terms

  • Adult
  • Cross-Over Studies
  • Double-Blind Method
  • Drinking Behavior / drug effects
  • Drinking Behavior / physiology
  • Energy Intake / drug effects*
  • Feeding Behavior / drug effects*
  • Feeding Behavior / physiology
  • Hormone Antagonists / pharmacology*
  • Humans
  • Hunger / drug effects
  • Hunger / physiology*
  • Male
  • Proglumide / analogs & derivatives*
  • Proglumide / pharmacology*
  • Random Allocation
  • Receptor, Cholecystokinin A
  • Receptors, Cholecystokinin / antagonists & inhibitors
  • Receptors, Cholecystokinin / physiology*
  • Reference Values
  • Satiation / drug effects*
  • Satiation / physiology

Substances

  • Hormone Antagonists
  • Receptor, Cholecystokinin A
  • Receptors, Cholecystokinin
  • loxiglumide
  • Proglumide