Effects of a lipase inhibitor (Orlistat) on cholecystokinin and appetite in response to a high-fat meal

Int J Obes Relat Metab Disord. 2003 Dec;27(12):1479-85. doi: 10.1038/sj.ijo.0802436.

Abstract

Objective: To examine the short-term effects of a lipase inhibitor (Orlistat) on physiological and behavioural measures of appetite in response to a high-fat meal.

Design: Randomised, single blind, placebo-controlled, crossover trial.

Subjects: A total of 19 healthy nonobese male subjects.

Procedures: After an overnight fast, subjects ingested a test meal of 2940 kJ (60% fat, 30% CHO, 10% protein) with Orlistat (120 mg) or a placebo, separated by 2 weeks. Appetite, as assessed by a standard line scale, and plasma cholecystokinin (CCK) concentrations were measured prior to and every hour after the test meal for 4 h. Thereafter, subjects ingested a quantified, but self-selected portion of a standardised lunch (15% protein, 37% fat and 45% CHO), before completing a final line scale questionnaire.

Results: The CCK response to the test meal was negatively correlated with BMI in both the Orlistat and placebo trials (R=-0.69 and -0.65, P<0.01). Orlistat administration did not significantly alter the CCK response to the test meal (6.30+/-3.27 vs 7.36+/-3.94 pM min, for Orlistat and placebo, P=0.193). Similarly, the line scale measures of appetite and subsequent intake (520+/-205 vs 554+/-197 g, P=0.48) were not different between the trials.

Conclusion: Orlistat administration did not alter short-term physiological or behavioural measures of satiety in response to a high-fat meal in healthy, nonobese subjects. The CCK response to a test meal may be partly determined by BMI.

Publication types

  • Clinical Trial
  • Randomized Controlled Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Anti-Obesity Agents / pharmacology
  • Appetite / drug effects*
  • Cholecystokinin / blood*
  • Cross-Over Studies
  • Dietary Fats / administration & dosage
  • Eating / drug effects
  • Enzyme Inhibitors / adverse effects
  • Enzyme Inhibitors / pharmacology*
  • Humans
  • Hunger / drug effects
  • Lactones / adverse effects
  • Lactones / pharmacology*
  • Lipase / antagonists & inhibitors*
  • Male
  • Orlistat
  • Satiation / drug effects
  • Single-Blind Method

Substances

  • Anti-Obesity Agents
  • Dietary Fats
  • Enzyme Inhibitors
  • Lactones
  • Cholecystokinin
  • Orlistat
  • Lipase