High-fat diet effects on gut motility, hormone, and appetite responses to duodenal lipid in healthy men

Am J Physiol Gastrointest Liver Physiol. 2003 Feb;284(2):G188-96. doi: 10.1152/ajpgi.00375.2002. Epub 2002 Oct 30.

Abstract

There is evidence that gastrointestinal function adapts in response to a high-fat (HF) diet. This study investigated the hypothesis that an HF diet modifies the acute effects of duodenal lipid on appetite, antropyloroduodenal pressures, plasma CCK and plasma glucagon-like peptide-1 (GLP-1) levels in humans. Twelve healthy men were studied twice in randomized, crossover fashion. The effects of a 90-min duodenal lipid infusion (6.3 kJ/min) on the above parameters were assessed immediately following 14-day periods on either an HF or a low-fat (LF) diet. After the HF diet, pyloric tonic and phasic pressures were attenuated, and the number of antropyloroduodenal pressure-wave sequences was increased when compared with the LF diet. Plasma CCK and GLP-1 levels did not differ between the two diets. Hunger was greater during the lipid infusion following the HF diet, but there was no difference in food intake. Therefore, exposure to an HF diet for 14 days attenuates the effects of duodenal lipid on antropyloroduodenal pressures and hunger without affecting food intake or plasma hormone levels.

Publication types

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

MeSH terms

  • Adult
  • Appetite / drug effects*
  • Cholecystokinin / blood
  • Diet*
  • Dietary Fats / administration & dosage
  • Dietary Fats / pharmacology*
  • Duodenum / physiology*
  • Eating / physiology
  • Energy Metabolism / physiology
  • Gastrointestinal Motility / physiology*
  • Glucagon / blood
  • Glucagon-Like Peptide 1
  • Hormones / blood*
  • Humans
  • Hunger / physiology
  • Intubation, Gastrointestinal
  • Male
  • Muscle Tonus / physiology
  • Peptide Fragments / blood
  • Protein Precursors / blood
  • Pylorus / physiology

Substances

  • Dietary Fats
  • Hormones
  • Peptide Fragments
  • Protein Precursors
  • Glucagon-Like Peptide 1
  • Glucagon
  • Cholecystokinin