Gastric distension and duodenal lipid infusion modulate intestinal gas transit and tolerance in humans

Am J Gastroenterol. 2002 Sep;97(9):2225-30. doi: 10.1111/j.1572-0241.2002.05976.x.

Abstract

Objective: Patients with unexplained abdominal complaints often attribute their symptoms to intestinal gas and indicate that symptoms are exacerbated by ingestion of a meal. However, the mechanisms responsible are unknown. Our aim was to analyze the specific influence of two meal-related factors, gastric distension, and intestinal nutrients, on intestinal gas dynamics and tolerance.

Methods: In 35 healthy subjects, gas evacuation and perception of jejunal gas infusion (12 ml/min) were measured for 3 h, during simultaneous duodenal infusion of saline, as control, lipids at 1 Kcal/min, or gastric distension.

Results: Infusion of lipids into the duodenum induced gas retention (584 +/- 154 ml, p < 0.05 vs 161 +/- 86 ml after saline infusion) without perception (2.2 +/- 0.5 score), whereas gastric distension induced perception (score 5.6 +/- 0.4, p < 0.05 vs score 1.9 +/- 0.4 after saline) without gas retention (7 +/- 205 ml).

Conclusions: Different meal-related factors exert specific effects on intestinal gas dynamics and tolerance, and these mechanisms may interact to produce postprandial gas symptoms.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Abdominal Pain / etiology*
  • Abdominal Pain / physiopathology*
  • Adolescent
  • Adult
  • Duodenum / drug effects*
  • Duodenum / physiopathology*
  • Fat Emulsions, Intravenous / administration & dosage
  • Fat Emulsions, Intravenous / pharmacology*
  • Female
  • Flatulence / complications*
  • Flatulence / physiopathology*
  • Gastrointestinal Transit / drug effects*
  • Gastrointestinal Transit / physiology*
  • Humans
  • Infusions, Parenteral
  • Male
  • Postprandial Period / drug effects
  • Postprandial Period / physiology
  • Reference Values
  • Stomach / drug effects*
  • Stomach / physiopathology*

Substances

  • Fat Emulsions, Intravenous