Physiological effects of enteral and parenteral feeding on pancreaticobiliary secretion in humans

Am J Physiol Gastrointest Liver Physiol. 2003 Jan;284(1):G27-36. doi: 10.1152/ajpgi.00155.2002.

Abstract

In the nutritional management of digestive disorders, it is important to know the relative secretory and metabolic responses to enteral and parenteral feeding. Twenty-seven healthy volunteers were studied while receiving either oral drinks or duodenal infusions of a complex formula diet, duodenal or intravenous infusions of elemental (protein as free amino acids, low fat) formulae, or saline. Pancreaticobiliary secretory responses were measured by nasoduodenal polyethylene glycol perfusion and aspiration, while monitoring blood hormone and nutrient levels. Diets were matched for protein (1.5 g x kg(-1) x d(-1)) and energy (40 kcal x kg(-1) x d(-1)). Compared with placebo, all oroenteral diets stimulated amylase, lipase, trypsin, and bile acid secretion and increased plasma concentrations of gastrin and cholecystokinin, whereas intravenous feeding did not. The complex formula produced a similar response whether given as drinks or duodenal infusions. Changing the duodenal formula to elemental reduced enzyme secretion by 50%, independently of CCK. Higher increases in plasma insulin, glucose, and amino acids were noted with intravenous feeding. Delivering food directly to the intestine by a feeding tube does not reduce pancreaticobiliary secretion. Enteral "elemental" formulae diminish, but only intravenous feeding avoids pancreatic stimulation. Intravenous administration impairs metabolic clearance.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Amino Acids / blood
  • Bile Ducts / metabolism*
  • Blood Glucose
  • Cholecystokinin / blood
  • Enteral Nutrition*
  • Fatty Acids, Nonesterified / blood
  • Female
  • Food, Formulated
  • Gastrins / blood
  • Humans
  • Insulin / blood
  • Male
  • Middle Aged
  • Nutrition Assessment
  • Pancreas / enzymology*
  • Pancreas / metabolism*
  • Parenteral Nutrition*

Substances

  • Amino Acids
  • Blood Glucose
  • Fatty Acids, Nonesterified
  • Gastrins
  • Insulin
  • Cholecystokinin