Reduction by morphine of human postprandial insulin release is secondary to inhibition of gastrointestinal motility

Diabetes. 1986 Mar;35(3):324-8. doi: 10.2337/diab.35.3.324.

Abstract

The effect of morphine (0.1 mg/kg) on insulin secretion stimulated by oral, intraduodenal, or intravenous administration of glucose was studied in seven healthy volunteers. When glucose was given intravenously, morphine had no effect on plasma glucose, insulin, glucose-dependent insulinotropic polypeptide (GIP), or pancreatic glucagon. Following oral glucose, morphine slowed gastric emptying and reduced plasma concentrations of glucose, insulin, and GIP. During intraduodenal infusion of glucose, insulin concentrations in plasma were also decreased by morphine, an effect best explained by decreased small intestinal transit with delayed absorption of glucose and delayed release of GIP. We conclude that clinically relevant doses of morphine have no direct effect on insulin secretion and that the changes observed were secondary to slowed gastric emptying and small intestinal transit.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Blood Glucose / analysis
  • Duodenum
  • Female
  • Gastric Emptying / drug effects
  • Gastric Inhibitory Polypeptide / blood
  • Gastrointestinal Motility / drug effects*
  • Glucagon-Like Peptides / blood
  • Glucose / administration & dosage
  • Glucose / pharmacology
  • Humans
  • Infusions, Parenteral
  • Insulin / blood
  • Insulin / metabolism*
  • Insulin Secretion
  • Male
  • Morphine / pharmacology*
  • Neurotensin / blood

Substances

  • Blood Glucose
  • Insulin
  • Neurotensin
  • Gastric Inhibitory Polypeptide
  • Glucagon-Like Peptides
  • Morphine
  • Glucose