Exendin-4 reduces fasting and postprandial glucose and decreases energy intake in healthy volunteers

Am J Physiol Endocrinol Metab. 2001 Jul;281(1):E155-61. doi: 10.1152/ajpendo.2001.281.1.E155.

Abstract

Exendin-4 is a long-acting potent agonist of the glucagon-like peptide 1 (GLP-1) receptor and may be useful in the treatment of type 2 diabetes and obesity. We examined the effects of an intravenous infusion of exendin-4 (0.05 pmol. kg(-1). min(-1)) compared with a control saline infusion in healthy volunteers. Exendin-4 reduced fasting plasma glucose levels and reduced the peak change of postprandial glucose from baseline (exendin-4, 1.5 +/- 0.3 vs. saline, 2.2 +/- 0.3 mmol/l, P < 0.05). Gastric emptying was delayed, as measured by the paracetamol absorption method. Volunteers consumed 19% fewer calories at a free-choice buffet lunch with exendin-4 (exendin-4, 867 +/- 79 vs. saline 1,075 +/- 93 kcal, P = 0.012), without reported side effects. Thus our results are in accord with the possibility that exendin-4 may be a potential treatment for type 2 diabetes, particularly for obese patients, because it acts to reduce plasma glucose at least partly by a delay in gastric emptying, as well as by reducing calorie intake.

MeSH terms

  • Acetaminophen / blood
  • Adult
  • Analgesics, Non-Narcotic / blood
  • Animals
  • Area Under Curve
  • Blood Glucose / metabolism*
  • Depression, Chemical
  • Energy Intake / drug effects*
  • Energy Metabolism / drug effects*
  • Exenatide
  • Fasting / metabolism
  • Female
  • Gastric Emptying / drug effects
  • Glucagon / blood
  • Glucagon-Like Peptide 1
  • Hormones / blood
  • Humans
  • Infusions, Intravenous
  • Insulin / blood
  • Lizards / physiology*
  • Male
  • Nausea / chemically induced
  • Peptide Fragments / blood
  • Peptides / administration & dosage
  • Peptides / adverse effects
  • Peptides / pharmacology*
  • Postprandial Period / drug effects
  • Postprandial Period / physiology
  • Protein Precursors / blood
  • Satiety Response / drug effects
  • Venoms / administration & dosage
  • Venoms / adverse effects
  • Venoms / pharmacology*

Substances

  • Analgesics, Non-Narcotic
  • Blood Glucose
  • Hormones
  • Insulin
  • Peptide Fragments
  • Peptides
  • Protein Precursors
  • Venoms
  • Acetaminophen
  • Glucagon-Like Peptide 1
  • Glucagon
  • Exenatide