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

Author:

Edwards C. Mark B.1,Stanley Sarah A.1,Davis Rachel2,Brynes Audrey E.2,Frost Gary S.2,Seal Leighton J.1,Ghatei Mohammad A.1,Bloom Stephen R.1

Affiliation:

1. Endocrine Unit, and

2. Department of Dietetics, Imperial College of Science, Technology and Medicine, Hammersmith Hospital, London W12 0NN, United Kingdom

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.

Publisher

American Physiological Society

Subject

Physiology (medical),Physiology,Endocrinology, Diabetes and Metabolism

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