Cholecystokinin-Induced Gallbladder Emptying and Single-Dose Metformin Elicit Additive Glucagon-Like Peptide-1 Responses

Ulrich Rohde, David Peick Sonne, Mikkel Christensen, Morten Hansen, Andreas Brønden, Signe Toräng, Jens Frederik Rehfeld, Jens Juul Holst, Tina Vilsbøll Lauritsen, Filip Krag Knop

16 Citations (Scopus)

Abstract

Context: Bile acids have been suggested to mediate glucagon-like peptide-1 (GLP-1) secretion. Metformin, too, has been shown to increase GLP-1 levels. The effect of gallbladder emptying, metformin, or a combination has, however, never been studied. Objective: We hypothesized that cholecystokinin (CCK)-8-induced gallbladder emptying stimulates human GLP-1 secretion and that metformin would potentiate this effect. Design: A double-blinded, randomized study. Setting: The study was conducted at a specialized research unit. Participants: Ten healthy male subjects with no family history of diabetes (age, 22 [range, 20-32] years; body mass index, 21.7 [19.3-24.2] kg/m2; fasting plasma glucose, 4.9 [4.7-5.3] mM; and glycosylated hemoglobin A1c, 5.1 [4.4-5.8] %). Intervention: On 4 separate days, the subjects received metformin or placebo and a concomitant 60-minute intravenous infusion of saline or CCK. Blood was sampled for 4 hours, and gallbladder volume was measured by ultrasound. Main Outcome Measures: Plasma levels of GLP-1. Results: CCK-induced gallbladder emptying and metformin alone (no observed effect on gallbladder emptying) both elicited significant and additive GLP-1 responses. Metformin alone or combined with gallbladder emptying elicited a significant peptide YY response. CCK-induced gallbladder emptying resulted in a short-lasting glucose-dependent insulinotropic polypeptide response independent of metformin. No effects were seen on plasma glucose, insulin, C-peptide, or gastrin. Conclusions: CCK-induced gallbladder emptying in healthy subjects elicits significant GLP-1 secretion, which can be potentiated by metformin.

Original languageEnglish
JournalThe Journal of clinical endocrinology and metabolism
Volume101
Issue number5
Pages (from-to)2076-2083
ISSN0021-972X
DOIs
Publication statusPublished - 1 May 2016

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