Effect of the artificial sweetener, sucralose, on gastric emptying and incretin hormone release in healthy subjects

The incretin hormones, glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), play an important role in glucose homeostasis in both health and diabetes. In mice, sucralose, an artificial sweetener, stimulates GLP-1 release via sweet taste receptors on enteroendocrine cells. We studied blood glucose, plasma levels of insulin, GLP-1, and GIP, and gastric emptying (by a breath test) in 7 healthy humans after intragastric infusions of 1) 50 g sucrose in water to a total volume of 500 ml (~290 mosmol/l), 2) 80 mg sucralose in 500 ml normal saline (~300 mosmol/1, 0.4 mM sucralose), 3) 800 mg sucralose in 500 ml normal saline (~300 mosmol/1, 4 mM sucralose), and 4) 500 ml normal saline (~300 mosmol/l), all labeled with 150 mg [sup.13]C-acetate. Blood glucose increased only in response to sucrose (P < 0.05). GLP-1, GIP, and insulin also increased after sucrose (P = 0.0001) but not after either load of sucralose or saline. Gastric emptying of sucrose was slower than that of saline ([t.sub.50]: 87.4 [+ or -] 4.1 min vs. 74.7 [+ or -] 3.2 min, P < 0.005), whereas there were no differences in [t.sub.50] between sucralose 0.4 mM (73.7 [+ or -] 3.1 min) or 4 mM (76.7 [+ or -] 3.1 min) and saline. We conclude that sucralose, delivered by intragastric infusion, does not stimulate insulin, GLP-1, or GIP release or slow gastric emptying in healthy humans.