Effect of the artificial sweetener, sucralose, on gastric emptying and incretin hormone release in healthy subjects
dc.contributor.author | Ma, J. | |
dc.contributor.author | Bellon, M. | |
dc.contributor.author | Wishart, J. | |
dc.contributor.author | Young, R. | |
dc.contributor.author | Blackshaw, L. | |
dc.contributor.author | Jones, K. | |
dc.contributor.author | Horowitz, M. | |
dc.contributor.author | Rayner, C. | |
dc.date.issued | 2009 | |
dc.description | Copyright © 2009 by the American Physiological Society | |
dc.description.abstract | 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 (approximately 290 mosmol/l), 2) 80 mg sucralose in 500 ml normal saline (approximately 300 mosmol/l, 0.4 mM sucralose), 3) 800 mg sucralose in 500 ml normal saline (approximately 300 mosmol/l, 4 mM sucralose), and 4) 500 ml normal saline (approximately 300 mosmol/l), all labeled with 150 mg 13C-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 (t50: 87.4+/-4.1 min vs. 74.7+/-3.2 min, P<0.005), whereas there were no differences in t50 between sucralose 0.4 mM (73.7+/-3.1 min) or 4 mM (76.7+/-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. | |
dc.description.statementofresponsibility | Jing Ma, Max Bellon, Judith M. Wishart, Richard Young, Ashley Blackshaw, Karen L. Jones, Michael Horowitz and Christopher K. Rayner | |
dc.identifier.citation | American Journal of Physiology - Gastrointestinal and Liver Physiology, 2009; 296(4):G735-G739 | |
dc.identifier.doi | 10.1152/ajpgi.90708.2008 | |
dc.identifier.issn | 0193-1857 | |
dc.identifier.issn | 1522-1547 | |
dc.identifier.orcid | Young, R. [0000-0001-5116-4951] [0009-0004-8274-9863] | |
dc.identifier.orcid | Blackshaw, L. [0000-0003-1565-0850] | |
dc.identifier.orcid | Jones, K. [0000-0002-1155-5816] | |
dc.identifier.orcid | Horowitz, M. [0000-0002-0942-0306] | |
dc.identifier.orcid | Rayner, C. [0000-0002-5527-256X] | |
dc.identifier.uri | http://hdl.handle.net/2440/53444 | |
dc.language.iso | en | |
dc.publisher | Amer Physiological Soc | |
dc.source.uri | https://doi.org/10.1152/ajpgi.90708.2008 | |
dc.subject | Stomach | |
dc.subject | Humans | |
dc.subject | Gastric Inhibitory Polypeptide | |
dc.subject | Insulin | |
dc.subject | Blood Glucose | |
dc.subject | Sucrose | |
dc.subject | Sweetening Agents | |
dc.subject | Single-Blind Method | |
dc.subject | Gastric Emptying | |
dc.subject | Dose-Response Relationship, Drug | |
dc.subject | Time Factors | |
dc.subject | Adult | |
dc.subject | Female | |
dc.subject | Male | |
dc.subject | Glucagon-Like Peptide 1 | |
dc.subject | Incretins | |
dc.subject | Young Adult | |
dc.title | Effect of the artificial sweetener, sucralose, on gastric emptying and incretin hormone release in healthy subjects | |
dc.type | Journal article | |
pubs.publication-status | Published |