T1R2 receptor-mediated glucose sensing in the upper intestine potentiates glucose absorption through activation of local regulatory pathways

Mol Metab. 2018 Nov:17:98-111. doi: 10.1016/j.molmet.2018.08.009. Epub 2018 Aug 27.

Abstract

Objective: Beyond the taste buds, sweet taste receptors (STRs; T1R2/T1R3) are also expressed on enteroendocrine cells, where they regulate gut peptide secretion but their regulatory function within the intestine is largely unknown.

Methods: Using T1R2-knock out (KO) mice we evaluated the role of STRs in the regulation of glucose absorption in vivo and in intact intestinal preparations ex vivo.

Results: STR signaling enhances the rate of intestinal glucose absorption specifically in response to the ingestion of a glucose-rich meal. These effects were mediated specifically by the regulation of GLUT2 transporter trafficking to the apical membrane of enterocytes. GLUT2 translocation and glucose transport was dependent and specific to glucagon-like peptide 2 (GLP-2) secretion and subsequent intestinal neuronal activation. Finally, high-sucrose feeding in wild-type mice induced rapid downregulation of STRs in the gut, leading to reduced glucose absorption.

Conclusions: Our studies demonstrate that STRs have evolved to modulate glucose absorption via the regulation of its transport and to prevent the development of exacerbated hyperglycemia due to the ingestion of high levels of sugars.

Keywords: GLP-2; GLUT2; Glucose homeostasis; Sweet taste receptors; T1R2.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Biological Transport
  • Energy Metabolism
  • Enteroendocrine Cells / metabolism
  • Female
  • Glucagon-Like Peptide 2 / metabolism
  • Glucose / metabolism*
  • Intestinal Absorption / drug effects
  • Intestinal Mucosa / metabolism*
  • Jejunum / metabolism
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Receptors, G-Protein-Coupled / deficiency
  • Receptors, G-Protein-Coupled / metabolism*
  • Signal Transduction / drug effects
  • Taste

Substances

  • Glucagon-Like Peptide 2
  • Receptors, G-Protein-Coupled
  • taste receptors, type 1
  • Glucose