Expression of the fatty acid receptor GPR120 in the gut of diet-induced-obese rats and its role in GLP-1 secretion

PLoS One. 2014 Feb 10;9(2):e88227. doi: 10.1371/journal.pone.0088227. eCollection 2014.

Abstract

Stimulation of the G protein coupled receptor GPR120 has been shown to have anti-inflammatory and insulin-sensitizing effects, to promote glucagon like peptide-1 (GLP-1) secretion, and to play a key role in sensing dietary fat and control energy balance. In a search for differentially expressed genes potentially involved in food intake and body-weight regulation we identified GPR120 to be differentially regulated in the intestine of selectively bred diet induced obese (DIO) and diet resistant (DR) rats. Subsequently we investigated the effect of GPR120 receptor stimulation with the long chain fatty acid alpha linolenic acid (ALA) on GLP-1 secretion in rats. Independent of diet (high or low fat), GPR120 expression showed a two-fold increase in the intestine of DIO compared to DR rats. In situ hybridization revealed a broad expression of GPR120 in the gut mucosa in both intestinal epithelial and endocrine cells. Using double in situ hybridization GPR120 mRNA did not appear to be enriched in preproglucagon expressing L-cells. In line with the anatomical data, ALA administration did not increase circulating GLP-1 levels. Our data shows a widespread expression of GPR120 in the gut epithelium and can not confirm a major role for GPR120 in the regulation of GLP-1 secretion. The broad expression of GPR120 in the gut epithelium supports reports indicating a putative role of GPR120 as a sensor of dietary fat.

MeSH terms

  • Administration, Oral
  • Animals
  • Caprylates / administration & dosage
  • Caprylates / pharmacology
  • Diet
  • Gastrointestinal Tract / drug effects
  • Gastrointestinal Tract / metabolism*
  • Glucagon-Like Peptide 1 / blood
  • Glucagon-Like Peptide 1 / metabolism*
  • Glucose / administration & dosage
  • Glucose / pharmacology
  • Insulin / blood
  • Linoleic Acid / administration & dosage
  • Linoleic Acid / pharmacology
  • Male
  • Multiplex Polymerase Chain Reaction
  • Obesity / blood
  • Obesity / metabolism*
  • Proglucagon / metabolism
  • Protein Transport / drug effects
  • Rats
  • Rats, Sprague-Dawley
  • Rats, Wistar
  • Receptors, G-Protein-Coupled / metabolism*

Substances

  • Caprylates
  • Ffar4 protein, rat
  • Insulin
  • Receptors, G-Protein-Coupled
  • Proglucagon
  • Glucagon-Like Peptide 1
  • Linoleic Acid
  • Glucose
  • octanoic acid

Grants and funding

The authors have no support or funding to report.