The Effect of High-Fat Diet-Induced Obesity on the Expression of Nutrient Chemosensors in the Mouse Stomach and the Gastric Ghrelin Cell

Nutrients. 2020 Aug 19;12(9):2493. doi: 10.3390/nu12092493.

Abstract

The stomach is the primary source of the orexigenic and adiposity-promoting hormone, ghrelin. There is emerging evidence on the nutrient-mediated modulation of gastric ghrelin secretion. However, limited information is available on gastric nutrient-sensing mechanisms in high-fat diet (HFD)-induced obesity. This study investigated the impact of HFD-induced obesity on the expression of nutrient chemosensors in mouse stomach, particularly ghrelin cells. Male C57BL/6 mice were fed either a standard laboratory diet (SLD) or HFD for 12 weeks. The expression of ghrelin, enzymes involved in ghrelin production (PC1/3, GOAT) and nutrient chemosensors (CD36, FFAR2&4, GPR93, CaSR, mGluR4 and T1R3) was determined by quantitative RT-PCR in the mouse corpus and antrum. Immunohistochemistry assessed the protein expression of CaSR and ghrelin in the corpus and antrum. Antral mRNA levels of CaSR and PC1/3 were increased in HFD compared to SLD mice, while mRNA levels of all other nutrient chemosensors examined remained unchanged. CaSR immunolabelling was observed in the gastric antrum only. Nearly 80% of antral ghrelin cells expressed CaSR, with a similar cell density and co-expression in SLD and HFD mice. In conclusion, HFD-induced obesity increased CaSR mRNA expression in mouse antrum. However, the high antral co-expression of CaSR and ghrelin was unaltered in HFD compared to SLD mice.

Keywords: CaSR; ghrelin; high-fat diet; nutrient sensing; obesity; stomach.

MeSH terms

  • Animals
  • CD36 Antigens / genetics
  • CD36 Antigens / metabolism
  • Diet, High-Fat / adverse effects*
  • Gastric Mucosa / cytology*
  • Gastric Mucosa / metabolism*
  • Gene Expression*
  • Ghrelin / genetics*
  • Ghrelin / metabolism*
  • Male
  • Mice, Inbred C57BL
  • Obesity / etiology*
  • Obesity / genetics
  • Obesity / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Receptors, Calcium-Sensing / genetics*
  • Receptors, Calcium-Sensing / metabolism*
  • Receptors, G-Protein-Coupled / genetics
  • Receptors, G-Protein-Coupled / metabolism
  • Receptors, Metabotropic Glutamate / genetics
  • Receptors, Metabotropic Glutamate / metabolism

Substances

  • CASR protein, mouse
  • CD36 Antigens
  • FFAR4 protein, mouse
  • Ffar2 protein, mouse
  • Ghrelin
  • RNA, Messenger
  • Receptors, Calcium-Sensing
  • Receptors, G-Protein-Coupled
  • Receptors, Metabotropic Glutamate
  • taste receptors, type 1
  • metabotropic glutamate receptor 4