Reduced GLP-1R expression in gastric glands of patients with type 2 diabetes mellitus

J Clin Endocrinol Metab. 2014 Sep;99(9):E1691-5. doi: 10.1210/jc.2014-1114. Epub 2014 May 30.

Abstract

Background: The incretin effect is reduced in type 2 diabetes mellitus (T2DM) patients. Whether the impaired function of the enteropancreatic axis in these patients is due to defective GLP-1 receptor (GLP-1R) expression in extrapancreatic target organs is not known.

Aims and methods: To compare the GLP-1R expression and distribution in gastric mucosa biopsies of patients with (n =22) and without (n =22) T2DM referred for routine esophagogastroduodenoscopies. GLP-1R mRNA levels were estimated by real-time PCR. The intensity of GLP-1R immunostaining, frequency, and types of glandular cells bearing GLP-1R and their glandular distribution in different stomach mucosa regions were evaluated by immunohistochemical morphological semiquantitative and quantitative analysis.

Results: Mean mRNA GLP-1R levels were significantly reduced in patients with T2DM compared with nondiabetic patients (P < .02). Immunohistochemical analysis revealed that the reduced GLP-1R expression in T2DM patients was due to a decreased intensity of immunostaining (P < .01). The number of glandular GLP-1R-bearing cells in both body and antrum mucosa was decreased in T2DM patients. Most notably, the frequency of GLP-1R immunoreactive acid-secreting parietal cells was reduced in the neck area of the gastric principal glands of T2DM patients (P < .01). No correlation was found between the reduced GLP-1R expression and clinical parameters including body mass index, age, glycosylated hemoglobin, and disease duration.

Conclusion: This is the first evidence of reduced GLP-1R expression in gastric glands of T2DM patients. These data demonstrate that the defective function of the incretin axis in T2DM may also result from decreased GLP-1R expression in its extrapancreatic target organs.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • Biopsy
  • Diabetes Mellitus, Type 2 / genetics*
  • Diabetes Mellitus, Type 2 / metabolism*
  • Endoscopy, Digestive System
  • Enteroendocrine Cells / cytology
  • Enteroendocrine Cells / physiology
  • Female
  • Gastric Mucosa / cytology
  • Gastric Mucosa / physiology*
  • Gene Expression Regulation
  • Glucagon-Like Peptide-1 Receptor
  • Humans
  • Male
  • Middle Aged
  • Parietal Cells, Gastric / cytology
  • Parietal Cells, Gastric / physiology
  • RNA, Messenger / metabolism
  • Receptors, Glucagon / genetics*
  • Receptors, Glucagon / metabolism*

Substances

  • GLP1R protein, human
  • Glucagon-Like Peptide-1 Receptor
  • RNA, Messenger
  • Receptors, Glucagon