Mas-related G protein-coupled receptors in gastrointestinal dysfunction and inflammatory bowel disease: A review

Br J Pharmacol. 2024 Jul;181(14):2197-2211. doi: 10.1111/bph.16059. Epub 2023 Mar 2.

Abstract

Inflammatory bowel disease (IBD) is a chronic debilitating condition, hallmarked by persistent inflammation of the gastrointestinal tract. Despite recent advances in clinical treatments, the aetiology of IBD is unknown, and a large proportion of patients are refractory to pharmacotherapy. Understanding IBD immunopathogenesis is crucial to discern the cause of IBD and optimise treatments. Mas-related G protein-coupled receptors (Mrgprs) are a family of approximately 50 G protein-coupled receptors that were first identified over 20 years ago. Originally known for their expression in skin nociceptors and their role in transmitting the sensation of itch in the periphery, new reports have described the presence of Mrgprs in the gastrointestinal tract. In this review, we consider the impact of these findings and assess the evidence that suggests that Mrgprs may be involved in the disrupted homeostatic processes that contribute to gastrointestinal disorders and IBD. LINKED ARTICLES: This article is part of a themed issue Therapeutic Targeting of G Protein-Coupled Receptors: hot topics from the Australasian Society of Clinical and Experimental Pharmacologists and Toxicologists 2021 Virtual Annual Scientific Meeting. To view the other articles in this section visit http://onlinelibrary.wiley.com/doi/10.1111/bph.v181.14/issuetoc.

Keywords: Mas‐related G protein‐coupled receptor; Mrgpr; enteric nervous system; gastrointestinal; inflammation; inflammatory bowel disease; mast cell; motility.

Publication types

  • Review

MeSH terms

  • Animals
  • Gastrointestinal Diseases* / drug therapy
  • Gastrointestinal Diseases* / metabolism
  • Gastrointestinal Diseases* / physiopathology
  • Humans
  • Inflammatory Bowel Diseases* / drug therapy
  • Inflammatory Bowel Diseases* / metabolism
  • Inflammatory Bowel Diseases* / physiopathology
  • Receptors, G-Protein-Coupled* / metabolism

Substances

  • Receptors, G-Protein-Coupled