Purinergic signaling in diabetes and metabolism

Biochem Pharmacol. 2021 May:187:114393. doi: 10.1016/j.bcp.2020.114393. Epub 2020 Dec 25.

Abstract

Purinergic signaling, a concept originally formulated by the late Geoffrey Burnstock (1929-2020), was found to modulate pathways in every physiological system. In metabolic disorders there is a role for both adenosine receptors and P2 (nucleotide) receptors, of which there are two classes, i.e. P2Y metabotropic and P2X ionotropic receptors. The individual roles of the 19 receptors encompassed by this family have been dissected - and in many cases the effects associated with specific cell types, including adipocytes, skeletal muscle, liver cells and immune cells. It is suggested that ligands selective for each of the four adenosine receptors (A1, A2A, A2B and A3), and several of the P2 subtypes (e.g. P2Y6 or P2X7 antagonists) might have therapeutic potential for treating diabetes and obesity. This is a developing story with some conflicting conclusions relevant to drug discovery, which we summarize here.

Keywords: Adenosine receptors; Diabetes; Obesity; P2X receptors; P2Y receptors.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Adenosine Triphosphate / metabolism*
  • Animals
  • Diabetes Mellitus / drug therapy
  • Diabetes Mellitus / metabolism*
  • Humans
  • Metabolic Diseases / drug therapy
  • Metabolic Diseases / metabolism
  • Purinergic Agonists / administration & dosage
  • Purinergic Antagonists / administration & dosage
  • Receptors, Purinergic / metabolism*
  • Signal Transduction / drug effects
  • Signal Transduction / physiology*

Substances

  • Purinergic Agonists
  • Purinergic Antagonists
  • Receptors, Purinergic
  • Adenosine Triphosphate