The Pharmacological Potential of Adenosine A 2A Receptor Antagonists for Treating Parkinson's Disease

Akihisa Mori, Jiang-Fan Chen, Shinichi Uchida, Cecile Durlach, Shelby M King, Peter Jenner

Research output: Contribution to journalArticlepeer-review

26 Citations (Scopus)
228 Downloads (Pure)

Abstract

The adenosine A2A receptor subtype is recognized as a non-dopaminergic pharmacological target for the treatment of neurodegenerative disorders, notably Parkinson's disease (PD). The selective A2A receptor antagonist istradefylline is approved in the US and Japan as an adjunctive treatment to levodopa/decarboxylase inhibitors in adults with PD experiencing OFF episodes or a wearing-off phenomenon; however, the full potential of this drug class remains to be explored. In this article, we review the pharmacology of adenosine A2A receptor antagonists from the perspective of the treatment of both motor and non-motor symptoms of PD and their potential for disease modification.

Original languageEnglish
Article number2366
JournalMolecules (Basel, Switzerland)
Volume27
Issue number7
Early online date6 Apr 2022
DOIs
Publication statusPublished - 6 Apr 2022

Keywords

  • non-dopaminergic target
  • Humans
  • istradefylline
  • Adenosine - pharmacology - therapeutic use
  • A2A receptors
  • adenosine
  • Receptor, Adenosine A2A
  • Adult
  • Parkinson Disease - drug therapy
  • Adenosine A2 Receptor Antagonists - pharmacology - therapeutic use
  • Levodopa - therapeutic use
  • G protein coupled receptor
  • Parkinson’s disease

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