Unit

UNIT 1.9 Characterization of P1 (Adenosine) Purinoceptors

  1. Michael F. Jarvis

Published Online: 1 MAY 2001

DOI: 10.1002/0471141755.ph0109s00

Current Protocols in Pharmacology

Current Protocols in Pharmacology

How to Cite

Jarvis, M. F. 2001. Characterization of P1 (Adenosine) Purinoceptors. Current Protocols in Pharmacology. 00:1.9:1.9.1–1.9.15.

Author Information

  1. Abbott Laboratories, Abbott Park, Illinois

Publication History

  1. Published Online: 1 MAY 2001
  2. Published Print: MAR 1998

This is not the most recent version of the article. View current version (8 OCT 2013)

Abstract

The purine nucleoside adenosine (ADO) is an important modulator of cellular function in mammalian tissues. ADO modulates neuronal excitability through an interaction with different cell surface receptor subtypes that are heterogeneously distributed in the mammalian central nervous system, as well as in many peripheral tissues. Four different ADO receptor subtypes have been cloned and characterized. Described in this unit are three radioligand binding assays for pharmacological characterization of the high-affinity ADO receptor subtypes A1, A2A, and A3 receptors. Pharmacological characterization of the low-affinity A2B receptor using radioligand binding has been limited by the paucity of potent and selective ligands for this subtype. Since receptor localization is an important criterion for differentiation of receptor subtypes, a support protocol that describes the methodology for the localization of ADO receptors in rat brain tissue using autoradiography is also included.