Adenosine A2 receptor-mediated modulation of contralateral rotation induced by metabotropic glutamate receptor activation

Eur J Pharmacol. 1995 Dec 12;287(2):115-20. doi: 10.1016/0014-2999(95)00479-3.

Abstract

Systemic pretreatment with the adenosine receptor antagonist theophylline significantly decreases contralateral rotation induced by unilateral intrastriatal 1-aminocyclopentane-1S,3R-dicarboxylic acid (1S,3R-ACPD). Intrastriatal or intrasubthalamic nucleus coadministration of theophylline and 1S,3R-ACPD significantly decreases contralateral rotation suggesting that metabotropic glutamate (mGlu) receptors and adenosine receptors interact locally. These appear to be adenosine A2 receptor effects as the adenosine A2 receptor antagonist 8-(3-chlorostyryl)caffeine (CSC) also decreases contralateral rotation induced by unilateral intrastriatal and intrasubthalamic nucleus administration of 1S,3R-ACPD, while the adenosine A1 receptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX) has no effect. Pretreatment with the adenosine A2 receptor agonist 2-p-(2-carboxyethyl)phenethylamino-5'-N-ethylcarboxamido adenosine hydrochloride (CGS 21680) potentiates contralateral rotation induced by unilateral striatal 1S,3R-ACPD, whereas pretreatment with the adenosine A1 receptor agonist N6-cyclopentyl-adenosine (CPA) has no effect. These results suggest that mGlu receptor effects may be due, in part, to modulation of adenosine action.

MeSH terms

  • Animals
  • Behavior, Animal / drug effects
  • Caffeine / pharmacology
  • Cycloleucine / analogs & derivatives
  • Cycloleucine / pharmacology
  • Male
  • Neurotoxins / pharmacology
  • Rats
  • Rats, Sprague-Dawley
  • Receptors, Metabotropic Glutamate / drug effects*
  • Receptors, Purinergic P1 / drug effects*
  • Rotation
  • Theophylline / pharmacology*

Substances

  • Neurotoxins
  • Receptors, Metabotropic Glutamate
  • Receptors, Purinergic P1
  • Cycloleucine
  • 1-amino-1,3-dicarboxycyclopentane
  • Caffeine
  • Theophylline