Intrathecal adenosine A1 receptor agonist attenuates hyperalgesia without inhibiting spinal glutamate release in the rat

Cell Mol Neurobiol. 2003 Apr;23(2):175-85. doi: 10.1023/a:1022997805525.

Abstract

The analgesia effects of intrathecal adenosine A1 receptor agonist, R-PIA, on the hyperalgesia and CSF-glutamate release after formalin injection into the rat paw were evaluated. R-PIA significantly and dose-dependently attenuated increases in flinching behavior, and this attenuating effect was reversed by the adenosine A1 receptor antagonist, aminophylline. Morphine blocked flinchs, however MK-801 partially abolished. The increase in CSF-glutamate release evoked by formalin stimulation was inhibited by morphine but not by either R-PIA or MK-801. These findings suggest that the intrathecal adenosine A1 receptor agonist provokes analgesic effect via the postsynaptic action independent of an effect upon spinal glutamate release.

Publication types

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

MeSH terms

  • Adenosine / administration & dosage*
  • Adenosine / analogs & derivatives*
  • Adenosine A1 Receptor Agonists*
  • Animals
  • Glutamic Acid / metabolism*
  • Hyperalgesia / drug therapy*
  • Injections, Spinal
  • Male
  • Pain Measurement / drug effects
  • Pain Measurement / methods
  • Rats
  • Rats, Sprague-Dawley
  • Receptor, Adenosine A1 / physiology
  • Spinal Cord / drug effects*
  • Spinal Cord / metabolism

Substances

  • Adenosine A1 Receptor Agonists
  • Receptor, Adenosine A1
  • N-(1-methyl-2-phenylethyl)adenosine
  • Glutamic Acid
  • Adenosine