Differential modulation by baclofen on antinociception induced by morphine and beta-endorphin administered intracerebroventricularly in the formalin test

Neuropeptides. 1999 Dec;33(6):534-41. doi: 10.1054/npep.1999.0775.

Abstract

Our previous studies have demonstrated that supraspinal GABAergic receptors are differentially involved in the antinociception induced by morphine and beta-endorphin given intracerebroventricularly (i.c.v.) in the tail-flick and hot-plate tests. These two models employed a phasic, thermal nociceptive stimulus. The present study was designed to examine the possible involvement of supraspinal GABAergic receptors in opioid-induced antinociception in the formalin test. Morphine (1 microg) and beta-endorphin (1 microg) given i.c.v. displayed the almost complete inhibitory effects against the hyperalgesic response in both phases. Muscimol (75-100 ng) and baclofen (5-10 ng) injected i.c.v. produced the hypoalgesic response in the both phases. The hypoalgesic response induced by muscimol and baclofen observed during the second phase was more pronounced than that observed during the second phase. Baclofen (2.5 ng), at the dose which did not affect the hyperalgesic response, resulted in a significant reversal of the i.c.v. administered beta-endorphin-induced hypoalgesic response observed during the second, but not the first, phase. However, the hypoalgesic response induced by i.c.v. administered morphine was not changed by the same dose of muscimol or baclofen injected i.c.v. Our results indicate that, at the supraspinal level, GABA(B)receptors appear to be involved in the modulation of antinociception induced by supraspinally administered beta-endorphin, but not morphine, in the formalin test model.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Analgesics, Opioid / pharmacology*
  • Animals
  • Baclofen / pharmacology*
  • Brain Chemistry / drug effects
  • Brain Chemistry / physiology
  • Fixatives
  • Formaldehyde
  • GABA Agonists / pharmacology*
  • Hot Temperature
  • Injections, Intraventricular
  • Male
  • Mice
  • Mice, Inbred ICR
  • Morphine / pharmacology*
  • Muscimol / pharmacology
  • Nociceptors / drug effects*
  • Pain Threshold / drug effects
  • Receptors, GABA-A / physiology
  • Receptors, GABA-B / physiology
  • beta-Endorphin / pharmacology*

Substances

  • Analgesics, Opioid
  • Fixatives
  • GABA Agonists
  • Receptors, GABA-A
  • Receptors, GABA-B
  • Formaldehyde
  • Muscimol
  • beta-Endorphin
  • Morphine
  • Baclofen