Differential potentiative effects of GABA receptor agonists in the production of antinociception induced by morphine and beta-endorphin administered intrathecally in the mouse

Citation
Hw. Suh et al., Differential potentiative effects of GABA receptor agonists in the production of antinociception induced by morphine and beta-endorphin administered intrathecally in the mouse, LIFE SCI, 66(4), 2000, pp. PL61-PL69
Citations number
37
Categorie Soggetti
Biochemistry & Biophysics
Journal title
LIFE SCIENCES
ISSN journal
00243205 → ACNP
Volume
66
Issue
4
Year of publication
2000
Pages
PL61 - PL69
Database
ISI
SICI code
0024-3205(2000)66:4<PL61:DPEOGR>2.0.ZU;2-8
Abstract
The effect of muscimol or baclofen injected intrathecally (i.t.) on the inh ibition of the tail-flick response induced by morphine and R-endorphin admi nistered i.t. was studied in ICR mice. The i.t. injection of muscimol (100 ng) or baclofen (10 np) alone did not affect the basal inhibition of the ta il-flick response. Morphine (0.2 mu g) and beta-endorphin (0.1 mu g) caused only slight inhibition of the tail-flick response. Baclofen, but not musci mol, injected i.t. enhanced the inhibition of the tail-flick response induc ed by i.t. administered morphine. Both muscimol and baclofen injected i.t, significantly enhanced i.t. injected beta-endorphin-induced inhibition of t he tail-flick response. Our results suggest that the GABA(B), but not GABA( A), receptors located in the spinal cord appear to be involved in enhancing the inhibition of the tail-flick response induced by morphine administered spinally. In addition, both GABA(A) and GABA(B) receptors are involved in enhancing the inhibition of the tail-flick response induced by beta-endorph in administered i.t. (C) 1999 Elsevier Science Inc.