Involvement of supraspinal GABA-ergic systems in clonidine-induced antinociception in the tail-pinch test in mice

Life Sci. 1997;61(11):1097-103. doi: 10.1016/s0024-3205(97)00618-8.

Abstract

We investigated the involvement of supraspinal GABAergic systems in the antinociceptive effect of clonidine using the tail-pinch test in mice. Muscimol (31.2-250 ng/mouse, i.c.v.) and R(+)-baclofen (10-100 ng/mouse, i.c.v.), selective agonists for the GABA(A) and GABA(B) receptors, respectively, significantly attenuated the antinociceptive effect of subcutaneously (s.c.) administered clonidine (1 mg/kg) in a dose-dependent manner. The attenuating effect of muscimol (62.5 ng/mouse, i.c.v.) on the clonidine-induced antinociception was significantly blocked by the GABA(A) antagonists bicuculline (100-400 ng/mouse, i.c.v.) and picrotoxin (250 ng/mouse, i.c.v.) but not by the GABA(B) antagonist 2-hydroxysaclofen (10 microg/mouse, i.c.v.). On the other hand, the attenuating effect of R(+)-baclofen (50 ng/mouse, i.c.v.) was blocked by the coadministration with 2-hydroxysaclofen (20 microg/mouse), but was not affected by the coadministration with bicuculline (400 ng/mouse). These results indicate that both supraspinal GABA(A) and GABA(B) receptors play inhibitory roles in the antinociception caused by systemically administered clonidine.

MeSH terms

  • Adrenergic alpha-2 Receptor Agonists
  • Analgesics / pharmacology*
  • Animals
  • Baclofen / analogs & derivatives
  • Baclofen / pharmacology
  • Bicuculline / pharmacology
  • Clonidine / pharmacology*
  • GABA Antagonists / pharmacology*
  • Male
  • Mice
  • Muscimol / pharmacology
  • Pain / physiopathology*
  • Picrotoxin / pharmacology
  • Receptors, GABA / physiology*
  • Tail
  • gamma-Aminobutyric Acid / physiology*

Substances

  • Adrenergic alpha-2 Receptor Agonists
  • Analgesics
  • GABA Antagonists
  • Receptors, GABA
  • Picrotoxin
  • Muscimol
  • gamma-Aminobutyric Acid
  • Baclofen
  • Clonidine
  • 2-hydroxysaclofen
  • Bicuculline