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Contribution of GABA(A) and GABA(B) receptors to the discriminative stimulus produced by gamma-hydroxybutyric acid.
- Source :
-
Pharmacology, biochemistry, and behavior [Pharmacol Biochem Behav] 1999 Oct; Vol. 64 (2), pp. 363-5. - Publication Year :
- 1999
-
Abstract
- The present study examined the involvement of GABA(A) and GABA(B) receptors in the discriminative stimulus effects of gamma-hydroxybutyric acid (GHB). Rats were trained to discriminate either 300 or 700 mg/kg GHB IG from water using a T-maze, food-reinforced drug-discrimination procedure. The direct GABA(B) agonist, baclofen, substituted completely for both training doses of GHB; its potency to substitute for GHB increased moderately as the training dose of GHB was increased. The positive GABA(A) modulator, diazepam, substituted partially for 300 mg/kg GHB, but failed to elicit GHB-appropriate responding in rats trained with the higher GHB dose. Finally, the GABA(B) antagonist, CGP 35348, completely blocked the discriminative stimulus effects of the high training dose of GHB, but only partially antagonized the effects of the low training dose. These results suggest that (a) GHB produces a compound stimulus, and (b) both GABA(B)- and GABA(A)-mediated cues are prominent components of this compound stimulus; the contribution of each component, however, appears to vary as the training dose of GHB is increased.
- Subjects :
- Animals
Baclofen pharmacology
Cues
Diazepam pharmacology
Dose-Response Relationship, Drug
GABA Agonists pharmacology
GABA Antagonists pharmacology
GABA Modulators pharmacology
GABA-A Receptor Agonists
GABA-A Receptor Antagonists
GABA-B Receptor Agonists
GABA-B Receptor Antagonists
Male
Motor Activity drug effects
Organophosphorus Compounds pharmacology
Rats
Rats, Long-Evans
Stimulation, Chemical
3-Hydroxybutyric Acid pharmacology
Discrimination, Psychological drug effects
Receptors, GABA-A drug effects
Receptors, GABA-B drug effects
Subjects
Details
- Language :
- English
- ISSN :
- 0091-3057
- Volume :
- 64
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Pharmacology, biochemistry, and behavior
- Publication Type :
- Academic Journal
- Accession number :
- 10515314
- Full Text :
- https://doi.org/10.1016/s0091-3057(99)00046-5