Résumé
1. 1. The role of both novel GABAB and classical GABAA receptors in GAG-induced antinociception was investigated using the tail flick and hot plate tests. To this end, manipulations known to increase baclofen-induced antinociception (GABAB) and the receptor antagonist bicuculline (GABAA) were used. 2. 2. Of the modifiers of monoamine function tested, only chlorpromazine and haloperidol significantly increased GAG-induced antinociception. 3. 3. Theophylline antagonized antinociception produced by both GAG and GVG. 4. 4. Bicuculline did not antagonize antinociception produced by either GAG or muscimol. 5. 5. GAG-induced antinociception does not appear to result from the activation of either classical or novel GABA receptors. An interaction with dopaminergic pathways appears to be involved.
Langue d'origine | English |
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Pages (de-à) | 603-607 |
Nombre de pages | 5 |
Journal | Vascular Pharmacology |
Volume | 14 |
Numéro de publication | 6 |
DOI | |
Statut de publication | Published - 1983 |
ASJC Scopus Subject Areas
- Pharmacology
PubMed: MeSH publication types
- Journal Article
- Research Support, Non-U.S. Gov't