Abstract
The anxiolytic property of R-(+)-8-OSO3CF3-PAT (R-(+)-8-[[(trifluoromethyl)sulfonyl]oxy]-2-(n-propyl-amino)tetralin), a 5-HT1A receptor agonist, was evaluated in Wistar rats by means of animal models of anxiety, the conditioned defensive burying model and the conditioned stress-induced freezing response followed by the elevated plus-maze tear, respectively, In addition, the 5-HIAA/5-HT ratio (5-hydroxy-indole acetic acid/5-hydroxytryptamine) of rat brain homogenates was studied. Acute drug administration resulted in abolition of the burying behaviour (3 mg/kg i.p.), a dose-dependent decrease of rearing and induction of hyperphagia. R-(+)8-OSO2CF3-PAT had no effect on conditioned footshock-induced freezing behaviour but increased open-arm activity in the rats on the plus-maze, The 5-HIAA/5-HT ratio was decreased in the lateral septum (1 and 3 mg/kg), dorsal hippocampus (3 mg/kg) and somatosensory cortex (3 mg/kg), implying that R-(+)-8-OSO2CF3-PAT affects particularly the limbic system in anxiety-inducing situations.
Original language | English |
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Pages (from-to) | 205-211 |
Number of pages | 7 |
Journal | European Journal of Pharmacology |
Volume | 297 |
Issue number | 3 |
Publication status | Published - 22 Feb 1996 |
Keywords
- 5-HT1A receptor
- defensive burying
- inescapable footshock
- plus-maze
- 5-HIAA/5-HT (5-hydroxy-indole acetic acid 5-hydroxytryptamine) ratio
- RAPHE NUCLEI
- BURYING TEST
- RAT-BRAIN
- SEROTONIN
- 8-OH-DPAT
- BUSPIRONE
- ANXIETY
- DORSAL
- DRUGS
- AUTORECEPTORS