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Vol. 284, Issue 1, 238-249, 1998
Centre de Recherche Pierre Fabre, 81106 Castres Cedex France
In this study we examined the effects of 5-HT1A ligands in
rats trained to discriminate 0.16 mg/kg i.p.
8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) from
saline in a two-lever, fixed ratio (FR)10 schedule of food
reinforcement, and in pigeons trained to discriminate 0.31 mg/kg i.m.
8-OH-DPAT from saline in a two-key, FR30 schedule of food
reinforcement. In both species, 8-OH-DPAT and a variety of structurally
unrelated 5-HT1A ligands occasioned dose-related, relatively high levels of drug-appropriate selection
(i.e.
67%). A significant positive correlation was
found between estimated ED50 values in both species
(r = 0.84, P < .001). Further,
5-HT1A antagonists, NAN-190, penbutolol, (
)-pindolol,
tertatolol and WAY-100635, produced dose-related decreases in
8-OH-DPAT-appropriate selection, and their potencies for antagonism in
rats and pigeons were highly correlated (r = 0.96, P < .01). The potency of WAY 100635 in rats and pigeons was
quantified by Schild analysis (apparent in vivo
pA2 values: 7.8 vs. 8.3, rat
vs. pigeon, respectively). Although most
5-HT1A agonists produced similar 8-OH-DPAT-like discriminative stimulus effects in both species, two compounds, lisuride and eltoprazine, occasioned high levels of drug-appropriate selection in pigeons, but not in rats. In contrast, idazoxan, yohimbine, LEK 8804 and BMY 7378 produced greater effects in rats. Among this latter group of compounds, only BMY 7378 blocked the discriminative stimulus effects of 8-OH-DPAT in pigeons, which suggested that intermediate levels of drug-appropriate selection observed with the remaining compounds are not necessarily the result of
low intrinsic activity. Overall, these results demonstrate similarities
in the discriminative stimulus effects of 8-OH-DPAT in rats and pigeons
despite different training conditions (e.g., training
dose and route of administration). Even so, the finding that some
5-HT1A ligands did not produce similar effects in rats and
pigeons illustrates the need to examine possible 8-OH-DPAT-like discriminative stimulus effects of compounds in both species.
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