Effects of fenfluramine on free-operant timing behaviour: evidence for involvement of 5-HT2A receptors

Psychopharmacology - Tập 176 - Trang 154-166 - 2004
S. Body1, S. Kheramin1, M.-Y. Ho1,2, F. Miranda Herrera1,3, C. M. Bradshaw1, E. Szabadi1
1Psychopharmacology Section, Division of Psychiatry, University of Nottingham, Nottingham, UK
2Institute of Clinical Behavioral Sciences, Chang Gung University, Tao Yuan County, Taiwan
3Facultad de Estudios Superiores Iztacala, Tlalnepantla Edo. Méx, Mexico, Mexico

Tóm tắt

Temporal differentiation in the free-operant psychophysical procedure is sensitive to the 5-hydroxytryptamine (5-HT)1A receptor agonist 8-hydroxy-2-(di-n-propylamino)-tetralin (8-OH-DPAT) and the 5-HT2 receptor agonist 2,5-dimethoxy-4-iodo-amphetamine (DOI); both drugs shift the psychophysical curve leftwards, reducing the indifference point, T 50. We have examined the effect of the 5-HT releasing agent fenfluramine on temporal differentiation. We examined whether fenfluramine’s effect on temporal differentiation can be antagonised by the 5-HT1A receptor antagonist N-[2-(4-[2-methoxy-phenyl]-1-piperazinyl)ethyl]-N-2-pyridinylcyclohexane-carboxamide (WAY-100635) and the 5-HT2A receptor antagonist ketanserin, and compared the effects of fenfluramine, DOI and 8-OH-DPAT in intact rats and rats whose 5-HTergic pathways had been destroyed by 5,7-dihydroxytryptamine. Rats were trained under the free-operant psychophysical procedure to press levers A and B in 50-s trials in which reinforcers were provided intermittently for responding on A in the first half, and B in the second half of the trial. Percent responding on B (%B) was recorded in successive 5-s epochs of the trials; logistic psychophysical curves were fitted to the data for derivation of timing indices (T 50, time corresponding to %B=50%, and Weber fraction). Experiment 1 examined the effects of acute treatment with fenfluramine, and the interaction between fenfluramine and the 5-HT1A and 5-HT2A receptor antagonists WAY-100635 and ketanserin; experiment 2 compared the effects of fenfluramine, 8-OH-DPAT and DOI in intact rats and rats whose 5-HTergic pathways had been destroyed by intra-raphe injection of 5,7-dihydroxytryptamine. Concentrations of 5-HT and catecholamines in the brain were measured by high-performance liquid chromatography. Experiment 1: fenfluramine (2 mg/kg) reduced T 50; this effect was attenuated by ketanserin (1.0 mg/kg) but not by WAY-100635 (100 μg/kg). Experiment 2: 8-OH-DPAT (100 μg/kg) and DOI (250 μg/kg) reduced T 50 in both groups; fenfluramine reduced T 50 only in the sham-lesioned group. Levels of 5-HT were reduced by 80% in the lesioned group; catecholamine levels were not affected. The results suggest that fenfluramine affects temporal differentiation via the release of endogenous 5-HT which acts mainly on postsynaptic 5-HT2A receptors.

Tài liệu tham khảo

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