The effects of the antidepressant drug, trazodone, on the extracellular 5-hydroxytryptamine 5-HT. levels in the frontal cortex of freely moving rats was investigated using microdialysis coupled to a high performance liquid chromatography HPLC. detection method. Systemic administration of 1.25 and 2.5 mgrkg s.c. of trazodone was followed by a rise in the 5-HT level which reached a 5-fold peak over the basal level 5 h after injection, and a 3-fold peak after 1 h. Higher doses had no effect. The increase was prevented by pretreatment with fluoxetine 10 mgrkg s.c.., a 5-HT uptake inhibitor. Direct administration of trazodone 0.03, 0.1, 1, 2 mgrml., by reverse dialysis into the frontal cortex, elicited a dose-dependent large increase in 5-HT levels. The increase was not prevented by systemic fluoxetine administration but was reduced by local perfusion of ketanserin 0.1 mgrml. a 5-HT2ArC receptor antagonist. Trazodone s.c. administration for 7 days did not increase 5-HT basal levels but enhanced the effects of challenge doses of 2.5 and 5 mgrkg s.c. The present work demonstrated that trazodone increases the 5-HT extracellular level through a double mechanism which involves the 5-HT transporter and 5-HT2ArC receptors. This increase may trigger the chain of events which lead to the therapeutic effects, similar to the case of many other antidepressant drugs.

Trazodone increases extracellular serotonin levels in the frontal cortex of rats / M. PAZZAGLI; M.G. GIOVANNINI; G. PEPEU. - In: EUROPEAN JOURNAL OF PHARMACOLOGY. - ISSN 0014-2999. - ELETTRONICO. - 383:(1999), pp. 249-257. [10.1016/S0014-2999(99)00644-5]

Trazodone increases extracellular serotonin levels in the frontal cortex of rats.

GIOVANNINI, MARIA GRAZIA;PEPEU, GIANCARLO
1999

Abstract

The effects of the antidepressant drug, trazodone, on the extracellular 5-hydroxytryptamine 5-HT. levels in the frontal cortex of freely moving rats was investigated using microdialysis coupled to a high performance liquid chromatography HPLC. detection method. Systemic administration of 1.25 and 2.5 mgrkg s.c. of trazodone was followed by a rise in the 5-HT level which reached a 5-fold peak over the basal level 5 h after injection, and a 3-fold peak after 1 h. Higher doses had no effect. The increase was prevented by pretreatment with fluoxetine 10 mgrkg s.c.., a 5-HT uptake inhibitor. Direct administration of trazodone 0.03, 0.1, 1, 2 mgrml., by reverse dialysis into the frontal cortex, elicited a dose-dependent large increase in 5-HT levels. The increase was not prevented by systemic fluoxetine administration but was reduced by local perfusion of ketanserin 0.1 mgrml. a 5-HT2ArC receptor antagonist. Trazodone s.c. administration for 7 days did not increase 5-HT basal levels but enhanced the effects of challenge doses of 2.5 and 5 mgrkg s.c. The present work demonstrated that trazodone increases the 5-HT extracellular level through a double mechanism which involves the 5-HT transporter and 5-HT2ArC receptors. This increase may trigger the chain of events which lead to the therapeutic effects, similar to the case of many other antidepressant drugs.
1999
383
249
257
M. PAZZAGLI; M.G. GIOVANNINI; G. PEPEU
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/211952
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