8-OH-DPAT, a 5-HT[sub 1A] agonist and ritanserin, a 5-HT[sub 2A/C] antagonist, reverse haloperidol-induced catalepsy in rats independently of striatal dopamine release.

Autor: Lucas, Guillaume, Bonhomme, Norbert, Deurwaerdère, Philippe De, Moal, Michel Le, Spampinato, U.
Předmět:
Zdroj: Psychopharmacology; 1997, Vol. 131 Issue 1, p57, 7p
Abstrakt: Abstract In this study, both catalepsy and changes in extracellular levels of striatal dopamine (DA) and dihydroxyphenyl acetic acid (DOPAC) induced by the typical neuroleptic haloperidol (HAL) were simultaneously assessed, using intracerebral microdialysis in freely moving rats, in the presence of either the 5-HT[sub 1A] agonist 8-OH-DPAT or the 5-HT[sub 2A/C] antagonist ritanserin. HAL (1 mg/kg, SC) elicited a strong cataleptic state, reaching its maximal intensity (about 240 s) 2 h after the drug administration. This effect was paralleled by a long-lasting enhancement of striatal DA and DOPAC extracellular levels, reaching 230 and 350% of basal values, respectively. 8-OH-DPAT (0.1 mg/kg, SC) given 2.5 h after, and ritanserin (0.63 and 1.25 mg/kg, IP), given 15 min prior to HAL, significantly reduced the neuroleptic-induced catalepsy. However, both 5-HT agents failed to modify basal DA and DOPAC striatal outflow as well as the stimulatory effect of HAL on these parameters. It can thus be concluded that the anticataleptic effect of these compounds is not related to an alteration of DA release within the striatum. [ABSTRACT FROM AUTHOR]
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