Effects of local application of 5-hydroxytryptamine into the dorsal or median raphe nuclei on haloperidol-induced catalepsy in the rat

Citation
Mlg. Wadenberg et al., Effects of local application of 5-hydroxytryptamine into the dorsal or median raphe nuclei on haloperidol-induced catalepsy in the rat, NEUROPHARM, 38(1), 1999, pp. 151-156
Citations number
35
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROPHARMACOLOGY
ISSN journal
00283908 → ACNP
Volume
38
Issue
1
Year of publication
1999
Pages
151 - 156
Database
ISI
SICI code
0028-3908(199901)38:1<151:EOLAO5>2.0.ZU;2-V
Abstract
The effects of local application of the endogenous brain neurotransmitter 5 -hydroxytryptamine (5-HT; serotonin) into the dorsal (DR) or median (MR) ra phe nuclei on haloperidol-induced catalepsy (CAT) in rats were studied. Loc al application of 5-HT (40 mu g, - 10 min) into the DR or MR, respectively, produced a significant reversal of haloperidol-induced CAT. Lower doses (5 or 25 mu g) of 5-HT were ineffective. Compared to previous studies using t he selective 5-HT1A receptor agonist 8-OH-DPAT, the non-selective endogenou s serotonin receptor agonist 5-HT was significantly less potent in this par adigm. Furthermore, the observed anticataleptic effect of 5-HT was seen fol lowing injections into both DR or MR nuclei. The reversal of CAT by local a pplication of 5-HT (40 mu g) into the DR was significant also at 70 min aft er 5-HT administration, with the same tendency for 5-HT injections into the MR. At this time interval, other serotonegic behavioral symptoms like head twitches and wet-dog shakes also emerged. The early reversal of CAT by loc al 5-HT administration into the MR is in all probability mediated via stimu lation of 5-HT1A autoreceptors on raphe serotonergic cell bodies. The rever sal of CAT following 5-HT injections into the DR might alternatively be med iated via functional mechanisms other than stimulation of 5-HT1A autorecept ors. The anticataleptic effects observed at the later observation time coul d be due to stimulation of postsynaptic 5-HT2 receptors following diffusion of 5-HT into 5-HT2 receptor rich areas of the brain. (C) 1999 Elsevier Sci ence Ltd. All rights reserved.