Interaction of serotonin autoreceptor antagonists in the rat dorsal raphe nucleus: an in vitro fast cyclic voltammetry study

Citation
C. Roberts et Gw. Price, Interaction of serotonin autoreceptor antagonists in the rat dorsal raphe nucleus: an in vitro fast cyclic voltammetry study, NEUROSCI L, 300(1), 2001, pp. 45-48
Citations number
10
Categorie Soggetti
Neurosciences & Behavoir
Journal title
NEUROSCIENCE LETTERS
ISSN journal
03043940 → ACNP
Volume
300
Issue
1
Year of publication
2001
Pages
45 - 48
Database
ISI
SICI code
0304-3940(20010302)300:1<45:IOSAAI>2.0.ZU;2-8
Abstract
5-HT1A, 5-HT18 and 5-HT1D receptors are known to function as 5-HT autorecep tors in the rat dorsal raphe nucleus (DRN), modulating local 5-HT efflux, H owever, there are no studies on the simultaneous blockade of these receptor s in the DRN. We investigated the effect of 5-HT18 and 5-HT1D receptor anta gonists on 5-HT efflux in rat DRN, alone and in the presence of 5-HT1A rece ptor antagonists, using the technique of fast cyclic voltammetry. The 5-HT, A receptor antagonist, WAY 100635, and the 5-HT1B receptor antagonist, SB-2 24289, had no effect on 5-HT efflux while the 5-HT1B/1D receptor antagonist , GR 127935, produced a small decrease in 5-HT afflux. In contrast, the 5-H T1D receptor antagonist, BRL 15572, produced a significant increase in 5-HT efflux. Go-perfusion of WAY 100635 and SB-224289 significantly increased 5 -HT efflux. In addition, WAY 100635 reversed the small inhibition of 5-HT e fflux observed with GR 127935 but had no effect on the BRL 15572-induced in crease. Antagonism of all three 5-HT autoreceptors with SB-224289, BRL 1557 2 and WAY 100635 significantly increased 5-HT afflux. These data confirm th at 5-HT afflux within the DRN is under the control of 5-HT1A, 5-HT1B and 5- HT1D autoreceptors and elevation of 5-HT efflux was greatest following anta gonism of 5-HT,A and 5-HT1B receptors. (C) 2001 Elsevier Science Ireland Lt d. All rights reserved.