The role of 5‐HT1B receptors in the regulation of serotonin cell firing and release in the rat brain
Open Access
- 1 October 2001
- journal article
- research article
- Published by Wiley in Journal of Neurochemistry
- Vol. 79 (1) , 172-182
- https://doi.org/10.1046/j.1471-4159.2001.00550.x
Abstract
The release of 5-HT in terminal areas of the rodent brain is regulated by 5-HT1B receptors. Here we examined the role of 5-HT1B receptors in the control of 5-HT output and firing in the dorsal raphe nucleus (DR), median raphe nucleus (MnR) and forebrain of the rat in vivo. The local perfusion (30–300 µm) of the selective 5-HT1B receptor agonist CP-93,129 to freely moving rats decreased 5-HT release in the DR and more markedly in the MnR. Likewise, 300 µm CP-93,129 reduced 5-HT output in substantia nigra pars reticulata, ventral pallidum, lateral habenula and the suprachiasmatic nucleus. The effect of CP-93,129 was prevented by SB-224289, but not by WAY-100635, selective 5-HT1B and 5-HT1A receptor antagonists, respectively. SB-224289 did not alter dialysate 5-HT in any raphe nuclei. The intravenous administration of the brain-penetrant selective 5-HT1B receptor agonist CP-94,253 (0.5–2.0 mg/kg) to anesthetized rats decreased dialysate 5-HT in dorsal hippocampus and globus pallidus, increased it in MnR and left it unaltered in the DR and medial prefrontal cortex. SB-224289, at a dose known to block 5-HT1B autoreceptor-mediated effects (5 mg/kg), did not prevent the effect of CP-94,253 on MnR 5-HT. The intravenous administration of CP-94,253 (0.05–1.6 mg/kg) to anesthetized rats increased the firing rate of MnR, but not DR-5-HT neurons. The local perfusion of CP-94,253 in the MnR showed a biphasic effect, with 5-HT reductions at 0.3–3 µm and increase at 300 µm. These results suggest that 5-HT cell firing and release in midbrain raphe nuclei (particularly in the MnR) are under control of 5-HT1B receptors. The activation of 5-HT1B autoreceptors (possibly located on 5-HT nerve endings and/or varicosities within DR and MnR) reduces 5-HT release. The effects of higher concentrations of 5-HT1B receptor agonists seem more compatible with the activation of 5-HT1B heteroreceptors on inhibitory neurons.Keywords
This publication has 67 references indexed in Scilit:
- Multiple 5-HT1 autoreceptor subtypes govern serotonin release in dorsal and median raphé nucleiNeuropharmacology, 2001
- Presynaptic inhibition by 5-HT1Breceptors of glutamatergic synaptic inputs onto serotonergic caudal raphe neurones in ratThe Journal of Physiology, 1998
- In situ hybridization evidence for the synthesis of 5‐HT1B receptor in serotoninergic neurons of anterior raphe nuclei in the rat brainSynapse, 1995
- Extracellular 5‐Hydroxytryptamine in Median Raphe Nucleus of the Conscious Rat Is Decreased by Nanomolar Concentrations of 8‐Hydroxy‐2‐(Di‐n‐Propylamino)tetralin and Is Sensitive to TetrodotoxinJournal of Neurochemistry, 1994
- Characterization of [3H]CP‐96,501 as a Selective Radioligand for the Serotonin 5‐HT1B Receptor: Binding Studies in Rat Brain MembranesJournal of Neurochemistry, 1992
- Binding and uptake studies with [3H]CP-93, 129, a radiolabeled selective 5-HT1B receptor ligandDrug Development Research, 1992
- Electrophysiological responses of serotoninergic dorsal raphe neurons to 5‐HT1A and 5‐HT1B agonistsSynapse, 1987
- Serotonin neurons of the midbrain raphe: Ascending projectionsJournal of Comparative Neurology, 1978
- An autoradiographic analysis of the differential ascending projections of the dorsal and median raphe nuclei in the ratJournal of Comparative Neurology, 1978
- Habenular and other midbrain raphe afferents demonstrated by a modified retrograde tracing techniqueBrain Research, 1977