5-HTID RECEPTORS REGULATE 5-HT RELEASE IN THE RAT RAPHE NUCLEI - IN-VIVO VOLTAMMETRY AND IN-VITRO SUPERFUSION STUDIES

The aim of the present study was to characterize the pharmacological p rofile of 5-hydroxytryptamine (5-HT) receptors modulating 5-HT release in the mesencephalic raphe region. In a first series of experiments, differential normal pulse voltammetry and nafion-coated electrodes wer e used to measure extracellular 5-HT in the dorsal raphe of anesthesiz ed rats. The intravenous administration of the selective 5-HT1A agonis t 8-OH-DPAT (30 mu g/kg) and the 5-HT1 agonist TFMPP (0.5 mg/kg) reduc ed the 5-hydroxyindole signal by 23% and 18%, respectively. Pretreatme nt with the 5-HT1A antagonist (+)WAY100135 (0.5 mg/kg IV) 30 minutes b efore the injection of the agonists, blocked the effect of 8-OH-DPAT b ut not that of TFMPP. The effect of TFMPP was blocked by (+)mianserin, a drug with high affinity for the rat 5-HT1D receptor, suggesting a r ole of this receptor subtype in the modulation of 5-HT release at the cell body level of 5-HT neurons. This was confirmed by in vitro superf usion experiments using mesencephalic raphe slices. The prototypical S -HT1 agonist 5-carboxy-amiditryptamine (5-CT) and the 5HT(1B/1D) agoni st sumatriptan (1-1,000 nM) induced a concentration-dependent inhibiti on of the electrically evoked release of [H-3]5-HT from preloaded raph e slices. 8-OH-DPAT (200 nM) produced an inhibitory effect similar to that of sumatriptan (100 nM). The selective 5-HT1B agonist CP 93129 (1 0-10,000 nM), had no effect in raphe slices, but it dose dependently i nhibited [H-3]5-HT release from hippocampal slices where autoreceptors are of the 5HT(1B) subtype. The inhibitory effect of 5-CT was blocked by the 5-HT1/2 antagonist methiothepin (1 mu M), the 5HT(1A) antagoni st S-UH-301 (1 mu M), and the 5-HT1B/1D antagonist GR 127935 (1 mu M). That of 8-OH-DPAT was blocked by S-UH-301 (1 mu M) but nor by GR 1279 35 (1 mu M), and that of sumatriptan was blocked by GR 127935 (1 mu M) but not by S-UH-301 (1 mu M). These results show that, together with 5-HT1A autoreceptors, 5-HT1D receptors negatively modulate the somatod endritic release of 5-HT.