Abstract
Serotoninergic transmission is implicated in the photic and non-photic regulation of circadian rhythms. 5-HT (1-100 μM), carboxamidotryptamine (5-CT 0.1-10 μM) and (+)-8-hydroxy-dipropylaminotetraline (8-OH-DPAT, 1-30 μM) dose-dependently activated an outward current (5-100 pA) in 30% of neurons voltage-clamped at -60 mV in the suprachiasmatic nucleus (SCN) in vitro slice. EC50 values were 7.0 μM for 5-HT and 0.2 μM for 5-CT. Serotonin-induced outward current was associated with an increase in input conductance, and the current was blocked by Ba2+ (1 mM). The amplitude of the current was enhanced by depolarization, reduced by hyperpolarization, and reversed its polarity during a hyperpolarization beyond the potassium equilibrium potential. Mean amplitudes of the 5-HT outward current changed with time of the subjective circadian day. The value near CT2 (23.8 pA) was about 4 times greater than that around CT14 (6.7 pA). Cells that responded with an outward current showed four types of morphology: monopolar, simple bipolar, curly bipolar and radial shaped; they were localized in all parts of the SCN. The EPSC evoked by retino-hypothalamic-tract (RHT) stimulation was inhibited 26% but the inward current induced by exogenously applied glutamate or NMDA was not affected by serotonin agonists. Focal stimulation-induced and spontaneous IPSC but not the exogenous GABA-induced outward current were inhibited by 5-HT agonists in a subpopulation of cells. In conclusion, 5-HT regulates SCN neurons by both pre- and post-synaptic inhibitory mechanisms; the latter may play a key role in modulating SCN circadian rhythm by activation of 5-HT receptors and opening of a potassium channel. Copyright (C) 2000 Elsevier Science B.V.
Original language | English (US) |
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Pages (from-to) | 247-256 |
Number of pages | 10 |
Journal | Brain research |
Volume | 866 |
Issue number | 1-2 |
DOIs | |
State | Published - Jun 2 2000 |
Keywords
- 5-HT receptor
- Circadian rhythm
- GABA
- Glutamate
- Serotonin
- Suprachiasmatic nucleus
- Synaptic inhibition
ASJC Scopus subject areas
- Neuroscience(all)
- Molecular Biology
- Clinical Neurology
- Developmental Biology