作者: S.Y. Wu , M.Y. Wang , N.J. Dun
DOI: 10.1016/0006-8993(91)90178-X
关键词: Afterhyperpolarization 、 Synaptic augmentation 、 Internal medicine 、 Inhibitory postsynaptic potential 、 Electrophysiology 、 Methysergide 、 Excitatory postsynaptic potential 、 Postsynaptic potential 、 Neuroscience 、 Neurotransmission 、 Endocrinology 、 Biology
摘要: Intracellular recordings were made from motoneurons in transverse spinal cord slices immature (12–20 day) rats and the effects of 5-HT on dorsal root evoked excitatory (EPSPs) inhibitory (IPSPs) postsynaptic potentials assessed. With or without causing a membrane polarization, (1–300 μM) depressed synaptic responses; IC50 was 6 μM. The effect potentiated by uptake inhibitor fluoxetine. 5-HT1A/1B agonists 5-CT 8-OH-DPAT 5-HT1B/1C agonist TFMPP reduced responses as well, with an 0.26, 2.2 0.28 μM, respectively. depressant not antagonized methysergide (0.1–1 μM), ketanserin (1–5 MDL 72222 (1–10 μM). Methysergide alone diminished some motoneurons. Spiperone partially fully 8-OH-DPAT, but ineffective against TFMPP. 5-HT-induced depression accompanied concomitant reduction glutamate-induced depolarization; latter enhanced after repeated exposure to Finally, afterhyperpolarization following single spike train spikes. results indicate that inhibits via presynaptic 5-HT1 receptors, activation which reduces liberation transmitters respective nerve endings.