Abstract
The actions of serotonin were investigated on motoneurons isolated from embryonic day 14 rat spinal cord and enriched by metrizamide density gradient centrifugation. Trophic support was provided by a spinal cord glial monolayer, ciliary neurotrophic factor and heat-inactivated serum. Cultures were maintained for 17–83 days and investigated using whole-cell patch-clamp recording. Serotonin evoked slow depolarizations (6.2±0.7 or 9.3±1.3 mV in the presence of 6-cyano-7-nitroquinoxaline-2,3-dione and strychnine, ec 50 8.2 nM), which were reversibly blocked by 0.1 μM ketanserin. Serotonin generated synaptic potentials in motoneurons, lowered the threshold for repetitive firing and changed the slope of the current intensity–firing frequency relationship. The inward current evoked by serotonin (−147±15.2 pA) was ascribed to a complex ionic mechanism, which varied amongst neurons in the sampled population. It was due to closure of barium-sensitive potassium channels, effects on I h and increase in a separate mixed cation current which comprised both transient voltage-sensitive and sustained components. We conclude that serotonergic responses develop in motoneurons cultured under these conditions in the absence of serotonergic input, sensory neurons or many interneurons.
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