Abstract
Activity-dependent changes in the short-term electrical properties of neurites were investigated in the anterior pagoda (AP) cell of leech. Imaging studies revealed that backpropagating Na+ spikes and synaptically evoked EPSPs caused Ca2+ entry through low-voltage-activated Ca2+ channels that are distributed throughout the neurites. Voltage-clamp recordings from the soma revealed a TEA-sensitive outward current that was reduced when Ca2+ entry was blocked with Co2+ or when the intracellular concentration of free Ca2+ was reduced by a high-affinity Ca2- buffer. Ca2+ released in the neurite from a caged Ca2+ compound caused a hyperpolarization of the membrane potential. These data imply that the AP cell expresses Ca2+- activated K+ conductances, and that these conductances are present in the neurites. When the Ca2+activated K+ current was reduced through the block of Ca2+ entry, backpropagating Na+ spikes and synaptically evoked EPSPs increased in amplitude. Hence, the activity-dependent changes in the intracellular [Ca2+] together with the Ca2+-activated K+ conductances participate in the regulation of dendritic signal propagation.
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Wessel, R., Kristan, W. B., & Kleinfeld, D. (1999). Dendritic Ca2+-activated K+ conductances regulate electrical signal propagation in an invertebrate neuron. Journal of Neuroscience, 19(19), 8319–8326. https://doi.org/10.1523/jneurosci.19-19-08319.1999
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