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Excitability of PFC Basal Dendrites (Acker and Antic 2009)
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".. We carried out multi-site voltage-sensitive dye imaging of membrane potential transients from thin basal branches of prefrontal cortical pyramidal neurons before and after application of channel blockers. We found that backpropagating action potentials (bAPs) are predominantly controlled by voltage-gated sodium and A-type potassium channels. In contrast, pharmacologically blocking the delayed rectifier potassium, voltage-gated calcium or Ih, conductance had little effect on dendritic action potential propagation. Optically recorded bAP waveforms were quantified and multicompartmental modeling (NEURON) was used to link the observed behavior with the underlying biophysical properties. The best-fit model included a non-uniform sodium channel distribution with decreasing conductance with distance from the soma, together with a non-uniform (increasing) A-type potassium conductance. AP amplitudes decline with distance in this model, but to a lesser extent than previously thought. We used this model to explore the mechanisms underlying two sets of published data involving high frequency trains of action potentials, and the local generation of sodium spikelets. ..."
Acker CD, Antic SD (2009) Quantitative assessment of the distributions of membrane conductances involved in action potential backpropagation along basal dendrites.
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Neuron or other electrically excitable cell;
Neocortex V1 L6 pyramidal corticothalamic GLU cell;
I L high threshold;
I T low threshold;
Dendritic Action Potentials;
Detailed Neuronal Models;
Acker, Corey [acker at uchc.edu];
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Neocortex V1 L6 pyramidal corticothalamic GLU cell
I L high threshold
I T low threshold
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