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PMID: 8845165 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S.

A model of spike initiation in neocortical pyramidal neurons.

Neuron ·Vol. 15 ·No. 6 ·1995-12-00 ·Pages 1427-39

Mainen ZF, Joerges J, Huguenard JR, Sejnowski TJ

Abstract

Neocortical pyramidal cells possess voltage-dependent dendritic sodium channels that promote propagation of action potentials into the dendritic tree but paradoxically may fail to originate dendritic spikes. A biophysical model was constructed to reconcile these observations with known anatomical and physiological properties. When dendritic and somatic sodium channel densities compatible with electrophysiological measurements were combined with much higher densities in the axon initial segment then, regardless of the site of stimulation, spikes initiated at the initial segment and subsequently invaded the dendrites. The lower initial segment threshold arose from high current density and electrical isolation from the soma. Failure of dendritic channels to initiate spikes was due to inactivation and source-load considerations, which were more favorable for conduction of back-propagated spikes.

MeSH Terms
Action Potentials Animals Axons/physiology Dendrites/physiology Models, Neurological Pyramidal Cells/physiology Rats
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Mainen Z F
Howard Hughes Medical Institute, Computational Neurobiology Laboratory, Salk Institute for Biological Studies, La Jolla, California 92037, USA.
Joerges J
Huguenard J R
Sejnowski T J
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1995-12-00
Pages
1427-39
Language
English
Region
United States
NLM ID
8809320
Subset
IM
Grants
NINDS NIH HHS · NS06477 · United States
NINDS NIH HHS · NS12151 · United States
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