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PMID: 7576650 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Amplification of EPSPs by axosomatic sodium channels in neocortical pyramidal neurons.

Neuron ·Vol. 15 ·No. 5 ·1995-11-00 ·Pages 1065-76

Stuart G, Sakmann B

Abstract

Simultaneous somatic and dendritic recordings were made from the same neocortical layer V pyramidal neuron, and current injection via the dendritic recording pipette was used to simulate the voltage change that occurs during an EPSP. At the soma, these simulated EPSPs increased nonlinearly with the amplitude of the dendritic current injection and with depolarization of the membrane potential. Bath application of the sodium channel blocker TTX decreased large (> 5 mV) EPSPs and also blocked amplification of EPSPs at depolarized membrane potentials, whereas calcium channel blockers had little effect. Local application of TTX to the soma and axon blocked EPSP amplification, whereas dendritic application had little effect. Simultaneous somatic and axonal recordings demonstrated that EPSP amplification was largest in the axon. These results show that EPSPs are amplified by voltage-activated sodium channels located close to the soma and in the axon.

MeSH Terms
Action Potentials Animals Axons/drug effects,physiology Calcium Channel Blockers/pharmacology Cerebral Cortex/physiology,ultrastructure Dendrites/drug effects,physiology Evoked Potentials Membrane Potentials Neurons/physiology,ultrastructure Rats Rats, Wistar Sodium Channels/physiology Tetrodotoxin/pharmacology
Chemicals
Calcium Channel Blockers Sodium Channels Tetrodotoxin
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
Stuart G
Abteilung Zellphysiologie, Max-Planck-Institut für medizinische Forschung, Heidelberg, Federal Republic of Germany.
Sakmann B
Article Info
Journal
Neuron
Abbr.
Neuron
ISSN
0896-6273
Published
1995-11-00
Pages
1065-76
Language
English
Region
United States
NLM ID
8809320
Subset
IM
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