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Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study

Unmyelinated C-fibers are a major type of sensory neurons conveying pain information. Action potential conduction is regulated by the bifurcation (T-junction) of sensory neuron axons within the dorsal root ganglia (DRG). Understanding how C-fiber signaling is influenced by the morphology of the T-ju...

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Autores principales: Sundt, Danielle, Gamper, Nikita, Jaffe, David B.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Physiological Society 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686302/
https://www.ncbi.nlm.nih.gov/pubmed/26334005
http://dx.doi.org/10.1152/jn.00226.2015
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author Sundt, Danielle
Gamper, Nikita
Jaffe, David B.
author_facet Sundt, Danielle
Gamper, Nikita
Jaffe, David B.
author_sort Sundt, Danielle
collection PubMed
description Unmyelinated C-fibers are a major type of sensory neurons conveying pain information. Action potential conduction is regulated by the bifurcation (T-junction) of sensory neuron axons within the dorsal root ganglia (DRG). Understanding how C-fiber signaling is influenced by the morphology of the T-junction and the local expression of ion channels is important for understanding pain signaling. In this study we used biophysical computer modeling to investigate the influence of axon morphology within the DRG and various membrane conductances on the reliability of spike propagation. As expected, calculated input impedance and the amplitude of propagating action potentials were both lowest at the T-junction. Propagation reliability for single spikes was highly sensitive to the diameter of the stem axon and the density of voltage-gated Na(+) channels. A model containing only fast voltage-gated Na(+) and delayed-rectifier K(+) channels conducted trains of spikes up to frequencies of 110 Hz. The addition of slowly activating KCNQ channels (i.e., K(V)7 or M-channels) to the model reduced the following frequency to 30 Hz. Hyperpolarization produced by addition of a much slower conductance, such as a Ca(2+)-dependent K(+) current, was needed to reduce the following frequency to 6 Hz. Attenuation of driving force due to ion accumulation or hyperpolarization produced by a Na(+)-K(+) pump had no effect on following frequency but could influence the reliability of spike propagation mutually with the voltage shift generated by a Ca(2+)-dependent K(+) current. These simulations suggest how specific ion channels within the DRG may contribute toward therapeutic treatments for chronic pain.
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spelling pubmed-46863022015-12-30 Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study Sundt, Danielle Gamper, Nikita Jaffe, David B. J Neurophysiol Sensory Processing Unmyelinated C-fibers are a major type of sensory neurons conveying pain information. Action potential conduction is regulated by the bifurcation (T-junction) of sensory neuron axons within the dorsal root ganglia (DRG). Understanding how C-fiber signaling is influenced by the morphology of the T-junction and the local expression of ion channels is important for understanding pain signaling. In this study we used biophysical computer modeling to investigate the influence of axon morphology within the DRG and various membrane conductances on the reliability of spike propagation. As expected, calculated input impedance and the amplitude of propagating action potentials were both lowest at the T-junction. Propagation reliability for single spikes was highly sensitive to the diameter of the stem axon and the density of voltage-gated Na(+) channels. A model containing only fast voltage-gated Na(+) and delayed-rectifier K(+) channels conducted trains of spikes up to frequencies of 110 Hz. The addition of slowly activating KCNQ channels (i.e., K(V)7 or M-channels) to the model reduced the following frequency to 30 Hz. Hyperpolarization produced by addition of a much slower conductance, such as a Ca(2+)-dependent K(+) current, was needed to reduce the following frequency to 6 Hz. Attenuation of driving force due to ion accumulation or hyperpolarization produced by a Na(+)-K(+) pump had no effect on following frequency but could influence the reliability of spike propagation mutually with the voltage shift generated by a Ca(2+)-dependent K(+) current. These simulations suggest how specific ion channels within the DRG may contribute toward therapeutic treatments for chronic pain. American Physiological Society 2015-09-02 2015-12-01 /pmc/articles/PMC4686302/ /pubmed/26334005 http://dx.doi.org/10.1152/jn.00226.2015 Text en Copyright © 2015 the American Physiological Society http://creativecommons.org/licenses/by/3.0/deed.en_US Licensed under Creative Commons Attribution CC-BY 3.0 (http://creativecommons.org/licenses/by/3.0/deed.en_US) : © the American Physiological Society.
spellingShingle Sensory Processing
Sundt, Danielle
Gamper, Nikita
Jaffe, David B.
Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study
title Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study
title_full Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study
title_fullStr Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study
title_full_unstemmed Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study
title_short Spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study
title_sort spike propagation through the dorsal root ganglia in an unmyelinated sensory neuron: a modeling study
topic Sensory Processing
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4686302/
https://www.ncbi.nlm.nih.gov/pubmed/26334005
http://dx.doi.org/10.1152/jn.00226.2015
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