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Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation

The ionic mechanism underlying optimal stimulus shapes that induce a neuron to fire an action potential, or spike, is relevant to understanding optimal information transmission and therapeutic stimulation in the nervous system. Here we analyze for the first time the ionic basis for stimulus optimali...

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Detalles Bibliográficos
Autores principales: Clay, John R., Forger, Daniel B., Paydarfar, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458826/
https://www.ncbi.nlm.nih.gov/pubmed/23049913
http://dx.doi.org/10.1371/journal.pone.0045983
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author Clay, John R.
Forger, Daniel B.
Paydarfar, David
author_facet Clay, John R.
Forger, Daniel B.
Paydarfar, David
author_sort Clay, John R.
collection PubMed
description The ionic mechanism underlying optimal stimulus shapes that induce a neuron to fire an action potential, or spike, is relevant to understanding optimal information transmission and therapeutic stimulation in the nervous system. Here we analyze for the first time the ionic basis for stimulus optimality in the Hodgkin and Huxley model and for eliciting a spike in squid giant axons, the preparation for which the model was devised. The experimentally determined stimulus is a smoothly varying biphasic current waveform having a relatively long and shallow hyperpolarizing phase followed by a depolarizing phase of briefer duration. The hyperpolarizing phase removes a small degree of the resting level of Na (+) channel inactivation. This result together with the subsequent depolarizing phase provides a signal that is energetically more efficient for eliciting spikes than rectangular current pulses. Sodium channel inactivation is the only variable that is changed during the stimulus waveform, other than the membrane potential, V. The activation variables for Na (+) and K (+) channels are unchanged throughout the stimulus. This result demonstrates how an optimal stimulus waveform relates to ionic dynamics and may have implications for energy efficiency of neural excitation in many systems including the mammalian brain.
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spelling pubmed-34588262012-10-03 Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation Clay, John R. Forger, Daniel B. Paydarfar, David PLoS One Research Article The ionic mechanism underlying optimal stimulus shapes that induce a neuron to fire an action potential, or spike, is relevant to understanding optimal information transmission and therapeutic stimulation in the nervous system. Here we analyze for the first time the ionic basis for stimulus optimality in the Hodgkin and Huxley model and for eliciting a spike in squid giant axons, the preparation for which the model was devised. The experimentally determined stimulus is a smoothly varying biphasic current waveform having a relatively long and shallow hyperpolarizing phase followed by a depolarizing phase of briefer duration. The hyperpolarizing phase removes a small degree of the resting level of Na (+) channel inactivation. This result together with the subsequent depolarizing phase provides a signal that is energetically more efficient for eliciting spikes than rectangular current pulses. Sodium channel inactivation is the only variable that is changed during the stimulus waveform, other than the membrane potential, V. The activation variables for Na (+) and K (+) channels are unchanged throughout the stimulus. This result demonstrates how an optimal stimulus waveform relates to ionic dynamics and may have implications for energy efficiency of neural excitation in many systems including the mammalian brain. Public Library of Science 2012-09-26 /pmc/articles/PMC3458826/ /pubmed/23049913 http://dx.doi.org/10.1371/journal.pone.0045983 Text en https://creativecommons.org/publicdomain/zero/1.0/ This is an open-access article distributed under the terms of the Creative Commons Public Domain declaration, which stipulates that, once placed in the public domain, this work may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose.
spellingShingle Research Article
Clay, John R.
Forger, Daniel B.
Paydarfar, David
Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation
title Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation
title_full Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation
title_fullStr Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation
title_full_unstemmed Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation
title_short Ionic Mechanism Underlying Optimal Stimuli for Neuronal Excitation: Role of Na (+) Channel Inactivation
title_sort ionic mechanism underlying optimal stimuli for neuronal excitation: role of na (+) channel inactivation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3458826/
https://www.ncbi.nlm.nih.gov/pubmed/23049913
http://dx.doi.org/10.1371/journal.pone.0045983
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