Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.

The mechanism(s) of action of most commonly used pharmacological blockers of voltage-gated ion channels are well understood; however, this knowledge is rarely considered when interpreting experimental data. Effects of blockade are often assumed to be equivalent, regardless of the mechanism of the bl...

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Main Authors: Ryan S Phillips, Jonathan E Rubin
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-08-01
Series:PLoS Computational Biology
Online Access:https://doi.org/10.1371/journal.pcbi.1006938
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author Ryan S Phillips
Jonathan E Rubin
author_facet Ryan S Phillips
Jonathan E Rubin
author_sort Ryan S Phillips
collection DOAJ
description The mechanism(s) of action of most commonly used pharmacological blockers of voltage-gated ion channels are well understood; however, this knowledge is rarely considered when interpreting experimental data. Effects of blockade are often assumed to be equivalent, regardless of the mechanism of the blocker involved. Using computer simulations, we demonstrate that this assumption may not always be correct. We simulate the blockade of a persistent sodium current (INaP), proposed to underlie rhythm generation in pre-Bötzinger complex (pre-BötC) respiratory neurons, via two distinct pharmacological mechanisms: (1) pore obstruction mediated by tetrodotoxin and (2) altered inactivation dynamics mediated by riluzole. The reported effects of experimental application of tetrodotoxin and riluzole in respiratory circuits are diverse and seemingly contradictory and have led to considerable debate within the field as to the specific role of INaP in respiratory circuits. The results of our simulations match a wide array of experimental data spanning from the level of isolated pre-BötC neurons to the level of the intact respiratory network and also generate a series of experimentally testable predictions. Specifically, in this study we: (1) provide a mechanistic explanation for seemingly contradictory experimental results from in vitro studies of INaP block, (2) show that the effects of INaP block in in vitro preparations are not necessarily equivalent to those in more intact preparations, (3) demonstrate and explain why riluzole application may fail to effectively block INaP in the intact respiratory network, and (4) derive the prediction that effective block of INaP by low concentration tetrodotoxin will stop respiratory rhythm generation in the intact respiratory network. These simulations support a critical role for INaP in respiratory rhythmogenesis in vivo and illustrate the importance of considering mechanism when interpreting and simulating data relating to pharmacological blockade.
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spelling doaj.art-e471841090744329a7dc5fa7d43b096b2022-12-21T19:55:36ZengPublic Library of Science (PLoS)PLoS Computational Biology1553-734X1553-73582019-08-01158e100693810.1371/journal.pcbi.1006938Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.Ryan S PhillipsJonathan E RubinThe mechanism(s) of action of most commonly used pharmacological blockers of voltage-gated ion channels are well understood; however, this knowledge is rarely considered when interpreting experimental data. Effects of blockade are often assumed to be equivalent, regardless of the mechanism of the blocker involved. Using computer simulations, we demonstrate that this assumption may not always be correct. We simulate the blockade of a persistent sodium current (INaP), proposed to underlie rhythm generation in pre-Bötzinger complex (pre-BötC) respiratory neurons, via two distinct pharmacological mechanisms: (1) pore obstruction mediated by tetrodotoxin and (2) altered inactivation dynamics mediated by riluzole. The reported effects of experimental application of tetrodotoxin and riluzole in respiratory circuits are diverse and seemingly contradictory and have led to considerable debate within the field as to the specific role of INaP in respiratory circuits. The results of our simulations match a wide array of experimental data spanning from the level of isolated pre-BötC neurons to the level of the intact respiratory network and also generate a series of experimentally testable predictions. Specifically, in this study we: (1) provide a mechanistic explanation for seemingly contradictory experimental results from in vitro studies of INaP block, (2) show that the effects of INaP block in in vitro preparations are not necessarily equivalent to those in more intact preparations, (3) demonstrate and explain why riluzole application may fail to effectively block INaP in the intact respiratory network, and (4) derive the prediction that effective block of INaP by low concentration tetrodotoxin will stop respiratory rhythm generation in the intact respiratory network. These simulations support a critical role for INaP in respiratory rhythmogenesis in vivo and illustrate the importance of considering mechanism when interpreting and simulating data relating to pharmacological blockade.https://doi.org/10.1371/journal.pcbi.1006938
spellingShingle Ryan S Phillips
Jonathan E Rubin
Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.
PLoS Computational Biology
title Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.
title_full Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.
title_fullStr Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.
title_full_unstemmed Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.
title_short Effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics.
title_sort effects of persistent sodium current blockade in respiratory circuits depend on the pharmacological mechanism of action and network dynamics
url https://doi.org/10.1371/journal.pcbi.1006938
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