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Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest

Acidosis and its associated pathologies predispose patients to develop cardiac arrhythmias and even cardiac arrest. These arrhythmias are assumed to be the result of membrane depolarization, however, the exact mechanism of depolarization during acidosis is not well defined. In our study, the model o...

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Autores principales: Ababneh, Omar, Qaswal, Abdallah Barjas, Alelaumi, Ahmad, Khreesha, Lubna, Almomani, Mujahed, Khrais, Majdi, Khrais, Oweiss, Suleihat, Ahmad, Mutleq, Shahed, Al-olaimat, Yazan, Nawafleh, Sager
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8830476/
https://www.ncbi.nlm.nih.gov/pubmed/35366283
http://dx.doi.org/10.3390/pathophysiology28030027
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author Ababneh, Omar
Qaswal, Abdallah Barjas
Alelaumi, Ahmad
Khreesha, Lubna
Almomani, Mujahed
Khrais, Majdi
Khrais, Oweiss
Suleihat, Ahmad
Mutleq, Shahed
Al-olaimat, Yazan
Nawafleh, Sager
author_facet Ababneh, Omar
Qaswal, Abdallah Barjas
Alelaumi, Ahmad
Khreesha, Lubna
Almomani, Mujahed
Khrais, Majdi
Khrais, Oweiss
Suleihat, Ahmad
Mutleq, Shahed
Al-olaimat, Yazan
Nawafleh, Sager
author_sort Ababneh, Omar
collection PubMed
description Acidosis and its associated pathologies predispose patients to develop cardiac arrhythmias and even cardiac arrest. These arrhythmias are assumed to be the result of membrane depolarization, however, the exact mechanism of depolarization during acidosis is not well defined. In our study, the model of quantum tunneling of protons is used to explain the membrane depolarization that occurs during acidosis. It is found that protons can tunnel through closed activation and inactivation gates of voltage-gated sodium channels Nav1.5 that are present in the membrane of cardiac cells. The quantum tunneling of protons results in quantum conductance, which is evaluated to assess its effect on membrane potential. The quantum conductance of extracellular protons is higher than that of intracellular protons. This predicts an inward quantum current of protons through the closed sodium channels. Additionally, the values of quantum conductance are influential and can depolarize the membrane potential according to the quantum version of the GHK equation. The quantum mechanism of depolarization is distinct from other mechanisms because the quantum model suggests that protons can directly depolarize the membrane potential, and not only through indirect effects as proposed by other mechanisms in the literature. Understanding the pathophysiology of arrhythmias mediated by depolarization during acidosis is crucial to treat and control them and to improve the overall clinical outcomes of patients.
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spelling pubmed-88304762022-03-23 Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest Ababneh, Omar Qaswal, Abdallah Barjas Alelaumi, Ahmad Khreesha, Lubna Almomani, Mujahed Khrais, Majdi Khrais, Oweiss Suleihat, Ahmad Mutleq, Shahed Al-olaimat, Yazan Nawafleh, Sager Pathophysiology Article Acidosis and its associated pathologies predispose patients to develop cardiac arrhythmias and even cardiac arrest. These arrhythmias are assumed to be the result of membrane depolarization, however, the exact mechanism of depolarization during acidosis is not well defined. In our study, the model of quantum tunneling of protons is used to explain the membrane depolarization that occurs during acidosis. It is found that protons can tunnel through closed activation and inactivation gates of voltage-gated sodium channels Nav1.5 that are present in the membrane of cardiac cells. The quantum tunneling of protons results in quantum conductance, which is evaluated to assess its effect on membrane potential. The quantum conductance of extracellular protons is higher than that of intracellular protons. This predicts an inward quantum current of protons through the closed sodium channels. Additionally, the values of quantum conductance are influential and can depolarize the membrane potential according to the quantum version of the GHK equation. The quantum mechanism of depolarization is distinct from other mechanisms because the quantum model suggests that protons can directly depolarize the membrane potential, and not only through indirect effects as proposed by other mechanisms in the literature. Understanding the pathophysiology of arrhythmias mediated by depolarization during acidosis is crucial to treat and control them and to improve the overall clinical outcomes of patients. MDPI 2021-09-03 /pmc/articles/PMC8830476/ /pubmed/35366283 http://dx.doi.org/10.3390/pathophysiology28030027 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Ababneh, Omar
Qaswal, Abdallah Barjas
Alelaumi, Ahmad
Khreesha, Lubna
Almomani, Mujahed
Khrais, Majdi
Khrais, Oweiss
Suleihat, Ahmad
Mutleq, Shahed
Al-olaimat, Yazan
Nawafleh, Sager
Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest
title Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest
title_full Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest
title_fullStr Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest
title_full_unstemmed Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest
title_short Proton Quantum Tunneling: Influence and Relevance to Acidosis-Induced Cardiac Arrhythmias/Cardiac Arrest
title_sort proton quantum tunneling: influence and relevance to acidosis-induced cardiac arrhythmias/cardiac arrest
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8830476/
https://www.ncbi.nlm.nih.gov/pubmed/35366283
http://dx.doi.org/10.3390/pathophysiology28030027
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