Cargando…

Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination

Introduction: Mechanisms underlying cardiac arrhythmias are typically driven by abnormalities in cardiac conduction and/or heterogeneities in repolarization time (RT) across the heart. While conduction slowing can be caused by either electrophysiological defects or physical blockade in cardiac tissu...

Descripción completa

Detalles Bibliográficos
Autores principales: Marchal, Gerard A., Biasci, Valentina, Loew, Leslie M., Biggeri, Annibale, Campione, Marina, Sacconi, Leonardo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196067/
https://www.ncbi.nlm.nih.gov/pubmed/37215182
http://dx.doi.org/10.3389/fphys.2023.1167524
_version_ 1785044265326346240
author Marchal, Gerard A.
Biasci, Valentina
Loew, Leslie M.
Biggeri, Annibale
Campione, Marina
Sacconi, Leonardo
author_facet Marchal, Gerard A.
Biasci, Valentina
Loew, Leslie M.
Biggeri, Annibale
Campione, Marina
Sacconi, Leonardo
author_sort Marchal, Gerard A.
collection PubMed
description Introduction: Mechanisms underlying cardiac arrhythmias are typically driven by abnormalities in cardiac conduction and/or heterogeneities in repolarization time (RT) across the heart. While conduction slowing can be caused by either electrophysiological defects or physical blockade in cardiac tissue, RT heterogeneities are mainly related to action potential (AP) prolongation or abbreviation in specific areas of the heart. Importantly, the size of the area with altered RT and the difference between the short RT and long RT (RT gradient) have been identified as critical determinators of arrhythmogenicity. However, current experimental methods for manipulating RT gradient rely on the use of ion channel inhibitors, which lack spatial and temporal specificity and are commonly only partially reversible. Therefore, the conditions facilitating sustained arrhythmia upon the presence of RT heterogeneities and/or defects in cardiac conduction remain to be elucidated. Methods: We here employ an approach based on optogenetic stimulation in a low-intensity fashion (sub-threshold illumination), to selectively manipulate cardiac electrical activity in defined areas of the heart. Results: As previously described, subthreshold illumination is a robust tool able to prolong action potentials (AP), decrease upstroke velocity as well as slow cardiac conduction, in a fully reversible manner. By applying a patterned sub-threshold illumination in intact mouse hearts constitutively expressing the light-gated ion channel channelrhodopsin-2 (ChR2), we optically manipulate RT gradients and cardiac conduction across the heart in a spatially selective manner. Moreover, in a proof-of-concept assessment we found that in the presence of patterned sub-threshold illumination, mouse hearts were more susceptible to arrhythmias. Hence, this optogenetic-based approach may be able to mimic conduction slowing and RT heterogeneities present in pathophysiological conditions.
format Online
Article
Text
id pubmed-10196067
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Frontiers Media S.A.
record_format MEDLINE/PubMed
spelling pubmed-101960672023-05-20 Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination Marchal, Gerard A. Biasci, Valentina Loew, Leslie M. Biggeri, Annibale Campione, Marina Sacconi, Leonardo Front Physiol Physiology Introduction: Mechanisms underlying cardiac arrhythmias are typically driven by abnormalities in cardiac conduction and/or heterogeneities in repolarization time (RT) across the heart. While conduction slowing can be caused by either electrophysiological defects or physical blockade in cardiac tissue, RT heterogeneities are mainly related to action potential (AP) prolongation or abbreviation in specific areas of the heart. Importantly, the size of the area with altered RT and the difference between the short RT and long RT (RT gradient) have been identified as critical determinators of arrhythmogenicity. However, current experimental methods for manipulating RT gradient rely on the use of ion channel inhibitors, which lack spatial and temporal specificity and are commonly only partially reversible. Therefore, the conditions facilitating sustained arrhythmia upon the presence of RT heterogeneities and/or defects in cardiac conduction remain to be elucidated. Methods: We here employ an approach based on optogenetic stimulation in a low-intensity fashion (sub-threshold illumination), to selectively manipulate cardiac electrical activity in defined areas of the heart. Results: As previously described, subthreshold illumination is a robust tool able to prolong action potentials (AP), decrease upstroke velocity as well as slow cardiac conduction, in a fully reversible manner. By applying a patterned sub-threshold illumination in intact mouse hearts constitutively expressing the light-gated ion channel channelrhodopsin-2 (ChR2), we optically manipulate RT gradients and cardiac conduction across the heart in a spatially selective manner. Moreover, in a proof-of-concept assessment we found that in the presence of patterned sub-threshold illumination, mouse hearts were more susceptible to arrhythmias. Hence, this optogenetic-based approach may be able to mimic conduction slowing and RT heterogeneities present in pathophysiological conditions. Frontiers Media S.A. 2023-05-05 /pmc/articles/PMC10196067/ /pubmed/37215182 http://dx.doi.org/10.3389/fphys.2023.1167524 Text en Copyright © 2023 Marchal, Biasci, Loew, Biggeri, Campione and Sacconi. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Marchal, Gerard A.
Biasci, Valentina
Loew, Leslie M.
Biggeri, Annibale
Campione, Marina
Sacconi, Leonardo
Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination
title Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination
title_full Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination
title_fullStr Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination
title_full_unstemmed Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination
title_short Optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination
title_sort optogenetic manipulation of cardiac repolarization gradients using sub-threshold illumination
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10196067/
https://www.ncbi.nlm.nih.gov/pubmed/37215182
http://dx.doi.org/10.3389/fphys.2023.1167524
work_keys_str_mv AT marchalgerarda optogeneticmanipulationofcardiacrepolarizationgradientsusingsubthresholdillumination
AT biascivalentina optogeneticmanipulationofcardiacrepolarizationgradientsusingsubthresholdillumination
AT loewlesliem optogeneticmanipulationofcardiacrepolarizationgradientsusingsubthresholdillumination
AT biggeriannibale optogeneticmanipulationofcardiacrepolarizationgradientsusingsubthresholdillumination
AT campionemarina optogeneticmanipulationofcardiacrepolarizationgradientsusingsubthresholdillumination
AT sacconileonardo optogeneticmanipulationofcardiacrepolarizationgradientsusingsubthresholdillumination