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Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation

Ventilator-induced diaphragm dysfunction (VIDD), a dysfunction of the diaphragm muscle caused by prolonged mechanical ventilation (MV), is an important factor that hinders successful weaning from ventilation. We evaluated the effects of electrical stimulation of the diaphragm muscle (pulsed current...

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Autores principales: Nakai, Hideki, Hirata, Yutaka, Furue, Hidemasa, Oku, Yoshitaka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656540/
https://www.ncbi.nlm.nih.gov/pubmed/37978221
http://dx.doi.org/10.1038/s41598-023-47093-w
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author Nakai, Hideki
Hirata, Yutaka
Furue, Hidemasa
Oku, Yoshitaka
author_facet Nakai, Hideki
Hirata, Yutaka
Furue, Hidemasa
Oku, Yoshitaka
author_sort Nakai, Hideki
collection PubMed
description Ventilator-induced diaphragm dysfunction (VIDD), a dysfunction of the diaphragm muscle caused by prolonged mechanical ventilation (MV), is an important factor that hinders successful weaning from ventilation. We evaluated the effects of electrical stimulation of the diaphragm muscle (pulsed current with off-time intervals) on genetic changes during 12 h of MV (E-V12). Rats were divided into four groups: control, 12-h MV, sham operation, and E-V12 groups. Transcriptome analysis using an RNA microarray revealed that 12-h MV caused upregulation of genes promoting muscle atrophy and downregulation of genes facilitating muscle synthesis, suggesting that 12-h MV is a reasonable method for establishing a VIDD rat model. Of the genes upregulated by 12-h MV, 18 genes were not affected by the sham operation but were downregulated by E-V12. These included genes related to catabolic processes, inflammatory cytokines, and skeletal muscle homeostasis. Of the genes downregulated by 12-h MV, 6 genes were not affected by the sham operation but were upregulated by E-V12. These included genes related to oxygen transport and mitochondrial respiration. These results suggested that 12-h MV shifted gene expression in the diaphragm muscle toward muscle degradation and that electrical stimulation counteracted this shift by suppressing catabolic processes and increasing mitochondrial respiration.
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spelling pubmed-106565402023-11-17 Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation Nakai, Hideki Hirata, Yutaka Furue, Hidemasa Oku, Yoshitaka Sci Rep Article Ventilator-induced diaphragm dysfunction (VIDD), a dysfunction of the diaphragm muscle caused by prolonged mechanical ventilation (MV), is an important factor that hinders successful weaning from ventilation. We evaluated the effects of electrical stimulation of the diaphragm muscle (pulsed current with off-time intervals) on genetic changes during 12 h of MV (E-V12). Rats were divided into four groups: control, 12-h MV, sham operation, and E-V12 groups. Transcriptome analysis using an RNA microarray revealed that 12-h MV caused upregulation of genes promoting muscle atrophy and downregulation of genes facilitating muscle synthesis, suggesting that 12-h MV is a reasonable method for establishing a VIDD rat model. Of the genes upregulated by 12-h MV, 18 genes were not affected by the sham operation but were downregulated by E-V12. These included genes related to catabolic processes, inflammatory cytokines, and skeletal muscle homeostasis. Of the genes downregulated by 12-h MV, 6 genes were not affected by the sham operation but were upregulated by E-V12. These included genes related to oxygen transport and mitochondrial respiration. These results suggested that 12-h MV shifted gene expression in the diaphragm muscle toward muscle degradation and that electrical stimulation counteracted this shift by suppressing catabolic processes and increasing mitochondrial respiration. Nature Publishing Group UK 2023-11-17 /pmc/articles/PMC10656540/ /pubmed/37978221 http://dx.doi.org/10.1038/s41598-023-47093-w Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Nakai, Hideki
Hirata, Yutaka
Furue, Hidemasa
Oku, Yoshitaka
Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation
title Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation
title_full Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation
title_fullStr Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation
title_full_unstemmed Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation
title_short Electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation
title_sort electrical stimulation mitigates muscle degradation shift in gene expressions during 12-h mechanical ventilation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656540/
https://www.ncbi.nlm.nih.gov/pubmed/37978221
http://dx.doi.org/10.1038/s41598-023-47093-w
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