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Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy

Neuromuscular electrical stimulation (NMES) allows activation of muscle fibers in the absence of voluntary force generation. NMES could have the potential to promote muscle homeostasis in the context of muscle disease, but the impacts of NMES on diseased muscle are not well understood. We used the z...

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Autores principales: Kilroy, Elisabeth A, Ignacz, Amanda C, Brann, Kaylee L, Schaffer, Claire E, Varney, Devon, Alrowaished, Sarah S, Silknitter, Kodey J, Miner, Jordan N, Almaghasilah, Ahmed, Spellen, Tashawna L, Lewis, Alexandra D, Tilbury, Karissa, King, Benjamin L, Kelley, Joshua B, Henry, Clarissa A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947762/
https://www.ncbi.nlm.nih.gov/pubmed/35324428
http://dx.doi.org/10.7554/eLife.62760
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author Kilroy, Elisabeth A
Ignacz, Amanda C
Brann, Kaylee L
Schaffer, Claire E
Varney, Devon
Alrowaished, Sarah S
Silknitter, Kodey J
Miner, Jordan N
Almaghasilah, Ahmed
Spellen, Tashawna L
Lewis, Alexandra D
Tilbury, Karissa
King, Benjamin L
Kelley, Joshua B
Henry, Clarissa A
author_facet Kilroy, Elisabeth A
Ignacz, Amanda C
Brann, Kaylee L
Schaffer, Claire E
Varney, Devon
Alrowaished, Sarah S
Silknitter, Kodey J
Miner, Jordan N
Almaghasilah, Ahmed
Spellen, Tashawna L
Lewis, Alexandra D
Tilbury, Karissa
King, Benjamin L
Kelley, Joshua B
Henry, Clarissa A
author_sort Kilroy, Elisabeth A
collection PubMed
description Neuromuscular electrical stimulation (NMES) allows activation of muscle fibers in the absence of voluntary force generation. NMES could have the potential to promote muscle homeostasis in the context of muscle disease, but the impacts of NMES on diseased muscle are not well understood. We used the zebrafish Duchenne muscular dystrophy (dmd) mutant and a longitudinal design to elucidate the consequences of NMES on muscle health. We designed four neuromuscular stimulation paradigms loosely based on weightlifting regimens. Each paradigm differentially affected neuromuscular structure, function, and survival. Only endurance neuromuscular stimulation (eNMES) improved all outcome measures. We found that eNMES improves muscle and neuromuscular junction morphology, swimming, and survival. Heme oxygenase and integrin alpha7 are required for eNMES-mediated improvement. Our data indicate that neuromuscular stimulation can be beneficial, suggesting that the right type of activity may benefit patients with muscle disease.
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spelling pubmed-89477622022-03-25 Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy Kilroy, Elisabeth A Ignacz, Amanda C Brann, Kaylee L Schaffer, Claire E Varney, Devon Alrowaished, Sarah S Silknitter, Kodey J Miner, Jordan N Almaghasilah, Ahmed Spellen, Tashawna L Lewis, Alexandra D Tilbury, Karissa King, Benjamin L Kelley, Joshua B Henry, Clarissa A eLife Developmental Biology Neuromuscular electrical stimulation (NMES) allows activation of muscle fibers in the absence of voluntary force generation. NMES could have the potential to promote muscle homeostasis in the context of muscle disease, but the impacts of NMES on diseased muscle are not well understood. We used the zebrafish Duchenne muscular dystrophy (dmd) mutant and a longitudinal design to elucidate the consequences of NMES on muscle health. We designed four neuromuscular stimulation paradigms loosely based on weightlifting regimens. Each paradigm differentially affected neuromuscular structure, function, and survival. Only endurance neuromuscular stimulation (eNMES) improved all outcome measures. We found that eNMES improves muscle and neuromuscular junction morphology, swimming, and survival. Heme oxygenase and integrin alpha7 are required for eNMES-mediated improvement. Our data indicate that neuromuscular stimulation can be beneficial, suggesting that the right type of activity may benefit patients with muscle disease. eLife Sciences Publications, Ltd 2022-03-24 /pmc/articles/PMC8947762/ /pubmed/35324428 http://dx.doi.org/10.7554/eLife.62760 Text en © 2022, Kilroy et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Developmental Biology
Kilroy, Elisabeth A
Ignacz, Amanda C
Brann, Kaylee L
Schaffer, Claire E
Varney, Devon
Alrowaished, Sarah S
Silknitter, Kodey J
Miner, Jordan N
Almaghasilah, Ahmed
Spellen, Tashawna L
Lewis, Alexandra D
Tilbury, Karissa
King, Benjamin L
Kelley, Joshua B
Henry, Clarissa A
Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy
title Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy
title_full Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy
title_fullStr Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy
title_full_unstemmed Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy
title_short Beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of Duchenne muscular dystrophy
title_sort beneficial impacts of neuromuscular electrical stimulation on muscle structure and function in the zebrafish model of duchenne muscular dystrophy
topic Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8947762/
https://www.ncbi.nlm.nih.gov/pubmed/35324428
http://dx.doi.org/10.7554/eLife.62760
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