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Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish

Age-related deficits in skeletal muscle function, termed sarcopenia, are due to loss of muscle mass and changes in the intrinsic mechanisms underlying contraction. Sarcopenia is associated with falls, functional decline, and mortality. Electrical impedance myography (EIM)—a minimally invasive, rapid...

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Autores principales: Rutkove, Seward B., Callegari, Santiago, Concepcion, Holly, Mourey, Tyler, Widrick, Jeffrey, Nagy, Janice A., Nath, Anjali K.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156759/
https://www.ncbi.nlm.nih.gov/pubmed/37137956
http://dx.doi.org/10.1038/s41598-023-34119-6
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author Rutkove, Seward B.
Callegari, Santiago
Concepcion, Holly
Mourey, Tyler
Widrick, Jeffrey
Nagy, Janice A.
Nath, Anjali K.
author_facet Rutkove, Seward B.
Callegari, Santiago
Concepcion, Holly
Mourey, Tyler
Widrick, Jeffrey
Nagy, Janice A.
Nath, Anjali K.
author_sort Rutkove, Seward B.
collection PubMed
description Age-related deficits in skeletal muscle function, termed sarcopenia, are due to loss of muscle mass and changes in the intrinsic mechanisms underlying contraction. Sarcopenia is associated with falls, functional decline, and mortality. Electrical impedance myography (EIM)—a minimally invasive, rapid electrophysiological tool—can be applied to animals and humans to monitor muscle health, thereby serving as a biomarker in both preclinical and clinical studies. EIM has been successfully employed in several species; however, the application of EIM to the assessment of zebrafish—a model organism amenable to high-throughput experimentation—has not been reported. Here, we demonstrated differences in EIM measures between the skeletal muscles of young (6 months of age) and aged (33 months of age) zebrafish. For example, EIM phase angle and reactance at 2 kHz showed significantly decreased phase angle (5.3 ± 2.1 versus 10.7 ± 1.5°; p = 0.001) and reactance (89.0 ± 3.9 versus 172.2 ± 54.8 ohms; p = 0.007) in aged versus young animals. Total muscle area, in addition to other morphometric features, was also strongly correlated to EIM 2 kHz phase angle across both groups (r = 0.7133, p = 0.01). Moreover, there was a strong correlation between 2 kHz phase angle and established metrics of zebrafish swimming performance, including turn angle, angular velocity, and lateral motion (r = 0.7253, r = 0.7308, r = 0.7857, respectively, p < 0.01 for all). In addition, the technique was shown to have high reproducibility between repeated measurements with a mean percentage difference of 5.34 ± 1.17% for phase angle. These relationships were also confirmed in a separate replication cohort. Together, these findings establish EIM as a fast, sensitive method for quantifying zebrafish muscle function and quality. Moreover, identifying the abnormalities in the bioelectrical properties of sarcopenic zebrafish provides new opportunities to evaluate potential therapeutics for age-related neuromuscular disorders and to interrogate the disease mechanisms of muscle degeneration.
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spelling pubmed-101567592023-05-05 Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish Rutkove, Seward B. Callegari, Santiago Concepcion, Holly Mourey, Tyler Widrick, Jeffrey Nagy, Janice A. Nath, Anjali K. Sci Rep Article Age-related deficits in skeletal muscle function, termed sarcopenia, are due to loss of muscle mass and changes in the intrinsic mechanisms underlying contraction. Sarcopenia is associated with falls, functional decline, and mortality. Electrical impedance myography (EIM)—a minimally invasive, rapid electrophysiological tool—can be applied to animals and humans to monitor muscle health, thereby serving as a biomarker in both preclinical and clinical studies. EIM has been successfully employed in several species; however, the application of EIM to the assessment of zebrafish—a model organism amenable to high-throughput experimentation—has not been reported. Here, we demonstrated differences in EIM measures between the skeletal muscles of young (6 months of age) and aged (33 months of age) zebrafish. For example, EIM phase angle and reactance at 2 kHz showed significantly decreased phase angle (5.3 ± 2.1 versus 10.7 ± 1.5°; p = 0.001) and reactance (89.0 ± 3.9 versus 172.2 ± 54.8 ohms; p = 0.007) in aged versus young animals. Total muscle area, in addition to other morphometric features, was also strongly correlated to EIM 2 kHz phase angle across both groups (r = 0.7133, p = 0.01). Moreover, there was a strong correlation between 2 kHz phase angle and established metrics of zebrafish swimming performance, including turn angle, angular velocity, and lateral motion (r = 0.7253, r = 0.7308, r = 0.7857, respectively, p < 0.01 for all). In addition, the technique was shown to have high reproducibility between repeated measurements with a mean percentage difference of 5.34 ± 1.17% for phase angle. These relationships were also confirmed in a separate replication cohort. Together, these findings establish EIM as a fast, sensitive method for quantifying zebrafish muscle function and quality. Moreover, identifying the abnormalities in the bioelectrical properties of sarcopenic zebrafish provides new opportunities to evaluate potential therapeutics for age-related neuromuscular disorders and to interrogate the disease mechanisms of muscle degeneration. Nature Publishing Group UK 2023-05-03 /pmc/articles/PMC10156759/ /pubmed/37137956 http://dx.doi.org/10.1038/s41598-023-34119-6 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
Rutkove, Seward B.
Callegari, Santiago
Concepcion, Holly
Mourey, Tyler
Widrick, Jeffrey
Nagy, Janice A.
Nath, Anjali K.
Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
title Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
title_full Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
title_fullStr Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
title_full_unstemmed Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
title_short Electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
title_sort electrical impedance myography detects age-related skeletal muscle atrophy in adult zebrafish
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10156759/
https://www.ncbi.nlm.nih.gov/pubmed/37137956
http://dx.doi.org/10.1038/s41598-023-34119-6
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