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Non-invasive muscle contraction assay to study rodent models of sarcopenia
BACKGROUND: Age-related sarcopenia is a disease state of loss of muscle mass and strength that affects physical function and mobility leading to falls, fractures, and disability. The need for therapies to treat age-related sarcopenia has attracted intensive preclinical research. To facilitate the di...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213194/ https://www.ncbi.nlm.nih.gov/pubmed/22035016 http://dx.doi.org/10.1186/1471-2474-12-246 |
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author | Chiu, Chi-Sung Weber, Hans Adamski, Sharon Rauch, Albert Gentile, Michael A Alves, Stephen E Kath, Gary Flores, Osvaldo Wilkinson, Hilary A |
author_facet | Chiu, Chi-Sung Weber, Hans Adamski, Sharon Rauch, Albert Gentile, Michael A Alves, Stephen E Kath, Gary Flores, Osvaldo Wilkinson, Hilary A |
author_sort | Chiu, Chi-Sung |
collection | PubMed |
description | BACKGROUND: Age-related sarcopenia is a disease state of loss of muscle mass and strength that affects physical function and mobility leading to falls, fractures, and disability. The need for therapies to treat age-related sarcopenia has attracted intensive preclinical research. To facilitate the discovery of these therapies, we have developed a non-invasive rat muscle functional assay system to efficiently measure muscle force and evaluate the efficacy of drug candidates. METHODS: The lower leg muscles of anesthetized rats are artificially stimulated with surface electrodes on the knee holders and the heel support, causing the lower leg muscles to push isometric pedals that are attached to force transducers. We developed a stimulation protocol to perform a fatigability test that reveals functional muscle parameters like maximal force, the rate of fatigue, fatigue-resistant force, as well as a fatigable muscle force index. The system is evaluated in a rat aging model and a rat glucocorticoid-induced muscle loss model RESULTS: The aged rats were generally weaker than adult rats and showed a greater reduction in their fatigable force when compared to their fatigue-resistant force. Glucocorticoid treated rats mostly lost fatigable force and fatigued at a higher rate, indicating reduced force from glycolytic fibers with reduced energy reserves. CONCLUSIONS: The involuntary contraction assay is a reliable system to assess muscle function in rodents and can be applied in preclinical research, including age-related sarcopenia and other myopathy. |
format | Online Article Text |
id | pubmed-3213194 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32131942011-11-11 Non-invasive muscle contraction assay to study rodent models of sarcopenia Chiu, Chi-Sung Weber, Hans Adamski, Sharon Rauch, Albert Gentile, Michael A Alves, Stephen E Kath, Gary Flores, Osvaldo Wilkinson, Hilary A BMC Musculoskelet Disord Research Article BACKGROUND: Age-related sarcopenia is a disease state of loss of muscle mass and strength that affects physical function and mobility leading to falls, fractures, and disability. The need for therapies to treat age-related sarcopenia has attracted intensive preclinical research. To facilitate the discovery of these therapies, we have developed a non-invasive rat muscle functional assay system to efficiently measure muscle force and evaluate the efficacy of drug candidates. METHODS: The lower leg muscles of anesthetized rats are artificially stimulated with surface electrodes on the knee holders and the heel support, causing the lower leg muscles to push isometric pedals that are attached to force transducers. We developed a stimulation protocol to perform a fatigability test that reveals functional muscle parameters like maximal force, the rate of fatigue, fatigue-resistant force, as well as a fatigable muscle force index. The system is evaluated in a rat aging model and a rat glucocorticoid-induced muscle loss model RESULTS: The aged rats were generally weaker than adult rats and showed a greater reduction in their fatigable force when compared to their fatigue-resistant force. Glucocorticoid treated rats mostly lost fatigable force and fatigued at a higher rate, indicating reduced force from glycolytic fibers with reduced energy reserves. CONCLUSIONS: The involuntary contraction assay is a reliable system to assess muscle function in rodents and can be applied in preclinical research, including age-related sarcopenia and other myopathy. BioMed Central 2011-10-28 /pmc/articles/PMC3213194/ /pubmed/22035016 http://dx.doi.org/10.1186/1471-2474-12-246 Text en Copyright ©2011 Chiu et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Chiu, Chi-Sung Weber, Hans Adamski, Sharon Rauch, Albert Gentile, Michael A Alves, Stephen E Kath, Gary Flores, Osvaldo Wilkinson, Hilary A Non-invasive muscle contraction assay to study rodent models of sarcopenia |
title | Non-invasive muscle contraction assay to study rodent models of sarcopenia |
title_full | Non-invasive muscle contraction assay to study rodent models of sarcopenia |
title_fullStr | Non-invasive muscle contraction assay to study rodent models of sarcopenia |
title_full_unstemmed | Non-invasive muscle contraction assay to study rodent models of sarcopenia |
title_short | Non-invasive muscle contraction assay to study rodent models of sarcopenia |
title_sort | non-invasive muscle contraction assay to study rodent models of sarcopenia |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3213194/ https://www.ncbi.nlm.nih.gov/pubmed/22035016 http://dx.doi.org/10.1186/1471-2474-12-246 |
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