Cargando…
The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design
In the field of muscular dystrophy, striated muscle function is often assessed in vitro in dystrophin-deficient mdx mice in order to test the impact of a potential treatment strategy. Although many past studies have assessed diaphragm contractile function at or near room temperature, the diaphragm p...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2012
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491430/ https://www.ncbi.nlm.nih.gov/pubmed/23162469 http://dx.doi.org/10.3389/fphys.2012.00422 |
_version_ | 1782248994916794368 |
---|---|
author | Murray, Jason D. Canan, Benjamin D. Martin, Christopher D. Stangland, Jenna E. Rastogi, Neha Rafael-Fortney, Jill A. Janssen, Paul M. L. |
author_facet | Murray, Jason D. Canan, Benjamin D. Martin, Christopher D. Stangland, Jenna E. Rastogi, Neha Rafael-Fortney, Jill A. Janssen, Paul M. L. |
author_sort | Murray, Jason D. |
collection | PubMed |
description | In the field of muscular dystrophy, striated muscle function is often assessed in vitro in dystrophin-deficient mdx mice in order to test the impact of a potential treatment strategy. Although many past studies have assessed diaphragm contractile function at or near room temperature, the diaphragm performs in vivo at 37°C. To improve translation of bench-top results to possible clinical application, we studied temperature-dependence of contractile performance in wild-type (C57BL/10) and mdx muscle strips at temperatures from 25°C to 37°C. Maximal tetanic force in wild-type muscles was higher at 37°C (198 ± 11 vs. 155 ± 9 mN/mm(2) at 25°C), while the difference between wild-type and mdx was extremely similar: wild-type muscles produced 45.9% and 45.1% more force at 25°C and 37°C respectively. At 37°C twitch contraction kinetics and 50% rise time to tetanic plateau were slower in mdx diaphragm. A fatigue/injury protocol indicated 2-fold fatigue/contraction-induced force deficit in mdx muscles. We conclude that assessment of diaphragm muscle strips can be reliably and reproducibly performed at 37°C. |
format | Online Article Text |
id | pubmed-3491430 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34914302012-11-16 The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design Murray, Jason D. Canan, Benjamin D. Martin, Christopher D. Stangland, Jenna E. Rastogi, Neha Rafael-Fortney, Jill A. Janssen, Paul M. L. Front Physiol Physiology In the field of muscular dystrophy, striated muscle function is often assessed in vitro in dystrophin-deficient mdx mice in order to test the impact of a potential treatment strategy. Although many past studies have assessed diaphragm contractile function at or near room temperature, the diaphragm performs in vivo at 37°C. To improve translation of bench-top results to possible clinical application, we studied temperature-dependence of contractile performance in wild-type (C57BL/10) and mdx muscle strips at temperatures from 25°C to 37°C. Maximal tetanic force in wild-type muscles was higher at 37°C (198 ± 11 vs. 155 ± 9 mN/mm(2) at 25°C), while the difference between wild-type and mdx was extremely similar: wild-type muscles produced 45.9% and 45.1% more force at 25°C and 37°C respectively. At 37°C twitch contraction kinetics and 50% rise time to tetanic plateau were slower in mdx diaphragm. A fatigue/injury protocol indicated 2-fold fatigue/contraction-induced force deficit in mdx muscles. We conclude that assessment of diaphragm muscle strips can be reliably and reproducibly performed at 37°C. Frontiers Media S.A. 2012-11-07 /pmc/articles/PMC3491430/ /pubmed/23162469 http://dx.doi.org/10.3389/fphys.2012.00422 Text en Copyright © 2012 Murray, Canan, Martin, Stangland, Rastogi, Rafael-Fortney and Janssen. http://www.frontiersin.org/licenseagreement This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Physiology Murray, Jason D. Canan, Benjamin D. Martin, Christopher D. Stangland, Jenna E. Rastogi, Neha Rafael-Fortney, Jill A. Janssen, Paul M. L. The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design |
title | The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design |
title_full | The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design |
title_fullStr | The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design |
title_full_unstemmed | The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design |
title_short | The force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design |
title_sort | force-temperature relationship in healthy and dystrophic mouse diaphragm; implications for translational study design |
topic | Physiology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3491430/ https://www.ncbi.nlm.nih.gov/pubmed/23162469 http://dx.doi.org/10.3389/fphys.2012.00422 |
work_keys_str_mv | AT murrayjasond theforcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT cananbenjamind theforcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT martinchristopherd theforcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT stanglandjennae theforcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT rastogineha theforcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT rafaelfortneyjilla theforcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT janssenpaulml theforcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT murrayjasond forcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT cananbenjamind forcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT martinchristopherd forcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT stanglandjennae forcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT rastogineha forcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT rafaelfortneyjilla forcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign AT janssenpaulml forcetemperaturerelationshipinhealthyanddystrophicmousediaphragmimplicationsfortranslationalstudydesign |