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...

Descripción completa

Detalles Bibliográficos
Autores principales: Murray, Jason D., Canan, Benjamin D., Martin, Christopher D., Stangland, Jenna E., Rastogi, Neha, Rafael-Fortney, Jill A., Janssen, Paul M. L.
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