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Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling
The murine spinotrapezius is a thin, superficial skeletal support muscle that extends from T3 to L4, and is easily accessible via dorsal skin incision. Its unique anatomy makes the spinotrapezius useful for investigation of ischemic injury and subsequent microvascular remodeling. Here, we demonstrat...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622090/ https://www.ncbi.nlm.nih.gov/pubmed/23486360 http://dx.doi.org/10.3791/50218 |
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author | Guendel, Alexander Michael Martin, Kyle S. Cutts, Joshua Foley, Patricia L. Bailey, Alexander M. Mac Gabhann, Feilim Cardinal, Trevor R. Peirce, Shayn M. |
author_facet | Guendel, Alexander Michael Martin, Kyle S. Cutts, Joshua Foley, Patricia L. Bailey, Alexander M. Mac Gabhann, Feilim Cardinal, Trevor R. Peirce, Shayn M. |
author_sort | Guendel, Alexander Michael |
collection | PubMed |
description | The murine spinotrapezius is a thin, superficial skeletal support muscle that extends from T3 to L4, and is easily accessible via dorsal skin incision. Its unique anatomy makes the spinotrapezius useful for investigation of ischemic injury and subsequent microvascular remodeling. Here, we demonstrate an arteriolar ligation model in the murine spinotrapezius muscle that was developed by our research team and previously published(1-3). For certain vulnerable mouse strains, such as the Balb/c mouse, this ligation surgery reliably creates skeletal muscle ischemia and serves as a platform for investigating therapies that stimulate revascularization. Methods of assessment are also demonstrated, including the use of intravital and confocal microscopy. The spinotrapezius is well suited to such imaging studies due to its accessibility (superficial dorsal anatomy) and relative thinness (60-200 μm). The spinotrapezius muscle can be mounted en face, facilitating imaging of whole-muscle microvascular networks without histological sectioning. We describe the use of intravital microscopy to acquire metrics following a functional vasodilation procedure; specifically, the increase in arterilar diameter as a result of muscle contraction. We also demonstrate the procedures for harvesting and fixing the tissues, a necessary precursor to immunostaining studies and the use of confocal microscopy. |
format | Online Article Text |
id | pubmed-3622090 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-36220902013-04-15 Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling Guendel, Alexander Michael Martin, Kyle S. Cutts, Joshua Foley, Patricia L. Bailey, Alexander M. Mac Gabhann, Feilim Cardinal, Trevor R. Peirce, Shayn M. J Vis Exp Biomedical Engineering The murine spinotrapezius is a thin, superficial skeletal support muscle that extends from T3 to L4, and is easily accessible via dorsal skin incision. Its unique anatomy makes the spinotrapezius useful for investigation of ischemic injury and subsequent microvascular remodeling. Here, we demonstrate an arteriolar ligation model in the murine spinotrapezius muscle that was developed by our research team and previously published(1-3). For certain vulnerable mouse strains, such as the Balb/c mouse, this ligation surgery reliably creates skeletal muscle ischemia and serves as a platform for investigating therapies that stimulate revascularization. Methods of assessment are also demonstrated, including the use of intravital and confocal microscopy. The spinotrapezius is well suited to such imaging studies due to its accessibility (superficial dorsal anatomy) and relative thinness (60-200 μm). The spinotrapezius muscle can be mounted en face, facilitating imaging of whole-muscle microvascular networks without histological sectioning. We describe the use of intravital microscopy to acquire metrics following a functional vasodilation procedure; specifically, the increase in arterilar diameter as a result of muscle contraction. We also demonstrate the procedures for harvesting and fixing the tissues, a necessary precursor to immunostaining studies and the use of confocal microscopy. MyJove Corporation 2013-03-03 /pmc/articles/PMC3622090/ /pubmed/23486360 http://dx.doi.org/10.3791/50218 Text en Copyright © 2013, Journal of Visualized Experiments http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs 3.0 Unported License. To view a copy of this license, visithttp://creativecommons.org/licenses/by-nc-nd/3.0/ |
spellingShingle | Biomedical Engineering Guendel, Alexander Michael Martin, Kyle S. Cutts, Joshua Foley, Patricia L. Bailey, Alexander M. Mac Gabhann, Feilim Cardinal, Trevor R. Peirce, Shayn M. Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling |
title | Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling |
title_full | Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling |
title_fullStr | Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling |
title_full_unstemmed | Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling |
title_short | Murine Spinotrapezius Model to Assess the Impact of Arteriolar Ligation on Microvascular Function and Remodeling |
title_sort | murine spinotrapezius model to assess the impact of arteriolar ligation on microvascular function and remodeling |
topic | Biomedical Engineering |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3622090/ https://www.ncbi.nlm.nih.gov/pubmed/23486360 http://dx.doi.org/10.3791/50218 |
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