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Whole Animal Perfusion Fixation for Rodents
The goal of fixation is to rapidly and uniformly preserve tissue in a life-like state. While placing tissue directly in fixative works well for small pieces of tissue, larger specimens like the intact brain pose a problem for immersion fixation because the fixative does not reach all regions of the...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MyJove Corporation
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476408/ https://www.ncbi.nlm.nih.gov/pubmed/22871843 http://dx.doi.org/10.3791/3564 |
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author | Gage, Gregory J. Kipke, Daryl R. Shain, William |
author_facet | Gage, Gregory J. Kipke, Daryl R. Shain, William |
author_sort | Gage, Gregory J. |
collection | PubMed |
description | The goal of fixation is to rapidly and uniformly preserve tissue in a life-like state. While placing tissue directly in fixative works well for small pieces of tissue, larger specimens like the intact brain pose a problem for immersion fixation because the fixative does not reach all regions of the tissue at the same rate (5,7). Often, changes in response to hypoxia begin before the tissue can be preserved (12). The advantage of directly perfusing fixative through the circulatory system is that the chemical can quickly reach every corner of the organism using the natural vascular network. In order to utilize the circulatory system most effectively, care must be taken to match physiological pressures (3). It is important to note that physiological pressures are dependent on the species used. Techniques for perfusion fixation vary depending on the tissue to be fixed and how the tissue will be processed following fixation. In this video, we describe a low-cost, rapid, controlled and uniform fixation procedure using 4% paraformaldehyde perfused via the vascular system: through the heart of the rat to obtain the best possible preservation of the brain for immunohistochemistry. The main advantage of this technique (vs. gravity-fed systems) is that the circulatory system is utilized most effectively. |
format | Online Article Text |
id | pubmed-3476408 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | MyJove Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-34764082012-10-24 Whole Animal Perfusion Fixation for Rodents Gage, Gregory J. Kipke, Daryl R. Shain, William J Vis Exp Neuroscience The goal of fixation is to rapidly and uniformly preserve tissue in a life-like state. While placing tissue directly in fixative works well for small pieces of tissue, larger specimens like the intact brain pose a problem for immersion fixation because the fixative does not reach all regions of the tissue at the same rate (5,7). Often, changes in response to hypoxia begin before the tissue can be preserved (12). The advantage of directly perfusing fixative through the circulatory system is that the chemical can quickly reach every corner of the organism using the natural vascular network. In order to utilize the circulatory system most effectively, care must be taken to match physiological pressures (3). It is important to note that physiological pressures are dependent on the species used. Techniques for perfusion fixation vary depending on the tissue to be fixed and how the tissue will be processed following fixation. In this video, we describe a low-cost, rapid, controlled and uniform fixation procedure using 4% paraformaldehyde perfused via the vascular system: through the heart of the rat to obtain the best possible preservation of the brain for immunohistochemistry. The main advantage of this technique (vs. gravity-fed systems) is that the circulatory system is utilized most effectively. MyJove Corporation 2012-07-30 /pmc/articles/PMC3476408/ /pubmed/22871843 http://dx.doi.org/10.3791/3564 Text en Copyright © 2012, 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 | Neuroscience Gage, Gregory J. Kipke, Daryl R. Shain, William Whole Animal Perfusion Fixation for Rodents |
title | Whole Animal Perfusion Fixation for Rodents |
title_full | Whole Animal Perfusion Fixation for Rodents |
title_fullStr | Whole Animal Perfusion Fixation for Rodents |
title_full_unstemmed | Whole Animal Perfusion Fixation for Rodents |
title_short | Whole Animal Perfusion Fixation for Rodents |
title_sort | whole animal perfusion fixation for rodents |
topic | Neuroscience |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3476408/ https://www.ncbi.nlm.nih.gov/pubmed/22871843 http://dx.doi.org/10.3791/3564 |
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