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Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation
Objective: Impaired microcirculation is one of the most important factors in delayed wound healing. The aim of the study was to investigate the influence of chemical and surgical interruption of sympathetic nerve fibers and α- and β-receptors blockers on muscular microcirculation. Methods: The exper...
Autores principales: | , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Open Science Company, LLC
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024898/ https://www.ncbi.nlm.nih.gov/pubmed/21283734 |
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author | Homann, Heinz H. Hirsch, Tobias Steinau, H.U. Muehlberger, Thomas Moll, Wibke Lehnhardt, Marcus Goertz, Ole |
author_facet | Homann, Heinz H. Hirsch, Tobias Steinau, H.U. Muehlberger, Thomas Moll, Wibke Lehnhardt, Marcus Goertz, Ole |
author_sort | Homann, Heinz H. |
collection | PubMed |
description | Objective: Impaired microcirculation is one of the most important factors in delayed wound healing. The aim of the study was to investigate the influence of chemical and surgical interruption of sympathetic nerve fibers and α- and β-receptors blockers on muscular microcirculation. Methods: The experiment was performed on a standardized cremaster muscle model of male Wistar rats (n=51). Microcirculation was recorded via transillumination microscopy on each of the 4 test groups and in a control group before and after their respective treatments with one of the following: topical application of bupivacaine, metoprolol, phentolamine, or surgical denervation. The arteriolar diameter and functional capillary density (FCD) as parameter for tissue perfusion were assessed. Results: The α-blocker phentolamine was the only agent that caused a significant dilation of the arteriolar diameter (76.6 ± 6.9 vs 100.0 ± 12.0 µm). However, like bupivacaine, metoprolol, and the surgical sympathectomy, it did not improve FCD as a parameter for tissue perfusion. The strongest vasoconstriction (35.9 ± 4.3 vs 28.6 ± 4.0) and impairment of the FCD (10.0 ± 0.7 vs 4.1 ± 0.9) was induced by the β-blocker metoprolol. Conclusions: This study shows that phentolamine could be an agent for dilating arteriolar diameter, but it did not improve FCD. Whereas the other agents, including sympathectomy, did not alter arteriolar diameter, the β-blocker worsened both investigated parameters. Our results raise the question whether β-blockers negatively influence microcirculation. Therefore, further studies are needed to investigate the potential adverse effects of β-blockers on wound healing. |
format | Text |
id | pubmed-3024898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Open Science Company, LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-30248982011-01-31 Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation Homann, Heinz H. Hirsch, Tobias Steinau, H.U. Muehlberger, Thomas Moll, Wibke Lehnhardt, Marcus Goertz, Ole Eplasty Journal Article Objective: Impaired microcirculation is one of the most important factors in delayed wound healing. The aim of the study was to investigate the influence of chemical and surgical interruption of sympathetic nerve fibers and α- and β-receptors blockers on muscular microcirculation. Methods: The experiment was performed on a standardized cremaster muscle model of male Wistar rats (n=51). Microcirculation was recorded via transillumination microscopy on each of the 4 test groups and in a control group before and after their respective treatments with one of the following: topical application of bupivacaine, metoprolol, phentolamine, or surgical denervation. The arteriolar diameter and functional capillary density (FCD) as parameter for tissue perfusion were assessed. Results: The α-blocker phentolamine was the only agent that caused a significant dilation of the arteriolar diameter (76.6 ± 6.9 vs 100.0 ± 12.0 µm). However, like bupivacaine, metoprolol, and the surgical sympathectomy, it did not improve FCD as a parameter for tissue perfusion. The strongest vasoconstriction (35.9 ± 4.3 vs 28.6 ± 4.0) and impairment of the FCD (10.0 ± 0.7 vs 4.1 ± 0.9) was induced by the β-blocker metoprolol. Conclusions: This study shows that phentolamine could be an agent for dilating arteriolar diameter, but it did not improve FCD. Whereas the other agents, including sympathectomy, did not alter arteriolar diameter, the β-blocker worsened both investigated parameters. Our results raise the question whether β-blockers negatively influence microcirculation. Therefore, further studies are needed to investigate the potential adverse effects of β-blockers on wound healing. Open Science Company, LLC 2011-01-20 /pmc/articles/PMC3024898/ /pubmed/21283734 Text en Copyright © 2011 The Author(s) http://creativecommons.org/licenses/by/2.0/ This is an open-access article whereby the authors retain copyright of the work. The article is distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Journal Article Homann, Heinz H. Hirsch, Tobias Steinau, H.U. Muehlberger, Thomas Moll, Wibke Lehnhardt, Marcus Goertz, Ole Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation |
title | Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation |
title_full | Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation |
title_fullStr | Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation |
title_full_unstemmed | Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation |
title_short | Influence of Receptor Antagonists, Local Anesthetics, and Denervation on Microcirculation |
title_sort | influence of receptor antagonists, local anesthetics, and denervation on microcirculation |
topic | Journal Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3024898/ https://www.ncbi.nlm.nih.gov/pubmed/21283734 |
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