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Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation
Arthritis of the knee is the most common type of joint inflammatory disorder and it is associated with pain and inflammation of the joint capsule. Few studies address the effects of the 810-nm laser in such conditions. Here we investigated the effects of low-level laser therapy (LLLT; infrared, 810-...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer-Verlag
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254867/ https://www.ncbi.nlm.nih.gov/pubmed/21484455 http://dx.doi.org/10.1007/s10103-011-0906-1 |
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author | Pallotta, Rodney Capp Bjordal, Jan Magnus Frigo, Lúcio Leal Junior, Ernesto Cesar Pinto Teixeira, Simone Marcos, Rodrigo Labat Ramos, Luciano de Moura Messias, Felipe Lopes-Martins, Rodrigo Álvaro Brandão |
author_facet | Pallotta, Rodney Capp Bjordal, Jan Magnus Frigo, Lúcio Leal Junior, Ernesto Cesar Pinto Teixeira, Simone Marcos, Rodrigo Labat Ramos, Luciano de Moura Messias, Felipe Lopes-Martins, Rodrigo Álvaro Brandão |
author_sort | Pallotta, Rodney Capp |
collection | PubMed |
description | Arthritis of the knee is the most common type of joint inflammatory disorder and it is associated with pain and inflammation of the joint capsule. Few studies address the effects of the 810-nm laser in such conditions. Here we investigated the effects of low-level laser therapy (LLLT; infrared, 810-nm) in experimentally induced rat knee inflammation. Thirty male Wistar rats (230–250 g) were anesthetized and injected with carrageenan by an intra-articular route. After 6 and 12 h, all animals were killed by CO(2) inhalation and the articular cavity was washed for cellular and biochemical analysis. Articular tissue was carefully removed for real-time PCR analysis in order to evaluate COX-1 and COX-2 expression. LLLT was able to significantly inhibit the total number of leukocytes, as well as the myeloperoxidase activity with 1, 3, and 6 J (Joules) of energy. This result was corroborated by cell counting showing the reduction of polymorphonuclear cells at the inflammatory site. Vascular extravasation was significantly inhibited at the higher dose of energy of 10 J. Both COX-1 and 2 gene expression were significantly enhanced by laser irradiation while PGE(2) production was inhibited. Low-level laser therapy operating at 810 nm markedly reduced inflammatory signs of inflammation but increased COX-1 and 2 gene expression. Further studies are necessary to investigate the possible production of antiinflammatory mediators by COX enzymes induced by laser irradiation in knee inflammation. |
format | Online Article Text |
id | pubmed-3254867 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Springer-Verlag |
record_format | MEDLINE/PubMed |
spelling | pubmed-32548672012-01-20 Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation Pallotta, Rodney Capp Bjordal, Jan Magnus Frigo, Lúcio Leal Junior, Ernesto Cesar Pinto Teixeira, Simone Marcos, Rodrigo Labat Ramos, Luciano de Moura Messias, Felipe Lopes-Martins, Rodrigo Álvaro Brandão Lasers Med Sci Original Article Arthritis of the knee is the most common type of joint inflammatory disorder and it is associated with pain and inflammation of the joint capsule. Few studies address the effects of the 810-nm laser in such conditions. Here we investigated the effects of low-level laser therapy (LLLT; infrared, 810-nm) in experimentally induced rat knee inflammation. Thirty male Wistar rats (230–250 g) were anesthetized and injected with carrageenan by an intra-articular route. After 6 and 12 h, all animals were killed by CO(2) inhalation and the articular cavity was washed for cellular and biochemical analysis. Articular tissue was carefully removed for real-time PCR analysis in order to evaluate COX-1 and COX-2 expression. LLLT was able to significantly inhibit the total number of leukocytes, as well as the myeloperoxidase activity with 1, 3, and 6 J (Joules) of energy. This result was corroborated by cell counting showing the reduction of polymorphonuclear cells at the inflammatory site. Vascular extravasation was significantly inhibited at the higher dose of energy of 10 J. Both COX-1 and 2 gene expression were significantly enhanced by laser irradiation while PGE(2) production was inhibited. Low-level laser therapy operating at 810 nm markedly reduced inflammatory signs of inflammation but increased COX-1 and 2 gene expression. Further studies are necessary to investigate the possible production of antiinflammatory mediators by COX enzymes induced by laser irradiation in knee inflammation. Springer-Verlag 2011-04-12 2012 /pmc/articles/PMC3254867/ /pubmed/21484455 http://dx.doi.org/10.1007/s10103-011-0906-1 Text en © The Author(s) 2011 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Noncommercial License which permits any noncommercial use, distribution, and reproduction in any medium, provided the original author(s) and source are credited. |
spellingShingle | Original Article Pallotta, Rodney Capp Bjordal, Jan Magnus Frigo, Lúcio Leal Junior, Ernesto Cesar Pinto Teixeira, Simone Marcos, Rodrigo Labat Ramos, Luciano de Moura Messias, Felipe Lopes-Martins, Rodrigo Álvaro Brandão Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation |
title | Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation |
title_full | Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation |
title_fullStr | Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation |
title_full_unstemmed | Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation |
title_short | Infrared (810-nm) low-level laser therapy on rat experimental knee inflammation |
title_sort | infrared (810-nm) low-level laser therapy on rat experimental knee inflammation |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3254867/ https://www.ncbi.nlm.nih.gov/pubmed/21484455 http://dx.doi.org/10.1007/s10103-011-0906-1 |
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