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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-...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer-Verlag 2011
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.
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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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