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Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures

Water-filtered infrared-A (wIRA) radiation has been described as supportive for tissue regeneration. We sought to investigate in detail the wIRA effect at different temperatures in 3T3 fibroblasts that were treated with glyoxal to induce formation of advanced glycation end products (AGEs). Nonirradi...

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Autores principales: Knels, Lilla, Valtink, Monika, De la Vega Marin, Jamlec, Steiner, Gerald, Roehlecke, Cora, Krueger, Alexander, Funk, Richard H. W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483822/
https://www.ncbi.nlm.nih.gov/pubmed/23125892
http://dx.doi.org/10.1155/2012/274953
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author Knels, Lilla
Valtink, Monika
De la Vega Marin, Jamlec
Steiner, Gerald
Roehlecke, Cora
Krueger, Alexander
Funk, Richard H. W.
author_facet Knels, Lilla
Valtink, Monika
De la Vega Marin, Jamlec
Steiner, Gerald
Roehlecke, Cora
Krueger, Alexander
Funk, Richard H. W.
author_sort Knels, Lilla
collection PubMed
description Water-filtered infrared-A (wIRA) radiation has been described as supportive for tissue regeneration. We sought to investigate in detail the wIRA effect at different temperatures in 3T3 fibroblasts that were treated with glyoxal to induce formation of advanced glycation end products (AGEs). Nonirradiated and nonglyoxal-treated cells served as controls. Experiments were carried out over a range of 37°–45°C with exact temperature monitoring to distinguish between temperature and wIRA effects. Metabolic activity was assessed by resazurin assay. Mitochondrial membrane potential was assessed by JC-1 vital staining. Apoptotic changes were determined by vital staining with annexin V and YO-PRO-1 and determination of subG1 DNA content. Temperature had a dominant effect overriding effects exerted by wIRA or glyoxal treatment. The number of apoptotic cells was significantly higher at 45°C, while the percentage of healthy cells was significantly lower at 45°C. WIRA irradiation itself or in combination with glyoxal treatment exerted no damaging effects on the fibroblasts at physiological (37°–40°C) or higher (42°–45°C) temperatures compared to untreated controls. Temperatures of 45°C, which can occur during inappropriate application of infrared irradiation, damage cells even in the absence of wIRA or glyoxal application.
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spelling pubmed-34838222012-11-02 Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures Knels, Lilla Valtink, Monika De la Vega Marin, Jamlec Steiner, Gerald Roehlecke, Cora Krueger, Alexander Funk, Richard H. W. Oxid Med Cell Longev Research Article Water-filtered infrared-A (wIRA) radiation has been described as supportive for tissue regeneration. We sought to investigate in detail the wIRA effect at different temperatures in 3T3 fibroblasts that were treated with glyoxal to induce formation of advanced glycation end products (AGEs). Nonirradiated and nonglyoxal-treated cells served as controls. Experiments were carried out over a range of 37°–45°C with exact temperature monitoring to distinguish between temperature and wIRA effects. Metabolic activity was assessed by resazurin assay. Mitochondrial membrane potential was assessed by JC-1 vital staining. Apoptotic changes were determined by vital staining with annexin V and YO-PRO-1 and determination of subG1 DNA content. Temperature had a dominant effect overriding effects exerted by wIRA or glyoxal treatment. The number of apoptotic cells was significantly higher at 45°C, while the percentage of healthy cells was significantly lower at 45°C. WIRA irradiation itself or in combination with glyoxal treatment exerted no damaging effects on the fibroblasts at physiological (37°–40°C) or higher (42°–45°C) temperatures compared to untreated controls. Temperatures of 45°C, which can occur during inappropriate application of infrared irradiation, damage cells even in the absence of wIRA or glyoxal application. Hindawi Publishing Corporation 2012 2012-10-17 /pmc/articles/PMC3483822/ /pubmed/23125892 http://dx.doi.org/10.1155/2012/274953 Text en Copyright © 2012 Lilla Knels et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article 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 Research Article
Knels, Lilla
Valtink, Monika
De la Vega Marin, Jamlec
Steiner, Gerald
Roehlecke, Cora
Krueger, Alexander
Funk, Richard H. W.
Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures
title Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures
title_full Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures
title_fullStr Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures
title_full_unstemmed Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures
title_short Effects of Temperature and Water-Filtered Infrared-A Alone or in Combination on Healthy and Glyoxal-Stressed Fibroblast Cultures
title_sort effects of temperature and water-filtered infrared-a alone or in combination on healthy and glyoxal-stressed fibroblast cultures
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3483822/
https://www.ncbi.nlm.nih.gov/pubmed/23125892
http://dx.doi.org/10.1155/2012/274953
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