Influência da radiação ultra-violeta-B na cicatrização em pele de ratos

Detalhes bibliográficos
Autor(a) principal: Korinfsky, Juliana Pedrosa [UNIFESP]
Data de Publicação: 2017
Tipo de documento: Tese
Idioma: por
Título da fonte: Repositório Institucional da UNIFESP
Texto Completo: https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=5034998
http://repositorio.unifesp.br/handle/11600/50360
Resumo: The integrity of the skin exerts a protective barrier against chemical and physical aggressors. One of the main agents external to its integrity is a direct exposure to sunlight for causing cumulative damage over time. Skin attacks are common event and triggered a series of biochemical events aimed at protection and repair. Exposure of the skin to solar radiation provides several photobiological effects, such as alterations in the shape and function of fibroblasts and the deposition of collagen in the skin. People exposed to intense ultraviolet radiation may have difficulty healing. Objective: To evaluate an influence of RUV-B on the skin healing of rats. Methods: Wistar rats (n = 50) with 3 months of age and weight of 250 g with distributed in 2 groups (experimental and control). No experimental group (n = 40) had a tricotomized back skin exposed to the RUV-B using a 306nm lamp, power 9J / s (W), installed in a wooden box, 15cm away from the animal's back, Seconds, three times a week. At the end of weeks 5, 10, 15 and 20, one exposed to interrupt in each subgroup (n = 10), a skin and photographed and biopsied in a standardized way. The control group was photographed and biopsied without any stimulus. Histopathological study was carried out and as photos were analyzed by 3 dermatologists unrelated to the experiment. As skin lesions were photographed daily up to 45 days later and an area of ​​the lesion was measured by the ImageJ program. It was statistically significant by the coefficient of agreement of Kendal and ANOVA with repetition.Results: Clinically the skin presented from the fifth week, erythematous lesions and over time the lesions become more chronic evolving until keratosis. The histological alterations presented inflammatory lymphomononuclear infiltrate, moderate atypia of basal keratinocytes and infiltration of the superficial dermis. These lesions over time evolved to more intense characteristics and in the twentieth week of exposure, hyperkeratosis and hyperparasqueratosis, atypical basal keratinocytes, epidermal atrophy, inflammatory infiltrate and cytoarchitectural disorganization became evident. There was an increase in the severity of the lesion as the exposure time to UVR increased, both macro- and microscopically. As for the collagen changes in the control group, there was minimal alteration, with total collagen regeneration at 45 days and in the experimental groups there was a reduction from 23% up to 37% and no regeneration at 45 days. The organization of the collagen fibers was less evident in the exposed groups. An inverse proportional relationship between exposure time and percentage of collagen was observed, that is, the longer the exposure time of the skin, the lower the percentage of collagen and, consequently, the longer the healing time of the skin. The control group had the shortest healing time of all the groups exposed, with a mean time of 16.4 days and the RUV20 group had the longest time, among all the exposed groups, 19.4 days. Conclusion: The skin that has been exposed to RUV-B for the longest time has had more severe macroscopic lesions and also more important microscopic changes, both with inflammatory characteristics. These changes may delay the healing process.
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spelling Influência da radiação ultra-violeta-B na cicatrização em pele de ratosInfluence of ultraviolet-B radiation on wound healing in mice skinHealingSkinSolar radiationCollagenCicatrizaçãoPeleRadiação solarColágenoThe integrity of the skin exerts a protective barrier against chemical and physical aggressors. One of the main agents external to its integrity is a direct exposure to sunlight for causing cumulative damage over time. Skin attacks are common event and triggered a series of biochemical events aimed at protection and repair. Exposure of the skin to solar radiation provides several photobiological effects, such as alterations in the shape and function of fibroblasts and the deposition of collagen in the skin. People exposed to intense ultraviolet radiation may have difficulty healing. Objective: To evaluate an influence of RUV-B on the skin healing of rats. Methods: Wistar rats (n = 50) with 3 months of age and weight of 250 g with distributed in 2 groups (experimental and control). No experimental group (n = 40) had a tricotomized back skin exposed to the RUV-B using a 306nm lamp, power 9J / s (W), installed in a wooden box, 15cm away from the animal's back, Seconds, three times a week. At the end of weeks 5, 10, 15 and 20, one exposed to interrupt in each subgroup (n = 10), a skin and photographed and biopsied in a standardized way. The control group was photographed and biopsied without any stimulus. Histopathological study was carried out and as photos were analyzed by 3 dermatologists unrelated to the experiment. As skin lesions were photographed daily up to 45 days later and an area of ​​the lesion was measured by the ImageJ program. It was statistically significant by the coefficient of agreement of Kendal and ANOVA with repetition.Results: Clinically the skin presented from the fifth week, erythematous lesions and over time the lesions become more chronic evolving until keratosis. The histological alterations presented inflammatory lymphomononuclear infiltrate, moderate atypia of basal keratinocytes and infiltration of the superficial dermis. These lesions over time evolved to more intense characteristics and in the twentieth week of exposure, hyperkeratosis and hyperparasqueratosis, atypical basal keratinocytes, epidermal atrophy, inflammatory infiltrate and cytoarchitectural disorganization became evident. There was an increase in the severity of the lesion as the exposure time to UVR increased, both macro- and microscopically. As for the collagen changes in the control group, there was minimal alteration, with total collagen regeneration at 45 days and in the experimental groups there was a reduction from 23% up to 37% and no regeneration at 45 days. The organization of the collagen fibers was less evident in the exposed groups. An inverse proportional relationship between exposure time and percentage of collagen was observed, that is, the longer the exposure time of the skin, the lower the percentage of collagen and, consequently, the longer the healing time of the skin. The control group had the shortest healing time of all the groups exposed, with a mean time of 16.4 days and the RUV20 group had the longest time, among all the exposed groups, 19.4 days. Conclusion: The skin that has been exposed to RUV-B for the longest time has had more severe macroscopic lesions and also more important microscopic changes, both with inflammatory characteristics. These changes may delay the healing process.A integridade da pele exerce barreira protetora contra os agressores químicos e físicos. Um dos principais agressores externos à sua integridade é a exposição direta à luz solar por provocar danos cumulativos ao longo do tempo. Agressões à pele é evento comum e desencadeiam de imediatamente uma série de eventos bioquímicos com objetivo de proteção e reparação. A exposição da pele às radiações solares proporciona diversos efeitos fotobiológicos, como a alteração na forma e funções dos fibroblastos e a deposição de colágenos na pele. As pessoas expostas à radiação ultravioleta intensa podem apresentar dificuldade de cicatrização. Objetivo: Avaliar a influência da RUV-B na cicatrização em pele de ratos. Métodos: Ratos Wistar (n=50) com 3 meses de idade e peso de 250g foram distribuídos em 2 grupos (experimental e controle). No grupo experimental (n=40) a pele tricotomizada do dorso foi exposta à RUV-B utilizando-se uma lâmpada de 306nm, potência 9J/s (W), instalada em caixa de madeira, distante 15cm do dorso do animal, cada exposição por 30 segundos, três vezes por semana. Ao final das semanas 5, 10, 15 e 20 a exposição foi interrompida em cada subgrupo (n=10), a pele foi fotografada e biopsiada de forma padronizada. O grupo controle foi fotografado e biopsiado sem qualquer estímulo. Realizou-se estudo histopatológico e as fotografias foram analisadas por 3 dermatologistas alheios ao experimento. As feridas na pele foram fotografadas diariamente até 45 dias depois e a área da lesão foi medida pelo programa ImageJ. Foi utilizada estatística pelo coeficiente de concordância de Kendal e ANOVA com repetição. Resultados: Clinicamente a pele apresentou desde a quinta semana, lesões eritematosas e ao passar do tempo as lesões se tornam mais crônicas evoluindo até ceratose. As alterações histológicas apresentaram infiltrado inflamatório linfomononuclear, moderada atipia de queratinócitos basais e infiltração na derme superficial. Estas lesões ao longo do tempo foram evoluindo para características mais intensas e na vigésima semana de exposição chegou a ser evidenciado hiperqueratose e hiperparaqueratose, atipia de queratinócitos basais, atrofia epidérmica, infiltrado inflamatório e desorganização citoarquitetural. Houve evolução da gravidade da lesão à medida que aumentou o tempo de exposição à RUV, macro e microscopicamente. Quanto às alterações de colágeno no grupo controle houve alteração mínima, com regeneração total do colágeno com 45 dias e nos grupos experimentais houve redução desde 23% chegando até a 37% e sem regeneração com 45 dias. A organização das fibras colágenas foi menos evidente nos grupos expostos. Percebeu-se uma relação inversamente proporcional entre o tempo de exposição e o percentual de colágeno, ou seja, quanto maior tempo de exposição da pele, menor é o percentual de colágeno e consequentemente, maior é o tempo de cicatrização da pele. O grupo Controle teve o menor tempo de cicatrização que todos os grupos expostos, com um tempo médio de 16,4 dias e o grupo RUV20 apresentou o maior tempo, entre todos os grupos expostos, 19,4 dias. Conclusão: A pele que por mais tempo foi exposta ao RUV-B apresentou lesões macroscópicas mais graves e também alterações microscópicas mais importantes, ambas com características inflamatórias. Estas alterações podem atrasar o processo de cicatrização.Dados abertos - Sucupira - Teses e dissertações (2017)Universidade Federal de São Paulo (UNIFESP)Plapler, Helio [UNIFESP]http://lattes.cnpq.br/2871630525937037http://lattes.cnpq.br/1777208206214708Universidade Federal de São Paulo (UNIFESP)Korinfsky, Juliana Pedrosa [UNIFESP]2019-06-19T14:57:48Z2019-06-19T14:57:48Z2017-05-30info:eu-repo/semantics/doctoralThesisinfo:eu-repo/semantics/publishedVersion57 f.application/pdfhttps://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=5034998http://repositorio.unifesp.br/handle/11600/50360porinfo:eu-repo/semantics/openAccessreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-08-02T16:42:11Zoai:repositorio.unifesp.br/:11600/50360Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-08-02T16:42:11Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false
dc.title.none.fl_str_mv Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
Influence of ultraviolet-B radiation on wound healing in mice skin
title Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
spellingShingle Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
Korinfsky, Juliana Pedrosa [UNIFESP]
Healing
Skin
Solar radiation
Collagen
Cicatrização
Pele
Radiação solar
Colágeno
title_short Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
title_full Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
title_fullStr Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
title_full_unstemmed Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
title_sort Influência da radiação ultra-violeta-B na cicatrização em pele de ratos
author Korinfsky, Juliana Pedrosa [UNIFESP]
author_facet Korinfsky, Juliana Pedrosa [UNIFESP]
author_role author
dc.contributor.none.fl_str_mv Plapler, Helio [UNIFESP]
http://lattes.cnpq.br/2871630525937037
http://lattes.cnpq.br/1777208206214708
Universidade Federal de São Paulo (UNIFESP)
dc.contributor.author.fl_str_mv Korinfsky, Juliana Pedrosa [UNIFESP]
dc.subject.por.fl_str_mv Healing
Skin
Solar radiation
Collagen
Cicatrização
Pele
Radiação solar
Colágeno
topic Healing
Skin
Solar radiation
Collagen
Cicatrização
Pele
Radiação solar
Colágeno
description The integrity of the skin exerts a protective barrier against chemical and physical aggressors. One of the main agents external to its integrity is a direct exposure to sunlight for causing cumulative damage over time. Skin attacks are common event and triggered a series of biochemical events aimed at protection and repair. Exposure of the skin to solar radiation provides several photobiological effects, such as alterations in the shape and function of fibroblasts and the deposition of collagen in the skin. People exposed to intense ultraviolet radiation may have difficulty healing. Objective: To evaluate an influence of RUV-B on the skin healing of rats. Methods: Wistar rats (n = 50) with 3 months of age and weight of 250 g with distributed in 2 groups (experimental and control). No experimental group (n = 40) had a tricotomized back skin exposed to the RUV-B using a 306nm lamp, power 9J / s (W), installed in a wooden box, 15cm away from the animal's back, Seconds, three times a week. At the end of weeks 5, 10, 15 and 20, one exposed to interrupt in each subgroup (n = 10), a skin and photographed and biopsied in a standardized way. The control group was photographed and biopsied without any stimulus. Histopathological study was carried out and as photos were analyzed by 3 dermatologists unrelated to the experiment. As skin lesions were photographed daily up to 45 days later and an area of ​​the lesion was measured by the ImageJ program. It was statistically significant by the coefficient of agreement of Kendal and ANOVA with repetition.Results: Clinically the skin presented from the fifth week, erythematous lesions and over time the lesions become more chronic evolving until keratosis. The histological alterations presented inflammatory lymphomononuclear infiltrate, moderate atypia of basal keratinocytes and infiltration of the superficial dermis. These lesions over time evolved to more intense characteristics and in the twentieth week of exposure, hyperkeratosis and hyperparasqueratosis, atypical basal keratinocytes, epidermal atrophy, inflammatory infiltrate and cytoarchitectural disorganization became evident. There was an increase in the severity of the lesion as the exposure time to UVR increased, both macro- and microscopically. As for the collagen changes in the control group, there was minimal alteration, with total collagen regeneration at 45 days and in the experimental groups there was a reduction from 23% up to 37% and no regeneration at 45 days. The organization of the collagen fibers was less evident in the exposed groups. An inverse proportional relationship between exposure time and percentage of collagen was observed, that is, the longer the exposure time of the skin, the lower the percentage of collagen and, consequently, the longer the healing time of the skin. The control group had the shortest healing time of all the groups exposed, with a mean time of 16.4 days and the RUV20 group had the longest time, among all the exposed groups, 19.4 days. Conclusion: The skin that has been exposed to RUV-B for the longest time has had more severe macroscopic lesions and also more important microscopic changes, both with inflammatory characteristics. These changes may delay the healing process.
publishDate 2017
dc.date.none.fl_str_mv 2017-05-30
2019-06-19T14:57:48Z
2019-06-19T14:57:48Z
dc.type.driver.fl_str_mv info:eu-repo/semantics/doctoralThesis
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format doctoralThesis
status_str publishedVersion
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http://repositorio.unifesp.br/handle/11600/50360
url https://sucupira.capes.gov.br/sucupira/public/consultas/coleta/trabalhoConclusao/viewTrabalhoConclusao.jsf?popup=true&id_trabalho=5034998
http://repositorio.unifesp.br/handle/11600/50360
dc.language.iso.fl_str_mv por
language por
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 57 f.
application/pdf
dc.publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
publisher.none.fl_str_mv Universidade Federal de São Paulo (UNIFESP)
dc.source.none.fl_str_mv reponame:Repositório Institucional da UNIFESP
instname:Universidade Federal de São Paulo (UNIFESP)
instacron:UNIFESP
instname_str Universidade Federal de São Paulo (UNIFESP)
instacron_str UNIFESP
institution UNIFESP
reponame_str Repositório Institucional da UNIFESP
collection Repositório Institucional da UNIFESP
repository.name.fl_str_mv Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)
repository.mail.fl_str_mv biblioteca.csp@unifesp.br
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