Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular

Detalhes bibliográficos
Autor(a) principal: Souza, Nathália Pereira de [UNESP]
Data de Publicação: 2015
Tipo de documento: Dissertação
Idioma: por
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://hdl.handle.net/11449/131943
http://www.athena.biblioteca.unesp.br/exlibris/bd/cathedra/11-11-2015/000853603.pdf
Resumo: The testicular dysgenesis syndrome (TDS) encompasses conditions such reduced semen quality, hypospadia, cryptorchidism and testicular germ cell tumors (TGCT), which may occur isolated or in association. The influence of environmental factors on TDS occurrence has become increasingly evident, special attention being paid to exogenous chemicals such phthalates and acrylamide (AA), well known testicular toxicants. Experimentally induced cryptorchidism can be an useful experimental tool to understand TDS pathogenesis. It has been reported that the testicular microenvironment is critically modified when rodents are experimentally exposed to dibutyl-phthalate (DBP), to AA or to cryptorchidism. However, the combined influence of cryptorchidism and testicular toxicants has not been explored. This study aimed to evaluate the morphological changes and the immunoexpression of the transcription factor binding octamer ¾ (OCT¾) and the luteinizing hormone receptor (LHR) in the testes of rats submitted to a model of testicular damage that associated chemicals (DBP or AA) and surgical (cryptorchidism/orchidopexy) treatments. In utero and postnatal DBP or AA exposures associated with surgically-established cryptorchidism induced disruption of spermatogenesis and increased the expression of OCT¾ in germ cells. Immunoreactivity of LHR was qualitatively decreased in the cryptorchid group also exposed to DBP. Exposures to DBP or AA did not alter the anogenital distance. All experimental groups showed decreased in the epididymis weights. Relative ventral prostate weights was decreased in cryptorchid animals and relative liver weights was decreased in DBP-exposed animals. The orchidopexy performed 3 weeks after cryptorchidism was effective to reestablish fairly the testes structure and reproductive organs weights. Our results indicate that the model used, which associated chemical exposures to surgical interventions, may be useful to understand TDS ...
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spelling Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicularAparelho genital masculinoTesticulos - DoençasToxicologiaAcrilamidaExpressão gênicaEspermatogeneseThe testicular dysgenesis syndrome (TDS) encompasses conditions such reduced semen quality, hypospadia, cryptorchidism and testicular germ cell tumors (TGCT), which may occur isolated or in association. The influence of environmental factors on TDS occurrence has become increasingly evident, special attention being paid to exogenous chemicals such phthalates and acrylamide (AA), well known testicular toxicants. Experimentally induced cryptorchidism can be an useful experimental tool to understand TDS pathogenesis. It has been reported that the testicular microenvironment is critically modified when rodents are experimentally exposed to dibutyl-phthalate (DBP), to AA or to cryptorchidism. However, the combined influence of cryptorchidism and testicular toxicants has not been explored. This study aimed to evaluate the morphological changes and the immunoexpression of the transcription factor binding octamer ¾ (OCT¾) and the luteinizing hormone receptor (LHR) in the testes of rats submitted to a model of testicular damage that associated chemicals (DBP or AA) and surgical (cryptorchidism/orchidopexy) treatments. In utero and postnatal DBP or AA exposures associated with surgically-established cryptorchidism induced disruption of spermatogenesis and increased the expression of OCT¾ in germ cells. Immunoreactivity of LHR was qualitatively decreased in the cryptorchid group also exposed to DBP. Exposures to DBP or AA did not alter the anogenital distance. All experimental groups showed decreased in the epididymis weights. Relative ventral prostate weights was decreased in cryptorchid animals and relative liver weights was decreased in DBP-exposed animals. The orchidopexy performed 3 weeks after cryptorchidism was effective to reestablish fairly the testes structure and reproductive organs weights. Our results indicate that the model used, which associated chemical exposures to surgical interventions, may be useful to understand TDS ...A Síndrome de Disgenesia Testicular (SDT) é caracterizada por baixa qualidade espermática, criptorquidia, hipospadia e tumores testiculares, sendo que essas condições podem aparecer isoladas ou variavelmente combinadas. Estudos recentes têm associado o aumento da incidência desta síndrome à exposição a agentes químicos exógenos e que sua origem esteja relacionada com distúrbios da esteroidogênese in utero. Modelos experimentais para o estudo da SDT devem utilizar substâncias tóxicas para células testiculares, como os ftalatos (DBP) e a acrilamida (ACR). Ainda, a criptorquidia, um componente da SDT, pode ser induzida experimentalmente e ser utilizada como ferramenta no estudo da patogênese desta síndrome. Exposição ao DBP, à ACR e a criptorquidia, quando estudados isoladamente, alteram o microambiente das células testiculares. Entretanto, os efeitos da combinação desta anomalia congênita com a exposição a tóxicos testiculares ainda não foram explorados. Este estudo teve como objetivo avaliar as alterações morfológicas e de imunoexpressão do fator de transcrição de ligação ao octâmero ¾ (OCT¾) e do receptor de hormônio luteinizante (LHR) nos testículos de ratos submetidos a um modelo de dano testicular que associa exposição química (DBP ou AA) e tratamentos cirúrgicos (criptorquidia/orquidopexia). Exposição in utero e pós-natal ao DBP e à AA associada à criptorquidia resultou em prejuízo da espermatogênese e aumentou a expressão de OCT¾ em células germinativas. A imunoexpressão de LHR foi qualitativamente reduzida no grupo expostos ao DBP e submetidos à criptorquidia. Exposição ao DBP ou à AA não alterou a distância anogenital. Todos os grupos experimentais apresentaram diminuição no peso relativo do epidídimo. O peso relativo da próstata ventral foi diminuído em animais criptorquídicos e o peso relativo do fígado diminuiu em animais expostos ao DBP e submetidos à...Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)FAPESP: 2012/098734Universidade Estadual Paulista (Unesp)Carvalho, João Lauro Viana de [UNESP]Pontes, Merielen Garcia Nascimento e [UNESP]Universidade Estadual Paulista (Unesp)Souza, Nathália Pereira de [UNESP]2015-12-10T14:22:41Z2015-12-10T14:22:41Z2015-02-27info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/masterThesis66 f.application/pdfSOUZA, Nathália Pereira de. Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular. 2015. 66 f. Dissertação (mestrado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Medicina de Botucatu, 2015.http://hdl.handle.net/11449/131943000853603http://www.athena.biblioteca.unesp.br/exlibris/bd/cathedra/11-11-2015/000853603.pdf33004064056P5Alephreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPporinfo:eu-repo/semantics/openAccess2023-11-17T06:09:14Zoai:repositorio.unesp.br:11449/131943Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-11-17T06:09:14Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
title Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
spellingShingle Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
Souza, Nathália Pereira de [UNESP]
Aparelho genital masculino
Testiculos - Doenças
Toxicologia
Acrilamida
Expressão gênica
Espermatogenese
title_short Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
title_full Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
title_fullStr Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
title_full_unstemmed Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
title_sort Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular
author Souza, Nathália Pereira de [UNESP]
author_facet Souza, Nathália Pereira de [UNESP]
author_role author
dc.contributor.none.fl_str_mv Carvalho, João Lauro Viana de [UNESP]
Pontes, Merielen Garcia Nascimento e [UNESP]
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Souza, Nathália Pereira de [UNESP]
dc.subject.por.fl_str_mv Aparelho genital masculino
Testiculos - Doenças
Toxicologia
Acrilamida
Expressão gênica
Espermatogenese
topic Aparelho genital masculino
Testiculos - Doenças
Toxicologia
Acrilamida
Expressão gênica
Espermatogenese
description The testicular dysgenesis syndrome (TDS) encompasses conditions such reduced semen quality, hypospadia, cryptorchidism and testicular germ cell tumors (TGCT), which may occur isolated or in association. The influence of environmental factors on TDS occurrence has become increasingly evident, special attention being paid to exogenous chemicals such phthalates and acrylamide (AA), well known testicular toxicants. Experimentally induced cryptorchidism can be an useful experimental tool to understand TDS pathogenesis. It has been reported that the testicular microenvironment is critically modified when rodents are experimentally exposed to dibutyl-phthalate (DBP), to AA or to cryptorchidism. However, the combined influence of cryptorchidism and testicular toxicants has not been explored. This study aimed to evaluate the morphological changes and the immunoexpression of the transcription factor binding octamer ¾ (OCT¾) and the luteinizing hormone receptor (LHR) in the testes of rats submitted to a model of testicular damage that associated chemicals (DBP or AA) and surgical (cryptorchidism/orchidopexy) treatments. In utero and postnatal DBP or AA exposures associated with surgically-established cryptorchidism induced disruption of spermatogenesis and increased the expression of OCT¾ in germ cells. Immunoreactivity of LHR was qualitatively decreased in the cryptorchid group also exposed to DBP. Exposures to DBP or AA did not alter the anogenital distance. All experimental groups showed decreased in the epididymis weights. Relative ventral prostate weights was decreased in cryptorchid animals and relative liver weights was decreased in DBP-exposed animals. The orchidopexy performed 3 weeks after cryptorchidism was effective to reestablish fairly the testes structure and reproductive organs weights. Our results indicate that the model used, which associated chemical exposures to surgical interventions, may be useful to understand TDS ...
publishDate 2015
dc.date.none.fl_str_mv 2015-12-10T14:22:41Z
2015-12-10T14:22:41Z
2015-02-27
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/masterThesis
format masterThesis
status_str publishedVersion
dc.identifier.uri.fl_str_mv SOUZA, Nathália Pereira de. Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular. 2015. 66 f. Dissertação (mestrado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Medicina de Botucatu, 2015.
http://hdl.handle.net/11449/131943
000853603
http://www.athena.biblioteca.unesp.br/exlibris/bd/cathedra/11-11-2015/000853603.pdf
33004064056P5
identifier_str_mv SOUZA, Nathália Pereira de. Criptorquidia e exposição in utero ao di(n-butil)-ftalato e à acrilamida: avaliação morfológica do dano testicular. 2015. 66 f. Dissertação (mestrado) - Universidade Estadual Paulista Júlio de Mesquita Filho, Faculdade de Medicina de Botucatu, 2015.
000853603
33004064056P5
url http://hdl.handle.net/11449/131943
http://www.athena.biblioteca.unesp.br/exlibris/bd/cathedra/11-11-2015/000853603.pdf
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dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
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dc.format.none.fl_str_mv 66 f.
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dc.publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
publisher.none.fl_str_mv Universidade Estadual Paulista (Unesp)
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reponame:Repositório Institucional da UNESP
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