In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales

Detalhes bibliográficos
Autor(a) principal: Pinto, Patricia
Data de Publicação: 2017
Outros Autores: Estêvão, M. Dulce, Santos, Soraia, Andrade, André, Power, Deborah
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.1/13022
Resumo: A wide range of estrogenic endocrine disruptors (EDCs) are accumulating in the environment and may disrupt the physiology of aquatic organisms. The effects of EDCs on fish have mainly been assessed using reproductive endpoints and in vivo animal experiments. We used a simple non-invasive assay to evaluate the impact of estrogens and EDCs on sea bass (Dicentrarchus labrax) and tilapia (Oreochromis mossambicus) scales. These were exposed to estradiol (E2), two phytoestrogens and six anthropogenic estrogenic/anti-estrogenic EDCs and activities of enzymes related to mineralized tissue turnover (TRAP, tartrate-resistant acid phosphatase and ALP, alkaline phosphatase) were measured. Semi-quantitative RT-PCR detected the expression of both membrane and nuclear estrogen receptors in the scales of both species, confirming scales as a target for E2 and EDCs through different mechanisms. Changes in TRAP or ALP activities after 30 minute and 24 h exposure were detected in sea bass and tilapia scales treated with E2 and three EDCs, although compound-, time- and dose-specific responses were observed for the two species. These results support again that the mineralized tissue turnover of fish is regulated by estrogens and reveals that the scales are a mineralized estrogen-responsive tissue that may be affected by some EDCs. The significance of these effects for whole animal physiology needs to be further explored. The in vitro fish scale bioassay is a promising non-invasive screening tool for E2 and EDCs effects, although the low sensitivity of TRAP/ALP quantification limits their utility and indicates that alternative endpoints are required.
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spelling In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scalesTrout Oncorhynchus-MykissLigand-binding domainRainbow-troutOsteoblastic activitiesZebrafish scaleTeleost fishBisphenol-AOsteoclastic activitiesBone metabolismReceptorAlkaline phosphataseBioassayEstradiolFish scalesTartrate-resistant acid phosphataseA wide range of estrogenic endocrine disruptors (EDCs) are accumulating in the environment and may disrupt the physiology of aquatic organisms. The effects of EDCs on fish have mainly been assessed using reproductive endpoints and in vivo animal experiments. We used a simple non-invasive assay to evaluate the impact of estrogens and EDCs on sea bass (Dicentrarchus labrax) and tilapia (Oreochromis mossambicus) scales. These were exposed to estradiol (E2), two phytoestrogens and six anthropogenic estrogenic/anti-estrogenic EDCs and activities of enzymes related to mineralized tissue turnover (TRAP, tartrate-resistant acid phosphatase and ALP, alkaline phosphatase) were measured. Semi-quantitative RT-PCR detected the expression of both membrane and nuclear estrogen receptors in the scales of both species, confirming scales as a target for E2 and EDCs through different mechanisms. Changes in TRAP or ALP activities after 30 minute and 24 h exposure were detected in sea bass and tilapia scales treated with E2 and three EDCs, although compound-, time- and dose-specific responses were observed for the two species. These results support again that the mineralized tissue turnover of fish is regulated by estrogens and reveals that the scales are a mineralized estrogen-responsive tissue that may be affected by some EDCs. The significance of these effects for whole animal physiology needs to be further explored. The in vitro fish scale bioassay is a promising non-invasive screening tool for E2 and EDCs effects, although the low sensitivity of TRAP/ALP quantification limits their utility and indicates that alternative endpoints are required.ElsevierSapientiaPinto, PatriciaEstêvão, M. DulceSantos, SoraiaAndrade, AndréPower, Deborah2019-11-20T15:07:24Z2017-092017-09-01T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.1/13022eng1532-045610.1016/j.cbpc.2017.06.002info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-07-24T10:25:02Zoai:sapientia.ualg.pt:10400.1/13022Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:04:14.543872Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
title In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
spellingShingle In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
Pinto, Patricia
Trout Oncorhynchus-Mykiss
Ligand-binding domain
Rainbow-trout
Osteoblastic activities
Zebrafish scale
Teleost fish
Bisphenol-A
Osteoclastic activities
Bone metabolism
Receptor
Alkaline phosphatase
Bioassay
Estradiol
Fish scales
Tartrate-resistant acid phosphatase
title_short In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
title_full In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
title_fullStr In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
title_full_unstemmed In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
title_sort In vitro screening for estrogenic endocrine disrupting compounds using Mozambique tilapia and sea bass scales
author Pinto, Patricia
author_facet Pinto, Patricia
Estêvão, M. Dulce
Santos, Soraia
Andrade, André
Power, Deborah
author_role author
author2 Estêvão, M. Dulce
Santos, Soraia
Andrade, André
Power, Deborah
author2_role author
author
author
author
dc.contributor.none.fl_str_mv Sapientia
dc.contributor.author.fl_str_mv Pinto, Patricia
Estêvão, M. Dulce
Santos, Soraia
Andrade, André
Power, Deborah
dc.subject.por.fl_str_mv Trout Oncorhynchus-Mykiss
Ligand-binding domain
Rainbow-trout
Osteoblastic activities
Zebrafish scale
Teleost fish
Bisphenol-A
Osteoclastic activities
Bone metabolism
Receptor
Alkaline phosphatase
Bioassay
Estradiol
Fish scales
Tartrate-resistant acid phosphatase
topic Trout Oncorhynchus-Mykiss
Ligand-binding domain
Rainbow-trout
Osteoblastic activities
Zebrafish scale
Teleost fish
Bisphenol-A
Osteoclastic activities
Bone metabolism
Receptor
Alkaline phosphatase
Bioassay
Estradiol
Fish scales
Tartrate-resistant acid phosphatase
description A wide range of estrogenic endocrine disruptors (EDCs) are accumulating in the environment and may disrupt the physiology of aquatic organisms. The effects of EDCs on fish have mainly been assessed using reproductive endpoints and in vivo animal experiments. We used a simple non-invasive assay to evaluate the impact of estrogens and EDCs on sea bass (Dicentrarchus labrax) and tilapia (Oreochromis mossambicus) scales. These were exposed to estradiol (E2), two phytoestrogens and six anthropogenic estrogenic/anti-estrogenic EDCs and activities of enzymes related to mineralized tissue turnover (TRAP, tartrate-resistant acid phosphatase and ALP, alkaline phosphatase) were measured. Semi-quantitative RT-PCR detected the expression of both membrane and nuclear estrogen receptors in the scales of both species, confirming scales as a target for E2 and EDCs through different mechanisms. Changes in TRAP or ALP activities after 30 minute and 24 h exposure were detected in sea bass and tilapia scales treated with E2 and three EDCs, although compound-, time- and dose-specific responses were observed for the two species. These results support again that the mineralized tissue turnover of fish is regulated by estrogens and reveals that the scales are a mineralized estrogen-responsive tissue that may be affected by some EDCs. The significance of these effects for whole animal physiology needs to be further explored. The in vitro fish scale bioassay is a promising non-invasive screening tool for E2 and EDCs effects, although the low sensitivity of TRAP/ALP quantification limits their utility and indicates that alternative endpoints are required.
publishDate 2017
dc.date.none.fl_str_mv 2017-09
2017-09-01T00:00:00Z
2019-11-20T15:07:24Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.1/13022
url http://hdl.handle.net/10400.1/13022
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 1532-0456
10.1016/j.cbpc.2017.06.002
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv Elsevier
publisher.none.fl_str_mv Elsevier
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron:RCAAP
instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
instacron_str RCAAP
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
collection Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
repository.name.fl_str_mv Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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