Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida
Autor(a) principal: | |
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Data de Publicação: | 2021 |
Tipo de documento: | Tese |
Idioma: | por |
Título da fonte: | Repositório Institucional da UFG |
dARK ID: | ark:/38995/00130000010fn |
Texto Completo: | http://repositorio.bc.ufg.br/tede/handle/tede/12190 |
Resumo: | Glyphosate (GLY) is the active ingredient of several herbicide formulations used to control weeds in agricultural and non-agricultural areas. Due to intensive use of GLY-based formulations and the repeated applications once weed resistance, some of their components, including the active ingredient, may reach the aquatic environment through direct run-off and leaching. The present study assessed the acute toxicity, after continuous and repeated exposures, and genotoxicity of the GLY-based formulation Atanor 48 (ATN) and its major constituents GLY, surfactant polyethoxylated tallow amine (POEA), as well as the main metabolite of GLY aminomethylphosphonic acid (AMPA) on zebrafish early life stages. Also, we evaluate larvae resilience after ATN, GLY and POEA pulsed-exposure. The toxic effects of these chemicals were evaluated in the fish embryo acute toxicity test with zebrafish (Danio rerio), while genotoxic effects were investigated in the comet assay with cells from zebrafish larvae and rainbow trout gonad-2 (RTG-2). GLY and AMPA caused no acute toxic effect after continuous exposure, while ATN and POEA induced significant lethal effects in zebrafish (LC50-96 h 76.50 mg/L and 5.49 mg/L, respectively. In summary, these data indicate that the lethal effects on zebrafish early-life stages can be ranked in the following order from most to least toxic: POEA > ATN > GLY ≈ AMPA. All compounds were genotoxic to zebrafish larvae (LOEC 1.7 mg/L for GLY, ATN, AMPA and 0.4 mg/L for POEA). Unlike in vivo. POEA induced DNA damage in RTG-2 cells (LOEC 1.6 mg/L), suggesting that it is a direct acting genotoxic agent. GLY caused no acute toxic effect after repeated pulse exposure. However, ATN showed significant mortality (LC50-96 h 148.80 mg/L) after 5 h pulse at 100 mg/L and POEA induced significant toxicity on zebrafish early life stages after 1, 2 and 5 h pulse with LC50-96 h of 43.49 mg/L, 47.23 mg/L and 11.61 mg/L, respectively. Zebrafish was not able to reverse the sublethal effects induced by ATN, GLY and POEA during the recovery period. The toxic effects induced by ATN and POEA after pulsed-exposure were less than continuous exposure. Therefore, its important to evaluate different toxicological endpoints with distinct exposure scenarios to predict the hazards of GLY-based formulations, their components and breakdown product to aquatic biota. |
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Oliveira, Gisele Augusto Rodrigues dehttp://lattes.cnpq.br/6221735418479539Oliveira, Gisele Augusto Rodrigues deFil, Eric de SouzaValadares, Marize CamposRocha, Thiago LopesSabóia-Morais, Simone Maria Teixeira dehttp://lattes.cnpq.br/0266761443016631Rodrigues, Laís de Brito2022-07-19T12:20:38Z2022-07-19T12:20:38Z2021-06-12RODRIGUES, L. B. Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida. 2022. 98 f. Tese (Doutorado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2021.http://repositorio.bc.ufg.br/tede/handle/tede/12190ark:/38995/00130000010fnGlyphosate (GLY) is the active ingredient of several herbicide formulations used to control weeds in agricultural and non-agricultural areas. Due to intensive use of GLY-based formulations and the repeated applications once weed resistance, some of their components, including the active ingredient, may reach the aquatic environment through direct run-off and leaching. The present study assessed the acute toxicity, after continuous and repeated exposures, and genotoxicity of the GLY-based formulation Atanor 48 (ATN) and its major constituents GLY, surfactant polyethoxylated tallow amine (POEA), as well as the main metabolite of GLY aminomethylphosphonic acid (AMPA) on zebrafish early life stages. Also, we evaluate larvae resilience after ATN, GLY and POEA pulsed-exposure. The toxic effects of these chemicals were evaluated in the fish embryo acute toxicity test with zebrafish (Danio rerio), while genotoxic effects were investigated in the comet assay with cells from zebrafish larvae and rainbow trout gonad-2 (RTG-2). GLY and AMPA caused no acute toxic effect after continuous exposure, while ATN and POEA induced significant lethal effects in zebrafish (LC50-96 h 76.50 mg/L and 5.49 mg/L, respectively. In summary, these data indicate that the lethal effects on zebrafish early-life stages can be ranked in the following order from most to least toxic: POEA > ATN > GLY ≈ AMPA. All compounds were genotoxic to zebrafish larvae (LOEC 1.7 mg/L for GLY, ATN, AMPA and 0.4 mg/L for POEA). Unlike in vivo. POEA induced DNA damage in RTG-2 cells (LOEC 1.6 mg/L), suggesting that it is a direct acting genotoxic agent. GLY caused no acute toxic effect after repeated pulse exposure. However, ATN showed significant mortality (LC50-96 h 148.80 mg/L) after 5 h pulse at 100 mg/L and POEA induced significant toxicity on zebrafish early life stages after 1, 2 and 5 h pulse with LC50-96 h of 43.49 mg/L, 47.23 mg/L and 11.61 mg/L, respectively. Zebrafish was not able to reverse the sublethal effects induced by ATN, GLY and POEA during the recovery period. The toxic effects induced by ATN and POEA after pulsed-exposure were less than continuous exposure. Therefore, its important to evaluate different toxicological endpoints with distinct exposure scenarios to predict the hazards of GLY-based formulations, their components and breakdown product to aquatic biota.O glifosato (GLI) é o ingrediente ativo encontrado em inúmeras formulações herbicidas úteis no controle de plantas daninhas em áreas agrícolas e não agrícolas. Em decorrência do uso indiscriminado de formulações a base de glifosato, alguns de seus componentes, incluindo o ingrediente ativo, podem alcançar ambientes aquáticos através de escoamento superficial e lixiviação. O presente estudo avaliou a toxicidade aguda após exposição única e repetida em pulsos, além da genotoxicidade da formulação a base de glifosato Atanor 48 (ATN) e seus principais constituintes: GLI, o surfactante polioxietilenoamina (POEA) e o ácido aminometilfosfônico (AMPA, principal produto de degradação de GLI) sobre estágios iniciais de zebrafish (Danio rerio). Além disso, a capacidade de resiliência das larvas após exposições repetidas a ATN, GLI e POEA também foi avaliada. Os efeitos tóxicos da formulação a base de GLI e seus principais constituintes foram avaliados utilizando o teste de toxicidade aguda com o estágio embrionário de zebrafish, enquanto os efeitos genotóxicos foram investigados utilizando o ensaio cometa com células de larvas de zebrafish e células gonadais (linhagem RTG-2) de truta arco-íris. GLI e AMPA não apresentaram efeitos tóxicos após exposição única, enquanto ATN e POEA induziram efeitos letais significativos em zebrafish (CL50-96 h 76,50 mg/L e 5,49 mg/L, respectivamente). Sendo assim, os efeitos agudos para o estágio embrio-larval de zebrafish após única exposição seguiu a seguinte ordem, do mais tóxico para o menos tóxico: POEA > ATN > GLI ≈ AMPA. Todas as substâncias foram genotóxicas para larvas de zebrafish (CEO 1,7 mg/L para GLI, ATN e AMPA e 0,4 mg/L para POEA). POEA também induziu dano ao DNA em células RTG-2 (CEO 1,6 mg/mL), indicando um genotoxicante de ação direta. GLI não induziu efeitos tóxicos após exposições repetidas em pulsos. No entanto, ATN induziu mortalidade significativa (CL50-96 h 148,80 mg/L) na maior concentração testada (100 mg/L) após pulsos de 5 horas. POEA induziu toxicidade aguda significativa em estágios iniciais de zebrafish após pulsos de 1, 2 e 5 horas com CL50-96 h de 43,49 mg/L, 47,23 mg/L e 11,61 mg/L, respectivamente. Durante o período de recuperação, não houve reversão de efeitos subletais. Os efeitos tóxicos induzidos por ATN e POEA após exposição repetida em pulsos foram menores quando comparados aos efeitos observados na exposição única. Em síntese, diferentes parâmetros toxicológicos em cenários de exposição distintos devem ser analisados para prever e entender a toxicidade de formulações a base de GLI e seus constituintes.Submitted by Marlene Santos (marlene.bc.ufg@gmail.com) on 2022-07-18T20:29:45Z No. of bitstreams: 2 Tese - Laís de Brito Rodrigues - 2022.pdf: 2570363 bytes, checksum: 8b1b5ddbb05b01a9c4f5368e7165bf3a (MD5) license_rdf: 805 bytes, checksum: 4460e5956bc1d1639be9ae6146a50347 (MD5)Approved for entry into archive by Luciana Ferreira (lucgeral@gmail.com) on 2022-07-19T12:20:38Z (GMT) No. of bitstreams: 2 Tese - Laís de Brito Rodrigues - 2022.pdf: 2570363 bytes, checksum: 8b1b5ddbb05b01a9c4f5368e7165bf3a (MD5) license_rdf: 805 bytes, checksum: 4460e5956bc1d1639be9ae6146a50347 (MD5)Made available in DSpace on 2022-07-19T12:20:38Z (GMT). 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dc.title.pt_BR.fl_str_mv |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida |
dc.title.alternative.eng.fl_str_mv |
Toxicicty evaluation of glyphosate-based formulation and its main constituents on the zebrafish early life stages: continuous and repeated pulse exposure |
title |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida |
spellingShingle |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida Rodrigues, Laís de Brito Surfactante AMPA FET Ensaio cometa Danio rerio Resiliência Surfactan Comet assay Resilience CIENCIAS BIOLOGICAS::FARMACOLOGIA::TOXICOLOGIA |
title_short |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida |
title_full |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida |
title_fullStr |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida |
title_full_unstemmed |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida |
title_sort |
Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida |
author |
Rodrigues, Laís de Brito |
author_facet |
Rodrigues, Laís de Brito |
author_role |
author |
dc.contributor.advisor1.fl_str_mv |
Oliveira, Gisele Augusto Rodrigues de |
dc.contributor.advisor1Lattes.fl_str_mv |
http://lattes.cnpq.br/6221735418479539 |
dc.contributor.referee1.fl_str_mv |
Oliveira, Gisele Augusto Rodrigues de |
dc.contributor.referee2.fl_str_mv |
Fil, Eric de Souza |
dc.contributor.referee3.fl_str_mv |
Valadares, Marize Campos |
dc.contributor.referee4.fl_str_mv |
Rocha, Thiago Lopes |
dc.contributor.referee5.fl_str_mv |
Sabóia-Morais, Simone Maria Teixeira de |
dc.contributor.authorLattes.fl_str_mv |
http://lattes.cnpq.br/0266761443016631 |
dc.contributor.author.fl_str_mv |
Rodrigues, Laís de Brito |
contributor_str_mv |
Oliveira, Gisele Augusto Rodrigues de Oliveira, Gisele Augusto Rodrigues de Fil, Eric de Souza Valadares, Marize Campos Rocha, Thiago Lopes Sabóia-Morais, Simone Maria Teixeira de |
dc.subject.por.fl_str_mv |
Surfactante AMPA FET Ensaio cometa Danio rerio Resiliência |
topic |
Surfactante AMPA FET Ensaio cometa Danio rerio Resiliência Surfactan Comet assay Resilience CIENCIAS BIOLOGICAS::FARMACOLOGIA::TOXICOLOGIA |
dc.subject.eng.fl_str_mv |
Surfactan Comet assay Resilience |
dc.subject.cnpq.fl_str_mv |
CIENCIAS BIOLOGICAS::FARMACOLOGIA::TOXICOLOGIA |
description |
Glyphosate (GLY) is the active ingredient of several herbicide formulations used to control weeds in agricultural and non-agricultural areas. Due to intensive use of GLY-based formulations and the repeated applications once weed resistance, some of their components, including the active ingredient, may reach the aquatic environment through direct run-off and leaching. The present study assessed the acute toxicity, after continuous and repeated exposures, and genotoxicity of the GLY-based formulation Atanor 48 (ATN) and its major constituents GLY, surfactant polyethoxylated tallow amine (POEA), as well as the main metabolite of GLY aminomethylphosphonic acid (AMPA) on zebrafish early life stages. Also, we evaluate larvae resilience after ATN, GLY and POEA pulsed-exposure. The toxic effects of these chemicals were evaluated in the fish embryo acute toxicity test with zebrafish (Danio rerio), while genotoxic effects were investigated in the comet assay with cells from zebrafish larvae and rainbow trout gonad-2 (RTG-2). GLY and AMPA caused no acute toxic effect after continuous exposure, while ATN and POEA induced significant lethal effects in zebrafish (LC50-96 h 76.50 mg/L and 5.49 mg/L, respectively. In summary, these data indicate that the lethal effects on zebrafish early-life stages can be ranked in the following order from most to least toxic: POEA > ATN > GLY ≈ AMPA. All compounds were genotoxic to zebrafish larvae (LOEC 1.7 mg/L for GLY, ATN, AMPA and 0.4 mg/L for POEA). Unlike in vivo. POEA induced DNA damage in RTG-2 cells (LOEC 1.6 mg/L), suggesting that it is a direct acting genotoxic agent. GLY caused no acute toxic effect after repeated pulse exposure. However, ATN showed significant mortality (LC50-96 h 148.80 mg/L) after 5 h pulse at 100 mg/L and POEA induced significant toxicity on zebrafish early life stages after 1, 2 and 5 h pulse with LC50-96 h of 43.49 mg/L, 47.23 mg/L and 11.61 mg/L, respectively. Zebrafish was not able to reverse the sublethal effects induced by ATN, GLY and POEA during the recovery period. The toxic effects induced by ATN and POEA after pulsed-exposure were less than continuous exposure. Therefore, its important to evaluate different toxicological endpoints with distinct exposure scenarios to predict the hazards of GLY-based formulations, their components and breakdown product to aquatic biota. |
publishDate |
2021 |
dc.date.issued.fl_str_mv |
2021-06-12 |
dc.date.accessioned.fl_str_mv |
2022-07-19T12:20:38Z |
dc.date.available.fl_str_mv |
2022-07-19T12:20:38Z |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/doctoralThesis |
format |
doctoralThesis |
status_str |
publishedVersion |
dc.identifier.citation.fl_str_mv |
RODRIGUES, L. B. Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida. 2022. 98 f. Tese (Doutorado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2021. |
dc.identifier.uri.fl_str_mv |
http://repositorio.bc.ufg.br/tede/handle/tede/12190 |
dc.identifier.dark.fl_str_mv |
ark:/38995/00130000010fn |
identifier_str_mv |
RODRIGUES, L. B. Avaliação toxicológica de uma formulação a base de glifosato e seus principais constituintes sobre o estágio embrio-larval de zebrafish: exposição única e repetida. 2022. 98 f. Tese (Doutorado em Ciências Farmacêuticas) - Universidade Federal de Goiás, Goiânia, 2021. ark:/38995/00130000010fn |
url |
http://repositorio.bc.ufg.br/tede/handle/tede/12190 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.program.fl_str_mv |
27 |
dc.relation.confidence.fl_str_mv |
500 500 500 500 |
dc.relation.department.fl_str_mv |
22 |
dc.relation.cnpq.fl_str_mv |
526 |
dc.relation.sponsorship.fl_str_mv |
1 |
dc.rights.driver.fl_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ info:eu-repo/semantics/openAccess |
rights_invalid_str_mv |
Attribution-NonCommercial-NoDerivatives 4.0 International http://creativecommons.org/licenses/by-nc-nd/4.0/ |
eu_rights_str_mv |
openAccess |
dc.publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.publisher.program.fl_str_mv |
Programa de Pós-graduação em Ciências Farmacêuticas (FF) |
dc.publisher.initials.fl_str_mv |
UFG |
dc.publisher.country.fl_str_mv |
Brasil |
dc.publisher.department.fl_str_mv |
Faculdade de Farmácia - FF (RG) |
publisher.none.fl_str_mv |
Universidade Federal de Goiás |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UFG instname:Universidade Federal de Goiás (UFG) instacron:UFG |
instname_str |
Universidade Federal de Goiás (UFG) |
instacron_str |
UFG |
institution |
UFG |
reponame_str |
Repositório Institucional da UFG |
collection |
Repositório Institucional da UFG |
bitstream.url.fl_str_mv |
http://repositorio.bc.ufg.br/tede/bitstreams/9519f2a1-e93f-400b-8829-1672edf8bdc1/download http://repositorio.bc.ufg.br/tede/bitstreams/54189d7e-2dcf-4f17-a850-beb972e5e86e/download http://repositorio.bc.ufg.br/tede/bitstreams/089d96d0-a2bf-49e5-8c8e-9a59cb931690/download |
bitstream.checksum.fl_str_mv |
8a4605be74aa9ea9d79846c1fba20a33 4460e5956bc1d1639be9ae6146a50347 8b1b5ddbb05b01a9c4f5368e7165bf3a |
bitstream.checksumAlgorithm.fl_str_mv |
MD5 MD5 MD5 |
repository.name.fl_str_mv |
Repositório Institucional da UFG - Universidade Federal de Goiás (UFG) |
repository.mail.fl_str_mv |
tasesdissertacoes.bc@ufg.br |
_version_ |
1815172519164903424 |