Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis
Autor(a) principal: | |
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Data de Publicação: | 2022 |
Outros Autores: | , , , , |
Tipo de documento: | Artigo |
Idioma: | por |
Título da fonte: | Revista Brasileira de Cancerologia (Online) |
Texto Completo: | https://rbc.inca.gov.br/index.php/revista/article/view/2787 |
Resumo: | This study describes the morphologic lesions that occur in the urinary bladder and colon of Wistar rats submitted to an alternative medium-term multi-organ assay for Chemical carcinogenesis. Developed by Japanese researchers with the Fischer 344 rat strain, in 1996 the bioassay was adopted by the Brazilian Agency for the Environment (IBAMA) as a source of evidence of Chemical carcinogenicity. The animais were allocated to six groups, one of them the non-treated control group. Groups 2, 3 and 4 were initiated for carcinogenesis with N-diethylnitrosamine (DEN, 100 mg/kg i.p.), N-methyl N-nitrosourea(MNU, 80 mg/kg i.p.), N-butyl-N-(4-hydroxybutil)nitrosamine (BBN 0.05 % drinking water, weeks 1 and 2), dimethyl-hidrazine (DMEt, 160 mg/kg, s.c.) and dihydroxi-propyl-nitrosamine (DEIPN 0.1% drinking water, weeks 3 e 4). Promotion of carcinogenesis was accomplished by phenobarbital 0.05% (groups 3 and 5) or 0.01% 2-acetilaminofluorene (2-AAF, groups 4 and 6) mixed in the diet. In the urinary bladder, the most relevant lesion found was the papillary/nodular hyperplasia, which was significantly more frequent in both male groups initiated and promoted for carcinogenesis. Lesions in the colon included aberrant crypt foci (ACF), adenomas and adenocarcinomas. Neoplasia ocurred in every male and female group initiated for carcinogenesis, but a significant incidence of adenocarcinomas occurred only in males also promoted by 2-AAF. The results indicate that the initiation of carcinogenesis was effective in the treated groups and document the lesion patterns that occur in the urinary bladder and colon of Wistar rats. |
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Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesisLesões da bexiga e do cólon de ratos wistar submetidos à carcinogênese química de duas etapasCancerígenos QuímicosTeste AlternativoRatos WistarBexigaCólonChemical CarcinogensAlternative BioassayWistar RatsColonUrinary BladderThis study describes the morphologic lesions that occur in the urinary bladder and colon of Wistar rats submitted to an alternative medium-term multi-organ assay for Chemical carcinogenesis. Developed by Japanese researchers with the Fischer 344 rat strain, in 1996 the bioassay was adopted by the Brazilian Agency for the Environment (IBAMA) as a source of evidence of Chemical carcinogenicity. The animais were allocated to six groups, one of them the non-treated control group. Groups 2, 3 and 4 were initiated for carcinogenesis with N-diethylnitrosamine (DEN, 100 mg/kg i.p.), N-methyl N-nitrosourea(MNU, 80 mg/kg i.p.), N-butyl-N-(4-hydroxybutil)nitrosamine (BBN 0.05 % drinking water, weeks 1 and 2), dimethyl-hidrazine (DMEt, 160 mg/kg, s.c.) and dihydroxi-propyl-nitrosamine (DEIPN 0.1% drinking water, weeks 3 e 4). Promotion of carcinogenesis was accomplished by phenobarbital 0.05% (groups 3 and 5) or 0.01% 2-acetilaminofluorene (2-AAF, groups 4 and 6) mixed in the diet. In the urinary bladder, the most relevant lesion found was the papillary/nodular hyperplasia, which was significantly more frequent in both male groups initiated and promoted for carcinogenesis. Lesions in the colon included aberrant crypt foci (ACF), adenomas and adenocarcinomas. Neoplasia ocurred in every male and female group initiated for carcinogenesis, but a significant incidence of adenocarcinomas occurred only in males also promoted by 2-AAF. The results indicate that the initiation of carcinogenesis was effective in the treated groups and document the lesion patterns that occur in the urinary bladder and colon of Wistar rats.Este estudo descreve as lesões morfológicas da bexiga e em cólon em ratos Wistar, de ambos os sexos, submetidos a um teste alternativo para a identificação de cancerígenos químicos. Desenvolvido por pesquisadores japoneses em ratos Fischer 344 machos, em 1996, este teste foi adotado, com algumas modificações, pelo Instituto Brasileiro do Meio Ambiente e Recursos Naturais Renováveis (IBAMA), como fonte de evidência de carcinogenicidade química. Os animais foram separados em seis grupos, um deles o controle não-tratado. Os grupos 2, 3 e 4 sofreram iniciação multi-orgânica da carcinogênese pelo tratamento sequencial com N-dietilnitrosamina (DEN, 100 mg/kg i.p.), N-metil-N-nitrosouréia (MNU, 80 mg/kg i.p.), N-butil-N-(4-hidroxibutil)nitrosamina (BBN 0,05 % via água de beber, semanas 1 e 2), dimetil-hidrazina (DMH, 160 mg/kg, s.c.) e dihidroxi-propil-nitrosamina (DHPN 0,1% via água de beber, semanas 3 e 4). A promoção da carcinogênese foi estabelecida à partir da 6a. semana, pela mistura, na ração, de 0,05% fenobarbital (grupos 3 e 5) ou 0,01% 2-acetilaminofluoreno (2-AAF, grupos 4 e 6), até o final do experimento, na 30a. semana. Na bexiga, a lesão vesical mais relevante foi a hiperplasia papilífera/nodular (HPN), particularmente nos grupos machos iniciados e promovidos para a carcinogênese. No cólon, ocorreram focos de criptas aberrantes (FCA), adenomas e adenocarcinomas. As neoplasias do cólon ocorreram em todos os grupos iniciados de ambos os sexos, mas aumento significativo da incidência de adenocarcinomas só ocorreu nos machos promovidos por 2-AAF. Os resultados indicam que a iniciação da carcinogênese foi efetiva nos animais tratados e documentam o padrão de lesões que ocorre na bexiga e cólon de ratos Wistar.INCA2022-07-11info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArtigos, Avaliado pelos paresapplication/pdfhttps://rbc.inca.gov.br/index.php/revista/article/view/278710.32635/2176-9745.RBC.1999v45n4.2787Revista Brasileira de Cancerologia; Vol. 45 No. 4 (1999): Oct./Nov./Dec.; 13-24Revista Brasileira de Cancerologia; Vol. 45 Núm. 4 (1999): oct./nov./dic.; 13-24Revista Brasileira de Cancerologia; v. 45 n. 4 (1999): out./nov./dez.; 13-242176-9745reponame:Revista Brasileira de Cancerologia (Online)instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)instacron:INCAporhttps://rbc.inca.gov.br/index.php/revista/article/view/2787/1664https://creativecommons.org/licenses/by/4.0info:eu-repo/semantics/openAccessBononi, Alexandra Procópio Caetano, Camila da Silva Rocha, Noeme de SouzaOliveira, Susie Vieira deSalvadori, Daisy Maria Fávero Camargo, João Lauro Viana de 2023-01-18T15:18:03Zoai:rbc.inca.gov.br:article/2787Revistahttps://rbc.inca.gov.br/index.php/revistaPUBhttps://rbc.inca.gov.br/index.php/revista/oairbc@inca.gov.br0034-71162176-9745opendoar:2023-01-18T15:18:03Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA)false |
dc.title.none.fl_str_mv |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis Lesões da bexiga e do cólon de ratos wistar submetidos à carcinogênese química de duas etapas |
title |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis |
spellingShingle |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis Bononi, Alexandra Procópio Cancerígenos Químicos Teste Alternativo Ratos Wistar Bexiga Cólon Chemical Carcinogens Alternative Bioassay Wistar Rats Colon Urinary Bladder |
title_short |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis |
title_full |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis |
title_fullStr |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis |
title_full_unstemmed |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis |
title_sort |
Bladder and colon lesions in wistar rats submitted to a two-stage Chemical carcinogenesis |
author |
Bononi, Alexandra Procópio |
author_facet |
Bononi, Alexandra Procópio Caetano, Camila da Silva Rocha, Noeme de Souza Oliveira, Susie Vieira de Salvadori, Daisy Maria Fávero Camargo, João Lauro Viana de |
author_role |
author |
author2 |
Caetano, Camila da Silva Rocha, Noeme de Souza Oliveira, Susie Vieira de Salvadori, Daisy Maria Fávero Camargo, João Lauro Viana de |
author2_role |
author author author author author |
dc.contributor.author.fl_str_mv |
Bononi, Alexandra Procópio Caetano, Camila da Silva Rocha, Noeme de Souza Oliveira, Susie Vieira de Salvadori, Daisy Maria Fávero Camargo, João Lauro Viana de |
dc.subject.por.fl_str_mv |
Cancerígenos Químicos Teste Alternativo Ratos Wistar Bexiga Cólon Chemical Carcinogens Alternative Bioassay Wistar Rats Colon Urinary Bladder |
topic |
Cancerígenos Químicos Teste Alternativo Ratos Wistar Bexiga Cólon Chemical Carcinogens Alternative Bioassay Wistar Rats Colon Urinary Bladder |
description |
This study describes the morphologic lesions that occur in the urinary bladder and colon of Wistar rats submitted to an alternative medium-term multi-organ assay for Chemical carcinogenesis. Developed by Japanese researchers with the Fischer 344 rat strain, in 1996 the bioassay was adopted by the Brazilian Agency for the Environment (IBAMA) as a source of evidence of Chemical carcinogenicity. The animais were allocated to six groups, one of them the non-treated control group. Groups 2, 3 and 4 were initiated for carcinogenesis with N-diethylnitrosamine (DEN, 100 mg/kg i.p.), N-methyl N-nitrosourea(MNU, 80 mg/kg i.p.), N-butyl-N-(4-hydroxybutil)nitrosamine (BBN 0.05 % drinking water, weeks 1 and 2), dimethyl-hidrazine (DMEt, 160 mg/kg, s.c.) and dihydroxi-propyl-nitrosamine (DEIPN 0.1% drinking water, weeks 3 e 4). Promotion of carcinogenesis was accomplished by phenobarbital 0.05% (groups 3 and 5) or 0.01% 2-acetilaminofluorene (2-AAF, groups 4 and 6) mixed in the diet. In the urinary bladder, the most relevant lesion found was the papillary/nodular hyperplasia, which was significantly more frequent in both male groups initiated and promoted for carcinogenesis. Lesions in the colon included aberrant crypt foci (ACF), adenomas and adenocarcinomas. Neoplasia ocurred in every male and female group initiated for carcinogenesis, but a significant incidence of adenocarcinomas occurred only in males also promoted by 2-AAF. The results indicate that the initiation of carcinogenesis was effective in the treated groups and document the lesion patterns that occur in the urinary bladder and colon of Wistar rats. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-07-11 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion Artigos, Avaliado pelos pares |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
https://rbc.inca.gov.br/index.php/revista/article/view/2787 10.32635/2176-9745.RBC.1999v45n4.2787 |
url |
https://rbc.inca.gov.br/index.php/revista/article/view/2787 |
identifier_str_mv |
10.32635/2176-9745.RBC.1999v45n4.2787 |
dc.language.iso.fl_str_mv |
por |
language |
por |
dc.relation.none.fl_str_mv |
https://rbc.inca.gov.br/index.php/revista/article/view/2787/1664 |
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https://creativecommons.org/licenses/by/4.0 info:eu-repo/semantics/openAccess |
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https://creativecommons.org/licenses/by/4.0 |
eu_rights_str_mv |
openAccess |
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application/pdf |
dc.publisher.none.fl_str_mv |
INCA |
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INCA |
dc.source.none.fl_str_mv |
Revista Brasileira de Cancerologia; Vol. 45 No. 4 (1999): Oct./Nov./Dec.; 13-24 Revista Brasileira de Cancerologia; Vol. 45 Núm. 4 (1999): oct./nov./dic.; 13-24 Revista Brasileira de Cancerologia; v. 45 n. 4 (1999): out./nov./dez.; 13-24 2176-9745 reponame:Revista Brasileira de Cancerologia (Online) instname:Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) instacron:INCA |
instname_str |
Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
instacron_str |
INCA |
institution |
INCA |
reponame_str |
Revista Brasileira de Cancerologia (Online) |
collection |
Revista Brasileira de Cancerologia (Online) |
repository.name.fl_str_mv |
Revista Brasileira de Cancerologia (Online) - Instituto Nacional de Câncer José Alencar Gomes da Silva (INCA) |
repository.mail.fl_str_mv |
rbc@inca.gov.br |
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1797042232911462400 |