Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents

Detalhes bibliográficos
Autor(a) principal: Favero Salvadori, Daisy Maria [UNESP]
Data de Publicação: 1998
Outros Autores: Barbisan, Luis Fernando [UNESP], Bazo, Ana Paula [UNESP], De Santana, Efigênia Queiroz, Denadai, Roberta [UNESP], De Oliveira, Susie Vieira [UNESP], Ribeiro, Lúcia Regina [UNESP], Viana De Camargo, João Lauro [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1002/(SICI)1520-6866(1998)18:4<199
http://hdl.handle.net/11449/226123
Resumo: The mutagenicity (clastogenicity) and the carcinogenicity (promoting potential) of cocaine were evaluated, respectively, by the mouse bone marrow micronucleus test (study I) and by the initiated rat liver bioassay (study II). In study I, two administration routes (i.p. and i.v.) and two sampling times (24 and 48 hours) after cocaine treatment were studied. Swiss male mice were treated with cocaine at doses of 0, 18, 37, and 75 mg/kg and 0, 2, 4, and 8 mg/kg by i.p. and i.v. routes, respectively. No significant differences were observed between treated and negative control groups regarding the frequencies of micronuclei and the polichromatic/normochromatic erythrocyte (PCE/NCE) ratios. In study II, the development of putative preneoplastic foci of hepatocytes expressing the enzyme glutathione S-transferase placental form (GST-P+) was utilized as the end-point marker in a 8-week rat liver bioassay. The animals were initiated for carcinogenesis by a single i.p. sub- carcinogenic dose of diethylnitrosamine (DEN). After a 6-week exposure to 5 or 10 mg/kg of cocaine i.v. twice a week there was no enhancement of GST-P+ foci development above the values of the control DEN-only treated animals. Also, cocaine did not induce any toxicity as evidenced by the absence of alterations of rat body and liver weights and of liver biochemical function and morphology. The results suggest that cocaine does not have a mutagenic effect on the mouse bone marrow cells or promoting activity on the rat hepatocarcinogenesis process.
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spelling Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodentsCocaineMicronucleus testMouse bone marrowRat liver carcinogenesis bioassayThe mutagenicity (clastogenicity) and the carcinogenicity (promoting potential) of cocaine were evaluated, respectively, by the mouse bone marrow micronucleus test (study I) and by the initiated rat liver bioassay (study II). In study I, two administration routes (i.p. and i.v.) and two sampling times (24 and 48 hours) after cocaine treatment were studied. Swiss male mice were treated with cocaine at doses of 0, 18, 37, and 75 mg/kg and 0, 2, 4, and 8 mg/kg by i.p. and i.v. routes, respectively. No significant differences were observed between treated and negative control groups regarding the frequencies of micronuclei and the polichromatic/normochromatic erythrocyte (PCE/NCE) ratios. In study II, the development of putative preneoplastic foci of hepatocytes expressing the enzyme glutathione S-transferase placental form (GST-P+) was utilized as the end-point marker in a 8-week rat liver bioassay. The animals were initiated for carcinogenesis by a single i.p. sub- carcinogenic dose of diethylnitrosamine (DEN). After a 6-week exposure to 5 or 10 mg/kg of cocaine i.v. twice a week there was no enhancement of GST-P+ foci development above the values of the control DEN-only treated animals. Also, cocaine did not induce any toxicity as evidenced by the absence of alterations of rat body and liver weights and of liver biochemical function and morphology. The results suggest that cocaine does not have a mutagenic effect on the mouse bone marrow cells or promoting activity on the rat hepatocarcinogenesis process.Departamento de Patologia Faculdade de Medicina UNESP, Botucatu, SPDepartamento de Nutrifarma USC, Bauru, SPDepartamento de Biologia UEFS, Feira de Santana, BADepartamento de Patologia Faculdade de Medicina Universidade Estadual Paulista, Botucatu, 18618-000, SPDepartamento de Patologia Faculdade de Medicina UNESP, Botucatu, SPDepartamento de Patologia Faculdade de Medicina Universidade Estadual Paulista, Botucatu, 18618-000, SPUniversidade Estadual Paulista (UNESP)USCUEFSFavero Salvadori, Daisy Maria [UNESP]Barbisan, Luis Fernando [UNESP]Bazo, Ana Paula [UNESP]De Santana, Efigênia QueirozDenadai, Roberta [UNESP]De Oliveira, Susie Vieira [UNESP]Ribeiro, Lúcia Regina [UNESP]Viana De Camargo, João Lauro [UNESP]2022-04-28T21:25:50Z2022-04-28T21:25:50Z1998-11-07info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article199-208http://dx.doi.org/10.1002/(SICI)1520-6866(1998)18:4<199Teratogenesis Carcinogenesis and Mutagenesis, v. 18, n. 4, p. 199-208, 1998.0270-3211http://hdl.handle.net/11449/22612310.1002/(SICI)1520-6866(1998)18:4<1992-s2.0-7844235806Scopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengTeratogenesis Carcinogenesis and Mutagenesisinfo:eu-repo/semantics/openAccess2022-04-28T21:25:50Zoai:repositorio.unesp.br:11449/226123Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462022-04-28T21:25:50Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
title Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
spellingShingle Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
Favero Salvadori, Daisy Maria [UNESP]
Cocaine
Micronucleus test
Mouse bone marrow
Rat liver carcinogenesis bioassay
title_short Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
title_full Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
title_fullStr Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
title_full_unstemmed Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
title_sort Cocaine mutagenicity and hepatocarcinogenicity evaluations in rodents
author Favero Salvadori, Daisy Maria [UNESP]
author_facet Favero Salvadori, Daisy Maria [UNESP]
Barbisan, Luis Fernando [UNESP]
Bazo, Ana Paula [UNESP]
De Santana, Efigênia Queiroz
Denadai, Roberta [UNESP]
De Oliveira, Susie Vieira [UNESP]
Ribeiro, Lúcia Regina [UNESP]
Viana De Camargo, João Lauro [UNESP]
author_role author
author2 Barbisan, Luis Fernando [UNESP]
Bazo, Ana Paula [UNESP]
De Santana, Efigênia Queiroz
Denadai, Roberta [UNESP]
De Oliveira, Susie Vieira [UNESP]
Ribeiro, Lúcia Regina [UNESP]
Viana De Camargo, João Lauro [UNESP]
author2_role author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (UNESP)
USC
UEFS
dc.contributor.author.fl_str_mv Favero Salvadori, Daisy Maria [UNESP]
Barbisan, Luis Fernando [UNESP]
Bazo, Ana Paula [UNESP]
De Santana, Efigênia Queiroz
Denadai, Roberta [UNESP]
De Oliveira, Susie Vieira [UNESP]
Ribeiro, Lúcia Regina [UNESP]
Viana De Camargo, João Lauro [UNESP]
dc.subject.por.fl_str_mv Cocaine
Micronucleus test
Mouse bone marrow
Rat liver carcinogenesis bioassay
topic Cocaine
Micronucleus test
Mouse bone marrow
Rat liver carcinogenesis bioassay
description The mutagenicity (clastogenicity) and the carcinogenicity (promoting potential) of cocaine were evaluated, respectively, by the mouse bone marrow micronucleus test (study I) and by the initiated rat liver bioassay (study II). In study I, two administration routes (i.p. and i.v.) and two sampling times (24 and 48 hours) after cocaine treatment were studied. Swiss male mice were treated with cocaine at doses of 0, 18, 37, and 75 mg/kg and 0, 2, 4, and 8 mg/kg by i.p. and i.v. routes, respectively. No significant differences were observed between treated and negative control groups regarding the frequencies of micronuclei and the polichromatic/normochromatic erythrocyte (PCE/NCE) ratios. In study II, the development of putative preneoplastic foci of hepatocytes expressing the enzyme glutathione S-transferase placental form (GST-P+) was utilized as the end-point marker in a 8-week rat liver bioassay. The animals were initiated for carcinogenesis by a single i.p. sub- carcinogenic dose of diethylnitrosamine (DEN). After a 6-week exposure to 5 or 10 mg/kg of cocaine i.v. twice a week there was no enhancement of GST-P+ foci development above the values of the control DEN-only treated animals. Also, cocaine did not induce any toxicity as evidenced by the absence of alterations of rat body and liver weights and of liver biochemical function and morphology. The results suggest that cocaine does not have a mutagenic effect on the mouse bone marrow cells or promoting activity on the rat hepatocarcinogenesis process.
publishDate 1998
dc.date.none.fl_str_mv 1998-11-07
2022-04-28T21:25:50Z
2022-04-28T21:25:50Z
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://dx.doi.org/10.1002/(SICI)1520-6866(1998)18:4<199
Teratogenesis Carcinogenesis and Mutagenesis, v. 18, n. 4, p. 199-208, 1998.
0270-3211
http://hdl.handle.net/11449/226123
10.1002/(SICI)1520-6866(1998)18:4<199
2-s2.0-7844235806
url http://dx.doi.org/10.1002/(SICI)1520-6866(1998)18:4<199
http://hdl.handle.net/11449/226123
identifier_str_mv Teratogenesis Carcinogenesis and Mutagenesis, v. 18, n. 4, p. 199-208, 1998.
0270-3211
10.1002/(SICI)1520-6866(1998)18:4<199
2-s2.0-7844235806
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Teratogenesis Carcinogenesis and Mutagenesis
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 199-208
dc.source.none.fl_str_mv Scopus
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
repository.mail.fl_str_mv
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