Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice
Autor(a) principal: | |
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Data de Publicação: | 2011 |
Outros Autores: | , |
Tipo de documento: | Artigo |
Idioma: | eng |
Título da fonte: | Repositório Institucional da UNIFESP |
Texto Completo: | http://dx.doi.org/10.1016/j.fct.2011.03.016 http://repositorio.unifesp.br/handle/11600/33716 |
Resumo: | Artesunate is a derivate of artemisinin that is both an antimalarial agent and acts cytotoxically on tumor cells. Despite its therapeutic use, its in vivo genotoxic potential has still not been evaluated. This study, therefore, was an investigation into the effects of a single oral administration of artesunate with an in vivo comet assay that analyzed leukocytes from peripheral blood and liver cells, and a micronucleus (MN) assay of bone marrow cells from male Swiss mice. the artesunate was administered by oral gavage at doses of 5, 50 and 100 mg/kg. Cytotoxicity was assessed by scoring 200 consecutive polychromatic (PCE) and normochromatic (NCE) erythrocytes (PCE/NCE ratio). the results demonstrate that artesunate induced significant DNA damage only in liver cells and that high doses of artesunate caused an increase in the mean number of micronucleated polychromatic erythrocytes (MNPCE). Under our experimental conditions, artesunate showed weak genotoxic effects at low doses and clastogenic effects at high doses. the PCE/NCE ratio indicated no cytotoxicity. the data obtained suggest caution about either continuous or high-dose use of artesunate by humans. (C) 2011 Elsevier B.V. All rights reserved. |
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Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of miceArtesunateArtemisinin derivateMicronucleus test comet assayClastogenicityArtesunate is a derivate of artemisinin that is both an antimalarial agent and acts cytotoxically on tumor cells. Despite its therapeutic use, its in vivo genotoxic potential has still not been evaluated. This study, therefore, was an investigation into the effects of a single oral administration of artesunate with an in vivo comet assay that analyzed leukocytes from peripheral blood and liver cells, and a micronucleus (MN) assay of bone marrow cells from male Swiss mice. the artesunate was administered by oral gavage at doses of 5, 50 and 100 mg/kg. Cytotoxicity was assessed by scoring 200 consecutive polychromatic (PCE) and normochromatic (NCE) erythrocytes (PCE/NCE ratio). the results demonstrate that artesunate induced significant DNA damage only in liver cells and that high doses of artesunate caused an increase in the mean number of micronucleated polychromatic erythrocytes (MNPCE). Under our experimental conditions, artesunate showed weak genotoxic effects at low doses and clastogenic effects at high doses. the PCE/NCE ratio indicated no cytotoxicity. the data obtained suggest caution about either continuous or high-dose use of artesunate by humans. (C) 2011 Elsevier B.V. All rights reserved.Univ Estadual Paulista, UNESP, Fac Filosofia & Ciencias, Dept Fonoaudiol, BR-17525900 Marilia, SP, BrazilUniv Estadual Paulista, UNESP, Inst Biociencias, Programa Posgrad Biol Geral & Aplicada, BR-18618970 Botucatu, SP, BrazilUniversidade Federal de São Paulo Unifesp, Dept Ciencias Exatas & Terra, BR-09972270 Diadema, SP, BrazilUniversidade Federal de São Paulo Unifesp, Dept Ciencias Exatas & Terra, BR-09972270 Diadema, SP, BrazilWeb of ScienceConselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)CNPq: 306544/2006-7FAPESP: 2008/51175-7Elsevier B.V.Univ Estadual PaulistaUniversidade de São Paulo (USP)Universidade Federal de São Paulo (UNIFESP)Aquino, IvaniPerazzo, Fábio Ferreira [UNIFESP]Maistro, Edson Luis2016-01-24T14:16:46Z2016-01-24T14:16:46Z2011-06-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersion1335-1339application/pdfhttp://dx.doi.org/10.1016/j.fct.2011.03.016Food and Chemical Toxicology. Oxford: Pergamon-Elsevier B.V., v. 49, n. 6, p. 1335-1339, 2011.10.1016/j.fct.2011.03.016WOS000291514800021.pdf0278-6915http://repositorio.unifesp.br/handle/11600/33716WOS:000291514800021engFood and Chemical Toxicologyinfo:eu-repo/semantics/openAccesshttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policyreponame:Repositório Institucional da UNIFESPinstname:Universidade Federal de São Paulo (UNIFESP)instacron:UNIFESP2024-07-31T20:30:27Zoai:repositorio.unifesp.br/:11600/33716Repositório InstitucionalPUBhttp://www.repositorio.unifesp.br/oai/requestbiblioteca.csp@unifesp.bropendoar:34652024-07-31T20:30:27Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP)false |
dc.title.none.fl_str_mv |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice |
title |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice |
spellingShingle |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice Aquino, Ivani Artesunate Artemisinin derivate Micronucleus test comet assay Clastogenicity |
title_short |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice |
title_full |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice |
title_fullStr |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice |
title_full_unstemmed |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice |
title_sort |
Genotoxicity assessment of the antimalarial compound artesunate in somatic cells of mice |
author |
Aquino, Ivani |
author_facet |
Aquino, Ivani Perazzo, Fábio Ferreira [UNIFESP] Maistro, Edson Luis |
author_role |
author |
author2 |
Perazzo, Fábio Ferreira [UNIFESP] Maistro, Edson Luis |
author2_role |
author author |
dc.contributor.none.fl_str_mv |
Univ Estadual Paulista Universidade de São Paulo (USP) Universidade Federal de São Paulo (UNIFESP) |
dc.contributor.author.fl_str_mv |
Aquino, Ivani Perazzo, Fábio Ferreira [UNIFESP] Maistro, Edson Luis |
dc.subject.por.fl_str_mv |
Artesunate Artemisinin derivate Micronucleus test comet assay Clastogenicity |
topic |
Artesunate Artemisinin derivate Micronucleus test comet assay Clastogenicity |
description |
Artesunate is a derivate of artemisinin that is both an antimalarial agent and acts cytotoxically on tumor cells. Despite its therapeutic use, its in vivo genotoxic potential has still not been evaluated. This study, therefore, was an investigation into the effects of a single oral administration of artesunate with an in vivo comet assay that analyzed leukocytes from peripheral blood and liver cells, and a micronucleus (MN) assay of bone marrow cells from male Swiss mice. the artesunate was administered by oral gavage at doses of 5, 50 and 100 mg/kg. Cytotoxicity was assessed by scoring 200 consecutive polychromatic (PCE) and normochromatic (NCE) erythrocytes (PCE/NCE ratio). the results demonstrate that artesunate induced significant DNA damage only in liver cells and that high doses of artesunate caused an increase in the mean number of micronucleated polychromatic erythrocytes (MNPCE). Under our experimental conditions, artesunate showed weak genotoxic effects at low doses and clastogenic effects at high doses. the PCE/NCE ratio indicated no cytotoxicity. the data obtained suggest caution about either continuous or high-dose use of artesunate by humans. (C) 2011 Elsevier B.V. All rights reserved. |
publishDate |
2011 |
dc.date.none.fl_str_mv |
2011-06-01 2016-01-24T14:16:46Z 2016-01-24T14:16:46Z |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://dx.doi.org/10.1016/j.fct.2011.03.016 Food and Chemical Toxicology. Oxford: Pergamon-Elsevier B.V., v. 49, n. 6, p. 1335-1339, 2011. 10.1016/j.fct.2011.03.016 WOS000291514800021.pdf 0278-6915 http://repositorio.unifesp.br/handle/11600/33716 WOS:000291514800021 |
url |
http://dx.doi.org/10.1016/j.fct.2011.03.016 http://repositorio.unifesp.br/handle/11600/33716 |
identifier_str_mv |
Food and Chemical Toxicology. Oxford: Pergamon-Elsevier B.V., v. 49, n. 6, p. 1335-1339, 2011. 10.1016/j.fct.2011.03.016 WOS000291514800021.pdf 0278-6915 WOS:000291514800021 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
Food and Chemical Toxicology |
dc.rights.driver.fl_str_mv |
info:eu-repo/semantics/openAccess http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy |
dc.format.none.fl_str_mv |
1335-1339 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier B.V. |
publisher.none.fl_str_mv |
Elsevier B.V. |
dc.source.none.fl_str_mv |
reponame:Repositório Institucional da UNIFESP instname:Universidade Federal de São Paulo (UNIFESP) instacron:UNIFESP |
instname_str |
Universidade Federal de São Paulo (UNIFESP) |
instacron_str |
UNIFESP |
institution |
UNIFESP |
reponame_str |
Repositório Institucional da UNIFESP |
collection |
Repositório Institucional da UNIFESP |
repository.name.fl_str_mv |
Repositório Institucional da UNIFESP - Universidade Federal de São Paulo (UNIFESP) |
repository.mail.fl_str_mv |
biblioteca.csp@unifesp.br |
_version_ |
1814268341436547072 |