Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes

Detalhes bibliográficos
Autor(a) principal: Araldi, Rodrigo Pinheiro
Data de Publicação: 2018
Outros Autores: dos Santos, Maristela Oliveira [UNESP], Barbon, Fabiane Faria [UNESP], Manjerona, Bruna Aparecida [UNESP], Meirelles, Bruno Rosa [UNESP], de Oliva Neto, Pedro [UNESP], da Silva, Pedro Ismael, dos Santos, Lucinéia [UNESP], Camargo, Isabel Cristina Cherici [UNESP], de Souza, Edislane Barreiros [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1016/j.biopha.2018.01.022
http://hdl.handle.net/11449/179500
Resumo: Brazilian Northeast is the world's largest producer of Agave sisalana Perrine for the supply of the sisal fiber. About 95% of plant biomass, which comprise the mucilage and sisal juice, is considered a waste residual is discarded in the soil. However, the sisal juice is rich in steroidal saponins, which exhibits different pharmacological properties. Despite this, natural products are not necessarily safe. Based on this, this study analyzed the antioxidant, cytotoxic and mutagenic potential of three extracts derived from acid hydrolysis (AHAS), dried precipitate (DPAS) and hexanic of A. sisalana (HAS). These analyses were performed by in vitro and in vivo methods, using Vero cells, human lymphocytes and mice. Results showed that AHAS 50 and 100 can be considered a useful antineoplastic candidate due to their antioxidant and cytotoxic activity, with no genotoxic/clastogenic potential in Vero cells and mice. Although the comet assay in human lymphocytes has showed that the AHAS 25, AHAS 50 and AHAS 100 can lead to DNA breaks, these extracts did not promote DNA damages in mice bone marrow. Considering the different mutagenic responses obtained with the different methods employed, this study suggest that the metabolizing pathways can produce by-products harmful to health. For this reason, it is mandatory to analyze the mutagenic potential by both in vitro and in vivo techniques, using cells derived from different species and origins.
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spelling Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytesAgave sisalanaComet assayHistone γ-H2AX assayMicronucleus testMutagenesisBrazilian Northeast is the world's largest producer of Agave sisalana Perrine for the supply of the sisal fiber. About 95% of plant biomass, which comprise the mucilage and sisal juice, is considered a waste residual is discarded in the soil. However, the sisal juice is rich in steroidal saponins, which exhibits different pharmacological properties. Despite this, natural products are not necessarily safe. Based on this, this study analyzed the antioxidant, cytotoxic and mutagenic potential of three extracts derived from acid hydrolysis (AHAS), dried precipitate (DPAS) and hexanic of A. sisalana (HAS). These analyses were performed by in vitro and in vivo methods, using Vero cells, human lymphocytes and mice. Results showed that AHAS 50 and 100 can be considered a useful antineoplastic candidate due to their antioxidant and cytotoxic activity, with no genotoxic/clastogenic potential in Vero cells and mice. Although the comet assay in human lymphocytes has showed that the AHAS 25, AHAS 50 and AHAS 100 can lead to DNA breaks, these extracts did not promote DNA damages in mice bone marrow. Considering the different mutagenic responses obtained with the different methods employed, this study suggest that the metabolizing pathways can produce by-products harmful to health. For this reason, it is mandatory to analyze the mutagenic potential by both in vitro and in vivo techniques, using cells derived from different species and origins.Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)Genetics Laboratory Butantan InstituteBiotechnology Interunit Post-Graduation Program Biomedical Science Institute University of São Paulo (USP)Department of Biotechnology School of Science Humanities and Languages São Paulo State University (UNESP), AssisCenter of Toxins Immune-Response and Cell Signaling (CeTICS/CEPID) Butantan InstituteDepartment of Biotechnology School of Science Humanities and Languages São Paulo State University (UNESP), AssisFAPESP: 2014/20617-5Butantan InstituteUniversidade de São Paulo (USP)Universidade Estadual Paulista (Unesp)Araldi, Rodrigo Pinheirodos Santos, Maristela Oliveira [UNESP]Barbon, Fabiane Faria [UNESP]Manjerona, Bruna Aparecida [UNESP]Meirelles, Bruno Rosa [UNESP]de Oliva Neto, Pedro [UNESP]da Silva, Pedro Ismaeldos Santos, Lucinéia [UNESP]Camargo, Isabel Cristina Cherici [UNESP]de Souza, Edislane Barreiros [UNESP]2018-12-11T17:35:26Z2018-12-11T17:35:26Z2018-02-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article873-885http://dx.doi.org/10.1016/j.biopha.2018.01.022Biomedicine and Pharmacotherapy, v. 98, p. 873-885.1950-60070753-3322http://hdl.handle.net/11449/17950010.1016/j.biopha.2018.01.0222-s2.0-850403421002-s2.0-85040342100.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengBiomedicine and Pharmacotherapy0,951info:eu-repo/semantics/openAccess2024-06-13T17:38:43Zoai:repositorio.unesp.br:11449/179500Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-08-05T21:19:46.527495Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
title Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
spellingShingle Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
Araldi, Rodrigo Pinheiro
Agave sisalana
Comet assay
Histone γ-H2AX assay
Micronucleus test
Mutagenesis
title_short Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
title_full Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
title_fullStr Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
title_full_unstemmed Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
title_sort Analysis of antioxidant, cytotoxic and mutagenic potential of Agave sisalana Perrine extracts using Vero cells, human lymphocytes and mice polychromatic erythrocytes
author Araldi, Rodrigo Pinheiro
author_facet Araldi, Rodrigo Pinheiro
dos Santos, Maristela Oliveira [UNESP]
Barbon, Fabiane Faria [UNESP]
Manjerona, Bruna Aparecida [UNESP]
Meirelles, Bruno Rosa [UNESP]
de Oliva Neto, Pedro [UNESP]
da Silva, Pedro Ismael
dos Santos, Lucinéia [UNESP]
Camargo, Isabel Cristina Cherici [UNESP]
de Souza, Edislane Barreiros [UNESP]
author_role author
author2 dos Santos, Maristela Oliveira [UNESP]
Barbon, Fabiane Faria [UNESP]
Manjerona, Bruna Aparecida [UNESP]
Meirelles, Bruno Rosa [UNESP]
de Oliva Neto, Pedro [UNESP]
da Silva, Pedro Ismael
dos Santos, Lucinéia [UNESP]
Camargo, Isabel Cristina Cherici [UNESP]
de Souza, Edislane Barreiros [UNESP]
author2_role author
author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Butantan Institute
Universidade de São Paulo (USP)
Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Araldi, Rodrigo Pinheiro
dos Santos, Maristela Oliveira [UNESP]
Barbon, Fabiane Faria [UNESP]
Manjerona, Bruna Aparecida [UNESP]
Meirelles, Bruno Rosa [UNESP]
de Oliva Neto, Pedro [UNESP]
da Silva, Pedro Ismael
dos Santos, Lucinéia [UNESP]
Camargo, Isabel Cristina Cherici [UNESP]
de Souza, Edislane Barreiros [UNESP]
dc.subject.por.fl_str_mv Agave sisalana
Comet assay
Histone γ-H2AX assay
Micronucleus test
Mutagenesis
topic Agave sisalana
Comet assay
Histone γ-H2AX assay
Micronucleus test
Mutagenesis
description Brazilian Northeast is the world's largest producer of Agave sisalana Perrine for the supply of the sisal fiber. About 95% of plant biomass, which comprise the mucilage and sisal juice, is considered a waste residual is discarded in the soil. However, the sisal juice is rich in steroidal saponins, which exhibits different pharmacological properties. Despite this, natural products are not necessarily safe. Based on this, this study analyzed the antioxidant, cytotoxic and mutagenic potential of three extracts derived from acid hydrolysis (AHAS), dried precipitate (DPAS) and hexanic of A. sisalana (HAS). These analyses were performed by in vitro and in vivo methods, using Vero cells, human lymphocytes and mice. Results showed that AHAS 50 and 100 can be considered a useful antineoplastic candidate due to their antioxidant and cytotoxic activity, with no genotoxic/clastogenic potential in Vero cells and mice. Although the comet assay in human lymphocytes has showed that the AHAS 25, AHAS 50 and AHAS 100 can lead to DNA breaks, these extracts did not promote DNA damages in mice bone marrow. Considering the different mutagenic responses obtained with the different methods employed, this study suggest that the metabolizing pathways can produce by-products harmful to health. For this reason, it is mandatory to analyze the mutagenic potential by both in vitro and in vivo techniques, using cells derived from different species and origins.
publishDate 2018
dc.date.none.fl_str_mv 2018-12-11T17:35:26Z
2018-12-11T17:35:26Z
2018-02-01
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/10.1016/j.biopha.2018.01.022
Biomedicine and Pharmacotherapy, v. 98, p. 873-885.
1950-6007
0753-3322
http://hdl.handle.net/11449/179500
10.1016/j.biopha.2018.01.022
2-s2.0-85040342100
2-s2.0-85040342100.pdf
url http://dx.doi.org/10.1016/j.biopha.2018.01.022
http://hdl.handle.net/11449/179500
identifier_str_mv Biomedicine and Pharmacotherapy, v. 98, p. 873-885.
1950-6007
0753-3322
10.1016/j.biopha.2018.01.022
2-s2.0-85040342100
2-s2.0-85040342100.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Biomedicine and Pharmacotherapy
0,951
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 873-885
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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