Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo

Detalhes bibliográficos
Autor(a) principal: Mauro, M. O. [UNESP]
Data de Publicação: 2013
Outros Autores: Monreal, M. T F D, Silva, M. T P [UNESP], Pesarini, J. R. [UNESP], Mantovani, M. S., Ribeiro, L. R. [UNESP], Dichi, J. B., Carreira, C. M., Oliveira, R. J.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.4238/2013.July.8.9
http://hdl.handle.net/11449/75931
Resumo: The incidence of colorectal cancer is growing worldwide. The characterization of compounds present in the human diet that can prevent the occurrence of colorectal tumors is vital. The oligosaccharide inulin is such a compound. The aim of this study was to evaluate the antigenotoxic, antimutagenic and anticarcinogenic effects of inulin in vivo. Our study is based on 3 assays that are widely used to evaluate chemoprevention (comet assay, micronucleus assay, and aberrant crypt focus assay) and tests 4 protocols of treatment with inulin (pre-treatment, simultaneous, post-treatment, and pre + continuous). Experiments were carried out in Swiss male mice of reproductive age. In order to induce DNA damage, we used the pro-carcinogenic agent 1,2-dimethylhydrazine. Inulin was administered orally at a concentration of 50 mg/kg body weight following the protocols mentioned above. Inulin was not administered to the control groups. Our data from the micronucleus assay reveal antimutagenic effects of inulin in all protocols. The percentage of inulin-induced damage reduction ranged from 47.25 to 141.75% across protocols. These data suggest that inulin could act through desmutagenic and bio-antimutagenic mechanisms. The anticarcinogenic activity (aberrant crypt focus assay) of inulin was observed in all protocols and the percentages of damage reduction ranged from 55.78 to 87.56% across protocols. Further tests, including human trials, will be necessary before this functional food can be proven to be effective in the prevention and treatment of colon cancer. © FUNPEC-RP.
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spelling Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivoChemopreventionFiberInulin1,2 dimethylhydrazineDNAinulinaberrant crypt focus assayanalytic methodanimal cellanimal experimentantigenotoxic activityantimutagenic activityantineoplastic activitybody weightcomet assayconcentration responseDNA damagedrug activitydrug determinationin vivo studymalemicronucleus testmousenonhumanThe incidence of colorectal cancer is growing worldwide. The characterization of compounds present in the human diet that can prevent the occurrence of colorectal tumors is vital. The oligosaccharide inulin is such a compound. The aim of this study was to evaluate the antigenotoxic, antimutagenic and anticarcinogenic effects of inulin in vivo. Our study is based on 3 assays that are widely used to evaluate chemoprevention (comet assay, micronucleus assay, and aberrant crypt focus assay) and tests 4 protocols of treatment with inulin (pre-treatment, simultaneous, post-treatment, and pre + continuous). Experiments were carried out in Swiss male mice of reproductive age. In order to induce DNA damage, we used the pro-carcinogenic agent 1,2-dimethylhydrazine. Inulin was administered orally at a concentration of 50 mg/kg body weight following the protocols mentioned above. Inulin was not administered to the control groups. Our data from the micronucleus assay reveal antimutagenic effects of inulin in all protocols. The percentage of inulin-induced damage reduction ranged from 47.25 to 141.75% across protocols. These data suggest that inulin could act through desmutagenic and bio-antimutagenic mechanisms. The anticarcinogenic activity (aberrant crypt focus assay) of inulin was observed in all protocols and the percentages of damage reduction ranged from 55.78 to 87.56% across protocols. Further tests, including human trials, will be necessary before this functional food can be proven to be effective in the prevention and treatment of colon cancer. © FUNPEC-RP.Centro de Estudos em Nutrição e Genética Toxicológica Centro Universitário Filadélfia, Londrina, PRInstituto de Biociências de Rio Claro Universidade Estadual Paulista, Rio Claro, SPCentro de Estudos em Celulas Tronco, Terapia Celular e Genética Toxicologica - CeTroGen Núcleo de Hospital Universitário Universidade Federal de Mato Grosso do Sul, Campo Grande, MSCentro de Ciências Biológicas e da Saúde Universidade Federal de Mato Grosso do Sul, Campo Grande, MSDepartamento de Biologia Centro de Ciências Biológicas Universidade Estadual de Londrina, Londrina, PRCentro de Ciências da Saúde Departamento de Ciências Farmacêuticas Universidade Estadual de Londrina, Londrina, PRUniversidade Federal de Mato Grosso do Sul, Campo Grande, MSInstituto de Biociências de Rio Claro Universidade Estadual Paulista, Rio Claro, SPCentro Universitário FiladélfiaUniversidade Estadual Paulista (Unesp)Universidade Federal de Mato Grosso do Sul (UFMS)Universidade Estadual de Londrina (UEL)Mauro, M. O. [UNESP]Monreal, M. T F DSilva, M. T P [UNESP]Pesarini, J. R. [UNESP]Mantovani, M. S.Ribeiro, L. R. [UNESP]Dichi, J. B.Carreira, C. M.Oliveira, R. J.2014-05-27T11:29:55Z2014-05-27T11:29:55Z2013-07-08info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article2281-2293application/pdfhttp://dx.doi.org/10.4238/2013.July.8.9Genetics and Molecular Research, v. 12, n. 3, p. 2281-2293, 2013.1676-5680http://hdl.handle.net/11449/7593110.4238/2013.July.8.9WOS:0003317174000122-s2.0-848801271162-s2.0-84880127116.pdfScopusreponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengGenetics and Molecular Research0,439info:eu-repo/semantics/openAccess2023-12-07T06:13:24Zoai:repositorio.unesp.br:11449/75931Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462023-12-07T06:13:24Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
title Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
spellingShingle Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
Mauro, M. O. [UNESP]
Chemoprevention
Fiber
Inulin
1,2 dimethylhydrazine
DNA
inulin
aberrant crypt focus assay
analytic method
animal cell
animal experiment
antigenotoxic activity
antimutagenic activity
antineoplastic activity
body weight
comet assay
concentration response
DNA damage
drug activity
drug determination
in vivo study
male
micronucleus test
mouse
nonhuman
title_short Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
title_full Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
title_fullStr Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
title_full_unstemmed Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
title_sort Evaluation of the antimutagenic and anticarcinogenic effects of inulin in vivo
author Mauro, M. O. [UNESP]
author_facet Mauro, M. O. [UNESP]
Monreal, M. T F D
Silva, M. T P [UNESP]
Pesarini, J. R. [UNESP]
Mantovani, M. S.
Ribeiro, L. R. [UNESP]
Dichi, J. B.
Carreira, C. M.
Oliveira, R. J.
author_role author
author2 Monreal, M. T F D
Silva, M. T P [UNESP]
Pesarini, J. R. [UNESP]
Mantovani, M. S.
Ribeiro, L. R. [UNESP]
Dichi, J. B.
Carreira, C. M.
Oliveira, R. J.
author2_role author
author
author
author
author
author
author
author
dc.contributor.none.fl_str_mv Centro Universitário Filadélfia
Universidade Estadual Paulista (Unesp)
Universidade Federal de Mato Grosso do Sul (UFMS)
Universidade Estadual de Londrina (UEL)
dc.contributor.author.fl_str_mv Mauro, M. O. [UNESP]
Monreal, M. T F D
Silva, M. T P [UNESP]
Pesarini, J. R. [UNESP]
Mantovani, M. S.
Ribeiro, L. R. [UNESP]
Dichi, J. B.
Carreira, C. M.
Oliveira, R. J.
dc.subject.por.fl_str_mv Chemoprevention
Fiber
Inulin
1,2 dimethylhydrazine
DNA
inulin
aberrant crypt focus assay
analytic method
animal cell
animal experiment
antigenotoxic activity
antimutagenic activity
antineoplastic activity
body weight
comet assay
concentration response
DNA damage
drug activity
drug determination
in vivo study
male
micronucleus test
mouse
nonhuman
topic Chemoprevention
Fiber
Inulin
1,2 dimethylhydrazine
DNA
inulin
aberrant crypt focus assay
analytic method
animal cell
animal experiment
antigenotoxic activity
antimutagenic activity
antineoplastic activity
body weight
comet assay
concentration response
DNA damage
drug activity
drug determination
in vivo study
male
micronucleus test
mouse
nonhuman
description The incidence of colorectal cancer is growing worldwide. The characterization of compounds present in the human diet that can prevent the occurrence of colorectal tumors is vital. The oligosaccharide inulin is such a compound. The aim of this study was to evaluate the antigenotoxic, antimutagenic and anticarcinogenic effects of inulin in vivo. Our study is based on 3 assays that are widely used to evaluate chemoprevention (comet assay, micronucleus assay, and aberrant crypt focus assay) and tests 4 protocols of treatment with inulin (pre-treatment, simultaneous, post-treatment, and pre + continuous). Experiments were carried out in Swiss male mice of reproductive age. In order to induce DNA damage, we used the pro-carcinogenic agent 1,2-dimethylhydrazine. Inulin was administered orally at a concentration of 50 mg/kg body weight following the protocols mentioned above. Inulin was not administered to the control groups. Our data from the micronucleus assay reveal antimutagenic effects of inulin in all protocols. The percentage of inulin-induced damage reduction ranged from 47.25 to 141.75% across protocols. These data suggest that inulin could act through desmutagenic and bio-antimutagenic mechanisms. The anticarcinogenic activity (aberrant crypt focus assay) of inulin was observed in all protocols and the percentages of damage reduction ranged from 55.78 to 87.56% across protocols. Further tests, including human trials, will be necessary before this functional food can be proven to be effective in the prevention and treatment of colon cancer. © FUNPEC-RP.
publishDate 2013
dc.date.none.fl_str_mv 2013-07-08
2014-05-27T11:29:55Z
2014-05-27T11:29:55Z
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/10.4238/2013.July.8.9
Genetics and Molecular Research, v. 12, n. 3, p. 2281-2293, 2013.
1676-5680
http://hdl.handle.net/11449/75931
10.4238/2013.July.8.9
WOS:000331717400012
2-s2.0-84880127116
2-s2.0-84880127116.pdf
url http://dx.doi.org/10.4238/2013.July.8.9
http://hdl.handle.net/11449/75931
identifier_str_mv Genetics and Molecular Research, v. 12, n. 3, p. 2281-2293, 2013.
1676-5680
10.4238/2013.July.8.9
WOS:000331717400012
2-s2.0-84880127116
2-s2.0-84880127116.pdf
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Genetics and Molecular Research
0,439
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 2281-2293
application/pdf
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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