Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA)
Descripción del Articulo
Objective: To determine the ameliorative effect of the ethanolic extract of Chuquiraga spinosa (ChS) on 7,12-Dimethylbenz[a]anthracene (DMBA)-induced breast cancer in rats. Methods: 36 female Holztman rats were divided into 6 groups. I) The negative control group received physiological saline (PS)....
Autores: | , , , , , , , , |
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Formato: | artículo |
Fecha de Publicación: | 2020 |
Institución: | Universidad Peruana de Ciencias Aplicadas |
Repositorio: | UPC-Institucional |
Lenguaje: | inglés |
OAI Identifier: | oai:repositorioacademico.upc.edu.pe:10757/655585 |
Enlace del recurso: | http://hdl.handle.net/10757/655585 |
Nivel de acceso: | acceso abierto |
Materia: | Anticarcinogenic agent Antioxidant Breast tumor Phytochemical Preventive medicine Toxicity 7,12 dimethylbenz[a]anthracene Alanine aminotransferasea Alkaline phosphatase Alkaloid derivative |
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dc.title.en_US.fl_str_mv |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) |
title |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) |
spellingShingle |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) Arroyo-Acevedo, Jorge Luis Anticarcinogenic agent Antioxidant Breast tumor Phytochemical Preventive medicine Toxicity 7,12 dimethylbenz[a]anthracene Alanine aminotransferasea Alkaline phosphatase Alkaloid derivative |
title_short |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) |
title_full |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) |
title_fullStr |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) |
title_full_unstemmed |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) |
title_sort |
Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA) |
author |
Arroyo-Acevedo, Jorge Luis |
author_facet |
Arroyo-Acevedo, Jorge Luis Herrera-Calderon, Oscar Tinco-Jayo, Johnny Aldo Rojas-Armas, Juan Pedro Rauf, Abdur Hañari-Quispe, Renán Figueroa-Salvador, Linder Fernández-Guzmán, Victor Yuli-Posadas, Ricardo Ángel |
author_role |
author |
author2 |
Herrera-Calderon, Oscar Tinco-Jayo, Johnny Aldo Rojas-Armas, Juan Pedro Rauf, Abdur Hañari-Quispe, Renán Figueroa-Salvador, Linder Fernández-Guzmán, Victor Yuli-Posadas, Ricardo Ángel |
author2_role |
author author author author author author author author |
dc.contributor.author.fl_str_mv |
Arroyo-Acevedo, Jorge Luis Herrera-Calderon, Oscar Tinco-Jayo, Johnny Aldo Rojas-Armas, Juan Pedro Rauf, Abdur Hañari-Quispe, Renán Figueroa-Salvador, Linder Fernández-Guzmán, Victor Yuli-Posadas, Ricardo Ángel |
dc.subject.en_US.fl_str_mv |
Anticarcinogenic agent Antioxidant Breast tumor Phytochemical Preventive medicine Toxicity 7,12 dimethylbenz[a]anthracene Alanine aminotransferasea Alkaline phosphatase Alkaloid derivative |
topic |
Anticarcinogenic agent Antioxidant Breast tumor Phytochemical Preventive medicine Toxicity 7,12 dimethylbenz[a]anthracene Alanine aminotransferasea Alkaline phosphatase Alkaloid derivative |
description |
Objective: To determine the ameliorative effect of the ethanolic extract of Chuquiraga spinosa (ChS) on 7,12-Dimethylbenz[a]anthracene (DMBA)-induced breast cancer in rats. Methods: 36 female Holztman rats were divided into 6 groups. I) The negative control group received physiological saline (PS). II) ChS-200 group received 200 mg/kg of ChS. III) DMBA group was induced with DMBA (20 mg/Kg) dissolved in PS and administrated orally for 15 weeks. IV) DMBA + ChS-50 group, V) DMBA + ChS-250 group, and VI) DMBA + ChS-500 group, which received the extract orally for 15 weeks after DMBA induction. All data were expressed as mean and standard deviation. One-way analysis of variance (ANOVA) followed by Dunnet test was carried out to compare the mean value of different groups Histopathological analysis was evaluated by using Image J software. Results: Hematology showed that the triglyceride level was significantly lowered (P< 0.01) and high-density lipoprotein (HDL) level was significantly increased (P <0.01) in groups III, IV and V. Also, ChS extract significantly lowered the C reactive protein (CRP) level (P <0.01) and malondialdehyde level (P<0.05). There was a significant decrease in the frequency of DMBA-induced micronucleated polychromatic erythrocyte (P<0.01). Conclusions: Chuquiraga spinosa showed an ameliorative effect on DMBA-induced breast cancer in rats as well as antioxidant, antitumor and antigenotoxic properties. |
publishDate |
2020 |
dc.date.accessioned.none.fl_str_mv |
2021-04-20T15:24:00Z |
dc.date.available.none.fl_str_mv |
2021-04-20T15:24:00Z |
dc.date.issued.fl_str_mv |
2020-05-01 |
dc.type.en_US.fl_str_mv |
info:eu-repo/semantics/article |
format |
article |
dc.identifier.doi.none.fl_str_mv |
10.5530/pj.2020.12.85 |
dc.identifier.uri.none.fl_str_mv |
http://hdl.handle.net/10757/655585 |
dc.identifier.eissn.none.fl_str_mv |
09753575 |
dc.identifier.journal.en_US.fl_str_mv |
Pharmacognosy Journal |
dc.identifier.eid.none.fl_str_mv |
2-s2.0-85084698852 |
dc.identifier.scopusid.none.fl_str_mv |
SCOPUS_ID:85084698852 |
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0000 0001 2196 144X |
identifier_str_mv |
10.5530/pj.2020.12.85 09753575 Pharmacognosy Journal 2-s2.0-85084698852 SCOPUS_ID:85084698852 0000 0001 2196 144X |
url |
http://hdl.handle.net/10757/655585 |
dc.language.iso.en_US.fl_str_mv |
eng |
language |
eng |
dc.relation.url.en_US.fl_str_mv |
https://www.phcogj.com/article/1146 |
dc.rights.en_US.fl_str_mv |
info:eu-repo/semantics/openAccess |
dc.rights.*.fl_str_mv |
Attribution-NonCommercial-ShareAlike 4.0 International |
dc.rights.uri.*.fl_str_mv |
http://creativecommons.org/licenses/by-nc-sa/4.0/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/ |
dc.format.en_US.fl_str_mv |
application/pdf |
dc.publisher.en_US.fl_str_mv |
EManuscript Technologies |
dc.source.es_PE.fl_str_mv |
Universidad Peruana de Ciencias Aplicadas (UPC) Repositorio Academico - UPC |
dc.source.none.fl_str_mv |
reponame:UPC-Institucional instname:Universidad Peruana de Ciencias Aplicadas instacron:UPC |
instname_str |
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institution |
UPC |
reponame_str |
UPC-Institucional |
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UPC-Institucional |
dc.source.journaltitle.none.fl_str_mv |
Pharmacognosy Journal |
dc.source.volume.none.fl_str_mv |
12 |
dc.source.issue.none.fl_str_mv |
3 |
dc.source.beginpage.none.fl_str_mv |
562 |
dc.source.endpage.none.fl_str_mv |
568 |
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I) The negative control group received physiological saline (PS). II) ChS-200 group received 200 mg/kg of ChS. III) DMBA group was induced with DMBA (20 mg/Kg) dissolved in PS and administrated orally for 15 weeks. IV) DMBA + ChS-50 group, V) DMBA + ChS-250 group, and VI) DMBA + ChS-500 group, which received the extract orally for 15 weeks after DMBA induction. All data were expressed as mean and standard deviation. One-way analysis of variance (ANOVA) followed by Dunnet test was carried out to compare the mean value of different groups Histopathological analysis was evaluated by using Image J software. Results: Hematology showed that the triglyceride level was significantly lowered (P< 0.01) and high-density lipoprotein (HDL) level was significantly increased (P <0.01) in groups III, IV and V. Also, ChS extract significantly lowered the C reactive protein (CRP) level (P <0.01) and malondialdehyde level (P<0.05). There was a significant decrease in the frequency of DMBA-induced micronucleated polychromatic erythrocyte (P<0.01). 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Nota importante:
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La información contenida en este registro es de entera responsabilidad de la institución que gestiona el repositorio institucional donde esta contenido este documento o set de datos. El CONCYTEC no se hace responsable por los contenidos (publicaciones y/o datos) accesibles a través del Repositorio Nacional Digital de Ciencia, Tecnología e Innovación de Acceso Abierto (ALICIA).