Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA)

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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)....

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Detalles Bibliográficos
Autores: 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
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
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dc.language.iso.en_US.fl_str_mv eng
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dc.source.es_PE.fl_str_mv Universidad Peruana de Ciencias Aplicadas (UPC)
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dc.source.volume.none.fl_str_mv 12
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dc.source.beginpage.none.fl_str_mv 562
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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). 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