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: | , , , , , , , , | 
|---|---|
| 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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                  2-s2.0-85084698852 | 
    
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                  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 | 
    
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                  http://creativecommons.org/licenses/by-nc-sa/4.0/ | 
    
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                  openAccess | 
    
| rights_invalid_str_mv | 
                  Attribution-NonCommercial-ShareAlike 4.0 International http://creativecommons.org/licenses/by-nc-sa/4.0/  | 
    
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                  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  | 
    
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                  reponame:UPC-Institucional instname:Universidad Peruana de Ciencias Aplicadas instacron:UPC  | 
    
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                  Universidad Peruana de Ciencias Aplicadas | 
    
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| 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).