Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA)
dc.contributor.author | Arroyo-Acevedo, Jorge Luis | |
dc.contributor.author | Herrera-Calderon, Oscar | |
dc.contributor.author | Tinco-Jayo, Johnny Aldo | |
dc.contributor.author | Rojas-Armas, Juan Pedro | |
dc.contributor.author | Rauf, Abdur | |
dc.contributor.author | Hañari-Quispe, Renán | |
dc.contributor.author | Figueroa-Salvador, Linder | |
dc.contributor.author | Fernández-Guzmán, Victor | |
dc.contributor.author | Yuli-Posadas, Ricardo Ángel | |
dc.date.accessioned | 2023-01-23T02:17:23Z | |
dc.date.available | 2023-01-23T02:17:23Z | |
dc.date.issued | 2020-05-07 | |
dc.description.abstract | 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. | en_EN |
dc.format | application/pdf | |
dc.identifier.citation | Arroyo-Acevedo, J. L., Herrera-Calderon, O., Tinco-Jayo, J. A., Rojas-Armas, J. P., Rauf, A., Hañari-Quispe, R., Figueroa-Salvador, L., Fernández-Guzmán, V., & Yuli-Posadas, R. A. (2020). Ameliorative Effect of the Oral Administration of Chuquiraga spinosa in a Murine Model of Breast Cancer Induced with 7,12-Dimethylbenz[a]anthracene (DMBA). Pharmacognosy Journal, 12(3), 562-568. https://doi.org/10.5530/pj.2020.12.85 | |
dc.identifier.doi | https://doi.org/10.5530/pj.2020.12.85 | |
dc.identifier.uri | https://hdl.handle.net/20.500.12640/3301 | |
dc.language | Inglés | |
dc.language.iso | eng | |
dc.publisher | Pharmacognosy Journal | |
dc.publisher.country | IN | |
dc.relation.ispartof | urn:issn:0975-3575 | |
dc.relation.uri | https://www.phcogj.com/sites/default/files/PharmacognJ-12-3-562.pdf | |
dc.rights | info:eu-repo/semantics/openAccess | * |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 International | en |
dc.rights.uri | https://creativecommons.org/licenses/by-nc-nd/4.0/ | |
dc.subject | Breast tumor | en_EN |
dc.subject | Preventive medicine | en_EN |
dc.subject | Phytochemical | en_EN |
dc.subject | Tumor de mama | es_ES |
dc.subject | Medicina preventiva | es_ES |
dc.subject | Antioxidant | en_EN |
dc.subject | Fitoquímico | es_ES |
dc.subject | Toxicity | en_EN |
dc.subject | Antioxidante | es_ES |
dc.subject | Toxicidad | es_ES |
dc.subject | Anticarcinogenic agent | en_EN |
dc.subject | Agente anticancerígeno | es_ES |
dc.subject.ocde | https://purl.org/pe-repo/ocde/ford#3.01.05 | |
dc.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) | en_EN |
dc.type | info:eu-repo/semantics/article | |
dc.type.other | Artículo | |
dc.type.version | info:eu-repo/semantics/publishedVersion | |
local.author.orcid | https://orcid.org/0000-0003-3271-2523 | |
oaire.citation.endPage | 568 | |
oaire.citation.issue | 3 | |
oaire.citation.startPage | 562 | |
oaire.citation.title | Pharmacognosy Journal | |
oaire.citation.volume | 12 |
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