dc.contributorMedeiros, Aldo da Cunha
dc.contributor
dc.contributor
dc.contributorCavalcanti Júnior, Geraldo Barroso
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dc.contributorFerreira, Lidiane Maria de Brito Macedo
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dc.contributorRego, Amália Cinthia Meneses do
dc.contributor
dc.contributorAzevedo, Eduardo Pereira de
dc.contributor
dc.creatorRocha, Keyla Borges Ferreira
dc.date.accessioned2020-03-20T17:56:47Z
dc.date.accessioned2022-10-05T23:10:14Z
dc.date.available2020-03-20T17:56:47Z
dc.date.available2022-10-05T23:10:14Z
dc.date.created2020-03-20T17:56:47Z
dc.date.issued2019-11-20
dc.identifierROCHA, Keyla Borges Ferreira. Efeito protetor do extrato de Arrabidaea chica contra o câncer de mama quimicamente induzido em modelo animal. 2019. 63f. Tese (Doutorado em Ciências da Saúde) - Centro de Ciências da Saúde, Universidade Federal do Rio Grande do Norte, Natal, 2019.
dc.identifierhttps://repositorio.ufrn.br/jspui/handle/123456789/28605
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/3948488
dc.description.abstractObjective: the aim of this study was to examine the effects of Arrabidaea chica (crajiru) extract, native plant of the Amazon, on a 7,12-dimethyl-benzanthracene (DMBA)-induced breast carcinoma model in Wistar rats. Methods: We compared the response of mammary carcinoma to the oral injected A. chica extract (ACE) for 16 weeks, associated or not with vincristine. Experimental design: normal control; DMBA group without treatment; DMBA+ACE (300 mg/kg) treatment; DMBA+vincristine. 500µg/kg injected i.p; DMBA+ACE+Vincristine 250µg/kg. Imaging using microPET and fluorescence, biochemistry, oxidative stress, hematology and histopathology were used to validate the treatments. Results: all animals survived. There was a gradual weight gain in all groups for 16 weeks, with no significant difference between them (p>0.05). The oral injection of ACE and ACE+vincristine 50% significantly reduced the incidence of breast tumors examined with PET-18FDG and fluorescence (p<0.001). Significant reduction of serum transaminases, oxidative stress and hematological toxicity were observed in these groups. Antioxidant enzyme levels in breast tissue were significantly higher compared to the DMBA and DMBA+vincristine groups. Conclusion: These results demonstrate that ACE positively influences the treatment of DMBA-induced breast cancer in animal model, suppressing abnormal cell proliferation and inducing a reduction in oxidative stress and chemotherapy toxicity. ACE may have clinical implication and be developed as a drug to reduce mortality and mitigate the toxicity of chemotherapy for breast cancer.
dc.publisherBrasil
dc.publisherUFRN
dc.publisherPROGRAMA DE PÓS-GRADUAÇÃO EM CIÊNCIAS DA SAÚDE
dc.rightsAcesso Aberto
dc.subjectCâncer de mama
dc.subject7,12-dimetil-benzantraceno
dc.subjectArrabidaea chica
dc.subjectVincristina
dc.subjectModelo animal
dc.titleEfeito protetor do extrato de Arrabidaea chica contra o câncer de mama quimicamente induzido em modelo animal
dc.typedoctoralThesis


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