Effect of Arrabidaea chica extract against chemically induced breast cancer in animal model

Acta Cir Bras. 2019 Dec 9;34(10):e201901001. doi: 10.1590/s0102-865020190100000001. eCollection 2019.

Abstract

Purpose: To examine the effects of Arrabidaa chica (Bignoniacea) extract, a native plant of the Amazon known as crajiru, on a 7,12-dimethyl-1,2-benzanthracene (DMBA)-induced breast cancer model in Wistar rats.

Methods: We compared the response of breast cancer to the oral administration of A. chica extract (ACE) for 16 weeks, associated or not with vincristine. Groups: normal control; DMBA (50mg/kg v.o,) without treatment; DMBA+ACE (300 mg/kg); DMBA+vincristine. 500μg/kg injected i.p; DMBA+ACE+Vincristine 250μg/kg i.p. Imaging by microPET and fluorescence, biochemistry, oxidative stress, hematology and histopathology were used to validate the treatments.

Results: All animals survived. A gradual weight gain in all groups was observed, with no significant difference (p>0.05). The oral administration of ACE and ACE+vincristine 50% significantly reduced breast tumors incidence 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 for the first time that ACE positively influences the treatment of DMBA-induced breast cancer in animal model, inducing a reduction in oxidative stress and chemotherapy toxicity, meaning that ACE may have clinical implication in further studies.

Publication types

  • Evaluation Study

MeSH terms

  • 9,10-Dimethyl-1,2-benzanthracene
  • Animals
  • Antineoplastic Agents / pharmacology*
  • Antineoplastic Agents / therapeutic use
  • Bignoniaceae / chemistry*
  • Breast Neoplasms / diagnostic imaging
  • Breast Neoplasms / drug therapy*
  • Breast Neoplasms / pathology
  • Carcinogens
  • Carcinoma / diagnostic imaging
  • Carcinoma / drug therapy*
  • Carcinoma / pathology
  • Catalase / analysis
  • Female
  • Fluorodeoxyglucose F18
  • Glutathione Peroxidase / analysis
  • Neoplasms, Experimental / diagnostic imaging
  • Neoplasms, Experimental / drug therapy*
  • Neoplasms, Experimental / pathology
  • Optical Imaging / methods
  • Oxidative Stress / drug effects
  • Plant Extracts / pharmacology*
  • Plant Extracts / therapeutic use
  • Positron-Emission Tomography / methods
  • Radiopharmaceuticals
  • Rats, Wistar
  • Reproducibility of Results
  • Superoxide Dismutase / analysis
  • Time Factors
  • Treatment Outcome
  • Vincristine / pharmacology
  • Vincristine / therapeutic use

Substances

  • Antineoplastic Agents
  • Carcinogens
  • Plant Extracts
  • Radiopharmaceuticals
  • Fluorodeoxyglucose F18
  • 9,10-Dimethyl-1,2-benzanthracene
  • Vincristine
  • Catalase
  • Glutathione Peroxidase
  • Superoxide Dismutase