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.
The present study aimed to determine whether the leaves of Turnera ulmifolia Linn. var. elegans extract exert significant antioxidant activity. The antioxidant activity of its hydroethanolic extract (HEETU) was evaluated by assessing (a) its radical scavenging ability in vitro, and (b) its in vivo effect on lipid peroxidation and antioxidant enzyme activities. The in vitro antioxidant assay (DPPH) clearly supported HEETU free radical scavenging potential. Moreover, glutathione content and antioxidant enzyme activities (glutathione peroxidase, superoxide dismutase and catalase) were significantly enhanced in CCl(4)-treated rats due to oral HEETU-treatment (500 mg/kgb.w.) over 7 and 21 days. In addition, an improvement was observed in lipid peroxidation and serum biochemical parameters (aspartate aminotransferase and alanine aminotransferase), indicating a protective effect against CCl(4)-induced liver injuries, confirmed by histopathological studies. The HEETU effect was comparable to the standard drug Legalon® (50 mg/kgb.w.) under the same experimental condition. Quantitative analysis of the HPLC extract revealed the presence of flavonoids, wich mediate the effects of antioxidant and oxidative stress. In conclusion, extract components exhibit antioxidant and hepatoprotective activities in vitro and in vivo.
1
1-Experimental SurgeryActa Cir Bras. 2017;32(2):90-97 Abstract Purpose: To evaluate the effect of tadalafil in renal ischemia/reperfusion (I/R) injury in rats. Methods: Group I/R saline rats (n=6) were subjected to 45 minutes of left renal ischemia and treated with saline; the I/R tadalafil rats (n=6) received oral 10mg/kg tadalafil microemulsion one hour before ischemia. In both groups, 8 hours after ischemia, laboratory analysis were performed. Results: Better tissue perfusion was lower in ischemic left/kidney than in right/kidney in saline group, suggesting reduced kidney clearance. Fluorescence in left/kidneys of tadalafil treated rats was lower than in right/kidneys (difference not significant). The fluorescence signal intensity in kidneys of tadafil treated rats was higher than in saline rats. TNF-α levels were significantly lower in I/R tadalafil group rats compared to I/R saline group (154±10.3 vs 391.3±12.3), as well as IL-1β (163.4±13.2 vs 279±11.5pg/dL), and IL-6 (122.9±8.1 vs 173.7±6.3 respectively; p=0.0001). Urea, creatinine and C-reactive protein were significantly lower in tadafil treated rats then in saline group. Conclusion: Tadalafil therapy decreased the expression of circulating pro-inflammatory cytokines in a renal I/R rodent model, while improving kidney function proofs.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.