Name: ANDREIA GOMES FREITAS FRIQUES

Publication date: 25/10/2019
Advisor:

Namesort descending Role
ELISARDO CORRAL VASQUEZ Advisor *

Examining board:

Namesort descending Role
DALTON VALENTIM VASSALLO Internal Examiner *
ELISARDO CORRAL VASQUEZ Advisor *
LUIZ CARLOS SCHENBERG Internal Examiner *

Summary: Although the harmful effects of Bisphenol A (BPA) contamination in infancy has been demonstrated, the mechanisms of action of cardiovascular outcomes still is scant. Here, we demonstrate the effects of BPA in infancy and the protective action of kefir.
Methods: Animals (25 days old) were treated with BPA (100 μg/Kg/day) for 60 days (BPA group), or administered with kefir (0.3 mL/100 g) in addition to BPA (BPA kefir group), compared with non-treated rats (Control group).The vascular endothelial function was evaluated in aortic rings through the relaxation response to acetylcholine (ACh) and specific blockers. The balance between reactive oxygen species (ROS) and nitric oxide (NO) synthase was assessed through flow cytometry in the vascular tissue.
Results: The BPA group developed high blood pressure (+10%) and the analysis of vascular reactivity showed an impaired ACh-induced relaxation (~80%). The further analysis by using NADPH, NOS and COX blockers revealed that the impaired vasorelaxation was due to increased ROS production (+12%), NO bioavailability (-12%) and increased vasoconstriction to prostanoids (+36%) compared with the Control group. Kefir treatment reverted those effects significantly. Analysis of the aortic cells showed increased •O2- production (1942±39 a.u.) and decreased NO bioavailability (1250±30 a.u.) compared with the Control group (1374±146 and 2777±25 a.u., P<.05) and kefir reverted these values (1298±57 and 2517±57 a.u.).
Conclusion: Contamination by BPA in this model caused hypertension and endothelial dysfunction and it was accompanied by a vascular ROS/NO imbalance, damage of endothelial layer and pro-apoptotic effects. The novelty is that the treatment using probiotic kefir was able to attenuate the progression of the above BPA effects.

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