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Bisphenol A contamination in infant rats: molecular, structural, and physiological cardiovascular changes and the protective role of kefir.
Friques, Andreia G F; Santos, Fernanda D N; Angeli, Daiany B; Silva, Fernanda Aldrigues Crispim; Dias, Ananda T; Aires, Rafaela; Leal, Marcos A S; Nogueira, Breno V; Amorim, Fernanda G; Campagnaro, Bianca P; Pereira, Thiago Melo C; Campos-Toimil, Manuel; Meyrelles, Silvana S; Vasquez, Elisardo C.
Afiliación
  • Friques AGF; Laboratory of Translational Physiology, Federal University of Espirito Santo (UFES), Vitoria, ES, Brazil. Electronic address: andreiafriques@hotmail.com.
  • Santos FDN; Emescam School of Health Sciences, Vitoria, ES, Brazil. Electronic address: fernanda.dornelasns@gmail.com.
  • Angeli DB; Emescam School of Health Sciences, Vitoria, ES, Brazil. Electronic address: daianyangeli2@gmail.com.
  • Silva FAC; Pharmaceutical Sciences Graduate Program, Vila Velha University (UVV), Vila Velha, ES, Brazil. Electronic address: nandaacs@hotmail.com.
  • Dias AT; Laboratory of Translational Physiology, Federal University of Espirito Santo (UFES), Vitoria, ES, Brazil. Electronic address: anandatd@yahoo.com.br.
  • Aires R; Laboratory of Translational Physiology, Federal University of Espirito Santo (UFES), Vitoria, ES, Brazil. Electronic address: rafaires2@gmail.com.
  • Leal MAS; Laboratory of Translational Physiology, Federal University of Espirito Santo (UFES), Vitoria, ES, Brazil. Electronic address: marcosleal.asl@gmail.com.
  • Nogueira BV; Laboratory of Cellular Ultrastructure, Department of Morphology, UFES, Health Sciences Center, UFES, Vitoria, ES, Brazil. Electronic address: brenovalentim@gmail.com.
  • Amorim FG; Pharmaceutical Sciences Graduate Program, Vila Velha University (UVV), Vila Velha, ES, Brazil. Electronic address: fernandagamorim@gmail.com.
  • Campagnaro BP; Pharmaceutical Sciences Graduate Program, Vila Velha University (UVV), Vila Velha, ES, Brazil. Electronic address: biancacampagnaro@yahoo.com.br.
  • Pereira TMC; Pharmaceutical Sciences Graduate Program, Vila Velha University (UVV), Vila Velha, ES, Brazil; Federal Institute of Education, Science and Technology (IFES), Vila Velha, ES, Brazil. Electronic address: pereiratmc@gmail.com.
  • Campos-Toimil M; Farmacología de las Enfermedades Crónicas (CDPHARMA), Centro de Investigación en Medicina Molecular y Enfermedades Crónicas (CIMUS), Universidade de Santiago de Compostela, Santiago de Compostela, Spain. Electronic address: manuel.campos@usc.es.
  • Meyrelles SS; Laboratory of Translational Physiology, Federal University of Espirito Santo (UFES), Vitoria, ES, Brazil. Electronic address: meyrelle.vix@terra.com.br.
  • Vasquez EC; Pharmaceutical Sciences Graduate Program, Vila Velha University (UVV), Vila Velha, ES, Brazil. Electronic address: evasquez@terra.com.br.
J Nutr Biochem ; 75: 108254, 2020 01.
Article en En | MEDLINE | ID: mdl-31707283
ABSTRACT
The effects of bisphenol A (BPA) contamination on the cardiovascular function still are not clear. Here, we evaluated the vascular effects of BPA and the protective actions of kefir in infant rats. Animals (25 days old) were treated with BPA (100 µg/Kg/day) for 60 days (BPA group), or administered 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 and specific blockers. The balance between reactive oxygen species (ROS) and nitric oxide (NO) was assessed through flow cytometry in the vascular tissue. 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.). 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 the above BPA effects.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Aorta / Fenoles / Compuestos de Bencidrilo / Especies Reactivas de Oxígeno / Kéfir / Hemodinámica Límite: Animals Idioma: En Revista: J Nutr Biochem Asunto de la revista: BIOQUIMICA / CIENCIAS DA NUTRICAO Año: 2020 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Aorta / Fenoles / Compuestos de Bencidrilo / Especies Reactivas de Oxígeno / Kéfir / Hemodinámica Límite: Animals Idioma: En Revista: J Nutr Biochem Asunto de la revista: BIOQUIMICA / CIENCIAS DA NUTRICAO Año: 2020 Tipo del documento: Article