Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage

Author:

Álvarez-González Isela1,Garcia-Melo Fernando1,Vásquez-Garzón Verónica R.2,Villa-Treviño Saúl2,Madrigal-Santillán E. Osiris3,Morales-González José A.3,Mendoza-Pérez Jorge A.4,Madrigal-Bujaidar Eduardo1

Affiliation:

1. Laboratorio de Genética, Escuela Nacional de Ciencias Biológicas, IPN, Unidad Profesional A. López Mateos, Avenida Wilfredo Massieu s/n, Zacatenco, Colonia, Lindavista, CP 07738, México, DF, Mexico

2. Departamento de Biología Celular, Centro de Investigación y Estudios Avanzados, IPN, Avenida Instituto Politécnico 2508, Colonia San Pedro Zacatenco, Del. Gustavo A. Madero, CP 06360, México, DF, Mexico

3. Laboratorio de Medicina de la Conservación, Escuela Superior de Medicina, IPN, Plan de San Luis y Díaz Mirón s/n, Casco de Santo Tomás, Del. Miguel Hidalgo, CP 11340, México, DF, Mexico

4. Laboratorio de Química Ambiental. Escuela Nacional de Ciencias Biológicas, IPN, Unidad Profesional A. López Mateos, Avenida Wilfredo Massieu s/n, Zacatenco, Colonia Lindavista, CP 07738, México, DF, Mexico

Abstract

Blueberry is a plant with a number of nutritional and biomedical capabilities. In the present study we initially evaluated the capacity of its juice (BJ) to inhibit the number of aberrant crypts (AC) induced with azoxymethane (AOM) in mouse. BJ was administered daily by the oral route to three groups of animals during four weeks (1.6, 4.1, and 15.0 μL/g), respectively, while AOM (10 mg/kg) was intraperitoneally injected to the mentioned groups, twice a week, in weeks two and three of the assay. We also included two control groups of mice, one administered distilled water and the other the high dose of BJ. A significant increase of AC was observed in the AOM treated animals, and a mean protection of 75.6% was determined with the two low doses of BJ tested; however, the high dose of the juice administered together with AOM increased the number of crypts more than four times the value observed in animals administered only AOM. Furthermore, we determined the antioxidant potential of BJ with anex vivoDPPH assay and found a dose-dependent decrease with a mean of 19.5%. We also determined the DNA oxidation/antioxidation by identifying 8-hydroxy-2′-deoxyguanosine adducts and found a mean decrease of 44.3% with the BJ administration with respect to the level induced by AOM. Our results show a complex differential effect of BJ related to the tested doses, opening the need to further evaluate a number of factors so as to determine the possibility of a cocarcinogenic potential.

Publisher

Hindawi Limited

Subject

Complementary and alternative medicine

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