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

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 group...

Full description

Bibliographic Details
Main Authors: Álvarez-González, Isela, Garcia-Melo, Fernando, Vásquez-Garzón, Verónica R., Villa-Treviño, Saúl, Madrigal-Santillán, E. Osiris, Morales-González, José A., Mendoza-Pérez, Jorge A., Madrigal-Bujaidar, Eduardo
Format: Online
Language:English
Published: Hindawi Publishing Corporation 2014
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166644/
id pubmed-4166644
recordtype oai_dc
spelling pubmed-41666442014-09-25 Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage Álvarez-González, Isela Garcia-Melo, Fernando Vásquez-Garzón, Verónica R. Villa-Treviño, Saúl Madrigal-Santillán, E. Osiris Morales-González, José A. Mendoza-Pérez, Jorge A. Madrigal-Bujaidar, Eduardo Research Article 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 an ex vivo DPPH 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. Hindawi Publishing Corporation 2014 2014-09-03 /pmc/articles/PMC4166644/ /pubmed/25258642 http://dx.doi.org/10.1155/2014/379890 Text en Copyright © 2014 Isela Álvarez-González et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Álvarez-González, Isela
Garcia-Melo, Fernando
Vásquez-Garzón, Verónica R.
Villa-Treviño, Saúl
Madrigal-Santillán, E. Osiris
Morales-González, José A.
Mendoza-Pérez, Jorge A.
Madrigal-Bujaidar, Eduardo
spellingShingle Álvarez-González, Isela
Garcia-Melo, Fernando
Vásquez-Garzón, Verónica R.
Villa-Treviño, Saúl
Madrigal-Santillán, E. Osiris
Morales-González, José A.
Mendoza-Pérez, Jorge A.
Madrigal-Bujaidar, Eduardo
Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage
author_facet Álvarez-González, Isela
Garcia-Melo, Fernando
Vásquez-Garzón, Verónica R.
Villa-Treviño, Saúl
Madrigal-Santillán, E. Osiris
Morales-González, José A.
Mendoza-Pérez, Jorge A.
Madrigal-Bujaidar, Eduardo
author_sort Álvarez-González, Isela
title Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage
title_short Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage
title_full Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage
title_fullStr Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage
title_full_unstemmed Evaluation of Blueberry Juice in Mouse Azoxymethane-Induced Aberrant Crypts and Oxidative Damage
title_sort evaluation of blueberry juice in mouse azoxymethane-induced aberrant crypts and oxidative damage
description 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 an ex vivo DPPH 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 Publishing Corporation
publishDate 2014
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166644/
_version_ 1613134723269263360