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Measurement of Redox Biomarkers in the Whole Blood and Red Blood Cell Lysates of Dogs

Authors :
Luis G. González-Arostegui
Alberto Muñoz-Prieto
Asta Tvarijonaviciute
José Joaquín Cerón
Camila Peres Rubio
Source :
Antioxidants, Vol 11, Iss 2, p 424 (2022)
Publication Year :
2022
Publisher :
MDPI AG, 2022.

Abstract

The evaluation of the biomarkers of oxidative status is usually performed in serum, however, other samples, such as red blood cells (RBCs) lysates or whole blood (WB), can be used. The objective of this study was to evaluate if a comprehensive panel of redox biomarkers can be measured in the WB and RBCs of dogs, and their possible changes “in vitro” after the addition of different concentrations of ascorbic acid. The panel was integrated by biomarkers of the antioxidant status, such as cupric reducing antioxidant capacity (CUPRAC), ferric reducing ability of plasma (FRAP), Trolox equivalent antioxidant capacity (TEAC), thiol and paraoxonase type 1 (PON-1), and of the oxidant status, such as total oxidant status (TOS), peroxide-activity (POX-Act), reactive oxygen-derived compounds (d-ROMs), advanced oxidation protein products (AOPP) and thiobarbituric acid reactive substances (TBARS). All the assays were precise and accurate in WB and RBCs lysates. In addition, they showed changes after ascorbic acid addition that are in line with previously published results, being WB more sensitive to detect these changes in our experimental conditions. In conclusion, the panel of assays used in this study can be measured in the WB and RBCs of the dog. In particular, the higher sensitivity to detect changes in our experimental conditions and its easier sample preparation makes WB a promising sample for the evaluation of redox status in dogs, with also potential applications to other animal species and humans.

Details

Language :
English
ISSN :
20763921
Volume :
11
Issue :
2
Database :
Directory of Open Access Journals
Journal :
Antioxidants
Publication Type :
Academic Journal
Accession number :
edsdoj.58b15f46c19542bda94d370413aa0c80
Document Type :
article
Full Text :
https://doi.org/10.3390/antiox11020424