Alterations in oxidative metabolism in liver of female rats: Effects of long-term vitamin A deficiency

Orozco Reina Agustina, Agüero Rocio, Razzeto Gabriela, Gimenez Maria Sofia and Vasquez Gomez Miriam Ester *

Department of Biochemistry and Biological Sciences, School of Chemistry, Biochemistry and Pharmacy, National University of San Luis, San Luis, Argentina.
 
Research Article
GSC Biological and Pharmaceutical Sciences, 2020, 13(01), 267-278.
Article DOI: 10.30574/gscbps.2020.13.1.0064
Publication history: 
Received on 12 March 2020; revised on 15 October 2020; accepted on 20 October 2020
 
Abstract: 
Background: The latest estimate by 5 UN agencies is that 821 million people globally are undernourished, which puts them at risk of vitamin and other nutrient deficiencies. Vitamin A deficiency remains a widespread public health problem among women and children in the developing world the role of vitamin A and its active metabolites in pathways involved in antioxidant protection and in the inhibition of important pathways that promote oxidative stress.
Objectives: Determine if vitamin A deficiency could influence oxidative metabolism in 6-month-old female wistar rats.
Materials and Methods: Determine the concentration of carbonyl proteins, as a marker of protein oxidation; TBARS, as a lipoperoxidation marker; and nitrotyrosine as a marker of oxidative stress dependent on nitric oxide. Quantify the expression of CAT, SOD, eNOS and iNOS in the liver and wistar rats deficient in vitamin A for 6 months.
Results:  An increase in the concentration of carbonyl protein and nitrotyrosine in the liver tissue deficient in vitamin A is observed. The expression of SOD, eNOS and iNOS decreased in the group with a private diet of vitamin A. From the regression analysis a positive correlation was established between hepatic retinoic acid levels and gene expression of eNOS, iNOS and SOD. A positive correlation between serum retinoic acid levels and gene expression of eNOS and iNOS was also observed.
Conclusions: It is possible to ratify the relationship between the development of stress and vitamin A levels; improving the understanding of hepatic metabolism and its response to the absence of this vitamin.
 
Keywords: 
Lipoperoxidation; Nitrotyrosine; Catalase; Superoxide dismutase; Nitric oxide synthetase
 
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