Affiliation:
1. Laboratorio de Biotecnologia Aplicada S. de R.L. de C.V., GRECA Inc., Carretera La Piedad-Carapan km 3.5, La Piedad, Michoacan, Mexico
2. Departamento de Biologia, Faculdade de Ciencias, Universidade do Porto, Rua do Campo Alegre, 4169-007 Porto, Portugal
Abstract
Background:
Oxygen is involved in a variety of physiological reactions in aerobic organisms, such as
those produced in the electron transport chain, hydroxylation, and oxygenation. Reactive oxygen species (ROS)
are naturally formed as byproducts from these previously reactions involving the O2 molecule; they are made up
of superoxide anion (O2−), hydroxyl radical (HO−), hydrogen peroxide (H2O2), nitric oxide (NO), peroxyl
(ROO−), and reactive aldehyde (ROCH). Under certain environmental stress conditions, ROS are accumulated
causing cellular damage but also triggering the overexpression of several enzyme classes such as superoxide
dismutases (SOD), catalases (CAT) and glutathione peroxidases (GPx), which represent an important intrinsic
antioxidant defence line. Liver is a key organ in vertebrates including farm animals and human. The oxidative
stress plays an important role in systemic malfunctions including hepatic, renal and immunological, disorders.
Methods:
This review presents a brief update about the relationship of oxidative stress with hepatic, renal and
immunological malfunctions in stressed organisms. Cellular and exogenous hepatoprotective compounds share
also the ability to scavenge ROS acting as antioxidants and in many cases as stimulators of immune response in
stressed organisms. We present the effect of some hepatoprotectors on the hepatic, renal and immunological function
in stressed mice by the jointed evaluation of biological and oxidative stress markers.
Conclusion:
Hepatoprotective effect of several exogenous compounds is very associated with their antioxidant
capacity. This fact is relevant for keeping oxidant/antioxidant balance in the respective organs, but also for maintaining
the physiological status of the whole organism.
Publisher
Bentham Science Publishers Ltd.
Subject
Drug Discovery,Pharmacology
Cited by
12 articles.
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