Abstract
Oxidative stress may initiate significant hepatocyte injury in subjects with fatty liver. We characterized changes in hepatic oxidative anti-oxidative parameters in rats given a fructose-enriched diet (FED) with and without medications to reduce blood pressure or plasma triglycerides. FED rats had an increase in malondialdehyde (MDA) concentration, a reduction in α-tocopherol concentration, a reduction in paraoxonase (PON) activity, an increase in glutathione peroxidase (GSH-Px), and glutathione reductase (GSSG-R) activity. Amlodipine increased PON and GSH-Px, but decreased GSSG-R activity and α-tocopherol concentration. Captopril decreased MDA concentration and the activity of both GSH-Px and GSSG-R, but increased α-tocopherol concentration and PON activity. Bezafibrate increased α-tocopherol concentration and PON activity, but decreased the activity of GSSG-R. Animals with fatty liver exhibit an increase in peroxidative stress but also a defect in anti-oxidative pathways. Drugs administered to treat hypertension and hypertriglyceridemia could lead to a variety of changes in the hepatic oxidative, anti-oxidative milieu.
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Abbreviations
- α-SMA:
-
α-Smooth muscle
- FED:
-
Fructose-enriched diet
- GSH-Px:
-
Glutathione peroxidase
- GSSG-R:
-
Glutathione reductase
- HIC:
-
Hepatic iron concentration
- HSC:
-
Hepatic stellate cell
- MDA:
-
Malondialdehyde
- NAFLD:
-
Non-alcoholic fatty liver disease
- NASH:
-
Non-alcoholic steatohepatitis
- PON:
-
Paraoxonase
- ROS:
-
Reactive oxygen species
- SRCD:
-
Standard rat chow diet
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Ackerman, Z., Oron-Herman, M., Rosenthal, T. et al. Effects of Amlodipine, Captopril, and Bezafibrate on Oxidative Milieu in Rats with Fatty Liver. Dig Dis Sci 53, 777–784 (2008). https://doi.org/10.1007/s10620-007-9911-4
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DOI: https://doi.org/10.1007/s10620-007-9911-4