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Effects of Amlodipine, Captopril, and Bezafibrate on Oxidative Milieu in Rats with Fatty Liver

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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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