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Erschienen in: Urolithiasis 2/2004

01.05.2004 | Original Paper

The effect of dehydroepiandrosterone on renal ischemia-reperfusion-induced oxidative stress in rabbits

verfasst von: Yılmaz Aksoy, Turgut Yapanoglu, Hülya Aksoy, A. Kadir Yildirim

Erschienen in: Urolithiasis | Ausgabe 2/2004

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Abstract

Reactive oxygen species (ROS) can play an important role in the pathogenesis of ischemia-reperfusion (I/R) injury. Dehydroepiandrosterone (DHEA) is one of the hormones secreted from adrenal glands, and in some studies it has been shown that DHEA has antioxidant properties. This experimental study was designed to determine the effect of DHEA on I/R-induced oxidative stress in rabbit kidney. Twenty-one rabbits were divided into three groups. Rabbits were subjected to 60 min of left renal pedicle occlusion followed by 24 h of reperfusion. DHEA (50 mg/kg) (I/R + DHEA group) or equal volume of vehicle (I/R group) was administered 3 h prior to ischemia. The control group received only laparotomy without I/R, DHEA or vehicle. At the end of the reperfusion periods, rabbits were decapitated. Renal tissues were taken for determination of malondialdehyde (MDA) levels as an indicator of lipid peroxidation and superoxide dismutase (SOD), catalase (CAT) and glutathione peroxidase (GPX) activities as antioxidant enzymes. In the I/R group, while renal SOD and CAT activities were significantly lower, MDA levels were significantly higher than in the I/R + DHEA group and controls. In the I/R + DHEA group, enzyme activities and MDA levels were similar to the controls. There was no significant difference in terms of renal GPX activity among the groups. DHEA may have a beneficial effect on renal tissue against oxidative damage due to I/R by preventing decreases in some antioxidant enzyme activities.
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Metadaten
Titel
The effect of dehydroepiandrosterone on renal ischemia-reperfusion-induced oxidative stress in rabbits
verfasst von
Yılmaz Aksoy
Turgut Yapanoglu
Hülya Aksoy
A. Kadir Yildirim
Publikationsdatum
01.05.2004
Verlag
Springer-Verlag
Erschienen in
Urolithiasis / Ausgabe 2/2004
Print ISSN: 2194-7228
Elektronische ISSN: 2194-7236
DOI
https://doi.org/10.1007/s00240-003-0382-6

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