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Different administration schedules of darbepoetin alfa affect oxidized and reduced glutathione levels to a similar extent in 5/6 nephrectomized rats
Authors:Péter Monostori  Gabriella F. Kocsis  Zsuzsanna Ökrös  Péter Bencsik  Orsolya Czétényi  Zoltán Kiss  Balázs Gellén  Csaba Bereczki  Imre Ocsovszki  Judit Pipis  János Pálóczi  Márta Sárközy  Szilvia Török  Ilona S. Varga  István Kiss  Eszter Fodor  Tamás Csont  Péter Ferdinandy  Sándor Túri
Affiliation:1. Department of Pediatrics, Albert Szent-Gy?rgyi Clinical Center, University of Szeged, Korányi fasor 14-15, Szeged, 6720, Hungary
2. Cardiovascular Research Group, Department of Biochemistry, University of Szeged, Dóm tér 9, Szeged, 6720, Hungary
3. Pharma Hungary Group, Dóm tér 9, Szeged, Szeged, 6720, Hungary
4. Department of Biochemistry and Molecular Biology, University of Szeged, K?zép fasor 52, Szeged, 6726, Hungary
5. Department of Nephrology-Hypertension, St Imre Teaching Hospital, Tétényi út 12-16, Budapest, 1115, Hungary
Abstract:

Background

The development of erythropoiesis-stimulating agents (ESAs) with extended serum half-lives has allowed marked prolongation of the administration intervals. The level of oxidative stress is increased in chronic kidney disease, and is reportedly decreased after long-term ESA treatment. However, the effect of different dosing regimens of ESAs on oxidative stress has not been elucidated.

Methods

Five-sixths nephrectomized (NX) rats received either 0.4 μg/kg darbepoetin alfa (DA) weekly or 0.8 μg/kg DA fortnightly between weeks 4 and 10. NX animals receiving saline and a sham-operated (SHAM) group served as controls. The levels of oxidized and reduced glutathione (GSSG, GSH) were followed from blood samples drawn fortnightly.

Results

During the follow-up, the ratios GSSG/GSH showed similar trends in both DA groups, levels being significantly lower than those in the SHAM group at weeks 8 and 10. GSSG levels were lower than the baseline throughout the study in all groups except for NX controls. The GSH levels were increased in all three NX groups (weeks 6–10) compared with both the baseline and the SHAM group

Conclusion

Our results suggest that the extent of oxidative stress is similar in response to different dosing regimens of DA in 5/6 NX rats when comparable hemoglobin levels are maintained. These findings remain to be confirmed in chronic kidney disease patients.
Keywords:
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