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Antioxidant and antiapoptotic effects of darbepoetin-α against traumatic brain injury in rats.

AbstractINTRODUCTION:
In this study, we tried to determine whether darbepoetin-α would protect the brain from oxidative stress and apoptosis in a rat traumatic brain injury model.
MATERIAL AND METHODS:
The animals were randomized into four groups; group 1 (sham), group 2 (trauma), group 3 (darbepoetin α), group 4 (methylprednisolone). In the sham group only the skin incision was performed. In all the other groups, a moderate traumatic brain injury modelwas applied.
RESULTS:
Following trauma both glutathione peroxidase, superoxide dismutase levels decreased (p < 0.001 for both); darbepoetin-α increased the activity of both antioxidant enzymes (p = 0.001 and p < 0.001 respectively). Trauma caused significant elevation in the nitric oxide synthetase and xanthine oxidase levels (p < 0.001 for both). Administration of darbepoetin-α significantly decreased the levels of nitric oxide synthetase and xanthine oxidase (p < 0.001 for both). Also, trauma caused significant elevation in the nitric oxide levels (p < 0.001); darbepoetin-α administration caused statistically significant reduction in the nitric oxide levels (p < 0.001). On the other hand, malondialdehyde levels were increased following trauma (p < 0.001), and darbepoetin α significantly reduced the malondialdehyde levels (p < 0.001). Due to the elevated apoptotic activity following the injury, caspase-3 activity increased significantly. Darbepoetin-α treatment significantly inhibited apoptosis by lowering the caspase-3 activity (p < 0.001). In the darbepoetin group, histopathological score was lower than the trauma group (p = 0.016).
CONCLUSIONS:
In this study, darbepoetin-α was shown to be at least as effective as methylprednisolone in protecting brain from oxidative stress, lipid peroxidation and apoptosis.
AuthorsHayri Kertmen, Bora Gürer, Erdal Resit Yilmaz, Mehmet Ali Kanat, Ata Türker Arikok, Berrin Imge Ergüder, Askin Esen Hasturk, Julide Ergil, Zeki Sekerci
JournalArchives of medical science : AMS (Arch Med Sci) Vol. 11 Issue 5 Pg. 1119-28 (Oct 12 2015) ISSN: 1734-1922 [Print] Poland
PMID26528358 (Publication Type: Journal Article)

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