Effect of Deferoxamine and Allopurinol on Non-protein-bound Iron Concentrations in Plasma and Cortical Brain Tissue of Newborn Lambs Following Hypoxia-ischemia
Overview
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Reduction of non-protein-bound iron (NPBI) using iron chelators may attenuate hypoxia-ischemia-induced reperfusion injury of the brain. This study investigated whether administration of low-dose deferoxamine and allopurinol, both having NPBI-chelating properties, reduced hypoxia-ischemia-induced NPBI formation in plasma effluent from the brain and in cerebral cortical tissue. Twenty-one newborn lambs underwent severe hypoxia-ischemia. Upon reperfusion and reoxygenation the lambs received either a placebo (n = 7), or deferoxamine 2.5 mg/kg (n = 7) or allopurinol 20 mg/kg (n = 7). The post-hypoxic-ischemic NPBI levels in plasma were significantly lower after deferoxamine but not after allopurinol as compared to placebo-treated lambs. Cortical NPBI levels in both deferoxamine and allopurinol-treated lambs were significantly lower than NPBI levels in placebo-treated lambs. We conclude that deferoxamine effectively lowers NPBI in plasma effluent from the brain, and that both, deferoxamine and allopurinol, lower NPBI in cortical brain tissue.
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Zhang M, Liu Q, Meng H, Duan H, Liu X, Wu J Signal Transduct Target Ther. 2024; 9(1):12.
PMID: 38185705 PMC: 10772178. DOI: 10.1038/s41392-023-01688-x.
Brain Iron Metabolism, Redox Balance and Neurological Diseases.
Gao G, You L, Zhang J, Chang Y, Yu P Antioxidants (Basel). 2023; 12(6).
PMID: 37372019 PMC: 10294882. DOI: 10.3390/antiox12061289.
Chen W, Wu P, Yu F, Luo G, Qing L, Tang J Cells. 2022; 11(22).
PMID: 36428981 PMC: 9688488. DOI: 10.3390/cells11223552.
Ferroptosis: A Promising Therapeutic Target for Neonatal Hypoxic-Ischemic Brain Injury.
Peeples E, Genaro-Mattos T Int J Mol Sci. 2022; 23(13).
PMID: 35806425 PMC: 9267109. DOI: 10.3390/ijms23137420.
Stegeman R, Nijman M, Breur J, Groenendaal F, Haas F, Derks J Trials. 2022; 23(1):174.
PMID: 35197082 PMC: 8867620. DOI: 10.1186/s13063-022-06098-y.