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   <subfield code="a">Deferoxamine Reduces Neuronal Death and Hematoma Lysis After Intracerebral Hemorrhage in Aged Rats</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Tetsuhiro Hatakeyama, Masanobu Okauchi, Ya Hua, Richard Keep, Guohua Xi]</subfield>
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   <subfield code="a">Intracerebral hemorrhage (ICH) is primarily a disease of the elderly. Deferoxamine (DFX), an iron chelator, reduces long-term neurological deficits and brain atrophy after ICH in aged rats. In the present study, we investigated whether DFX can reduce acute ICH-induced neuronal death and whether it affects the endogenous response to ICH (ferritin upregulation and hematoma resolution) in aged rats. Male Fischer 344 rats (18months old) had an intracaudate injection of 100μL autologous whole blood into the right basal ganglia and were treated with DFX (100mg/kg) or vehicle 2h post-ICH and then every 12h up to 7days. Rats were euthanized 1, 3, or 7days later for neuronal death and ferritin and hematoma size measurements. Plasma ferritin levels and behavioral outcome following ICH were also examined. DFX treatment significantly reduced ICH-induced neuronal death and neurological deficits. DFX also suppressed ferritin upregulation in the ipsilateral basal ganglia after ICH and hematoma lysis (hematoma volume at day7, 13.2 ± 4.9 vs. 3.8 ± 1.2mm3 in vehicle-treated group, p &lt; 0.01). However, effects of DFX on plasma ferritin levels after ICH did not reach significance. In conclusion, DFX reduces neuronal death and neurological deficits after ICH in aged rats. It also affects the endogenous response to ICH.</subfield>
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