Deferoxamine Treatment for Intracerebral Hemorrhage in Aged Rats Therapeutic Time Window and Optimal Duration

被引:103
作者
Okauchi, Masanobu
Keep, Richard F. [2 ]
Morgenstern, Lewis B. [2 ]
Schallert, Timothy [3 ]
Xi, Guohua [1 ,2 ]
机构
[1] Univ Michigan, Dept Neurosurg, BSRB, Ann Arbor, MI 48109 USA
[2] Univ Michigan, Stroke Program, Ann Arbor, MI 48109 USA
[3] Univ Texas Austin, Dept Psychol, Austin, TX 78712 USA
基金
美国国家卫生研究院;
关键词
behavior; brain atrophy; brain edema; cerebral hemorrhage; deferoxamine; iron; BRAIN EDEMA; NEURONAL DEATH; IRON; HEMATOMA; INJURY; MODEL;
D O I
10.1161/STROKEAHA.109.569830
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background and Purpose-Deferoxamine (DFX) reduces brain edema, neurological deficits, and brain atrophy after intracerebral hemorrhage (ICH) in aged and young rats. Our previous study found that 50 mg/kg is an effective dose in aged rats. In the present study, we explored potential therapeutic time windows and optimal therapeutic durations. Methods-Aged male Fischer 344 rats (18 months old) sustained an intracaudate injection of 100 mu L autologous whole blood, followed by intramuscular DFX or vehicle beginning at different time points, or continuing for different durations. Subgroups of rats were euthanized at day 3 for brain edema measurement and day 56 for brain atrophy determination. Behavioral tests were performed on days 1, 28, and 56 after ICH. Results-Systemic administration of DFX, when begun within 12 hours after ICH, reduced brain edema. DFX treatment started 2 hours after ICH and administered for >= 7 days attenuated ICH-induced ventricle enlargement, caudate atrophy, and neurological deficits. DFX attenuated ICH-induced brain atrophy and neurological deficits without detectable side effects when begun within 24 hours and administered for 7 days. Conclusions-To the extent that these results can be translated to humans, the therapeutic time window and the optimal duration for DFX in this aged rat model of ICH may provide useful information for an ongoing DFX-ICH clinical trial. (Stroke. 2010; 41: 375-382.)
引用
收藏
页码:375 / 382
页数:8
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