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Submitted on March 13, 2007
From the Departments of Neurosurgery (S.S., Y.H., R.F.K., J.T.H., G.X.), and Physiology (R.F.K.), University of Michigan, Ann Arbor. * To whom correspondence should be addressed. E-mail: guohuaxi{at}umich.edu.
Background and Purpose—There is an urgent need to develop a model in which to study the mechanism of intracerebral hemorrhage-induced neuronal death in vivo. Methods—This study was divided into 2 parts: (1) Rats received either an infusion of hemoglobin, ferrous iron, or saline into the right hippocampus; (2) Rats had an infusion of hemoglobin and then were treated with either deferoxamine or vehicle. Rats were killed for hippocampus size, DNA damage, and neuronal death measurements. Results—Compared with saline, hemoglobin or iron injection caused hippocampal neuronal death. Systemic use of deferoxamine reduced hemoglobin-induced DNA damage, hippocampal neuronal death, and atrophy. Conclusions—This article demonstrates a new model and indicates that iron has a key role in hemoglobin–induced neuronal death.
Accepted on April 10, 2007
A New Hippocampal Model for Examining Intracerebral Hemorrhage-Related Neuronal Death. Effects of Deferoxamine on Hemoglobin-Induced Neuronal Death
Shuijiang Song MD;
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