Hemorrhage is the primary event in approximately 15% of strokes, and accompanies most significant brain trauma. A growing body of experimental evidence suggests that hemoglobin release from lysing erythrocytes may contribute to oxidative injury to tissue surrounding a hematoma. Prior studies have demonstrated that hemoglobin toxicity is mediated by transfer of its heme moieties to nearby cells, which is facilitated by its spontaneous oxidation to methemoglobin. Hemin, the oxidized form of heme, is then catabolized by the heme oxygenase enzymes to iron, carbon monoxide, and biliverdin. The cytoprotective effects of the latter two products may be overwhelmed if iron sequestration is inadequate. Astrocytes respond to hemoglobin exposure by rapidly inducing ferritin, a 24-mer heteropolymer with a capacity for over 4000 iron atoms in its mineral core. However, cortical neurons in cell culture and in vivo express very little ferritin after hemoglobin treatment. Cell ferritin levels are primarily regulated by iron regulatory proteins (IRP1 and IRP2), which bind to an iron responsive element (IRE) in the 5'-untranslated region of its mRNA and repress translation. In vitro studies using cell lines have demonstrated that inhibitors of IRP binding increase ferritin expression and protect against oxidative injury. In order to evaluate the therapeutic potential of this approach in attenuating hemoglobin neurotoxicity, we have established colonies of IRP1 and IRP2 knockout mice. In completed studies, we have observed that: 1) Ferritin is overexpressed by IRP2 knockout neurons at baseline and after oxidant exposure, while IRP1 knockout has a much weaker and variable effect;2) IRP2 gene knockout markedly reduces neuronal vulnerability to hemoglobin and hydrogen peroxide;3) Oxidative injury surrounding a striatal hematoma is attenuated in IRP2 knockout mice. The goal of this competitive revision application is to compare functional recovery in wild-type and IRP2 knockout mice after experimental intracerebral hemorrhage, using both direct blood injection and collagenase injection models. In addition to standard behavioral tests, we propose to quantify functional deficits via an approach that is novel in hemorrhagic stroke research: automated analysis of home cage locomotor behavior, testing proprietary software marketed by two U.S.-based companies. Specifically, mouse activity will be video recorded for 24 hour intervals. Activity levels, turning/circling, and stereotypic behaviors will be quantified with ANY-maze and HomeCageScan software.

Public Health Relevance

The information gained in this project may lead to new treatments for victims of hemorrhagic stroke and head trauma. The ultimate goal is to reduce brain injury in tissue surrounding a blood clot by detoxifying iron, and to thereby improve the likelihood of survival and return to an independent, productive life.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
3R01NS042273-07S1
Application #
7830896
Study Section
Special Emphasis Panel (ZRG1-BDCN-Y (95))
Program Officer
Jacobs, Tom P
Project Start
2001-07-01
Project End
2012-05-31
Budget Start
2009-09-15
Budget End
2012-05-31
Support Year
7
Fiscal Year
2009
Total Cost
$289,925
Indirect Cost
Name
Thomas Jefferson University
Department
Emergency Medicine
Type
Schools of Medicine
DUNS #
053284659
City
Philadelphia
State
PA
Country
United States
Zip Code
19107
Chen-Roetling, Jing; Liu, Wenpei; Regan, Raymond F (2012) Hemopexin decreases hemin accumulation and catabolism by neural cells. Neurochem Int 60:488-94
Chen-Roetling, Jing; Sinanan, Jesse; Regan, Raymond F (2012) Effect of iron chelators on methemoglobin and thrombin preconditioning. Transl Stroke Res 3:452-9
Chen, Lifen; Zhang, Xuefeng; Chen-Roetling, Jing et al. (2011) Increased striatal injury and behavioral deficits after intracerebral hemorrhage in hemopexin knockout mice. J Neurosurg 114:1159-67
Chen-Roetling, Jing; Liu, Wenpei; Regan, Raymond F (2011) Iron accumulation and neurotoxicity in cortical cultures treated with holotransferrin. Free Radic Biol Med 51:1966-74
Chen-Roetling, Jing; Chen, Lifen; Regan, Raymond F (2011) Apotransferrin protects cortical neurons from hemoglobin toxicity. Neuropharmacology 60:423-31
Jaremko, Kellie M; Chen-Roetling, Jing; Chen, Lifen et al. (2010) Accelerated hemolysis and neurotoxicity in neuron-glia-blood clot co-cultures. J Neurochem 114:1063-73
Chen, Mai; Awe, Olatilewa O; Chen-Roetling, Jing et al. (2010) Iron regulatory protein-2 knockout increases perihematomal ferritin expression and cell viability after intracerebral hemorrhage. Brain Res 1337:95-103
Chen-Roetling, Jing; Chen, Lifen; Regan, Raymond F (2009) Minocycline attenuates iron neurotoxicity in cortical cell cultures. Biochem Biophys Res Commun 386:322-6
Li, Zhi; Chen-Roetling, Jing; Regan, Raymond F (2009) Increasing expression of H- or L-ferritin protects cortical astrocytes from hemin toxicity. Free Radic Res 43:613-21
Regan, Raymond F; Chen, Mai; Li, Zhi et al. (2008) Neurons lacking iron regulatory protein-2 are highly resistant to the toxicity of hemoglobin. Neurobiol Dis 31:242-9

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