Recent clinical trials have shown that early treatment using the thrombolytic agent, rt-PA, can improve the clinical outcome in certain patients with ischemic stroke. But even when treatment is initiated within the 3 hour """"""""therapeutic window of opportunity"""""""", there are few cases that derive significant benefit from rt-PA and some patients may actually deteriorate. The development of more effective treatment options and extension of the therapeutic window to later time points will depend on the ability of clinicians to differentiate patients with ischemic stroke that have the potential to benefit from thrombolysis (or some other therapy) from those that will model to differentiate ischemic brain tissue, prior to reperfusion, with the potential for recovery (i.e. receptive to therapeutic intervention) from irreversibly damaged tissues (i.e. no response or may worsen with thrombolysis) for the purpose of selecting treatment options. Our approach is based on a mechanistic hypothesis that multi-parameter MRI, by accounting for the multiple biophysical states of water in tissue and tissue perfusion, will yield a more complete classification of ischemic brain tissue than any single MRI parameter. A secondary goal of the project will be to define post reperfusion MRI indications of treatment efficacy in terms of successful or unsuccessful reperfusion and the implications for recovery, no change in status or further deterioration of the involved tissue. Based on development of MRI based tissue models to predict ischemic histopathology and eventual outcome during the current funding period, we propose to accomplish these objectives using a multi- parameter MRI data approach in conjunction with sophisticated data analysis routines.

Project Start
2002-09-01
Project End
2003-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
15
Fiscal Year
2002
Total Cost
$173,158
Indirect Cost
Name
Henry Ford Health System
Department
Type
DUNS #
073134603
City
Detroit
State
MI
Country
United States
Zip Code
48202
Knight, R A; Nagaraja, T N; Li, L et al. (2016) A Prospective Safety Trial of Atorvastatin Treatment to Assess Rebleeding after Spontaneous Intracerebral Hemorrhage: A Serial MRI Investigation. Austin J Cerebrovasc Dis Stroke 3:
Ding, Guang-Liang; Chopp, Michael; Li, Lian et al. (2014) Magnetic Resonance Imaging of Stroke in the Rat. Bo Pu Xue Za Zhi 31:116-132
Pindolia, Kirit; Li, Hong; Cardwell, Cisley et al. (2014) Characterization and functional analysis of cellular immunity in mice with biotinidase deficiency. Mol Genet Metab 112:49-56
Yan, Tao; Chopp, Michael; Ning, Ruizhuo et al. (2013) Intracranial aneurysm formation in type-one diabetes rats. PLoS One 8:e67949
Hernández-Vázquez, A; Wolf, B; Pindolia, K et al. (2013) Biotinidase knockout mice show cellular energy deficit and altered carbon metabolism gene expression similar to that of nutritional biotin deprivation: clues for the pathogenesis in the human inherited disorder. Mol Genet Metab 110:248-54
Xiong, Ye; Mahmood, Asim; Chopp, Michael (2013) Animal models of traumatic brain injury. Nat Rev Neurosci 14:128-42
Wang, Shiyang; Chopp, Michael; Nazem-Zadeh, Mohammad-Reza et al. (2013) Comparison of neurite density measured by MRI and histology after TBI. PLoS One 8:e63511
Cui, Xu; Chopp, Michael; Zacharek, Alex et al. (2013) The neurorestorative benefit of GW3965 treatment of stroke in mice. Stroke 44:153-61
Zhang, Rui Lan; Zhang, Zheng Gang; Chopp, Michael (2013) Targeting nitric oxide in the subacute restorative treatment of ischemic stroke. Expert Opin Investig Drugs 22:843-51
Santra, Manoranjan; Chopp, Michael; Zhang, Zheng Gang et al. (2012) Thymosin ? 4 mediates oligodendrocyte differentiation by upregulating p38 MAPK. Glia 60:1826-38

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