The objective is a better understanding of the pathophysiology of stroke. The program features an integration of the research activities of the Departments of Neurology, Neurosurgery, Neuropsychology and Diagnostic Radiology in the study of cerebral vascular disease. The research emphasizes and explores the utility of 31-P Topical Nuclear Magnetic Resonance (TMR) proton spectroscopy and proton NMR imaging in the study of brain anatomy, cerebral blood flow (CBF) and energy phosphate metabolism in clinical patients with stroke. Administrative, statistical and methodological cores and four individual projects are proposed. The methodological cores describe the NMR facility, CBF laboratory and Neuropsychological laboratories. Project 1 proposes early experiments towards the development of NMR methods for the eventual autoradiographic measurement of CBF. The second project explores the dynamic changes in cerebral energy metabolism as measured by 31-P NMR and 1-H in a cat models of global and focal cerebral ischemia. Studies of the clinical patient with stroke begin in Project 3 with a proposal to improve and explore the utility of the 133-Xenon inhalation technique for the measurement of CBF and to establish abnormal CBF as a risk factor for stroke. Project 4 proposes to apply 31-P and 1-H spectroscopy together with NMR imaging to the study of the clinical patient with diffuse hemispheric ischemia and focal ischemic infarction. The eventual goals of this Program Project are to establish noninvasive techniques to identify hemodynamic and metabolic markers which permit the logical and safe therapy of acute and chronic ischemia in cerebrovascular disease by either medical or surgical means.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
1P01NS023393-01
Application #
3100062
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Project Start
1986-04-01
Project End
1989-03-31
Budget Start
1986-04-01
Budget End
1987-03-31
Support Year
1
Fiscal Year
1986
Total Cost
Indirect Cost
Name
Henry Ford Health System
Department
Type
DUNS #
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
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
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
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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