This proposal is two separate Cores summed into one administrative unit, representing two research groups in Henry Ford Health Systems; the Neurology NMR laboratory, which will oversee the Magnetic Resonance Imaging (MRI) sections of the proposed Program Project, and the Radiology Image Analysis Laboratory, which will oversee the visualization and combination of MRI (and other) images. It is the focus of Neurology NMR, and its responsibility in this Core, to parameterize MRI data in animal models of cerebral ischemia, and in humans with acute and chronic stroke. Neurology NMR is charged with data acquisition and data processing to produce maps of such parameters as proton density, T1, T2, cerebral blood flow (CBF), the apparent diffusion coefficient of water (ADC/W), the apparent forward magnetization transfer rate, K(fa), etcetera, in order to construct physical and physiological models of cerebral tissue across the phases of cerebral ischemia. To this end, the practices and principles of the MRI image acquisition and data processing used in the various Projects of the Program Project Proposal are presented in this Core, Section A. It has been the focus of the Radiology Image Analysis Laboratory to combine MRI (and other image data) in humans and animal models. In large part, because of the signal-to-noise advantage gained, image intensities alone (e.g., a set of spin-echo images, rather than a T2 map) are input to the algorithms employed by this group. Given an identified pure tissue signal, it has been possible to employ image processing algorithms in the identification of regions of irreversible tissue damage versus borderline regions, versus undamaged regions, versus regions with partial-volume effects. These techniques particularly the Eigenimage and ISODATA filters, are valuable because they employ all the information in an image set and, with experience, they allow the non-invasive identification of different tissue types. The practices and principles of Image Processing used in the various Projects of this Program Project proposal are presented in this Core, Section B. Finally, it is the purpose of this core to apply the work of both groups to the MRI study of cerebral infarction in animals and humans, and to combine their work so that the results of the image processing approaches can be mapped across field strengths and species.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
3P01NS023393-14A1S1
Application #
6573863
Study Section
Special Emphasis Panel (ZNS1)
Project Start
2001-09-01
Project End
2002-08-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
14
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
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

Showing the most recent 10 out of 319 publications