This is an application for the Institutional Development Award (IdeA) to establish a Center for Biomedical Research Excellence (COBRE) at the University of New Mexico (UNM) for carrying our research in CNS injury and pathophysiology using an integrative approach with a neuroimaging focus. One goal is to strengthen our existing unique neuroimaging facilities so that they become integrated into a state-of-the- art Center for applying functional neuroimaging techniques in brain research. UNM has developed a unique niche in neuroimaging over the past ten years with strengths in a number of areas including Magnetoencephalography (MEG), Magnetic Resonance Spectroscopy (MRS), and Optimal Imaging. We are also in the process of constructing an Electron Paramagnetic Resonance (EPR) facility for non-invasive measurements of free radicals in in vivo preparations. Four pieces of major equipment requested for the core of this COBRE would substantially strengthen our Center, enabling us to complete at the national level in various areas of neuroimaging applications. This includes the upgrades of an existing 4.7T MR scanner and in vivo EPR spectrometer for animal studies, and a photodiode array and a two-photon laser scanning microscope for cellular optimal imaging studies using in vitro and in vivo preparations. Our second goal is to utilize this research environment for increasing the productivity and quality of research of our faculty, especially the junior faculty members, so that we can increase the number of funded investigators at the regular individual NIH grant (R01) level. At UNM there is a group of successful senior investigators with active regular individual NIH grant (RO1) level. At UNM there is a group of senior investigators with active RO1-level funding in the area of CNS injury and pathophysiology with a neuroimaging focus who can establish a collaborative research team that can service to create an exciting and stimulating environment for fostering faculty development. The increase in the number of active investigators at our institution over the past decade makes the COBRE an ideal vehicle for faculty development. We have identified four promising junior faculty members working in the area of CNS injury and pathophysiology who can be directly helped with support from this IdeA grant to become independent scientists from R01- level funding. The COBRE Director and the senior investigator our team will serve as the mentors. The proposed research by these mentored investigators is multi-disciplinary and integrative, designed to produce a useful systematic longitudinal characterization of each type of pathophysiology and to provide new insights into the possible mechanisms of brain injury and recovery. To help create a stimulating research milieu, we propose to initiate a formal seminar series on neuro- pathophysiology, to annually organize a mini-symposium on timely thematic topics, and to administer a visiting scientist program. We have also formed a national advisory committee consisting of prominent scientists in our field who can guide us in the development of our COBRE, The progress of the junior faculty members in their scientific work will be monitored according to our mentorship program.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
5P20RR015636-02
Application #
6499491
Study Section
Special Emphasis Panel (ZRR1-RCMI-2 (02))
Program Officer
Sayre, Michael
Project Start
2001-02-23
Project End
2006-01-31
Budget Start
2002-02-01
Budget End
2003-01-31
Support Year
2
Fiscal Year
2002
Total Cost
$1,913,708
Indirect Cost
Name
University of New Mexico
Department
Neurology
Type
Schools of Medicine
DUNS #
829868723
City
Albuquerque
State
NM
Country
United States
Zip Code
87131
Yamashiro, Kunihiko; Fujii, Yuki; Maekawa, Shohei et al. (2017) Multiple pathways for elevating extracellular adenosine in the rat hippocampal CA1 region characterized by adenosine sensor cells. J Neurochem 140:24-36
Pan, Rong; Liu, Ke Jian (2016) ZNT-1 Expression Reduction Enhances Free Zinc Accumulation in Astrocytes After Ischemic Stroke. Acta Neurochir Suppl 121:257-61
Kimura-Ohba, Shihoko; Yang, Yi (2016) Oxidative DNA Damage Mediated by Intranuclear MMP Activity Is Associated with Neuronal Apoptosis in Ischemic Stroke. Oxid Med Cell Longev 2016:6927328
Dai, Xingping; Bragina, Olga; Zhang, Tongsheng et al. (2016) High Intracranial Pressure Induced Injury in the Healthy Rat Brain. Crit Care Med 44:e633-8
Liu, Jie; Weaver, John; Jin, Xinchun et al. (2016) Nitric Oxide Interacts with Caveolin-1 to Facilitate Autophagy-Lysosome-Mediated Claudin-5 Degradation in Oxygen-Glucose Deprivation-Treated Endothelial Cells. Mol Neurobiol 53:5935-5947
Welch, J H; Mayfield, J J; Leibowitz, A L et al. (2016) Third trimester-equivalent ethanol exposure causes micro-hemorrhages in the rat brain. Neuroscience 324:107-18
Yang, Yi; Rosenberg, Gary A (2015) Matrix metalloproteinases as therapeutic targets for stroke. Brain Res 1623:30-8
Topper, Lauren A; Baculis, Brian C; Valenzuela, C Fernando (2015) Exposure of neonatal rats to alcohol has differential effects on neuroinflammation and neuronal survival in the cerebellum and hippocampus. J Neuroinflammation 12:160
Pan, Rong; Timmins, Graham S; Liu, Wenlan et al. (2015) Autophagy Mediates Astrocyte Death During Zinc-Potentiated Ischemia--Reperfusion Injury. Biol Trace Elem Res 166:89-95
Nemoto, Edwin M; Bragin, Denis E; Statom, Gloria et al. (2014) Role of microvascular shunts in the loss of cerebral blood flow autoregulation. Adv Exp Med Biol 812:43-49

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