The purpose of the electrophysiology and behavior core (COBRE Core D) is to provide a battery of standard tests and techniques that are needed to assess the function of animals and their spinal cords after injury and treatment, and to facilitate the development of more specialized techniques and tests that may be needed for the COBRE projects. The core will provide transcranial magnetic motor evoked potentials (tcMMEP), somatosensory evoke potentials (acute and chronic), Hoffman and crossed extensor reflexes, cutaneous reflexes, somatosensory evoked potentials, and field potential mapping. In addition, the core will provide for in vitro extracellular recording of white matter (demyelination/remyelination), intracellular recording from in vitro preparations and whole-cell recording that could be performed in thin slice or tissue culture. Behaviorally, the core will provide the BBB and grid walking tests for hindlimbs, the food retrieval tests for forelimbs, and footprint and gait analysis that examines both forelimbs and hindlimbs. Apart from the footprint and gait analysis, these are currently available in our research group. In addition to providing the tests and techniques listed above, core personnel will pursue independent studies using the animal models and cell types available in the COBRE cores to generate the preliminary studies necessary to become competitive for additional extramural support.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Exploratory Grants (P20)
Project #
1P20RR015576-01
Application #
6383610
Study Section
Special Emphasis Panel (ZRR1)
Project Start
2000-09-15
Project End
2005-07-31
Budget Start
Budget End
Support Year
1
Fiscal Year
2000
Total Cost
Indirect Cost
Name
University of Louisville
Department
Type
DUNS #
City
Louisville
State
KY
Country
United States
Zip Code
40292
Kuypers, Nicholas J; Bankston, Andrew N; Howard, Russell M et al. (2016) Remyelinating Oligodendrocyte Precursor Cell miRNAs from the Sfmbt2 Cluster Promote Cell Cycle Arrest and Differentiation. J Neurosci 36:1698-710
Myers, Scott A; Bankston, Andrew N; Burke, Darlene A et al. (2016) Does the preclinical evidence for functional remyelination following myelinating cell engraftment into the injured spinal cord support progression to clinical trials? Exp Neurol 283:560-72
Ward, P J; Herrity, A N; Harkema, S J et al. (2016) Training-Induced Functional Gains following SCI. Neural Plast 2016:4307694
May, Zacnicte; Fouad, Karim; Shum-Siu, Alice et al. (2015) Challenges of animal models in SCI research: Effects of pre-injury task-specific training in adult rats before lesion. Behav Brain Res 291:26-35
Jagadapillai, Rekha; Mellen, Nicholas M; Sachleben Jr, Leroy R et al. (2014) Ceftriaxone preserves glutamate transporters and prevents intermittent hypoxia-induced vulnerability to brain excitotoxic injury. PLoS One 9:e100230
Nielson, Jessica L; Guandique, Cristian F; Liu, Aiwen W et al. (2014) Development of a database for translational spinal cord injury research. J Neurotrauma 31:1789-99
Ward, Patricia J; Herrity, April N; Smith, Rebecca R et al. (2014) Novel multi-system functional gains via task specific training in spinal cord injured male rats. J Neurotrauma 31:819-33
Kuypers, Nicholas J; James, Kurtis T; Enzmann, Gaby U et al. (2013) Functional consequences of ethidium bromide demyelination of the mouse ventral spinal cord. Exp Neurol 247:615-22
Schultz, R L; Kullman, E L; Waters, R P et al. (2013) Metabolic adaptations of skeletal muscle to voluntary wheel running exercise in hypertensive heart failure rats. Physiol Res 62:361-9
Burke, Darlene A; Whittemore, Scott R; Magnuson, David S K (2013) Consequences of common data analysis inaccuracies in CNS trauma injury basic research. J Neurotrauma 30:797-805

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