Injury to the spinal cord or the central nervous system in general initiates a cascade of complex events, the net effect of which is a limiting neurological deficit. The magnitude of the deficit is determined not only by the extent of the initial injury but also, by variation within the events that follow. Many studies point to the realization that in order to understand these events, and perhaps devise strategies that can improve the likelihood of a more favorable neurological outcome, we must first understand the fundamental cellular mechanisms influencing degenerative and regenerative events within the CNS. The ultimate goal of the projects described in this program proposal is to develop a body of knowledge that will help us to identify basic mechanisms that may be susceptible to intervention strategies that would improve outcome following injury. The program is divided into 6 major areas: 1) A Core facility providing support for electron microscopy and administration; 2) Studies designed to test specific hypotheses about postsynaptic mechanisms that influence the response to injury; 3) The influence of trophic mechanisms including specific membrane bound proteins on attempts at regeneration; 4) Studies on the role of intrinsic local circuits and descending circuits in the development of post-injury abnormal sensory responses; 5) Experiments designed to explore the effects of injury on membrane mechanisms of excitability such as voltage-gated channels; and 6) Experiments designed to test the hypothesis that the placement of an axotomy is an important determinant in the subsequent response of the neuron. Pursuing these studies will fill critical gaps in our current understanding of degenerative/regenerative processes occurring within the central nervous system. This knowledge is essential for the development of treatment strategies directed not only at the spinal cord but the central nervous system in general.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Specialized Center (P50)
Project #
5P50NS010174-23
Application #
2262164
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Project Start
1978-09-01
Project End
1997-08-31
Budget Start
1994-09-01
Budget End
1995-08-31
Support Year
23
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Yale University
Department
Surgery
Type
Schools of Medicine
DUNS #
082359691
City
New Haven
State
CT
Country
United States
Zip Code
06520
Radtke, Christine; Akiyama, Yukinori; Brokaw, Jane et al. (2004) Remyelination of the nonhuman primate spinal cord by transplantation of H-transferase transgenic adult pig olfactory ensheathing cells. FASEB J 18:335-7
Liu, Chang-Ning; Devor, Marshall; Waxman, Stephen G et al. (2002) Subthreshold oscillations induced by spinal nerve injury in dissociated muscle and cutaneous afferents of mouse DRG. J Neurophysiol 87:2009-17
Akiyama, Yukinori; Radtke, Christine; Honmou, Osamu et al. (2002) Remyelination of the spinal cord following intravenous delivery of bone marrow cells. Glia 39:229-36
Akiyama, Yukinori; Radtke, Christine; Kocsis, Jeffery D (2002) Remyelination of the rat spinal cord by transplantation of identified bone marrow stromal cells. J Neurosci 22:6623-30
Lankford, Karen L; Imaizumi, Toshio; Honmou, Osamu et al. (2002) A quantitative morphometric analysis of rat spinal cord remyelination following transplantation of allogenic Schwann cells. J Comp Neurol 443:259-74
Everill, B; Cummins, T R; Waxman, S G et al. (2001) Sodium currents of large (Abeta-type) adult cutaneous afferent dorsal root ganglion neurons display rapid recovery from inactivation before and after axotomy. Neuroscience 106:161-9
Sasaki, M; Honmou, O; Akiyama, Y et al. (2001) Transplantation of an acutely isolated bone marrow fraction repairs demyelinated adult rat spinal cord axons. Glia 35:26-34
Kohama, I; Lankford, K L; Preiningerova, J et al. (2001) Transplantation of cryopreserved adult human Schwann cells enhances axonal conduction in demyelinated spinal cord. J Neurosci 21:944-50
Yan, H; Nie, X; Kocsis, J D (2001) Hepatocyte growth factor is a mitogen for olfactory ensheathing cells. J Neurosci Res 66:698-704
Kato, T; Honmou, O; Uede, T et al. (2000) Transplantation of human olfactory ensheathing cells elicits remyelination of demyelinated rat spinal cord. Glia 30:209-18

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