The purpose of the proposed research is to determine the mechanisms which contribute to recovery of function after spinal cord injury. By developing methods which can enhance these mechanisms, we will attempt to increase the extent of recovery. We will examine two consequences of axotomy that are important to recovery: 1) cell survival after axotomy and 2) responses of the surviving cells that support axonal growth. Factors that we will study that affect cell survival are: a) the influence of the target; b) the influence of afferents; c) sprouting of undamaged neurons; and d) changes in protein synthesis. Quantitative morphological and electrophysiological methods will be used to identify characteristics of cells that survive axotomy and to characterize the responses required for regeneration. The influence of natural targets and afferents on cell survival will be tested using in vivo and in vitro methods; we will then determine whether supplying a surrogate target of fetal tissue will enhance the likelihood of neuronal survival and axonal outgrowth. Sprouting and synaptogenesis of undamaged neurons which are spared by the lesion can also mediate recovery by compensation; some of the functional consequences of sprouting will be tested. In order to investigate methods for enhancing recovery we will identify changes in axotomized cells that are correlated with the regenerative response. We will use electrophysiological methods, in situ hybridization and studies of protein synthetic changes to characterize the successful regenerative response, and we will also examine the factors that stimulate axonal outgrowth in developing neurons. We will use fetal spinal cord transplants to identify the way in which the transplanted tissue encourages metabolic activity supportive of regeneration by axotomized cells. The functional consequences of spinal cord regeneration mediated by the presence of transplanted fetal tissue will be assessed using quantitative methods developed to evaluate recovery of motor behavior. In addition to the six projects, we are proposing six core facilities, including new tissue culture, image analysis and motion analysis cores. These core facilities will make advanced technology available to all projects, and promote development of new methods for the analysis of the recovery of function after spinal cord injury. The proposed experimental program should permit identification of some of the mechanisms underlying recovery and development of ways to enhance these mechanisms in order to increase the extent of recovery following spinal cord injury.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Program Projects (P01)
Project #
5P01NS024707-08
Application #
2265327
Study Section
Neurological Disorders Program Project Review A Committee (NSPA)
Project Start
1987-04-01
Project End
1995-06-30
Budget Start
1994-04-01
Budget End
1995-06-30
Support Year
8
Fiscal Year
1994
Total Cost
Indirect Cost
Name
Allegheny University of Health Sciences
Department
Anatomy/Cell Biology
Type
Schools of Medicine
DUNS #
City
Philadelphia
State
PA
Country
United States
Zip Code
19129
Dugan, Elizabeth A; Shumsky, Jed S (2015) A combination therapy of neural and glial restricted precursor cells and chronic quipazine treatment paired with passive cycling promotes quipazine-induced stepping in adult spinalized rats. J Spinal Cord Med 38:792-804
Moxon, Karen A; Kao, Tina; Shumsky, Jed S (2013) Role of cortical reorganization on the effect of 5-HT pharmacotherapy for spinal cord injury. Exp Neurol 240:17-27
Kao, T; Shumsky, J S; Knudsen, E B et al. (2011) Functional role of exercise-induced cortical organization of sensorimotor cortex after spinal transection. J Neurophysiol 106:2662-74
Hayashi, Y; Jacob-Vadakot, S; Dugan, E A et al. (2010) 5-HT precursor loading, but not 5-HT receptor agonists, increases motor function after spinal cord contusion in adult rats. Exp Neurol 221:68-78
Giszter, Simon F; Hockensmith, Greg; Ramakrishnan, Arun et al. (2010) How spinalized rats can walk: biomechanics, cortex, and hindlimb muscle scaling--implications for rehabilitation. Ann N Y Acad Sci 1198:279-93
Kao, Tina; Shumsky, Jed S; Murray, Marion et al. (2009) Exercise induces cortical plasticity after neonatal spinal cord injury in the rat. J Neurosci 29:7549-57
Boyce, Vanessa S; Lemay, Michel A (2009) Modularity of endpoint force patterns evoked using intraspinal microstimulation in treadmill trained and/or neurotrophin-treated chronic spinal cats. J Neurophysiol 101:1309-20
Stackhouse, Scott K; Murray, Marion; Shumsky, Jed S (2008) Effect of cervical dorsolateral funiculotomy on reach-to-grasp function in the rat. J Neurotrauma 25:1039-47
Zottoli, S J; Freemer, M M (2003) Recovery of C-starts, equilibrium and targeted feeding after whole spinal cord crush in the adult goldfish Carassius auratus. J Exp Biol 206:3015-29
Zottoli, S J; Newman, B C; Rieff, H I et al. (1999) Decrease in occurrence of fast startle responses after selective Mauthner cell ablation in goldfish (Carassius auratus). J Comp Physiol A 184:207-18