Chondroitinase ABC promotes recovery of adaptive limb movements and enhances axonal growth caudal to a spinal hemisection.

作者: S. C. Jefferson , N. J. Tester , D. R. Howland

DOI: 10.1523/JNEUROSCI.4459-10.2011

关键词:

摘要: A number of studies have shown that chondroitinase ABC (Ch9ase ABC) digestion inhibitory chondroitin sulfate glycosaminoglycans significantly enhances axonal growth and recovery in rodents following spinal cord injury (SCI). Further, our group has improved SCI the larger cat model. The purpose current study was to determine whether intraspinal delivery Ch9ase ABC, T10 hemisections adult cats, adaptive movement features during a skilled locomotor task and/or promotes plasticity supraspinal circuitry. Here, we show enhanced crossing peg walkway post-SCI ipsilateral hindlimb trajectories integration into functional forelimb–hindlimb coordination pattern. Recovery these complex movements associated with significant increases neurofilament immunoreactivity immediately below white ( p = 0.033) contralateral gray matter 0.003). rubrospinal tract is critical normal require accurate paw placements like those seen crossing. Rubrospinal connections were assessed Fluoro-Gold injections, caudal hemisection. Significantly more retrogradely labeled right (axotomized) red nucleus (RN) neurons ABC-treated (23%) compared control-treated cats (8%; 0.032) indicating RN had axons lesion level. Thus, SCI, may facilitate at level, enhance locomotion, affect circuitry known support behaviors cat.

参考文章(94)
S. Miller, J. Van Der Burg, F.G.A. Van Der Meché, Locomotion in the cat: Basic programmes of movement Brain Research. ,vol. 91, pp. 239- 253 ,(1975) , 10.1016/0006-8993(75)90545-4
T Drew, W Jiang, B Kably, S Lavoie, Role of the motor cortex in the control of visually triggered gait modifications Canadian Journal of Physiology and Pharmacology. ,vol. 74, pp. 426- 442 ,(1996) , 10.1139/Y96-043
D M Armstrong, D E Marple-Horvat, Role of the cerebellum and motor cortex in the regulation of visually controlled locomotion Canadian Journal of Physiology and Pharmacology. ,vol. 74, pp. 443- 455 ,(1996) , 10.1139/Y96-044
E. D. Blagoveshchenskii, L.-G. Pettersson, S. N. Perfil’ev, Control of fine movements mediated by propriospinal neurons. Neuroscience and Behavioral Physiology. ,vol. 35, pp. 299- 304 ,(2005) , 10.1007/S11055-005-0061-X
V. J. Tom, H. R. Sandrow-Feinberg, K. Miller, L. Santi, T. Connors, M. A. Lemay, J. D. Houle, Combining Peripheral Nerve Grafts and Chondroitinase Promotes Functional Axonal Regeneration in the Chronically Injured Spinal Cord The Journal of Neuroscience. ,vol. 29, pp. 14881- 14890 ,(2009) , 10.1523/JNEUROSCI.3641-09.2009
D.M. Armstrong, Supraspinal contributions to the initiation and control of locomotion in the cat Progress in Neurobiology. ,vol. 26, pp. 273- 361 ,(1986) , 10.1016/0301-0082(86)90021-3
Mindy F. Levin, Jeffrey A. Kleim, Steven L. Wolf, What Do Motor “Recovery” and “Compensation” Mean in Patients Following Stroke? Neurorehabilitation and Neural Repair. ,vol. 23, pp. 313- 319 ,(2009) , 10.1177/1545968308328727
S. Miller, F.G.A. van der Meché, Movements of the forelimbs of the cat during stepping on a treadmill Brain Research. ,vol. 91, pp. 255- 269 ,(1975) , 10.1016/0006-8993(75)90546-6
Dámaso Crespo, Richard A. Asher, Rachel Lin, Kate E. Rhodes, James W. Fawcett, How does chondroitinase promote functional recovery in the damaged CNS Experimental Neurology. ,vol. 206, pp. 159- 171 ,(2007) , 10.1016/J.EXPNEUROL.2007.05.001
Nicole J. Tester, Anna H. Plaas, Dena R. Howland, Effect of body temperature on chondroitinase ABC's ability to cleave chondroitin sulfate glycosaminoglycans. Journal of Neuroscience Research. ,vol. 85, pp. 1110- 1118 ,(2007) , 10.1002/JNR.21199