Promoting plasticity in the spinal cord with chondroitinase improves functional recovery after peripheral nerve repair.

Functional recovery after peripheral nerve repair in humans is often disappointing. A major reason for this is the inaccuracy of re-innervation of muscles and sensory structures. We hypothesized that promoting plasticity in the spinal cord, through digestion of chondroitin sulphate proteoglycans (CSPGs) with chondroitinase ABC (ChABC), might allow the CNS to compensate for inaccurate peripheral re-innervation and improve functional recovery. The median and ulnar nerves were injured and repaired to produce three grades of inaccuracy of peripheral re-innervation by (i) crush of both nerves; (ii) correct repair of median to median and ulnar to ulnar; and (iii) crossover of the median and ulnar nerves. Mapping of the motor neuron pool of the flexor carpi radialis muscle showed precise re-innervation after nerve crush, inaccurate regeneration after correct repair, more inaccurate after crossover repair. Recovery of forelimb function, assessed by skilled paw reaching, grip strength and sensory testing varied with accuracy of re-innervation. This was not due to differences in the number of regenerated axons. Single injections of ChABC into the spinal cord led to long-term changes in the extracellular matrix, with hyaluronan and neurocan being removed and not fully replaced after 8 weeks. ChABC treatment produce increased sprouting visualized by MAP1BP staining and improved functional recovery in skilled paw reaching after correct repair and in grip strength after crossover repair. There was no hyperalgesia. Enhanced plasticity in the spinal cord, therefore, allows the CNS to compensate for inaccurate motor and sensory re-innervation of the periphery, and may be a useful adjunct therapy to peripheral nerve repair.

[1]  Nakaakira Tsukahara,et al.  Reorganization of corticorubral synapses following cross-innervation of flexor and extensor nerves of adult cat: a quantitative electron microscopic study , 1984, Brain Research.

[2]  J. Sanes,et al.  Pre-existing pathways promote precise projection patterns , 2002, Nature Neuroscience.

[3]  J. Bertelli,et al.  The rat brachial plexus and its terminal branches: An experimental model for the study of peripheral nerve regeneration , 1995, Microsurgery.

[4]  J. Wall,et al.  Human brain plasticity: an emerging view of the multiple substrates and mechanisms that cause cortical changes and related sensory dysfunctions after injuries of sensory inputs from the body , 2002, Brain Research Reviews.

[5]  L. Maffei,et al.  Synergistic Effects of Brain-Derived Neurotrophic Factor and Chondroitinase ABC on Retinal Fiber Sprouting after Denervation of the Superior Colliculus in Adult Rats , 2003, The Journal of Neuroscience.

[6]  M. Murray,et al.  Expression of a phosphorylated isoform of MAP1B is maintained in adult central nervous system areas that retain capacity for structural plasticity , 1996, The Journal of comparative neurology.

[7]  A. Bringmann,et al.  In vivo and in vitro labelling of perineuronal nets in rat brain , 1996, Brain Research.

[8]  I. Fischer,et al.  Microtubule-associated protein 1b (MAP1b) is concentrated in the distal region of growing axons , 1994, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[9]  S. Dunnett,et al.  A lateralised grip strength test to evaluate unilateral nigrostriatal lesions in rats , 1998, Neuroscience Letters.

[10]  M. Schachner,et al.  Reduced Perisomatic Inhibition, Increased Excitatory Transmission, and Impaired Long-Term Potentiation in Mice Deficient for the Extracellular Matrix Glycoprotein Tenascin-R , 2001, Molecular and Cellular Neuroscience.

[11]  L. G. Cohen,et al.  Nervous system reorganization following injury , 2002, Neuroscience.

[12]  L. Maffei,et al.  Reactivation of Ocular Dominance Plasticity in the Adult Visual Cortex , 2002, Science.

[13]  F. Rossi,et al.  Degradation of Chondroitin Sulfate Proteoglycans Induces Sprouting of Intact Purkinje Axons in the Cerebellum of the Adult Rat , 2005, The Journal of Neuroscience.

[14]  A. Irintchev,et al.  Opposite impacts of tenascin‐C and tenascin‐R deficiency in mice on the functional outcome of facial nerve repair , 2005, The European journal of neuroscience.

[15]  G. Lundborg Nerve injury and repair – a challenge to the plastic brain , 2003 .

[16]  Shuhei Yamada,et al.  Oversulfated Chondroitin/Dermatan Sulfates Containing GlcAβ1/IdoAα1–3GalNAc(4,6-O-disulfate) Interact with L- and P-selectin and Chemokines* , 2002, The Journal of Biological Chemistry.

[17]  T. Murakami,et al.  Three-dimensional microanatomy of perineuronal proteoglycan nets enveloping motor neurons in the rat spinal cord , 1998, Journal of neurocytology.

[18]  M. Botte,et al.  Inaccurate projection of rat soleus motoneurons: A comparison of nerve repair techniques , 1997, Muscle & nerve.

[19]  James W. Fawcett,et al.  Chondroitinase ABC promotes functional recovery after spinal cord injury , 2002, Nature.

[20]  M. Miyasaka,et al.  Oversulfated chondroitin/dermatan sulfates containing GlcAbeta1/IdoAalpha1-3GalNAc(4,6-O-disulfate) interact with L- and P-selectin and chemokines. , 2002, The Journal of biological chemistry.

[21]  Birgitta Rosén,et al.  Sensory relearning after nerve repair , 2001, The Lancet.

[22]  S. McMahon,et al.  Muscle Afferents Innervating Skin Form Somatotopically Appropriate Connections in the Adult Rat Dorsal Horn , 1993, The European journal of neuroscience.

[23]  Nobuyuki Itoh,et al.  Specific Molecular Interactions of Oversulfated Chondroitin Sulfate E with Various Heparin-binding Growth Factors , 2002, The Journal of Biological Chemistry.

[24]  A. Haunsø,et al.  Morphology of perineuronal nets in tenascin-R and parvalbumin single and double knockout mice , 2000, Brain Research.

[25]  K. Horie,et al.  Two Distinct Chondroitin Sulfate ABC Lyases , 1997, The Journal of Biological Chemistry.

[26]  Michael J. Hansen,et al.  Semaphorin 5A Is a Bifunctional Axon Guidance Cue Regulated by Heparan and Chondroitin Sulfate Proteoglycans , 2004, Neuron.

[27]  M. Schachner,et al.  The extracellular matrix and synapses , 2006, Cell and Tissue Research.

[28]  I. Whishaw,et al.  Varieties of paw and digit movement during spontaneous food handling in rats: Postures, bimanual coordination, preferences, and the effect of forelimb cortex lesions , 1996, Behavioural Brain Research.

[29]  X. Navarro,et al.  Peripheral and spinal motor reorganization after nerve injury and repair. , 2004, Journal of neurotrauma.

[30]  J. Winn,et al.  Brain , 1878, The Lancet.

[31]  S. Rossignol,et al.  Adaptive changes of locomotion after central and peripheral lesions. , 2004, Canadian journal of physiology and pharmacology.

[32]  M. Schachner,et al.  Modification of extracellular matrix by enzymatic removal of chondroitin sulfate and by lack of tenascin-R differentially affects several forms of synaptic plasticity in the hippocampus , 2001, Neuroscience.

[33]  Xiang Yang Chen,et al.  Probable corticospinal tract control of spinal cord plasticity in the rat. , 2002, Journal of neurophysiology.

[34]  S. Hovius,et al.  Median, ulnar, and combined median-ulnar nerve injuries: functional outcome and return to productivity. , 2001, The Journal of trauma.

[35]  J. Fawcett,et al.  Characterization of tests of functional recovery after median and ulnar nerve injury and repair in the rat forelimb , 2007, Journal of the peripheral nervous system : JPNS.

[36]  S. Dunnett,et al.  Environmental enrichment affects striatal graft morphology and functional recovery , 2004, The European journal of neuroscience.

[37]  R. Kalb,et al.  Large diameter primary afferent input is required for expression of the cat-301 proteoglycan on the surface of motor neurons , 1990, Neuroscience.

[38]  F. S. Haddad,et al.  Handcuff related injuries , 1997 .

[39]  D. Snow,et al.  Embryonic Neurons Adapt to the Inhibitory Proteoglycan Aggrecan by Increasing Integrin Expression , 1999, The Journal of Neuroscience.

[40]  R. Coggeshall,et al.  Peripheral nerve injury triggers central sprouting of myelinated afferents , 1992, Nature.

[41]  S. Dunnett,et al.  The “staircase test”: a measure of independent forelimb reaching and grasping abilities in rats , 1991, Journal of Neuroscience Methods.

[42]  J. Maurissen,et al.  Factors affecting grip strength testing. , 2003, Neurotoxicology and teratology.

[43]  Jon H. Kaas,et al.  Central reorganization of sensory pathways following peripheral nerve regeneration in fetal monkeys , 1996, Nature.

[44]  D. Hudson,et al.  Primary epineural repair of the median nerve in children. , 1997, Journal of hand surgery.

[45]  Takao K. Hensch,et al.  Controlling the critical period , 2003, Neuroscience Research.

[46]  J W Fawcett,et al.  Chondroitin sulphate proteoglycans: preventing plasticity or protecting the CNS? , 2004, Journal of anatomy.

[47]  I. Fischer,et al.  Phosphorylated MAP1B is induced in central sprouting of primary afferents in response to peripheral injury but not in response to rhizotomy , 2002, The European journal of neuroscience.

[48]  J. Klooster,et al.  Semaphorin 3A displays a punctate distribution on the surface of neuronal cells and interacts with proteoglycans in the extracellular matrix , 2005, Molecular and Cellular Neuroscience.

[49]  M. Schachner,et al.  High Affinity Binding and Overlapping Localization of Neurocan and Phosphacan/Protein-tyrosine Phosphatase-ζ/β with Tenascin-R, Amphoterin, and the Heparin-binding Growth-associated Molecule* , 1998, The Journal of Biological Chemistry.

[50]  J. Silver,et al.  Chondroitinase ABC Digestion of the Perineuronal Net Promotes Functional Collateral Sprouting in the Cuneate Nucleus after Cervical Spinal Cord Injury , 2006, The Journal of Neuroscience.

[51]  C. Woolf,et al.  Neuronal plasticity: increasing the gain in pain. , 2000, Science.

[52]  E. Almquist,et al.  Nerve conduction velocity, microscopic, and electron microscopy studies comparing repaired adult and baby monkey median nerves. , 1983, The Journal of hand surgery.

[53]  A. Bringmann,et al.  Acute and long-lasting changes in extracellular-matrix chondroitin-sulphate proteoglycans induced by injection of chondroitinase ABC in the adult rat brain , 1998, Experimental Brain Research.

[54]  M. Noda,et al.  A Chondroitin Sulfate Proteoglycan PTPζ/RPTPβ Regulates the Morphogenesis of Purkinje Cell Dendrites in the Developing Cerebellum , 2003, The Journal of Neuroscience.

[55]  S. Hockfield,et al.  Molecular evidence for early activity-dependent development of hamster motor neurons , 1988, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[56]  I. Apostolova,et al.  Tenascin-R Restricts Posttraumatic Remodeling of Motoneuron Innervation and Functional Recovery after Spinal Cord Injury in Adult Mice , 2006, The Journal of Neuroscience.

[57]  J Schouenborg,et al.  Developmental Adaptation of Rat Nociceptive Withdrawal Reflexes after Neonatal Tendon Transfer , 1997, The Journal of Neuroscience.

[58]  J. Fawcett,et al.  Regeneration of CNS axons back to their target following treatment of adult rat brain with chondroitinase ABC , 2001, Nature Neuroscience.

[59]  M. Beattie,et al.  An Analysis of Changes in Sensory Thresholds to Mild Tactile and Cold Stimuli after Experimental Spinal Cord Injury in the Rat , 2000, Neurorehabilitation and neural repair.