Abstract

While several cellular and pharmacological treatments have been evaluated following spinal cord injury (SCI) in animal models, it is increasingly recognized that approaches to address the glial scar, including the use of chondroitinase ABC (ChABC), can facilitate neuroanatomical plasticity. Moreover, increasing evidence suggests that combinatorial strategies are key to unlocking the plasticity that is enabled by ChABC. Given this, we evaluated the anatomical and functional consequences of ChABC in a combinatorial approach that also included growth factor (EGF, FGF2 and PDGF-AA) treatments and daily treadmill training on the recovery of hindlimb locomotion in rats with mid thoracic clip compression SCI. Using quantitative neuroanatomical and kinematic assessments, we demonstrate that the combined therapy significantly enhanced the neuroanatomical plasticity of major descending spinal tracts such as corticospinal and serotonergic-spinal pathways. Additionally, the pharmacological treatment attenuated chronic astrogliosis and inflammation at and adjacent to the lesion with the modest synergistic effects of treadmill training. We also observed a trend for earlier recovery of locomotion accompanied by an improvement of the overall angular excursions in rats treated with ChABC and growth factors in the first 4 weeks after SCI. At the end of the 7-week recovery period, rats from all groups exhibited an impressive spontaneous recovery of the kinematic parameters during locomotion on treadmill. However, although the combinatorial treatment led to clear chronic neuroanatomical plasticity, these structural changes did not translate to an additional long-term improvement of locomotor parameters studied including hindlimb-forelimb coupling. These findings demonstrate the beneficial effects of combined ChABC, growth factors and locomotor training on the plasticity of the injured spinal cord and the potential to induce earlier neurobehavioral recovery. However, additional approaches such as stem cell therapies or a more adapted treadmill training protocol may be required to optimize this repair strategy in order to induce sustained functional locomotor improvement.

Highlights

  • Spinal cord injury (SCI) results in motor deficits below the level of injury that can be temporary or permanent, incomplete or complete depending on the severity of the lesion [1,2,3,4]

  • We have shown that degradation of chondroitin sulfate proteoglycans (CSPGs) in the glial scar with chondroitinase ABC (ChABC) was needed to improve the outcomes of transplanting neural precursor cells (NPCs) in chronic spinal cord injury (SCI) [11] or efficient activation and oligodendrocyte replacement of endogenous spinal cord precursor cells in subacute SCI [15]

  • Our quantitative analysis showed no statistically significant difference in tissue sparing across the experimental groups suggesting that ChABC, growth factor (GF) and training had no beneficial effects on attenuating tissue degeneration following injury

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Summary

Introduction

Spinal cord injury (SCI) results in motor deficits below the level of injury that can be temporary or permanent, incomplete or complete depending on the severity of the lesion [1,2,3,4]. Various cellular and neurochemical repair strategies have been evaluated in experimental models of SCI for their efficacy in promoting neuroplasticity, axon regeneration, remyelination, and re-establishment of spinal circuitry to improve motor recovery following such injury [6,7,8,9,10,11,12,13] Among these treatment strategies, targeting the inhibitory properties of chondroitin sulfate proteoglycans (CSPGs) located in the extracellular matrix of glial scar has shown promising potential in enhancing SCI repair [11,12,14,15,16,17,18,19,20,21]. ChABC treatment has shown the potential to enhance locomotion in combination with other therapies in models of transection or compressive/contusive SCI [11,14,21]

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