Method Article

Combining Peripheral Nerve Grafting and Matrix Modulation to Repair the Injured Rat Spinal Cord

DOI:

10.3791/1324

November 20th, 2009

In This Article

Summary

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Traumatic injury to the spinal cord disrupts communication with the brain. To restore lost connectivity we utilize a peripheral nerve graft to provide a substratum for regenerating fibers in combination with neurotrophic factors and matrix-modulating enzymes to remove inhibitory molecules to promote long distance growth.

Abstract

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Traumatic injury to the spinal cord (SCI) causes death of neurons, disruption of motor and sensory nerve fiber (axon) pathways and disruption of communication with the brain. One of the goals of our research is to promote axon regeneration to restore connectivity across the lesion site. To accomplish this we developed a peripheral nerve (PN) grafting technique where segments of sciatic nerve are either placed directly between the damaged ends of the spinal cord or are used to form a bridge across the lesion. There are several advantages to this approach compared to transplantation of other neural tissues; regenerating axons can be directed towards a specific target area, the number and source of regenerating axons is easily determined by tracing techniques, the graft can be used for electrophysiological experiments to measure functional recovery associated with axons in the graft, and it is possible to use an autologous nerve to reduce the possibility of graft rejection. In our lab we have performed both autologous (donor and recipient are the same animal) and heterologous (donor and recipient are different animals) grafts with comparable results. This approach has been used successfully in both acute and chronic injury situations. Regenerated axons that reach the distal end of the PN graft often fail to extend back into the spinal cord, so we use microinjections of chondroitinase to degrade inhibitory molecules associated with the scar tissue surrounding the area of SCI. At the same time we have found that providing exogenous growth and trophic molecules encourages longer distance axonal regrowth into the spinal cord. Several months after transplantation we perform a variety of anatomical, behavioral and electrophysiological tests to evaluate the recovery of function in our spinal cord injured animals. This experimental approach has been used successfully in several spinal cord injury models, at different levels of injury and in different species (mouse, rat and cat). Importantly, the peripheral nerve grafting approach is effective in promoting regeneration by acute and chronically injured neurons.

Protocol

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1) Preparation for microscopic surgery

  1. The surgical station needs to be clean and sanitized with a dilute bleach solution prior to setting out instruments and accessory materials. Instruments will be autoclaved 1 day prior to surgery and stored in a sterile container. Turn on the Hot Bead Sterilizer (Fine Science Tools) used to remove pathogens and microbial contaminants from instruments between procedures on different animals.
  2. Plug in the thermal barrier used to maintain body temperature during the surgical procedure. Set out cotton swabs and gauze pads used to control bleeding. Prepare small (< 2mm3) pieces of Gel Foam to be....

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Discussion

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  1. For reproducibility of the experiment it is important that the level of spinal cord injury be consistent from animal to animal. Therefore it is critical that the appropriate vertebral process for laminectomy be identified. Because we are using a hemisection or transection lesion model for this study there is no ambiguity about the size of the lesion or whether specific spinal tracts were injured or spared.
  2. It is necessary that the peripheral nerve be pre-degenerated before transplantation because this initiates digestion.......

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Acknowledgements

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This work was supported by NIH/NINDS Grants NS26380 and NS55976, the Christopher and Dana Reeve Foundation and the Daniel Heumann Fund for Spinal Cord Research. The Drexel University College of Medicine Spinal Cord Research Center provides support for core facilities used to complete this work.

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Materials

List of materials used in this article
NameCompanyCatalog NumberComments
10-0 silk sutureArosSurgicalT5A10N10
6-0 silk sutureMcKesson2693
AmpicillinMcKesson483549
Antibody to cFosSigma-AldrichF7799
Biotinylated dextran AmineInvitrogenD7135
Buprenorphin (.3mg/ml)McKesson12496075701
Chondroitinase ABCAssociates of Cape Cod100332-1A
EuthasolWebster Veterinary07-805-9296
Hanks Balanced Salt SolutionCellgro21-021-CV
IsofluraneHenry Schein209-1966
Michel Wound ClipsFine Science Tools12040-02
Neurotrace KitInvitrogenN7167
True BlueSigma-AldrichT5891
XenodineWebster Veterinary92201
Hot Bead SterilizerFine Science Tools
Forced Exercise WheelLafayette Instruments
TreadScan SystemClever System
Infinite Horizon Impact DevicePrecision Systems and Instrumentation
Magnetic Stimulation DeviceMagstim

References

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  1. Houle, J. D. Demonstration of the potential for chronically injured neurons to regenerate axons into intraspinal peripheral nerve grafts. Exp. Neurol. 113, 1-9 (1991).
  2. Ye, J. H., Houle, J. D.

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Tags

Peripheral Nerve GraftingSpinal Cord InjuryChondroitinase TreatmentAxon RegenerationSciatic Nerve TransectionHemi Section LesionGel Foam HemostasisMicroinjection ProcedureFunctional Connectivity AssessmentBiotinylated Dextrin Amine

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