Implantation of cauda equina nerve roots through a biodegradable scaffold at the conus medullaris in rat

Abstract Background context Traumatic injuries occurring at the conus medullaris of the spinal cord cause permanent damage both to the central nervous system and to the cauda equina nerve roots. Purpose This proof-of-concept study was to determine whether implanting the nerve roots into a biodegrada...

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Veröffentlicht in:The spine journal 2014-09, Vol.14 (9), p.2172-2177
Hauptverfasser: Grahn, Peter J., BA, Vaishya, Sandeep, MD, Knight, Andrew M., PhD, Chen, Bingkun K., MD, PhD, Schmeichel, Ann M, Currier, Bradford L., MD, Spinner, Robert J., MD, Yaszemski, Michael J., MD, PhD, Windebank, Anthony J., MD
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Sprache:eng
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Zusammenfassung:Abstract Background context Traumatic injuries occurring at the conus medullaris of the spinal cord cause permanent damage both to the central nervous system and to the cauda equina nerve roots. Purpose This proof-of-concept study was to determine whether implanting the nerve roots into a biodegradable scaffold would improve regeneration after injury. Methods All experimental works involving rats were performed according to the approved guidelines by the Mayo Clinic Institutional Animal Care and Use Committee. Surgical procedures were performed on 32 Sprague-Dawley rats. Four ventral cauda equina nerve roots were reimplanted either directly into the ventral cord stump or through a poly(lactic -co -glycolic acid) (PLGA) scaffold. These experimental groups were compared with a control group in which the nerves were inserted into a muscle fascia barrier that was placed between the spinal cord and the nerve roots. Animals were sacrificed at 4 weeks. Results There was no difference in motor neuron counts in the spinal cord rostral to the injury in all treatment groups, implying equal potential for the regeneration into implanted nerve roots. One-way analysis of variance testing, with Tukey post hoc test, showed a statistically significant improvement in axon regeneration through the injury in the PLGA scaffold treatment group compared with the control (p
ISSN:1529-9430
1878-1632
DOI:10.1016/j.spinee.2014.01.059