Grahn Peter J, Vaishya Sandeep, Knight Andrew M, Chen Bingkun K, Schmeichel Ann M, Currier Bradford L, Spinner Robert J, Yaszemski Michael J, Windebank Anthony J
Mayo Graduate School, Mayo Clinic, Rochester, 200 First Street SW, MN 55905, USA.
Department of Neurology, Mayo Clinic, Rochester, 200 First Street SW, MN 55905, USA.
Spine J. 2014 Sep 1;14(9):2172-7. doi: 10.1016/j.spinee.2014.01.059. Epub 2014 Feb 6.
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.
This proof-of-concept study was to determine whether implanting the nerve roots into a biodegradable scaffold would improve regeneration after injury.
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.
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<.05, scaffold n=11, control n=11).
This pilot study demonstrated that a PLGA scaffold improved regeneration of axons into peripheral nerve roots. However, the number of regenerating axons observed was limited and did not lead to functional recovery. Future experiments will employ a different scaffold material and possible growth factors or enzymes to increase axon populations.
脊髓圆锥处发生的创伤性损伤会对中枢神经系统和马尾神经根造成永久性损伤。
本概念验证研究旨在确定将神经根植入可生物降解支架是否能改善损伤后的再生情况。
所有涉及大鼠的实验工作均按照梅奥诊所机构动物护理和使用委员会批准的指南进行。对32只Sprague-Dawley大鼠进行手术。将四条腹侧马尾神经根直接重新植入腹侧脊髓残端或通过聚乳酸-乙醇酸共聚物(PLGA)支架进行植入。这些实验组与一个对照组进行比较,对照组中神经被插入置于脊髓和神经根之间的肌肉筋膜屏障中。在4周时对动物实施安乐死。
所有治疗组中,损伤部位头侧脊髓中的运动神经元数量没有差异,这意味着植入神经根后再生的潜力相同。通过单因素方差分析及Tukey事后检验发现,与对照组相比,PLGA支架治疗组损伤部位的轴突再生有统计学意义上的显著改善(p<0.05,支架组n = 11,对照组n = 11)。
这项初步研究表明,PLGA支架可改善轴突向周围神经根的再生。然而,观察到的再生轴突数量有限,并未导致功能恢复。未来的实验将采用不同的支架材料以及可能的生长因子或酶来增加轴突数量。