Department of Clinical Neuroscience, Division of Neurosurgery, Karolinska University Hospital, Stockholm, Sweden; Department of Anesthesiology & Perioperative Care, University of California at Irvine, Irvine, CA, USA.
Neuroscience. 2013 Oct 10;250:129-39. doi: 10.1016/j.neuroscience.2013.06.054. Epub 2013 Jul 2.
Here, we have translated from the rat to the non-human primate a unilateral lumbosacral injury as a model for cauda equina injury. In this morphological study, we have investigated retrograde effects of a unilateral L6-S2 ventral root avulsion (VRA) injury as well as the long-term effects of Wallerian degeneration on avulsed ventral roots at 6-10 months post-operatively in four adult male rhesus monkeys. Immunohistochemistry for choline acetyl transferase and glial fibrillary acidic protein demonstrated a significant loss of the majority of the axotomized motoneurons in the affected L6-S2 segments and signs of an associated astrocytic glial response within the ventral horn of the L6 and S1 spinal cord segments. Quantitative analysis of the avulsed ventral roots showed that they exhibited normal size and were populated by a normal number of myelinated axons. However, the myelinated axons in the avulsed ventral roots were markedly smaller in caliber compared to the fibers of the intact contralateral ventral roots, which served as controls. Ultrastructural studies confirmed the presence of small myelinated axons and a population of unmyelinated axons within the avulsed roots. In addition, collagen fibers were readily identified within the endoneurium of the avulsed roots. In summary, a lumbosacral VRA injury resulted in retrograde motoneuron loss and astrocytic glial activation in the ventral horn. Surprisingly, the Wallerian degeneration of motor axons in the avulsed ventral roots was followed by a repopulation of the avulsed roots by small myelinated and unmyelinated fibers. We speculate that the small axons may represent sprouting or axonal regeneration by primary afferents or autonomic fibers.
在这里,我们将大鼠的单侧腰骶部损伤转化为非人类灵长类动物的马尾损伤模型。在这项形态学研究中,我们调查了单侧 L6-S2 腹根撕脱伤(VRA)后的逆行效应,以及 Wallerian 变性对术后 6-10 个月时撕脱腹根的长期影响,研究对象为 4 只成年雄性恒河猴。胆碱乙酰转移酶和神经胶质酸性蛋白的免疫组织化学染色显示,受影响的 L6-S2 节段中大多数轴突切断的运动神经元明显丧失,L6 和 S1 脊髓节段腹角存在与之相关的星形胶质细胞反应的迹象。对撕脱腹根的定量分析表明,它们的大小正常,并且有正常数量的有髓轴突。然而,与作为对照的完整对侧腹根纤维相比,撕脱的腹根中的有髓轴突明显变细。超微结构研究证实了撕脱根内存在小有髓轴突和无髓轴突群体。此外,在撕脱根的神经内膜内很容易识别胶原纤维。总之,腰骶部 VRA 损伤导致腹角中的运动神经元逆行性丧失和星形胶质细胞激活。令人惊讶的是,撕脱腹根中的运动轴突的 Wallerian 变性后,被小的有髓和无髓纤维重新占据。我们推测,这些小轴突可能代表初级传入纤维或自主纤维的发芽或轴突再生。