Smith Peter M, Jeffery Nick D
Neurosciences Group, Department of Veterinary Medicine, University of Cambridge, Cambridge, UK.
Brain Pathol. 2006 Apr;16(2):99-109. doi: 10.1111/j.1750-3639.2006.00001.x.
Detailed analysis of the structural changes that follow human clinical spinal cord injury is limited by difficulties in achieving adequate tissue fixation. This study bypasses this obstacle by examining the spinal cord from paraplegic domestic animals, enabling us to document the ultrastructural changes at different times following injury. In all but one case, injury resulted from a combination of contusion and compression. There was infarction and hemorrhage, followed by gray matter destruction and the rapid development of a variety of white matter changes including axon swelling and myelin degeneration. Axons greater than 5 microm in diameter were more susceptible to degenerative changes, whereas smaller axons, particularly those in the subpial region, were relatively well preserved. Demyelinated axons were seen within 2 weeks after injury and, at later time points, both Schwann cell and oligodendrocyte remyelination was common. More subtle white matter abnormalities were identified by examining sagittal sections, including focal accumulation of organelles in the axoplasm and partial and paranodal myelin abnormalities. These observations serve to validate observations from experimental models of spinal contusion but also highlight the complexity of naturally occurring (ie, clinical) spinal injury. They also raise the possibility that focal abnormalities such as paranodal demyelination may contribute to early axonal dysfunction and possibly to progressive tissue damage.
对人类临床脊髓损伤后结构变化的详细分析因难以实现充分的组织固定而受到限制。本研究通过检查截瘫家畜的脊髓绕过了这一障碍,使我们能够记录损伤后不同时间的超微结构变化。除1例病例外,其余损伤均由挫伤和压迫共同导致。出现了梗死和出血,随后是灰质破坏以及包括轴突肿胀和髓鞘变性在内的多种白质变化迅速发展。直径大于5微米的轴突更容易发生退行性变化,而较小的轴突,尤其是软膜下区域的轴突,相对保存完好。损伤后2周内可见脱髓鞘轴突,在后期,施万细胞和少突胶质细胞的髓鞘再生都很常见。通过检查矢状切片发现了更细微的白质异常,包括轴浆内细胞器的局灶性聚集以及节段旁和结旁髓鞘异常。这些观察结果有助于验证脊髓挫伤实验模型中的观察结果,但也突出了自然发生(即临床)脊髓损伤的复杂性。它们还提出了节段旁脱髓鞘等局灶性异常可能导致早期轴突功能障碍并可能导致进行性组织损伤的可能性。