Saggu S K, Chotaliya H P, Cai Z, Blumbergs P, Casson R J
Department of Ophthalmology and Visual Sciences, The University of Adelaide, SA-5000, Australia.
Exp Neurol. 2008 May;211(1):52-8. doi: 10.1016/j.expneurol.2007.12.022. Epub 2008 Jan 8.
To describe the spatiotemporal pattern of somal and axonal pathologic changes after perikaryal excitotoxic injury to retinal ganglion cells in-vivo.
40 male Sprague-Dawley rats were killed at 0 h, 24 h, 72 h and 7 days after injecting 20 nM N-methyl-D-aspartate (NMDA) into the vitreous chamber of left eye. Saline-injected right eyes served as control. After perfusion fixation, the eyes and retrobulbar optic nerves from half of the animals in each group were embedded in paraffin and tissues from the other half embedded in resin. Paraffin-embedded eyes and resin-embedded proximal (intraorbital) and distal (intracranial) optic nerve segments were evaluated by light microscopy. Light microscopic photographs of proximal and distal optic nerve segments were compared using the following parameters: axon counts, axonal swellings and myelin changes.
Retinas showed cell loss in ganglion cell layer (GCL) and reduction in inner retinal thickness at 72 h after NMDA injection (p<0.05), with changes becoming more advanced after 7 days (p<0.001). The cell count in GCL correlated strongly with the axonal counts (R=0.929, p<0.001). Axon loss, axon swellings and myelin damage were seen in both proximal and distal segments of optic nerves 72 h post-NMDA exposure (p<0.05), with changes increasing further at 7 days (p<0.001). Pathological changes were more prominent in the distal segments (p<0.05).
Excitotoxic perikaryal injury causes an axonopathy, which is synchronous with the somal degeneration and which is most prominent in the distal portions of the axon, consistent with "dying-back like neuropathy".
描述体内视网膜神经节细胞胞体兴奋性毒性损伤后胞体和轴突病理变化的时空模式。
将20 nM N-甲基-D-天冬氨酸(NMDA)注入40只雄性Sprague-Dawley大鼠的左眼玻璃体内,分别于注射后0小时、24小时、72小时和7天处死大鼠。右眼注射生理盐水作为对照。灌注固定后,每组一半动物的眼睛和球后视神经用石蜡包埋,另一半动物的组织用树脂包埋。通过光学显微镜评估石蜡包埋的眼睛以及树脂包埋的视神经近端(眶内)和远端(颅内)节段。使用以下参数比较视神经近端和远端节段的光学显微镜照片:轴突计数、轴突肿胀和髓鞘变化。
NMDA注射后72小时,视网膜神经节细胞层(GCL)出现细胞丢失,视网膜内层厚度减小(p<0.05),7天后变化更明显(p<0.001)。GCL中的细胞计数与轴突计数密切相关(R=0.929,p<0.001)。NMDA暴露72小时后,视神经近端和远端节段均出现轴突丢失、轴突肿胀和髓鞘损伤(p<0.05),7天时变化进一步加重(p<0.001)。远端节段的病理变化更明显(p<0.05)。
兴奋性毒性胞体损伤导致轴突病,与胞体变性同步,且在轴突远端最为明显,符合“回返性神经病样”表现。