Huang Jufang, Zhou Lihong, Wang Hui, Luo Jia, Xiong Kun, Zeng Leping, Chen Dan
Department of Anatomy and Neurobiology, Xiangya School of Medicine, Central South University, Changsha 410013, Hunan Province, China.
Neural Regen Res. 2012 Jun 5;7(16):1234-40. doi: 10.3969/j.issn.1673-5374.2012.16.005.
A rat model of acute high intraocular pressure was established by injecting saline into the anterior chamber of the left eye. Synaptophysin expression was increased in the inner plexiform layer at 2 hours following injury, and was widely distributed in the outer plexiform layer at 3-7 days, and then decreased to the normal level at 14 days. This suggests that expression of this presynaptic functional protein experienced spatiotemporal alterations after elevation of intraocular pressure. There was no significant change in the fluorescence intensity and distribution pattern for synapse-associated protein 102 following elevated intraocular pressure. Synapse-associated protein 102 immunoreactivity was confined to the outer plexiform layer, while synaptophysin immunoreactivity spread into the outer plexiform layer and the outer nuclear layer at 3 and 7 days following injury. These alterations in presynaptic elements were not accompanied by changes in postsynaptic components.
通过向左眼前房注射生理盐水建立急性高眼压大鼠模型。损伤后2小时,突触素表达在内网状层增加,在3 - 7天广泛分布于外网状层,然后在14天降至正常水平。这表明该突触前功能蛋白的表达在眼压升高后经历了时空变化。眼压升高后,突触相关蛋白102的荧光强度和分布模式无显著变化。突触相关蛋白102免疫反应局限于外网状层,而突触素免疫反应在损伤后3天和7天扩散到外网状层和外核层。突触前成分的这些改变并未伴随突触后成分的变化。