Department of Ophthalmology, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.
Exp Eye Res. 2011 Feb;92(2):104-11. doi: 10.1016/j.exer.2010.12.010. Epub 2010 Dec 25.
The site of outflow resistance leading to elevated intraocular pressure in primary open-angle glaucoma is believed to be located in the region of Schlemm's canal inner wall endothelium, its basement membrane and the adjacent juxtacanalicular tissue. Evidence also suggests collector channels and intrascleral vessels may have a role in intraocular pressure in both normal and glaucoma eyes. Traditional imaging modalities limit the ability to view both proximal and distal portions of the trabecular outflow pathway as a single unit. In this study, we examined the effectiveness of three-dimensional micro-computed tomography (3D micro-CT) as a potential method to view the trabecular outflow pathway. Two normal human eyes were used: one immersion fixed in 4% paraformaldehyde and one with anterior chamber perfusion at 10 mmHg followed by perfusion fixation in 4% paraformaldehyde/2% glutaraldehyde. Both eyes were postfixed in 1% osmium tetroxide and scanned with 3D micro-CT at 2 μm or 5 μm voxel resolution. In the immersion fixed eye, 24 collector channels were identified with an average orifice size of 27.5 ± 5 μm. In comparison, the perfusion fixed eye had 29 collector channels with a mean orifice size of 40.5 ± 13 μm. Collector channels were not evenly dispersed around the circumference of the eye. There was no significant difference in the length of Schlemm's canal in the immersed versus the perfused eye (33.2 versus 35.1 mm). Structures, locations and size measurements identified by 3D micro-CT were confirmed by correlative light microscopy. These findings confirm 3D micro-CT can be used effectively for the non-invasive examination of the trabecular meshwork, Schlemm's canal, collector channels and intrascleral vasculature that comprise the distal outflow pathway. This imaging modality will be useful for non-invasive study of the role of the trabecular outflow pathway as a whole unit.
人们认为原发性开角型青光眼导致眼内压升高的流出阻力部位位于施莱姆氏管内壁内皮细胞、其基底膜和相邻的小梁间隙组织区域。有证据表明,在正常眼和青光眼眼中,收集管和巩膜内血管可能在眼内压中起作用。传统的成像方式限制了将作为一个整体单元的小梁流出途径的近侧和远侧部分进行单一视图的能力。在这项研究中,我们检验了三维微计算机断层扫描(3D 微 CT)作为观察小梁流出途径的一种潜在方法的有效性。使用了两只正常的人眼:一只在 4%多聚甲醛中浸泡固定,另一只在前房以 10mmHg 灌注,然后在 4%多聚甲醛/2%戊二醛中灌注固定。两只眼睛都用 1%锇四氧化物后固定,并以 2μm 或 5μm 体素分辨率用 3D 微 CT 扫描。在浸泡固定的眼中,鉴定出 24 个收集管,平均口大小为 27.5±5μm。相比之下,灌注固定的眼中有 29 个收集管,平均口大小为 40.5±13μm。收集管不是均匀地分布在眼球的圆周周围。在浸泡眼和灌注眼之间,施莱姆氏管的长度没有显著差异(33.2 与 35.1mm)。3D 微 CT 确定的结构、位置和尺寸测量值通过相关的光学显微镜得到了证实。这些发现证实,3D 微 CT 可有效地用于非侵入性检查构成远侧流出途径的小梁网、施莱姆氏管、收集管和巩膜内血管结构。这种成像方式将有助于对整个小梁流出途径作为一个整体单元的作用进行非侵入性研究。