Downs J Crawford, Yang Hongli, Girkin Christopher, Sakata Lisandro, Bellezza Anthony, Thompson Hilary, Burgoyne Claude F
Devers Eye Institute, Legacy Health System, Portland, Oregon 97208-3950, USA.
Invest Ophthalmol Vis Sci. 2007 Jul;48(7):3195-208. doi: 10.1167/iovs.07-0021.
To delineate three dimensionally the neural canal landmarks-Bruch's membrane opening (BMO), anterior sclera canal opening (ASCO), anterior laminar insertion (ALI), posterior laminar insertion (PLI), and posterior scleral canal opening (PSCO)-and the anterior-most aspect of the subarachnoid space (ASAS), within digital three-dimensional (3-D) reconstructions of the monkey optic nerve head (ONH).
The trephinated ONH and peripapillary sclera from both eyes of three early glaucoma (EG) monkeys (one eye normal, one eye with laser-induced EG) were serial sectioned at 3-microm thickness, with the embedded tissue block face stained and imaged after each cut. The images were aligned and stacked in a 3-D volume, within which the BMO, ASCO, ALI, PLI, PSCO, and ASAS were delineated in 40 digital, radial, and sagittal sections. An ellipse was fitted to the 80 BMO points to establish a BMO zero reference plane, on which all other points were projected. The distance from each projected point to the BMO centroid (offset) and BMO zero reference plane (depth) were calculated and compared regionally between normal and EG eyes, both overall and within each monkey, by analysis of variance.
BMO was the clinically visible optic disc margin in all six eyes. The neural canal architecture was highly variable in the three normal eyes. Radial expansion of the neural canal was greatest posteriorly in the EG eyes. Axial elongation of the canal was less pronounced overall but was regionally present within all three EG eyes. ASAS was regionally radially expanded and anteriorly displaced within two of the three EG eyes.
Profound deformation of the neural canal and ASAS architecture are present in young adult monkey eyes at the onset of ONH surface change in early experimental glaucoma.
在猴视神经乳头(ONH)的数字三维(3-D)重建中,从三维角度描绘神经管标志——布鲁赫膜开口(BMO)、前巩膜管开口(ASCO)、前板层插入(ALI)、后板层插入(PLI)和后巩膜管开口(PSCO),以及蛛网膜下腔最前端(ASAS)。
对三只早期青光眼(EG)猴(一只眼正常,一只眼激光诱导性EG)双眼的环切ONH和视乳头周围巩膜进行连续切片,切片厚度为3微米,每次切割后对包埋组织块表面进行染色和成像。将图像对齐并堆叠成三维体积,在40个数字、径向和矢状切片中描绘BMO、ASCO、ALI、PLI、PSCO和ASAS。对80个BMO点拟合椭圆以建立BMO零参考平面,将所有其他点投影到该平面上。通过方差分析计算每个投影点到BMO质心的距离(偏移量)和到BMO零参考平面的距离(深度),并在正常眼和EG眼之间进行整体和每只猴内的区域比较。
在所有六只眼中,BMO是临床上可见的视盘边缘。三只正常眼中神经管结构高度可变。EG眼中神经管的径向扩张在后部最大。神经管的轴向伸长总体上不太明显,但在所有三只EG眼中局部存在。在三只EG眼中的两只眼中,ASAS局部径向扩张并向前移位。
在早期实验性青光眼中,成年猴眼在ONH表面变化开始时,神经管和ASAS结构存在深刻变形。