Kerrison J B, Buchanan K, Rosenberg M L, Clark R, Andreason K, Alfaro D V, Grossniklaus H E, Kerrigan-Baumrind L A, Kerrigan D F, Miller N R, Quigley H A
Wilmer Ophthalmological Institute, Johns Hopkins Hospital, Baltimore, MD, USA.
Arch Ophthalmol. 2001 Sep;119(9):1333-41. doi: 10.1001/archopht.119.9.1333.
To quantify the amount of optic nerve axonal loss associated with the presence of a mild relative afferent pupillary defect (RAPD) in an experimental monkey model.
The right macula of 5 rhesus monkeys (Macaca mulatta) was treated with concentrically enlarging diode laser burns until an RAPD was detected using a transilluminator light and measured with neutral density filters. Intervals between treatments were 3 to 7 days over a period of 2 months. Pupillary responses to light stimulation were recorded with a monocular infrared television pupillometer. Two months after detection of an RAPD, 5 treated and 4 control monkeys underwent euthanasia and enucleation. Histopathologic analysis and quantification of optic nerve axon counts using an image analysis system were performed.
No RAPD was observed despite an estimated ganglion cell loss of up to 26%. A 0.6 log unit RAPD was present in 5 monkeys when the laser scar incorporated the entire macula within the temporal vascular arcades. One eye had progressive vitreomacular traction with worsening of the RAPD to 1.8 log units without further laser treatment. Histopathologic evaluation disclosed complete loss of the normal retinal architecture within the macula. The average fiber loss for the 4 treated eyes with 0.6 log unit RAPDs compared with fellow eyes was 53.3% (95% confidence interval [CI], 45.0%-61.6%). The average difference in axon counts between untreated pairs of optic nerves was 12.8% (95% CI, 10.0%-15.6%). Optic nerve axon loss between pairs of experimental and control eyes was statistically significant (P<.001).
In rhesus monkeys, an RAPD develops after an approximate unilateral loss between 25% and 50% of retinal ganglion cells.
Owing to redundancy in the anterior visual pathways, unilateral retinal ganglion cell loss may occur prior to the observation of an RAPD. The presence of an RAPD measuring 0.6 log units implies that significant retinal ganglion cell injury has occurred.
在实验性猴模型中量化与轻度相对性传入性瞳孔障碍(RAPD)存在相关的视神经轴突损失量。
对5只恒河猴(猕猴)的右眼黄斑进行同心扩大的二极管激光烧灼,直至使用透照光检测到RAPD,并使用中性密度滤光片进行测量。治疗间隔为3至7天,为期2个月。用单眼红外电视瞳孔计记录对光刺激的瞳孔反应。在检测到RAPD两个月后,对5只接受治疗的猴子和4只对照猴子实施安乐死并摘除眼球。进行组织病理学分析,并使用图像分析系统对视神经轴突计数进行量化。
尽管估计神经节细胞损失高达26%,但未观察到RAPD。当激光瘢痕累及颞侧血管弓内的整个黄斑时,5只猴子出现了0.6对数单位的RAPD。一只眼睛出现进行性玻璃体黄斑牵引,RAPD恶化至1.8对数单位,未进行进一步激光治疗。组织病理学评估显示黄斑内正常视网膜结构完全丧失。与对侧眼相比,4只RAPD为0.6对数单位的治疗眼的平均纤维损失为53.3%(95%置信区间[CI],45.0%-61.6%)。未治疗的视神经对之间的轴突计数平均差异为12.8%(95%CI,10.0%-15.6%)。实验眼与对照眼之间的视神经轴突损失具有统计学意义(P<0.001)。
在恒河猴中,视网膜神经节细胞单侧损失约25%至50%后会出现RAPD。
由于前视觉通路的冗余性,在观察到RAPD之前可能发生单侧视网膜神经节细胞损失。测量为0.6对数单位的RAPD的存在意味着已发生显著的视网膜神经节细胞损伤。