Murphy C G, Johnson M, Alvarado J A
Department of Ophthalmology, University of California School of Medicine, San Francisco 94143.
Arch Ophthalmol. 1992 Dec;110(12):1779-85. doi: 10.1001/archopht.1992.01080240119043.
We tested the hypothesis that obstruction of the juxtacanalicular tissues, by melanin granules in pigmentary glaucoma and by other impermeable material in primary open angle glaucoma, leads to the development of a chronic glaucomatous condition. The distribution and concentration of melanin and other impermeable materials in the juxtacanalicular tissues and elsewhere in the trabecular meshwork was determined in 13 specimens. Six specimens were from patients with pigmentary glaucoma, two from patients with pigment dispersion syndrome, and three from patients with primary open angle glaucoma, as well as two from normal subjects. The effect of these materials on flow resistance was estimated using two hydrodynamic models. In model A, the electron-lucent spaces of the juxtacanalicular tissue were assumed to be open spaces, while in model B, these spaces and spaces filled with ground substance were assumed to be gel filled. In pigmentary glaucoma, 3.5% of the pigment was found in the juxtacanalicular tissue, while 96.5% was found in the corneoscleral and uveoscleral tissues. Permeabilities calculated according to model A were much higher than those expected from estimates of outflow facility in all groups, in agreement with the previous report of Ethier et al. The gel-filled spaces available for fluid flow, as determined by model B, showed no statistically demonstrable differences (pigmentary glaucoma, 32.9%; primary open angle glaucoma, 36.6%; pigment dispersion syndrome, 43.4%; normal, 44.1%). Furthermore, the amount of pigment present in the juxtacanalicular tissue was determined to have a negligible influence on permeability. Thus, the development of the chronic glaucomatous condition cannot be directly attributed to pigment accumulation in the juxtacanalicular tissue in pigmentary glaucoma.
在色素性青光眼中,黑色素颗粒以及在原发性开角型青光眼中的其他不可渗透物质对小管周组织的阻塞会导致慢性青光眼状态的发展。在13个标本中测定了黑色素和其他不可渗透物质在小管周组织及小梁网其他部位的分布和浓度。6个标本来自色素性青光眼患者,2个来自色素播散综合征患者,3个来自原发性开角型青光眼患者,还有2个来自正常受试者。使用两个流体动力学模型估计了这些物质对流动阻力的影响。在模型A中,假定小管周组织的电子透亮空间为开放空间,而在模型B中,假定这些空间以及充满基质的空间为凝胶填充。在色素性青光眼中,3.5%的色素存在于小管周组织,而96.5%存在于角巩膜和葡萄膜巩膜组织。根据模型A计算的渗透率远高于所有组根据房水流畅系数估计值所预期的渗透率,这与埃蒂尔等人之前的报告一致。由模型B确定的可用于流体流动的凝胶填充空间在统计学上没有显示出明显差异(色素性青光眼,32.9%;原发性开角型青光眼,36.6%;色素播散综合征,43.4%;正常,44.1%)。此外,确定小管周组织中存在的色素量对渗透率的影响可忽略不计。因此,慢性青光眼状态的发展不能直接归因于色素性青光眼中色素在小管周组织中的积累。