Mestriner A C, Haddad A
Departamento de Morfologia Faculdade de Medicina de Ribeirão Preto, S.P. Brasil.
Graefes Arch Clin Exp Ophthalmol. 1994 Apr;232(4):242-51. doi: 10.1007/BF00184013.
In order to check the entrance site of serum albumin into the aqueous humor, rabbits were injected intravenously either with Evans blue (which reacts very quickly with albumin) or horseradish peroxidase. The Evans blue-albumin complex (Eb-a) was traced to the posterior chamber as early as 1 min after injection by examining frozen half eyes. The Eb-a was localized in frozen sections by fluorescence microscopy in the stroma of the ciliary and iridial processes, as well as in the lumen of all blood vessels from 1 to 60 min after injection even at doses as low as 3 mg/kg. The peroxidase activity was also localized on these same structures from 8 min to 4.5 h. Neither tracer was visualized in the iris stroma outside the lumen of blood vessels. This was also true for experiments with Eb (75 mg/kg) in which the blood-aqueous barrier was disrupted. The concentration (m/v) of Evans blue and the peroxidase activity in the aqueous humor of the anterior chamber were estimated by spectrophotometry. The morphological integrity of the blood-aqueous barrier was demonstrated by electron microscopy in all peroxidase-injected rabbits. Considering that (a) the Eb-a appeared first in the posterior chamber, (b) there was a high concentration of tracers in the stroma of the ciliary and iridial processes, (c) neither tracer was visualized in the iris stroma, (d) there was no evidence of disruption of the blood-aqueous barrier, and (e) the concentration of both tracers in the aqueous humor kept increasing up to 4 h after injection, it was assumed that serum macromolecules entered first the posterior chamber and subsequently migrated to the anterior chamber. Most likely they passed in between the cells of the inner layer of the ciliary epithelium, the site of the so-called blood-aqueous barrier. No evidence was found indicating migration of macromolecules from the stroma of the processes directly to the anterior chamber via the iris root.
为了检查血清白蛋白进入房水的入口部位,给兔子静脉注射伊文思蓝(它与白蛋白反应非常迅速)或辣根过氧化物酶。通过检查冷冻的半侧眼球,早在注射后1分钟就追踪到了伊文思蓝 - 白蛋白复合物(Eb - a)进入后房。注射后1至60分钟,即使剂量低至3mg/kg,通过荧光显微镜在冷冻切片中发现Eb - a定位于睫状突和虹膜突的基质以及所有血管腔内。过氧化物酶活性在注射后8分钟至4.5小时也定位于这些相同结构上。在血管腔外的虹膜基质中未观察到任何一种示踪剂。对于用伊文思蓝(75mg/kg)破坏血 - 房水屏障的实验也是如此。通过分光光度法估计前房房水中伊文思蓝的浓度(m/v)和过氧化物酶活性。在所有注射过氧化物酶的兔子中,通过电子显微镜证实了血 - 房水屏障的形态完整性。考虑到(a)Eb - a首先出现在后房,(b)在睫状突和虹膜突的基质中有高浓度的示踪剂,(c)在虹膜基质中未观察到任何一种示踪剂,(d)没有血 - 房水屏障破坏的证据,以及(e)两种示踪剂在房水中的浓度在注射后长达4小时持续增加,推测血清大分子首先进入后房,随后迁移到前房。它们很可能通过所谓血 - 房水屏障部位的睫状上皮内层细胞之间进入。未发现有证据表明大分子从突的基质通过虹膜根部直接迁移到前房。