Grimes P A
Department of Ophthalmology, University of Pennsylvania School of Medicine, Philadelphia 19104.
Exp Eye Res. 1988 May;46(5):769-83. doi: 10.1016/s0014-4835(88)80063-0.
Carboxyfluorescein levels in ocular tissues of normal rats were measured using quantitative fluorescence microscopy and compared with fluorescein levels to determine the extent to which blood-retinal barrier permeability is affected by the difference in lipid solubility of these two dyes. Retinal fluorescence intensity measurements at 2 min after i.v. dye injection were very much lower for carboxyfluorescein than for fluorescein despite similar plasma free dye concentrations. Marked leakage of dye from the optic disc into peripapillary retina was identified. At 1- and 2 hr, retinal levels of the two dyes became more similar, because fluorescein was removed from retina faster than carboxyfluorescein. After sodium-iodate-induced damage of the pigment epithelium, high levels of both dyes were evident in retina, but carboxyfluorescein was localized chiefly within extracellular space whereas fluorescein also densely stained cell somata. The fluorescence intensity levels recorded, which are proportional to the total mass of dye in the tissue, were correspondingly lower for carboxyfluorescein than for fluorescein, indicating that they were markedly affected by the different distribution of the two dyes. To relate tissue fluorescence intensity directly to dye concentration in the extracellular fluid, measurements were obtained from isolated retinas incubated in dye solutions of known concentration. Log-log plots demonstrated a linear relation between fluorescence intensity and medium concentration for both dyes, but retinal fluorescence of carboxyfluorescein, in correspondence with its limited distribution in the tissue space, was consistently less than that of fluorescein. The ratio of carboxyfluorescein to fluorescein fluorescence varied with the retinal layers but was constant for each layer over the concentration range tested. These fluorescence intensity ratios then were used to adjust the in vivo data so that comparison between the two dyes more closely reflected their extracellular dye concentration. With this correction the amount of carboxyfluorescein present in outer retina shortly after dye injection was approx. 1/10 that of fluorescein, indicating that carboxyfluorescein penetrates the pigment epithelium less readily than fluorescein, as expected from the difference in lipid solubility of the two dyes. However, fluorescence of both dyes in retina and presumably in vitreous humor eventually reached similar levels. This is attributed to entry of the dyes at sites of barrier discontinuity, as at the optic disc, and by a difference in their rates of removal from the intraocular compartment.
使用定量荧光显微镜测量正常大鼠眼组织中的羧基荧光素水平,并与荧光素水平进行比较,以确定这两种染料的脂溶性差异对血视网膜屏障通透性的影响程度。静脉注射染料后2分钟时,尽管血浆中游离染料浓度相似,但羧基荧光素的视网膜荧光强度测量值远低于荧光素。观察到染料从视盘明显渗漏到视乳头周围视网膜。在1小时和2小时时,两种染料的视网膜水平变得更加相似,因为荧光素从视网膜中清除的速度比羧基荧光素快。在碘酸钠诱导色素上皮损伤后,视网膜中两种染料的水平都很高,但羧基荧光素主要定位于细胞外间隙,而荧光素也使细胞体密集染色。记录的荧光强度水平与组织中染料的总质量成正比,羧基荧光素的荧光强度水平相应低于荧光素,这表明它们受到两种染料不同分布的显著影响。为了将组织荧光强度与细胞外液中的染料浓度直接相关联,从在已知浓度染料溶液中孵育的分离视网膜中进行测量。对数-对数图显示两种染料的荧光强度与培养基浓度之间呈线性关系,但羧基荧光素的视网膜荧光,与其在组织空间中的有限分布一致,始终低于荧光素。羧基荧光素与荧光素荧光的比率随视网膜层而变化,但在测试的浓度范围内,每层的比率是恒定的。然后使用这些荧光强度比率来调整体内数据,以便两种染料之间的比较更紧密地反映它们的细胞外染料浓度。通过这种校正,染料注射后不久外层视网膜中存在的羧基荧光素量约为荧光素的1/10,这表明羧基荧光素比荧光素更不容易穿透色素上皮,正如两种染料脂溶性差异所预期的那样。然而,视网膜中以及可能在玻璃体液中两种染料的荧光最终达到相似水平。这归因于染料在屏障不连续部位的进入,如在视盘处,以及它们从眼内腔室中清除速率的差异。