Wiig H
Department of Physiology, University of Bergen, Norway.
Exp Eye Res. 1990 Mar;50(3):261-7. doi: 10.1016/0014-4835(90)90210-l.
Transport of radiolabelled albumin in vivo has been measured in cornea. In anaesthetized rabbits, a 1-10 nl mixture of either 125I- or 131I-labelled human serum albumin and fluorescinthiocarbamoyldextran was injected with micropipettes under guidance of a fluorescent microscope. The injection sites were a spot 3 mm from limbus and the cornea centre, and the sites were localized by a template fitting the cornea exactly. Four, 12, 20 and 30 hr after the injection, the rabbits were reanaesthetized, and enucleated after being killed with an overdose of anaesthetic. The bulbi were frozen, and dissection of cornea performed in the cold room using the template described above and a stereomicroscope. Numbered samples were obtained, and isotope distribution measured. In the experiments lasting for 20 hr, about 55% of the isotope was recovered, giving a transfer coefficient of 0.4-0.5 per day. A common pattern of isotope distribution was observed independent of duration of isotope equilibration; peripherally injected isotope moved preferentially in central direction, indicating that fluid is transported by bulk flow and diffusion from peripheral to central cornea. Centrally injected isotope moved symmetrically from the injection point, as expected from transport by diffusion alone. Data from experiments with isotope injection in the cornea centre allowed the calculation of a diffusion coefficient for albumin along cornea of 2.19 x 10(-7) cm2 sec-1.
已对角膜中放射性标记白蛋白的体内转运进行了测量。在麻醉的兔子中,在荧光显微镜引导下用微量移液器注射125I或131I标记的人血清白蛋白与荧光素硫代氨基甲酰葡聚糖的1-10 nl混合物。注射部位是距角膜缘和角膜中心3 mm处的一个点,这些部位通过与角膜精确适配的模板进行定位。注射后4、12、20和30小时,兔子再次麻醉,用过量麻醉剂处死之后摘眼球。眼球冷冻后,在冷藏室中使用上述模板和体视显微镜进行角膜解剖。获取编号样本并测量同位素分布。在持续20小时的实验中,约55%的同位素被回收,每天的转移系数为0.4 - 0.5。观察到同位素分布的常见模式,与同位素平衡持续时间无关;周边注射的同位素优先向中心方向移动,表明液体通过整体流动和扩散从周边角膜向中央角膜运输。如仅由扩散运输所预期的那样,中央注射的同位素从注射点对称移动。角膜中心同位素注射实验的数据使得能够计算白蛋白沿角膜的扩散系数为2.19×10(-7) cm2 sec-1。