Kojima M
Department of Experimental Ophthalmology, University of Bonn, F.R.G.
Lens Eye Toxic Res. 1990;7(3-4):547-61.
As the UV-B cataract and early stages of diabetic cataract in rats only touches the epithelium and anterior superficial cortex, a whole lens analysis is not meaningful, but a regional analysis with the freeze-sectioning device has to be performed. Scheimpflug photography with microdensitometric image analysis enables the scientist to discern in vivo single layers along the optical axis of the lens. UV-B cataracts (0.2 J/cm2, every 2nd day) and diabetic cataracts (Streptozotocin (STZ), 70 mg/kg BW) were induced in Brown-Norway rats. The stages of lens opacification were documented by Scheimpflug photography. 8 weeks after start of UV-B treatment and at several dates before onset of visible diabetic cataractous changes, the animals were sacrificed. The lenses were divided reproducibly into 4 or 7 parts such as an equatorial ring and several layers of the central cylinder from anterior to posterior part. The enzyme activity spectrum shows highly region related pattern that would not have been found in a whole lens analysis. Aldose reductase was activated before appearance of visible cataractous changes due to diabetes compared to normal lenses. In contrast Fructose-1,6-biphosphate-aldolase activity was lower before onset of visible changes than in normal lenses, but only within the 1st section where later visible cataractous changes of UV-B cataract could be detected.
由于大鼠中的UV-B白内障和糖尿病性白内障早期仅累及晶状体上皮和前表面皮质,因此对整个晶状体进行分析并无意义,而必须使用冷冻切片装置进行区域分析。带有显微密度图像分析的Scheimpflug摄影技术使科学家能够在体内沿晶状体光轴分辨单层结构。在棕色挪威大鼠中诱导产生UV-B白内障(0.2 J/cm²,每隔一天一次)和糖尿病性白内障(链脲佐菌素(STZ),70 mg/kg体重)。通过Scheimpflug摄影记录晶状体混浊的阶段。在UV-B治疗开始8周后以及在可见糖尿病性白内障变化出现之前的几个时间点,处死动物。将晶状体可重复地分为4或7部分,例如一个赤道环和从晶状体前部到后部的中央圆柱体的几层。酶活性谱显示出高度与区域相关的模式,这在对整个晶状体的分析中是无法发现的。与正常晶状体相比,在因糖尿病出现可见白内障变化之前,醛糖还原酶就已被激活。相比之下,在可见变化出现之前,果糖-1,6-二磷酸醛缩酶的活性低于正常晶状体,但仅在第一个切片中,在该切片中后来可以检测到UV-B白内障的可见变化。