Meyer Linda M, Söderberg Per, Dong Xiuqin, Wegener Alfred
Research Department, St Erik's Eye Hospital, Karolinska Institutet, Polhemsgatan 50, SE-112 82 Stockholm, Sweden.
Exp Eye Res. 2005 Oct;81(4):389-94. doi: 10.1016/j.exer.2005.02.009.
The evolution of the morphological appearance and intensity of light scattering in C57 mice lenses after exposure to ultraviolet radiation type B (UVR-B) was investigated. A total of 80, 6-week-old female C57BL/6 mice were divided into four groups (n=20). One eye in each animal was exposed in vivo to UVR-B in the 300 nm wavelength region (UVR-B-300 nm) to a dose of 5 kJm(-2) for 15 min. The radiation output had lambda(max) at 302 nm with 5 nm [FWHM]. The animals were consecutively sacrificed at 1, 2, 4 and 8 days after the exposure. Macroscopic lens changes were documented using grid- and dark field illumination photography. Light scattering in the exposed and contralateral not exposed lens was measured quantitatively. Morphological lens changes were documented using grid- and dark field illumination photography. In vivo exposure to UVR-B-300 nm induced subcapsular cataract in all exposed lenses and occasionally cortical and nuclear cataract at all investigated time points. Exposed lenses scattered light significantly higher on all investigated days compared to contralateral non-exposed lenses. A transient increase of light scattering peaking at day 2 in exposed as well as in contralateral not exposed lenses was identified. Light scattering of the lenses varies with latency time after exposure. A dose of 5 kJm(-2) UVR-B-300 nm induces light scattering in C57 mice lenses. The increase has a transient peak at 2 days after exposure. The variation of light scattering among days 1, 2, 4, and 8 indicates a dynamic change of scattering characteristics in the mouse lens following unilateral in vivo exposure to 5 kJm(-2) UVR-B-300 nm.
研究了C57小鼠晶状体在暴露于B型紫外线(UVR-B)后光散射的形态外观和强度的演变。总共80只6周龄雌性C57BL/6小鼠被分为四组(n = 20)。每只动物的一只眼睛在体内暴露于波长为300 nm的UVR-B(UVR-B-300 nm),剂量为5 kJm(-2),持续15分钟。辐射输出的λ(max)为302 nm,半高宽为5 nm。在暴露后1、2、4和8天连续处死动物。使用网格照明和暗场照明摄影记录晶状体的宏观变化。对暴露的晶状体和对侧未暴露的晶状体中的光散射进行定量测量。使用网格照明和暗场照明摄影记录晶状体的形态变化。在所有研究时间点,体内暴露于UVR-B-300 nm均在所有暴露的晶状体中诱发了囊下白内障,偶尔还诱发了皮质和核性白内障。与对侧未暴露的晶状体相比,在所有研究日中,暴露的晶状体散射的光明显更高。在暴露的以及对侧未暴露的晶状体中,均发现光散射在第2天出现短暂增加并达到峰值。晶状体的光散射随暴露后的潜伏时间而变化。5 kJm(-2)的UVR-B-300 nm剂量会在C57小鼠晶状体中诱导光散射增加。这种增加在暴露后2天出现短暂峰值。第1、2、4和8天之间光散射的变化表明,在小鼠晶状体单侧体内暴露于5 kJm(-2)的UVR-B-300 nm后,散射特性发生了动态变化。