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使用完整晶状体的体外紫外线诱导白内障的作用光谱和恢复情况

Action spectrum and recovery for in vitro UV-induced cataract using whole lenses.

作者信息

Oriowo O M, Cullen A P, Chou B R, Sivak J G

机构信息

School of Optometry, University of Waterloo, Ontario, Canada.

出版信息

Invest Ophthalmol Vis Sci. 2001 Oct;42(11):2596-602.

Abstract

PURPOSE

To establish the in vitro action spectrum for acute UV cataractogenesis using whole cultured lenses. The recovery pattern of the induced cataract was also investigated.

METHODS

Aseptically dissected porcine lenses were cultured in glass chambers. At 1 week, lenses were exposed to a predetermined UV energy (J/cm(2)) at specific wavebands ranging from 270 to 370 nm at 5- and 10-nm intervals. The UV energy was generated by a PRA integrated arc lamp system using a water-cooled 1000 W, high-pressure xenon lamp. The lamp output was limited using a deionized water filter, a monochromator, and secondary optics. An electronic shutter was used to control the exposure time. The median effective dose, ED(50) (i.e., UV energy threshold) for each waveband was statistically determined using probit analysis. Irradiated spots (3.06 mm(2)) on the lenses were monitored every 6 to 12 hours up to 48 hours postirradiation for any UV-induced opacity with a dissecting microscope and photomicrography. The ED(50)s were plotted against wavelengths to obtain the action spectrum.

RESULTS

The threshold values for 270, 300, and 365 nm were 0.057, 0.069, and 137.19 J/cm(2), respectively. Permanent UV-induced cataract was obtained at twice the threshold values for UVB and UVA.

CONCLUSIONS

An action spectrum for in vitro UV-induced cataract using whole cultured lens is established. These data are comparable to published in vitro (with isolated lens epithelial cells) and in vivo action spectra. The recovery pattern appears to be similar to the in vivo situation.

摘要

目的

利用全培养晶状体建立急性紫外线致白内障形成的体外作用光谱。同时研究诱导性白内障的恢复模式。

方法

无菌解剖猪晶状体并培养于玻璃小室中。1周后,晶状体在特定波段(270至370nm,间隔5nm和10nm)下暴露于预定的紫外线能量(J/cm²)。紫外线能量由PRA集成弧光灯系统产生,该系统使用水冷1000W高压氙灯。通过去离子水滤光片、单色仪和二级光学器件限制灯的输出。使用电子快门控制曝光时间。使用概率分析统计确定每个波段的半数有效剂量(ED50)(即紫外线能量阈值)。在照射后长达48小时内,每6至12小时用解剖显微镜和显微摄影监测晶状体上的照射点(3.06mm²)是否有紫外线诱导的混浊。将ED50值与波长作图以获得作用光谱。

结果

270nm、300nm和365nm的阈值分别为0.057、0.069和137.19J/cm²。在UVB和UVA阈值的两倍时可获得永久性紫外线诱导的白内障。

结论

建立了利用全培养晶状体的体外紫外线诱导白内障的作用光谱。这些数据与已发表的体外(分离的晶状体上皮细胞)和体内作用光谱相当。恢复模式似乎与体内情况相似。

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