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紫外线A辐射对器官培养中晶状体上皮钠钾ATP酶的影响。

Effects of UV-A radiation on lens epithelial NaK-ATPase in organ culture.

作者信息

Dovrat A, Weinreb O

机构信息

B. Rappaport Faculty of Medicine, Technion-Israel Institute of Technology, Haifa.

出版信息

Invest Ophthalmol Vis Sci. 1999 Jun;40(7):1616-20.

Abstract

PURPOSE

To investigate the mechanisms involved in the damage caused by UV-A irradiation at 365 nm on the eye lens.

METHODS

Bovine lenses obtained from animals 1 to 5 years of age were placed in specially designed organ culture chambers for preincubation. Twenty-four hours later, the lenses were irradiated by 33 J/cm2 UV-A at 365 nm. During irradiation, the lenses were oriented in the culture so that the anterior surface faced the incident UV-A radiation source. After irradiation, lens optical quality was monitored throughout the 8 days of the culture period, and lens samples were taken for analysis of NaK-ATPase activity.

RESULTS

Lens optics and NaK-ATPase activity were affected by irradiation of 33 J/cm2. The effects on lens epithelial NaK-ATPase activity were stronger at the equators than at the center. The damage to the activity at the center was reversible, as the lens optically recovered from the LW-A damage.

CONCLUSIONS

Lens NaK-ATPase activity can recover from damage caused by UV-A at 365 nm. When the lenses received irradiation of 33 J/cm2, NaK-ATPase activity recovered from the damage during the culture period only at the center and not at the equators of the epithelium.

摘要

目的

研究365nm的UV-A辐射对眼晶状体造成损伤的相关机制。

方法

将取自1至5岁动物的牛晶状体置于专门设计的器官培养室中进行预孵育。24小时后,用33J/cm²的365nm UV-A对晶状体进行照射。照射期间,将晶状体在培养中定向,使前表面面对入射的UV-A辐射源。照射后,在整个8天的培养期内监测晶状体的光学质量,并采集晶状体样本分析NaK-ATP酶活性。

结果

33J/cm²的照射影响了晶状体光学和NaK-ATP酶活性。对晶状体上皮NaK-ATP酶活性的影响在赤道处比在中心更强。中心处活性的损伤是可逆的,因为晶状体从LW-A损伤中光学恢复。

结论

晶状体NaK-ATP酶活性可从365nm的UV-A造成的损伤中恢复。当晶状体接受33J/cm²的照射时,NaK-ATP酶活性仅在培养期内在上皮中心而非赤道处从损伤中恢复。

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