老年性白内障患者晶状体上皮细胞DNA氧化损伤水平与总抗氧化能力(TAC)是否相关?

Kranti S. Sorte Gawali, Avinash Jadhao, Manoj C. Lokhnade
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引用次数: 0

摘要

背景:各种实验证据表明,在白内障发病过程中,氧化应激在DNA损伤中起重要作用,但关于DNA损伤的体内评估和抗氧化剂的作用尚缺乏相关数据。目的:直接测定白内障患者晶状体上皮细胞中DNA损伤的百分比和总抗氧化能力(TAC),并与对照组进行比较,观察老年性白内障患者DNA氧化损伤与总抗氧化能力之间是否存在统计学相关性。患者和方法:选取我院眼科白内障手术收治的30例50 ~ 80岁老年性白内障患者,采用彗星法和TAC法体外评估人晶状体上皮细胞DNA损伤。从健康尸体或其亲属捐献的眼睛进行TAC分析中收集12例对照。结果:老年性白内障患者晶状体上皮细胞DNA氧化损伤水平与晶状体上皮细胞水提液中TAC含量无关。结论:本研究不应认为通过饮食补充抗氧化剂对预防氧化性DNA损伤没有作用。可能还有另一种机制导致DNA氧化损伤。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Is the Oxidative DNA Damage Level of Human Lens Epithelial Cells Correlated with the Total Antioxidant Capacity (TAC) in Aqueous Extract of HLECs in Senile Cataract Patients?
Background: Various experimental evidence suggests that in cataract pathogenesis oxidative stress plays an important role in causing DNA damage, but there is still a lack of data on in vivo assessment of DNA damage and the role of antioxidants. Objectives: To measure the percentage of DNA damage and the total antioxidant capacity (TAC) of patients with cataracts directly in human lens epithelial cells and compare these with a control group followed by whether there is any statistical correlation between oxidative DNA damage and total antioxidant status in senile cataract patients. Patients and methods: A total number of capsulorhexis from thirty senile cataract cases aged 50-80 years, who were admitted to the ophthalmology ward of AVBRH for cataract surgery, were used for in vitro assessment of DNA damage in human lens epithelial cells by Comet assay and TAC assays. 12 controls were collected from healthy cadavers who or their relatives donated their eyes for TAC assays. Results : Oxidative DNA damage level of human lens epithelial cells is not correlated with the TAC in aqueous extract of HLECs in senile cataract patients . Conclusion: The conclusion in the present study should not be taken that supplementing antioxidants through diet has no role in the prevention of oxidative DNA damage against oxidants. There may be another mechanism may be responsible for oxidative DNA damage.
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