首页> 外文期刊>Mutation Research: International Journal on Mutagenesis, Chromosome Breakage and Related Subjects >DNA damage and antioxidant defense in peripheral leukocytes of patients with Type I diabetes mellitus.
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DNA damage and antioxidant defense in peripheral leukocytes of patients with Type I diabetes mellitus.

机译:I型糖尿病患者外周血白细胞的DNA损伤和抗氧化防御作用。

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We determined relationship among DNA damage, nitric oxide (NO) and antioxidant defense in leukocytes of patients with Type 1 DM. DNA damage was evaluated as strand breakage and formamidopyrimidine DNA glycosylase (Fpg)-sensitive sites by the comet assay in DNA from leukocytes of the subjects. Nitrite level, as a product of NO, superoxide dismutase (SOD) activity and glutathione peroxidase (G-Px) activity of the leukocytes were measured by spectrophotometric kits. Serum glucose level and glycosylated haemoglobin (HbA(1c)) were higher in the patients, as expected. Differences in measured parameters between controls and patients were assessed in men and women separately. There was no significant difference between patient and control groups in neither men nor women for nitrite level. Strand breakage and Fpg-sensitive sites were found to be increased, SOD and G-Px activities of the leukocytes were found to be decreased in both men and women of patient group as compared to their respective controls. Significant correlations were determined between strand breakage and HbA(1c) (r = 0.37, P<0.05); Fpg-sensitive sites and HbA(1c) (r = 0.59, P<0.01); Fpg-sensitive sites and glucose (r = 0.45, P<0.02); Fpg-sensitive sites and SOD (r = -0.48, P<0.02); HbA(1c) and SOD (r = -0.50, P<0.02). In conclusion, impaired antioxidant defense in leukocytes of patients with Type 1 DM may be one of the responsible mechanisms for increased DNA damage in those patients.
机译:我们确定了1型DM患者白细胞的DNA损伤,一氧化氮(NO)和抗氧化防御之间的关系。通过彗星试验测定受试者白细胞DNA中的DNA损伤,以链断裂和甲酰嘧啶DNA糖基化酶(Fpg)敏感位点进行评估。用分光光度法测定白细胞中亚硝酸盐水平(作为NO,超氧化物歧化酶(SOD)活性和谷胱甘肽过氧化物酶(G-Px)活性的产物)。如预期的那样,患者的血清葡萄糖水平和糖基化血红蛋白(HbA(1c))较高。分别评估了男性和女性在对照组和患者之间的测量参数差异。男女患者亚硝酸盐水平无明显差异。与对照组相比,患者组的男性和女性均发现链断裂和Fpg敏感位点增加,白细胞的SOD和G-Px活性降低。确定了链断裂与HbA(1c)之间的显着相关性(r = 0.37,P <0.05); Fpg敏感位点和HbA(1c)(r = 0.59,P <0.01); Fpg敏感位点和葡萄糖(r = 0.45,P <0.02); Fpg敏感位点和SOD(r = -0.48,P <0.02); HbA(1c)和SOD(r = -0.50,P <0.02)。总之,1型糖尿病患者白细胞中抗氧化防御能力的受损可能是导致这些患者DNA损伤增加的原因之一。

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