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慢性肾衰竭患者的微量元素与脂质过氧化异常

Trace elements and lipid peroxidation abnormalities in patients with chronic renal failure.

作者信息

Richard M J, Arnaud J, Jurkovitz C, Hachache T, Meftahi H, Laporte F, Foret M, Favier A, Cordonnier D

机构信息

Laboratoire de Biochimie C, CHRUG, Grenoble, France.

出版信息

Nephron. 1991;57(1):10-5. doi: 10.1159/000186208.

Abstract

Plasma selenium (Se), zinc (Zn) and copper (Cu) levels and antioxidant metalloenzymes, glutathione peroxidase (GPX) and superoxide dismutase (SOD), were studied in 17 patients on maintenance hemodialysis (HD) (group I), 14 uremic patients (group II) and 14 healthy subjects (group III). Plasma Se levels and erythrocyte GPX were significantly lower in the HD group (for Se: 0.69 +/- 0.12 vs. 1.05 +/- 0.13 mumol/l in controls; for erythrocyte GPX: 34.4 +/- 6.4 vs. 49.2 +/- 9 IU/g hemoglobin in controls) and a significant correlation was found between the two parameters (r = 0.66, p less than 0.005). There was also a correlation between decreased plasma Zn and erythrocyte SOD activity (r = 0.58, p less than 0.02) and between decreased plasma Cu and erythrocyte SOD (r = 0.60, p less than 0.02). Plasma malondialdehyde levels were augmented in HD patients (5.08 +/- 0.26 vs. 2.55 +/- 0.15 mumol/l in controls and 2.79 +/- 0.40 mumol/l in the uremic group). The catalase activity was increased in HD patients (202 +/- 24 vs. 140 +/- 40 IU/mg hemoglobin in group III). A defective antioxidant activity may thus contribute to increased peroxidative damage to cells in the course of dialysis.

摘要

对17例维持性血液透析(HD)患者(I组)、14例尿毒症患者(II组)和14例健康受试者(III组)的血浆硒(Se)、锌(Zn)和铜(Cu)水平以及抗氧化金属酶谷胱甘肽过氧化物酶(GPX)和超氧化物歧化酶(SOD)进行了研究。HD组的血浆Se水平和红细胞GPX显著降低(Se:HD组为0.69±0.12μmol/L,对照组为1.05±0.13μmol/L;红细胞GPX:HD组为34.4±6.4IU/g血红蛋白,对照组为49.2±9IU/g血红蛋白),且发现这两个参数之间存在显著相关性(r = 0.66,p<0.005)。血浆Zn降低与红细胞SOD活性降低之间也存在相关性(r = 0.58,p<0.02),血浆Cu降低与红细胞SOD之间也存在相关性(r = 0.60,p<0.02)。HD患者的血浆丙二醛水平升高(HD组为5.08±0.26μmol/L,对照组为2.55±0.15μmol/L,尿毒症组为2.79±0.40μmol/L)。HD患者的过氧化氢酶活性增加(HD组为202±24IU/mg血红蛋白,III组为140±40IU/mg血红蛋白)。因此,抗氧化活性缺陷可能导致透析过程中细胞过氧化损伤增加。

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