SELENIUM – GLUTATHIONE PEROXIDASE RELATION IN ERYTHROCYTES WITH G-6-PDH DEFICIENCY AND THE GP ACTIVITY DEVIATION DURING OXIDATION BY SELENIUM. MINI-REVIEW

T. M. Huseynov, R. T. Guliyeva
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Abstract

Selenium status and glutathione peroxidase (GP) activity were investigated in patients with normal and glucose-6-phosphate dehydrogenase (G-6-PDH) deficient erythrocytes among Azerbaijani population. It has been shown that the content of Se in G-6-PDH-deficient erythrocytes is a little (≈16%) different from the norm, while GP activity of in them is substantially lower (≈ 50%). The low activity of GP probably is due to decreased production of GSH, the basic substrate for GP, in G-6-PDH-deficient erythrocytes. Addition of GSH precursor (N-acetylcysteine) to the incubation medium increases the GP activity, suggesting that the low level of GP activity is possibly connected with low level of GSH. G-6-PDH-deficient erythrocytes demonstrate significantly greater susceptibility to oxidative stress than normal ones when exposed to ultraviolet radiation of the small (7 kJ/m2) and moderate (15 kJ/m2) doses, and to high tension electric field (HTEF ≈ 60 kV/m × 5 hours). In particular, the accumulation of lipid peroxidation products (malonic dialdehyde) under visible UV irradiation in G-6-PDH-deficient erythrocytes is ≈50-80% higher, than in the control. Nevertheless, in G-6-PDH-deficient erythrocytes HTEF have no significant effect on the accumulation of malonic dialdehyde, though the GP and catalase activity are falling faster than normal, and have initially lower level.
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硒氧化过程中g-6-pdh缺乏症红细胞中硒-谷胱甘肽过氧化物酶与gp活性偏差的关系。本文着重
研究了阿塞拜疆人群中正常红细胞和谷胱甘肽过氧化物酶(GP)活性和葡萄糖-6-磷酸脱氢酶(G-6-PDH)缺陷红细胞的硒状态。结果表明,g -6- pdh缺陷红细胞中Se的含量与正常值相差不大(≈16%),而GP的活性则明显降低(≈50%)。GP活性低可能是由于GSH (GP的基本底物)在g -6- pdh缺乏的红细胞中产生减少。在培养液中加入谷胱甘肽前体(n -乙酰半胱氨酸)可使谷胱甘肽活性增加,提示谷胱甘肽活性低可能与谷胱甘肽水平低有关。g -6- pdh缺陷红细胞暴露于小剂量(7 kJ/m2)和中等剂量(15 kJ/m2)的紫外线辐射和高压电场(HTEF≈60 kV/m × 5小时)下,对氧化应激的敏感性明显高于正常红细胞。特别是,在可见紫外线照射下,g -6- pdh缺陷红细胞中脂质过氧化产物(丙二醛)的积累比对照组高约50-80%。然而,在g -6- pdh缺乏的红细胞中,HTEF对丙二醛的积累没有显著影响,尽管GP和过氧化氢酶活性下降速度比正常快,并且初始水平较低。
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