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Enhancement of lipid peroxidation and its amelioration by vitamin E in a subject with mutations in the SBP2 gene

机译:SBP2基因突变的受试者体内脂质过氧化作用的增强和维生素E的改善

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摘要

Selenocysteine (Sec) insertion sequence-binding protein 2 (SBP2) is essential for the biosynthesis of Sec-containing proteins, termed selenoproteins. Subjects with mutations in the SBP2 gene have decreased levels of several selenoproteins, resulting in a complex phenotype. Selenoproteins play a significant role in antioxidative defense, and deficiencies in these proteins can lead to increased oxidative stress. However, lipid peroxidation and the effects of antioxidants in subjects with SBP2 gene mutations have not been studied. In the present study, we evaluated the lipid peroxidation products in the blood of a subject (the proband) with mutations in the SBP2 gene. We found that the proband had higher levels of free radical-mediated lipid peroxidation products, such as 7β-hydroxycholesterol, than the control subjects. Treatment of the proband with vitamin E (α-tocopherol acetate, 100 mg/day), a lipid-soluble antioxidant, for 2 years reduced lipid peroxidation product levels to those of control subjects. Withdrawal of vitamin E treatment for 7 months resulted in an increase in lipid peroxidation products. Collectively, these results clearly indicate that free radical-mediated oxidative stress is increased in the subject with SBP2 gene mutations and that vitamin E treatment effectively inhibits the generation of lipid peroxidation products.
机译:硒代半胱氨酸(Sec)插入序列结合蛋白2(SBP2)对于生物合成含硒的蛋白(称为硒蛋白)至关重要。 SBP2基因突变的受试者的几种硒蛋白水平降低,导致复杂的表型。硒蛋白在抗氧化防御中起着重要作用,这些蛋白的缺乏会导致氧化应激增加。然而,尚未研究脂质过氧化和抗氧化剂在具有SBP2基因突变的受试者中的作用。在本研究中,我们评估了受试者(先证者)的血液中的脂质过氧化产物,其SBP2基因发生了突变。我们发现,先证者具有比对照受试者更高水平的自由基介导的脂质过氧化产物,例如7β-羟基胆固醇。用维生素E(醋酸α-生育酚,100 mg /天)(一种脂溶性抗氧化剂)治疗先证者2年,与对照对象相比,脂类过氧化产物的水平降低了。停用维生素E治疗7个月导致脂质过氧化产物增加。总的来说,这些结果清楚地表明,自由基介导的氧化应激在具有SBP2基因突变的受试者中增加,并且维生素E处理有效地抑制了脂质过氧化产物的产生。

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