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Polymorphism in the manganese superoxide dismutase gene

机译:锰超氧化物歧化酶基因的多态性

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Oxidative stress and mitochondrial damage occur in sepsis. Manganese superoxide dismutase (MnSOD) provides the main defence against oxidative stress within mitochondria. Ala9Val is a single nucleotide polymorphism (SNP) in the MnSOD gene, predicted to affect intra- mitochondrial transport of the enzyme. We found a significant difference in the genotype frequency between healthy subjects (n = 100) and patients with sepsis (n = 40, p = 0.009). For assessment of functionality ten healthy subjects of each homozygous genotype (A/ A or V/ V) were studied. Peripheral blood mononuclear cells were separated and incubated for 18 h with lipopolysaccharide (LPS), followed by analysis of mitochondrial and cytosolic fractions. There was no difference between genotypes in MnSOD activity and cytochrome c concentration, and minor differences in total antioxidant capacity (TAC) and mitochondrial membrane potential, which did not affect response to LPS. Despite predictions from structural enzyme studies that mitochondrial trafficking would be affected by the Ala9Val polymorphism of the MnSOD gene had little functional effect.
机译:氧化应激和线粒体损伤发生在败血症中。锰超氧化物歧化酶(MnSOD)提供了针对线粒体内氧化应激的主要防御作用。 Ala9Val是MnSOD基因中的单核苷酸多态性(SNP),预计会影响酶的线粒体内转运。我们发现健康受试者(n = 100)和败血症患者(n = 40,p = 0.009)之间的基因型频率有显着差异。为了评估功能,研究了每种纯合基因型(A / A或V / V)的十名健康受试者。分离外周血单个核细胞,并与脂多糖(LPS)孵育18 h,然后分析线粒体和胞质组分。 MnSOD活性和细胞色素c浓度的基因型之间没有差异,总抗氧化剂能力(TAC)和线粒体膜电位的细微差异也没有,这不影响对LPS的反应。尽管从结构酶研究中预测到,MnSOD基因的Ala9Val多态性会影响线粒体运输,但功能影响很小。

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