抑制高铁血红蛋白形成对红细胞抗氧化防御的影响

IF 3.8 3区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of biochemistry and biophysics Pub Date : 2024-08-14 DOI:10.1016/j.abb.2024.110121
Daniela Melo , Susana Coimbra , Susana Rocha , Alice Santos-Silva
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引用次数: 0

摘要

我们的目的是研究防止高铁血红蛋白(metHb)形成对过氧化物歧化酶 2(Prx2)、谷胱甘肽过氧化物酶(GPx)和过氧化氢酶(CAT)在红细胞抗氧化防御系统中的作用的影响。我们使用健康的红细胞进行了体外试验,在抑制或不抑制 Hb 自氧化(一氧化碳饱和)的情况下,然后进行 H2O2 诱导的氧化应激。我们评估了红细胞(RBC)细胞质和细胞膜中 CAT、GPx 和 Prx2 的酶活性和数量,以及氧化应激的几种生物标志物,如还原和氧化谷胱甘肽水平、硫代巴比妥酸活性物质(TBARS)水平、膜结合血红蛋白和总抗氧化状态。当 Hb 的自氧化受到抑制时,GPx 和 CAT 没有发现明显的变化;Prx2 仅在细胞质中以单体形式存在,没有与膜结合。阻断 Hb 作为伪过氧化物酶的功能似乎不会对红细胞过氧化物酶的功能产生影响。
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Influence of inhibiting methemoglobin formation on erythrocyte antioxidant defense

We aimed to study the influence of preventing methemoglobin (metHb) formation, in the roles of peroxiredoxin 2 (Prx2), glutathione peroxidase (GPx) and catalase (CAT) on the erythrocyte antioxidant defense system. We performed in vitro assays using healthy erythrocytes, with and without inhibition of autoxidation of Hb (saturation with carbon monoxide), followed by H2O2-induced oxidative stress. We assessed the enzyme activities and amounts of CAT, GPx and Prx2 in the red blood cell (RBC) cytosol and membrane and several biomarkers of oxidative stress, such as the reduced and oxidized glutathione levels, thiobarbituric acid reactive substances (TBARS) levels, membrane bound hemoglobin and total antioxidant status. When autoxidation of Hb was inhibited, no significant changes were found for GPx and CAT; Prx2 was observed only in the monomeric form in the cytosol and none bound to the membrane. Blocking the function of Hb as a pseudo-peroxidase does not seem to have an impact on the function of the RBC peroxidases.

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来源期刊
Archives of biochemistry and biophysics
Archives of biochemistry and biophysics 生物-生化与分子生物学
CiteScore
7.40
自引率
0.00%
发文量
245
审稿时长
26 days
期刊介绍: Archives of Biochemistry and Biophysics publishes quality original articles and reviews in the developing areas of biochemistry and biophysics. Research Areas Include: • Enzyme and protein structure, function, regulation. Folding, turnover, and post-translational processing • Biological oxidations, free radical reactions, redox signaling, oxygenases, P450 reactions • Signal transduction, receptors, membrane transport, intracellular signals. Cellular and integrated metabolism.
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