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首页> 外文期刊>Free radical research >The reduction of nitroblue tetrazolium by red blood cells: a measure of Red Cell membrane antioxidant capacity and hemoglobin-membrane binding sites.
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The reduction of nitroblue tetrazolium by red blood cells: a measure of Red Cell membrane antioxidant capacity and hemoglobin-membrane binding sites.

机译:红细胞对硝基蓝四唑的还原作用:红细胞膜抗氧化能力和血红蛋白-膜结合位点的量度。

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摘要

The reduction of nitroblue tetrazolium (NBT) with intact Red Blood Cells (RBCs) is biphasic with an initial rapid reduction followed by a slower second phase. This biphasic kinetics has been explained with the initial rapid phase attributed to antioxidants in the red cell which reduce membrane bound NBT and the slower phase associated with the reaction of NBT with membrane bound hemoglobin. This model has been confirmed by a utilization of a number of red cell modifications which either increase the red cell antioxidants (vitamin C and vitamin E) or damage the red cell membrane (cumene hydroperoxide and N-ethylmaleimide). The utilization of this assay for human blood samples was investigated by studying a series of 20 human subjects ranging between 34 and 87 years of age. It was possible to fit all of these samples with two adjustable parameters which reflect the red cell membrane antioxidant capacity (x) and the hemoglobin membrane interactions (m). The antioxidant capacity shows a significant (p < .002; R = -.67) decrease with age. This finding is consistent with a decrease in the level of antioxidants in aged subjects. In addition, the number of hemoglobin membrane sites are negatively correlated with the antioxidant capacity (p < .02; R = -.52) suggesting that the oxidative stress associated with reduced antioxidants results in increased hemoglobin-membrane interactions.
机译:完整的红血球(RBC)还原硝基蓝四唑(NBT)是双相的,最初是快速还原,然后是较慢的第二相。已经解释了这种双相动力学,其初始快速相归因于红细胞中的抗氧化剂,其减少了与膜结合的NBT的抗氧化剂,以及与NBT与膜结合的血红蛋白反应相关的较慢的相。该模型已通过利用多种红细胞修饰得到证实,这些修饰可增加红细胞抗氧化剂(维生素C和维生素E)或损坏红细胞膜(氢过氧化枯烯和N-乙基马来酰亚胺)。通过研究一系列年龄在34至87岁之间的20名人类受试者,研究了该测定法在人类血液样本中的利用。可以用反映红细胞膜抗氧化能力(x)和血红蛋白膜相互作用(m)的两个可调参数来拟合所有这些样品。随着年龄的增长,抗氧化能力显着下降(p <.002; R = -.67)。这一发现与老年受试者中抗氧化剂水平的降低是一致的。此外,血红蛋白膜位点的数量与抗氧化能力呈负相关(p <.02; R = -.52),表明与减少的抗氧化剂相关的氧化应激导致血红蛋白与膜的相互作用增加。

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