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Snapshot situation of oxidative degradation of the nervous system, kidney, and adrenal glands biomarkers-neuroprostane and dihomo-isoprostanes-urinary biomarkers from infancy to elderly adults

机译:从婴儿期到老年人的神经系统,肾脏和肾上腺生物标记物-神经前列腺素和二高异异前列腺素-尿液生物标记物氧化降解的快照情况

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We analyzed biomarkers of lipid peroxidation of the nervous system -F2-dihomo-isoprostanes, F3-neuroprostanes, and F4-neuroprostanes- in urine samples from 158 healthy volunteers ranging from 4 to 88 years old with the aim of analyzing possible associations between their excretion values and age (years). Ten biomarkers were screened in the urine samples by UHPLC-QqQ-MS/MS. Four F2-dihomo-isoprostanes ( ent ?7-( R )?7-F2t-dihomo-isoprostane, ent ?7- epi ?7-F2t-dihomo-isoprostane, 17-F2t-dihomo-isoprostane, 17- epi ?17-F2t-dihomo-isoprostane), and one DPA-neuroprostane (4-F3t-neuroprostane) were detected in the samples. On the one hand, we found a significant, positive correlation (Rho: 0.197, P =0.015) between the age increase and the amount of total F2-dihomo-IsoPs. On the other hand, the values were significantly higher in the childhood group (4–12 years old), when compared to the adolescence group (13–17 years old) and the young adult group (18–35 years old). Surprisingly, no significant differences were found between the middle-aged adults (36–64 years old) and the elderly adults (65–88 years old). We display a snapshot situation of excretory values of oxidative stress biomarkers of the nervous system, using healthy volunteers representative of the different stages of human growth and development. The values reported in this study could be used as a basal or starting point in clinical interventions related to aging processes and/or pathologies associated with the nervous system.
机译:我们分析了神经系统脂质过氧化的生物标志物-F 2 -二高异异前列腺素,F 3 -神经前列腺素和F 4 -神经前列腺素-从158名4至88岁的健康志愿者的尿液样本中进行分析,目的是分析其排泄值与年龄(岁)之间的可能联系。通过UHPLC-QqQ-MS / MS在尿液样品中筛选出十种生物标志物。四个F 2 -二高异前列腺素(ent?7-(R)?7-F 2t -二高异前列腺素,ent?7- Epi?7-F 2t -dihomo-isoprostane,17-F 2t- dihomo-isoprostane,17- Epi?17-F 2t -dihomo-isoprostane)和一个样品中检出了DPA-神经前列腺素(4-F 3t -神经前列腺素)。一方面,我们发现年龄增加与F 2 -dihomo-IsoPs总量之间存在显着的正相关(Rho:0.197,P = 0.015)。另一方面,与青春期组(13-17岁)和青年组(18-35岁)相比,儿童组(4-12岁)中的值明显更高。令人惊讶的是,中年人(36-64岁)和老年人(65-88岁)之间没有发现显着差异。我们使用代表人类生长和发育不同阶段的健康志愿者来显示神经系统氧化应激生物标记物排泄值的快照情况。这项研究中报道的值可以用作与神经系统相关的衰老过程和/或病理相关的临床干预的基础或起点。

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