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Increased ROS production and DNA damage in monocytes are biomarkers of aging and atherosclerosis

机译:单核细胞中ROS产生增加和DNA损伤是衰老和动脉粥样硬化的生物标志

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摘要

BackgroundNew evidence demonstrates that aging and dyslipidemia are closely associated with oxidative stress, DNA damage and apoptosis in some cells and extravascular tissues. However, in monocytes, which are naturally involved in progression and/or resolution of plaque in atherosclerosis, this concurrence has not yet been fully investigated. In this study, we evaluated the influence of aging and hypercholesterolemia on serum pro-inflammatory cytokines, oxidative stress, DNA damage and apoptosis in monocytes from apolipoprotein E-deficient (apoE−/−) mice compared with age-matched wild-type C57BL/6 (WT) mice. Experiments were performed in young (2-months) and in old (18-months) male wild-type (WT) and apoE−/− mice.
机译:背景新证据表明衰老和血脂异常与某些细胞和血管外组织的氧化应激,DNA损伤和细胞凋亡密切相关。然而,在自然参与动脉粥样硬化斑块的发展和/或消退的单核细胞中,这种并发性尚未得到充分研究。在这项研究中,我们评估了衰老和高胆固醇血症对载脂蛋白E缺乏症(apoE -// )小鼠的血清促炎细胞因子,氧化应激,DNA损伤和单核细胞凋亡的影响与年龄的关系。匹配的野生型C57BL / 6(WT)小鼠。实验是在雄性野生型(WT)和apoE -// 小鼠的年轻(2个月)和大龄(18个月)中进行的。

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