Tsakanova Gohar, Arakelova Elina, Ayvazyan Violetta, Ayvazyan Anna, Tatikyan Stepan, Grigoryan Ruzanna, Sargsyan Natalya, Arakelyan Arsen
Institute of Molecular Biology of National Academy of Sciences of Republic of Armenia, 7 Hasratyan str., 0014, Yerevan, Armenia.
CANDLE Synchrotron Research Institute, 31 Acharyan str., 0040, Yerevan, Armenia.
Biomed Opt Express. 2020 Jun 2;11(7):3444-3454. doi: 10.1364/BOE.393898. eCollection 2020 Jul 1.
According to the "oxidative stress theory" of aging, this process is accompanied by a progressive and irreversible accumulation of oxidative damage caused by reactive oxygen species (ROS). This, in turn, has a deleterious impact on molecular mechanisms in aging thereby altering the physiological function of the organism, increasing the risk of different aging-related diseases, as well as impacting the life span. The aim of the current study was to investigate oxidative stress in living red blood cells (RBCs) in human aging as an oxidative stress-related pathological condition. Two-photon laser scanning and light microscopy techniques were applied to analyze the oxidative stress in RBCs and the cell viability. Spectrophotometric analyzes were performed to determine the percentage of RBC hemolysis, activities of superoxide dismutase and catalase in RBCs, as well as the ferroxidase activities of ceruloplasmin in blood plasma samples. The studies included three human aging groups, young, middle-aged, and elderly. According to the results, the two-photon fluorescence of carboxy-DCFDA, indicating the intensity of oxidative stress, significantly increase in RBCs by the increase of age ( < 0.05), and these intensities are in statistically significant positive correlation with age ( < 0.001) and a strong negative correlation ( < 0.05) with the activity of catalase in RBCs and ferroxidase activity of ceruloplasmin in plasma. In conclusion, two-photon fluorescent imaging of oxidative stress in human living RBCs is a valuable and accurate method for the determination of aging processes in humans and can be suggested as a novel indicator for human aging processes in individual aging.
根据衰老的“氧化应激理论”,这一过程伴随着活性氧(ROS)引起的氧化损伤的逐渐且不可逆的积累。反过来,这对衰老过程中的分子机制产生有害影响,从而改变生物体的生理功能,增加与衰老相关的不同疾病的风险,并影响寿命。本研究的目的是调查人类衰老过程中活红细胞(RBC)中的氧化应激,这是一种与氧化应激相关的病理状况。应用双光子激光扫描和光学显微镜技术分析红细胞中的氧化应激和细胞活力。进行分光光度分析以确定红细胞溶血百分比、红细胞中超氧化物歧化酶和过氧化氢酶的活性,以及血浆样本中铜蓝蛋白的亚铁氧化酶活性。研究包括三个人类衰老组,即青年、中年和老年组。结果显示,羧基 - DCFDA的双光子荧光表明氧化应激强度,随着年龄增长在红细胞中显著增加(<0.05),并且这些强度与年龄呈统计学显著正相关(<0.001),与红细胞中过氧化氢酶活性和血浆中铜蓝蛋白的亚铁氧化酶活性呈强负相关(<0.05)。总之,人类活红细胞氧化应激的双光子荧光成像对于确定人类衰老过程是一种有价值且准确的方法,可被建议作为个体衰老中人类衰老过程的新指标。