He Jingyi, Li Tingyu, Chen Jie, Liu Youxue, Xiong Feng, Yang Jing, Song Cui
Children Nutrition Research Center, Ministry of Education Key Laboratory of Child Development and Disorders, Key Laboratory of Pediatrics in Chongqing, CSTC2009 CA5002, Chongqing International Science and Technology Cooperation Center for Child Development and Disorders, Children's Hospital of Chongqing Medical University, Chongqing 400014, PR China.
Children's Hospital of Chongqing Medical University, Central District, Chongqing, PR China.
Clin Biochem. 2016 Jan;49(1-2):61-5. doi: 10.1016/j.clinbiochem.2015.08.026. Epub 2015 Sep 2.
Oxidative stress (OS) may play a critical role in cell aging and neurologic disorders that are often seen in Down syndrome (DS) patients. The aim of this study was to determine the antioxidant enzyme level and lipoperoxidation status in blood from DS children.
In a cross-sectional study, we recruited a total of 36 DS children and 40 healthy controls (HCs). All subjects were free of infection according to the C reactive protein (CRP) value and routine peripheral blood profile. The activities of total superoxide dismutases (SODs), extracellular glutathione peroxidase (GPx3),malondialdehyde (MDA) and nitric oxide synthase (NOS) concentrations in peripheral blood were measured by spectrophotometric methods. The relationship of SOD and GPx3 was analyzed in the two groups.
The two groups were similar with respect to age, gender and peripheral blood profiles. The total SOD activity was significantly increased, while the GPx3 activity was significantly reduced in the DS group compared to the HCs (p=0.000, p=0.033 respectively). The MDA level was higher in DS children (p=0.013). There was no significant difference in NOS between DS and HCs (p=0.708). A significant negative correlation between GPx3 and SOD activity was identified in DS (r=-0.14, p=0.018) but not in the HC group.
Abnormal redox metabolism takes place in DS individuals. Reducing GPx3 may be a compensatory mechanism of protection against intracellular OS. Moreover, monitoring of decreases in GPx3 activity may be a useful biomarker for evaluating OS in DS patients.
氧化应激(OS)可能在细胞衰老以及唐氏综合征(DS)患者中常见的神经疾病中起关键作用。本研究的目的是测定DS儿童血液中的抗氧化酶水平和脂质过氧化状态。
在一项横断面研究中,我们共招募了36名DS儿童和40名健康对照(HC)。根据C反应蛋白(CRP)值和常规外周血检查,所有受试者均无感染。采用分光光度法测定外周血中总超氧化物歧化酶(SOD)、细胞外谷胱甘肽过氧化物酶(GPx3)、丙二醛(MDA)和一氧化氮合酶(NOS)的浓度。分析两组中SOD和GPx3的关系。
两组在年龄、性别和外周血检查方面相似。与HC组相比,DS组的总SOD活性显著升高,而GPx3活性显著降低(分别为p = 0.000,p = 0.033)。DS儿童的MDA水平较高(p = 0.013)。DS组和HC组之间的NOS无显著差异(p = 0.708)。在DS组中,GPx3与SOD活性之间存在显著负相关(r = -0.14,p = 0.018),而在HC组中未发现。
DS个体存在异常的氧化还原代谢。降低GPx3可能是一种针对细胞内OS的代偿性保护机制。此外,监测GPx3活性的降低可能是评估DS患者OS的有用生物标志物。