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不同压力和浓度氧气治疗后氧化应激和炎症、miRNA、血红蛋白变化的随机试验。

Oxidative Stress and Inflammation, MicroRNA, and Hemoglobin Variations after Administration of Oxygen at Different Pressures and Concentrations: A Randomized Trial.

机构信息

Department of Biomedical Sciences, University of Padova, 35131 Padova, Italy.

Institute of Clinical Physiology, National Research Council (CNR), 20162 Milan, Italy.

出版信息

Int J Environ Res Public Health. 2021 Sep 16;18(18):9755. doi: 10.3390/ijerph18189755.

Abstract

Exercise generates reactive oxygen species (ROS), creating a redox imbalance towards oxidation when inadequately intense. Normobaric and hyperbaric oxygen (HBO) breathed while not exercising induces antioxidant enzymes expression, but literature is still poor. Twenty-two athletes were assigned to five groups: controls; 30%, or 50% O; 100% O (HBO) at 1.5 or 2.5 atmosphere absolute (ATA). Twenty treatments were administered on non-training days. Biological samples were collected at T0 (baseline), T1 (end of treatments), and T2 (1 month after) to assess ROS, antioxidant capacity (TAC), lipid peroxidation, redox (amino-thiols) and inflammatory (IL-6, 10, TNF-α) status, renal function (i.e., neopterin), miRNA, and hemoglobin. At T1, O mixtures and HBO induced an increase of ROS, lipid peroxidation and decreased TAC, counterbalanced at T2. Furthermore, 50% O and HBO treatments determined a reduced state in T2. Neopterin concentration increased at T1 breathing 50% O and HBO at 2.5 ATA. The results suggest that 50% O treatment determined a reduced state in T2; HBO at 1.5 and 2.5 ATA similarly induced protective mechanisms against ROS, despite the latter could expose the body to higher ROS levels and neopterin concentrations. HBO resulted in increased Hb levels and contributed to immunomodulation by regulating interleukin and miRNA expression.

摘要

运动产生活性氧(ROS),在强度不足时会导致氧化还原失衡。非运动时吸入常压低氧(NBO)和高压氧(HBO)会诱导抗氧化酶的表达,但文献仍然较少。22 名运动员被分为五组:对照组;30%或 50%O;100%O(HBO)在 1.5 或 2.5 个绝对大气压(ATA)。在非训练日进行 20 次治疗。在 T0(基线)、T1(治疗结束)和 T2(治疗结束后 1 个月)收集生物样本,以评估 ROS、抗氧化能力(TAC)、脂质过氧化、氧化还原(氨基酸硫醇)和炎症(IL-6、10、TNF-α)状态、肾功能(即新蝶呤)、miRNA 和血红蛋白。在 T1 时,O 混合物和 HBO 引起 ROS、脂质过氧化增加,TAC 降低,但在 T2 时得到了平衡。此外,50%O 和 HBO 处理在 T2 时使机体处于还原状态。在 T1 时,50%O 和 HBO 2.5ATA 呼吸会增加新蝶呤浓度。结果表明,50%O 处理在 T2 时使机体处于还原状态;1.5 和 2.5ATA 的 HBO 同样诱导了针对 ROS 的保护机制,尽管后者可能使机体暴露于更高的 ROS 水平和新蝶呤浓度下。HBO 导致血红蛋白水平升高,并通过调节白细胞介素和 miRNA 表达来促进免疫调节。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9dca/8468581/811aa76c2053/ijerph-18-09755-g001.jpg

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