Koike Shin, Sudo Haruka, Turudome Satori, Ueyama Masako, Tanaka Yoshiaki, Kimura Hiroshi, Ishida Yo-Ichi, Ogasawara Yuki
Department of Analytical Biochemistry, Meiji Pharmaceutical University, 2-522-1 Noshio, Kiyose, Tokyo 204-8588, Japan.
Laboratory of Biochemistry, Department of Clinical Pharmacy, Faculty of Pharmaceutical Sciences, Shonan University of Medical Sciences, 16-10 Kamishinano, Totsuka-ku, Yokohama, Kanagawa 244-0806, Japan.
Antioxidants (Basel). 2022 Dec 17;11(12):2486. doi: 10.3390/antiox11122486.
Peroxiredoxin (Prx) 2 in red blood cells (RBCs) reacts with various reactive oxygen species and changes to hyperoxidized Prx2 (Prx2-SO). Therefore, Prx2 may serve as an indicator of oxidative stress in vivo. This study aimed to analyze Prx2-SO levels in clinical samples to examine whether the oxidation state of Prx2 in human RBCs reflects the pathological condition of oxidative stress diseases. We first focused on obstructive sleep apnea (OSA), a hypoxic stress-induced disease of the respiratory system, and investigated the levels of Prx2-SO accumulated in the RBCs of OSA patients. In measurements on a small number of OSA patients and healthy subjects, levels of Prx2-SO accumulation in patients with OSA were clearly increased compared to those in healthy subjects. Hence, we proceeded to validate these findings with more samples collected from patients with OSA. The results revealed significantly higher levels of erythrocytic Prx2-SO in patients with OSA than in healthy subjects, as well as a positive correlation between the severity of OSA and Prx2-SO levels in the RBCs. Moreover, we performed a chromatographic study to show the structural changes of Prx2 due to hyperoxidation. Our findings demonstrated that the Prx2-SO molecules in RBCs from patients with OSA were considerably more hydrophilic than the reduced form of Prx2. These results implicate Prx2-SO as a promising candidate biomarker for OSA.
红细胞(RBC)中的过氧化物酶(Prx)2可与多种活性氧发生反应,并转变为高度氧化的Prx2(Prx2-SO)。因此,Prx2可能作为体内氧化应激的一个指标。本研究旨在分析临床样本中Prx2-SO的水平,以检验人红细胞中Prx2的氧化状态是否反映氧化应激疾病的病理状况。我们首先聚焦于阻塞性睡眠呼吸暂停(OSA),这是一种由低氧应激诱发的呼吸系统疾病,并研究了OSA患者红细胞中积累的Prx2-SO水平。在对少数OSA患者和健康受试者的检测中,与健康受试者相比,OSA患者中Prx2-SO的积累水平明显升高。因此,我们继续用从OSA患者收集的更多样本验证这些发现。结果显示,OSA患者红细胞中的Prx2-SO水平显著高于健康受试者,并且OSA的严重程度与红细胞中Prx2-SO水平之间呈正相关。此外,我们进行了一项色谱研究,以显示Prx2因过度氧化而发生的结构变化。我们的研究结果表明,OSA患者红细胞中的Prx2-SO分子比还原形式的Prx2亲水性强得多。这些结果表明Prx2-SO有望成为OSA的生物标志物。