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氧化应激生物标志物:脐血中异前列腺素、晚期氧化蛋白产物和硝基酪氨酸苯酯参考值的确定。

Oxidative Stress Biomarkers: Establishment of Reference Values for Isoprostanes, AOPP, and NPBI in Cord Blood.

作者信息

Longini Mariangela, Belvisi Elisa, Proietti Fabrizio, Bazzini Francesco, Buonocore Giuseppe, Perrone Serafina

机构信息

Department of Molecular and Developmental Medicine, University of Siena, Siena, Italy.

UOC Clinical Pathology AOU Senese, Siena, Italy.

出版信息

Mediators Inflamm. 2017;2017:1758432. doi: 10.1155/2017/1758432. Epub 2017 Apr 23.

Abstract

Oxidative stress (OS) is a common pathogenic factor involved in the onset of several diseases in humans, from immunologic disorders to malignancy, being a serious public health problem. In perinatal period, OS has been associated with adverse outcome of pregnancy and neonatal diseases. Dangerous effects of OS are mediated by increased production of free radicals (FRs) following various mechanisms, such as hypoxia, ischemia reperfusion, hyperoxia, inflammation, mitochondrial dysfunction, Fenton chemistry, and prostaglandin metabolism. FRs have short half-life, and their measurement in vivo is faced with many challenges. However, oxyradical derivatives are stable and thus may be measured and monitored repeatedly. The quantification of OS is based on the measurement of specific biomarkers in biologic fluids and tissues, which reflect induced oxidative damage to lipids, proteins, and DNA. Prostanoids, non-protein-bound iron (NPBI), and advanced oxidation protein products (AOPP) are actually considered truly specific and reliable for neonatal injury. Defining reference values for these biomarkers is necessary to investigate their role in neonatal diseases or also to evaluate the success of treatments. In this work, we wanted to define laboratory reference values for biomarkers of OS in a healthy population of term newborns.

摘要

氧化应激(OS)是人类多种疾病发病过程中涉及的常见致病因素,从免疫紊乱到恶性肿瘤,是一个严重的公共卫生问题。在围产期,OS与妊娠不良结局和新生儿疾病有关。OS的危险作用是由多种机制导致的自由基(FRs)产生增加介导的,如缺氧、缺血再灌注、高氧、炎症、线粒体功能障碍、芬顿化学反应和前列腺素代谢。FRs半衰期短,其体内测量面临诸多挑战。然而,氧自由基衍生物稳定,因此可以反复测量和监测。OS的量化基于生物体液和组织中特定生物标志物的测量,这些生物标志物反映了对脂质、蛋白质和DNA的氧化损伤。前列腺素、非蛋白结合铁(NPBI)和晚期氧化蛋白产物(AOPP)实际上被认为对新生儿损伤具有真正的特异性和可靠性。确定这些生物标志物的参考值对于研究它们在新生儿疾病中的作用或评估治疗效果是必要的。在这项工作中,我们想确定足月健康新生儿群体中OS生物标志物的实验室参考值。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bbe7/5420435/65101f923f45/MI2017-1758432.001.jpg

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