Panasenko O M, Gorudko I V, Sokolov A V
Research Institute of Physico-Chemical Medicine, Moscow, 119435, Russia.
Biochemistry (Mosc). 2013 Dec;78(13):1466-89. doi: 10.1134/S0006297913130075.
Hypochlorous acid (HOCl) is produced in the human body by the family of mammalian heme peroxidases, mainly by myeloperoxidase, which is secreted by neutrophils and monocytes at sites of inflammation. This review discusses the reactions that occur between HOCl and the major classes of biologically important molecules (amino acids, proteins, nucleotides, nucleic acids, carbohydrates, lipids, and inorganic substances) to form free radicals. The generation of such free radical intermediates by HOCl and other reactive halogen species is accompanied by the development of halogenative stress, which causes a number of socially important diseases, such as cardiovascular, neurodegenerative, infectious, and other diseases usually associated with inflammatory response and characterized by the appearance of biomarkers of myeloperoxidase and halogenative stress. Investigations aimed at elucidating the mechanisms regulating the activity of enzyme systems that are responsible for the production of reactive halogen species are a crucial step in opening possibilities for control of the development of the body's inflammatory response.
次氯酸(HOCl)在人体中由哺乳动物血红素过氧化物酶家族产生,主要由髓过氧化物酶产生,髓过氧化物酶由炎症部位的中性粒细胞和单核细胞分泌。本综述讨论了HOCl与主要类别的生物重要分子(氨基酸、蛋白质、核苷酸、核酸、碳水化合物、脂质和无机物)之间发生的反应,以形成自由基。HOCl和其他活性卤素物种产生此类自由基中间体伴随着卤化应激的发展,卤化应激会引发一些具有社会重要性的疾病,如心血管疾病、神经退行性疾病、感染性疾病以及其他通常与炎症反应相关且以髓过氧化物酶和卤化应激生物标志物出现为特征的疾病。旨在阐明负责产生活性卤素物种的酶系统活性调节机制的研究,是为控制机体炎症反应发展开辟可能性的关键一步。