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Chlorinative stress: An under appreciated mediator of neurodegeneration?

机译:氯化应激:神经退行性疾病的受人赞赏的媒介?

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Oxidative stress has been implicated as playing a role in neurodegenerative disorders, such as ischemic stroke, Alzheimer's, Huntington's, and Parkinson's disease. Persuasive evidences have shown that microglial-mediated oxidative stress contributes significantly to cell loss and accompanying cognitive decline characteristic of the diseases. Based on the facts that (i) levels of catalytically active myeloperoxidase are elevated in diseased brains and (ii) myeloperoxidase polymorphism is associated with the risk of developing neurodegenerative disorders, HOCl as a major oxidant produced by activated phagocytes in the presence of myeloperoxidase is therefore suggested to be involved in neurodegeneration. Its association with neurodegeneration is further showed by elevated level of 3-chlorotyrosine (bio-marker of HOCl in vivo) in affected brain regions as well as HOCl scavenging ability of neuroprotectants, desferrioxamine and uric acid. In this review, we will summary the current understanding concerning the association of HOCl and neuronal cell death where production of HOCl will lead to further formation of reactive nitrogen and oxygen species. In addition, HOCl also causes tissue destruction and cellular damage leading cell death. (c) 2006 Published by Elsevier Inc.
机译:氧化应激被认为在神经变性疾病如缺血性中风,阿尔茨海默氏病,亨廷顿氏病和帕金森氏病中起作用。有说服力的证据表明,小胶质细胞介导的氧化应激显着促进了疾病的细胞丧失和伴随的认知能力下降。基于以下事实:(i)在患病的大脑中催化活性髓过氧化物酶水平升高,并且(ii)髓过氧化物酶多态性与发生神经退行性疾病的风险相关,因此,HOCl是在髓过氧化物酶存在下由活化吞噬细胞产生的主要氧化剂。建议参与神经变性。其与神经退行性的关联进一步通过在受影响的大脑区域中升高水平的3-氯酪氨酸(体内HOCl的生物标记)以及神经保护剂,去铁胺和尿酸对HOCl的清除能力来进一步证明。在这篇综述中,我们将总结关于HOCl与神经元细胞死亡的关联的当前理解,其中HOCl的产生将导致活性氮和氧物种的进一步形成。另外,HOC1还引起组织破坏和细胞损伤,导致细胞死亡。 (c)2006年由Elsevier Inc.发布。

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