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氧化应激、抗氧化治疗与慢性肾脏病。

Oxidative stress, anti-oxidant therapies and chronic kidney disease.

机构信息

Centre for Kidney Disease Research, School of Medicine, The University of Queensland, Queensland, Australia.

出版信息

Nephrology (Carlton). 2012 May;17(4):311-21. doi: 10.1111/j.1440-1797.2012.01572.x.

DOI:10.1111/j.1440-1797.2012.01572.x
PMID:22288610
Abstract

Chronic kidney disease (CKD) is a common and serious problem that adversely affects human health, limits longevity and increases costs to health-care systems worldwide. Its increasing incidence cannot be fully explained by traditional risk factors. Oxidative stress is prevalent in CKD patients and is considered to be an important pathogenic mechanism. Oxidative stress develops from an imbalance between free radical production often increased through dysfunctional mitochondria formed with increasing age, type 2 diabetes mellitus, inflammation, and reduced anti-oxidant defences. Perturbations in cellular oxidant handling influence downstream cellular signalling and, in the kidney, promote renal cell apoptosis and senescence, decreased regenerative ability of cells, and fibrosis. These factors have a stochastic deleterious effect on kidney function. The majority of studies investigating anti-oxidant treatments in CKD patients show a reduction in oxidative stress and many show improved renal function. Despite heterogeneity in the oxidative stress levels in the CKD population, there has been little effort to measure patient oxidative stress levels before the use of any anti-oxidants therapies to optimize outcome. This review describes the development of oxidative stress, how it can be measured, the involvement of mitochondrial dysfunction and the molecular pathways that are altered, the role of oxidative stress in CKD pathogenesis and an update on the amelioration of CKD using anti-oxidant therapies.

摘要

慢性肾脏病(CKD)是一种常见且严重的问题,它会对人类健康造成不良影响,限制寿命并增加全球医疗保健系统的成本。其发病率的增加不能完全用传统的危险因素来解释。氧化应激在 CKD 患者中很常见,被认为是一个重要的致病机制。氧化应激是由自由基产生的不平衡引起的,自由基的产生通常通过功能失调的线粒体增加,这些线粒体随着年龄的增长、2 型糖尿病、炎症和抗氧化防御能力的降低而形成。细胞内氧化剂处理的紊乱会影响下游的细胞信号转导,在肾脏中,促进肾细胞凋亡和衰老、细胞再生能力下降以及纤维化。这些因素对肾功能有随机的有害影响。大多数研究表明,抗氧化治疗可以降低 CKD 患者的氧化应激水平,许多研究表明可以改善肾功能。尽管 CKD 患者的氧化应激水平存在异质性,但在使用任何抗氧化治疗之前,很少有努力测量患者的氧化应激水平,以优化治疗效果。本文综述了氧化应激的发展、如何测量氧化应激、线粒体功能障碍的参与以及改变的分子途径、氧化应激在 CKD 发病机制中的作用以及抗氧化治疗改善 CKD 的最新进展。

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