糖尿病肾病的氧化还原调节。

IF 3.7 2区 医学 Q1 PHYSIOLOGY
Ilse S Daehn, Ubong S Ekperikpe, Krisztian Stadler
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引用次数: 0

摘要

糖尿病肾病(DKD)是糖尿病最具破坏性的并发症之一,目前尚无治疗方法。导致这种并发症的发病机制有多种,其中氧化应激是关键因素之一。在过去的几十年中,有大量关于这一主题各个方面的论文发表;然而,DKD 中氧化还原调节的具体细节仍不清楚。部分原因是氧化还原生物学非常复杂,再加上器官复杂且异质,细胞类型众多。此外,"氧化应激 "或活性氧等术语常常被用作一个笼统的术语,以涵盖种类繁多的活性物种及其不同的反应。然而,活性氧的种类并不相同,并非所有活性氧都能产生与生物相关的反应或 "氧化还原信号"。本综述的目的是提供一系列在肾脏中具有不同反应性和特异性的特定反应性氧种类的生化背景,并重点介绍氧化还原生物学的一些进展,这些进展为更好地了解 DKD 的发展和风险铺平了道路。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Redox regulation in diabetic kidney disease.

Redox regulation in diabetic kidney disease.

Redox regulation in diabetic kidney disease.

Redox regulation in diabetic kidney disease.

Diabetic kidney disease (DKD) is one of the most devastating complications of diabetes mellitus, where currently there is no cure available. Several important mechanisms contribute to the pathogenesis of this complication, with oxidative stress being one of the key factors. The past decades have seen a large number of publications with various aspects of this topic; however, the specific details of redox regulation in DKD are still unclear. This is partly because redox biology is very complex, coupled with a complex and heterogeneous organ with numerous cell types. Furthermore, often times terms such as "oxidative stress" or reactive oxygen species are used as a general term to cover a wide and rich variety of reactive species and their differing reactions. However, no reactive species are the same, and not all of them are capable of biologically relevant reactions or "redox signaling." The goal of this review is to provide a biochemical background for an array of specific reactive oxygen species types with varying reactivity and specificity in the kidney as well as highlight some of the advances in redox biology that are paving the way to a better understanding of DKD development and risk.

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来源期刊
CiteScore
8.40
自引率
7.10%
发文量
154
审稿时长
2-4 weeks
期刊介绍: The American Journal of Physiology - Renal Physiology publishes original manuscripts on timely topics in both basic science and clinical research. Published articles address a broad range of subjects relating to the kidney and urinary tract, and may involve human or animal models, individual cell types, and isolated membrane systems. Also covered are the pathophysiological basis of renal disease processes, regulation of body fluids, and clinical research that provides mechanistic insights. Studies of renal function may be conducted using a wide range of approaches, such as biochemistry, immunology, genetics, mathematical modeling, molecular biology, as well as physiological and clinical methodologies.
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