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早期 db/db 小鼠肾病中 RNA 的氧化损伤增加。

Increased Oxidative Damage of RNA in Early-Stage Nephropathy in db/db Mice.

机构信息

The MOH Key Laboratory of Geriatrics, Beijing Hospital, National Center of Gerontology, Beijing 100730, China.

Department of Laboratory Medicine, Gansu Provincial Hospital, Lanzhou, Gansu 730000, China.

出版信息

Oxid Med Cell Longev. 2017;2017:2353729. doi: 10.1155/2017/2353729. Epub 2017 Oct 19.

DOI:10.1155/2017/2353729
PMID:29201270
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5671745/
Abstract

To evaluate RNA oxidation in the early stage of diabetic nephropathy, we applied an accurate method based on isotope dilution high-performance liquid chromatography-triple quadruple mass spectrometry to analyze the oxidatively generated guanine nucleosides in renal tissue and urine from db/db mice of different ages. We further investigated the relationship between these oxidative stress markers, microalbumin excretion, and histological changes. We found that the levels of 8-oxo-7,8-dihydroguanosine (8-oxoGuo) and 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxodGuo) were increased in the urine and renal tissue of db/db mice and db/db mice with early symptoms of diabetic nephropathy suffered from more extensive oxidative damage than lean littermate control db/m mice. Importantly, in contrast to the findings in db/m mice, the 8-oxoGuo levels in the urine and renal tissue of db/db mice were higher than those of 8-oxodGuo at four weeks. These results indicate that RNA oxidation is more apparent than DNA oxidation in the early stage of diabetic nephropathy. RNA oxidation may provide new insight into the pathogenesis of diabetic nephropathy, and urinary 8-oxoGuo may represent a novel, noninvasive, and easily detected biomarker of diabetic kidney diseases if further study could clarify its source and confirm these results in a large population study.

摘要

为了评估糖尿病肾病早期的 RNA 氧化,我们应用了一种基于同位素稀释高效液相色谱-三重四极杆质谱的准确方法,来分析不同年龄 db/db 小鼠肾脏组织和尿液中氧化生成的鸟嘌呤核苷。我们进一步研究了这些氧化应激标志物与微量白蛋白排泄和组织学变化之间的关系。我们发现,8-氧代-7,8-二氢鸟苷(8-oxoGuo)和 8-氧代-7,8-二氢-2'-脱氧鸟苷(8-oxodGuo)的水平在 db/db 小鼠的尿液和肾脏组织中升高,且患有早期糖尿病肾病症状的 db/db 小鼠比瘦型同窝对照 db/m 小鼠遭受更广泛的氧化损伤。重要的是,与 db/m 小鼠的发现相反,db/db 小鼠尿液和肾脏组织中的 8-oxoGuo 水平在四周时高于 8-oxodGuo。这些结果表明,在糖尿病肾病早期,RNA 氧化比 DNA 氧化更为明显。RNA 氧化可能为糖尿病肾病的发病机制提供新的见解,如果进一步的研究能够阐明其来源并在大规模人群研究中证实这些结果,那么尿中 8-oxoGuo 可能成为一种新的、非侵入性和易于检测的糖尿病肾病生物标志物。

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本文引用的文献

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Oxid Med Cell Longev. 2016;2016:4323198. doi: 10.1155/2016/4323198. Epub 2015 Dec 7.
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氧化RNA损伤在2型糖尿病发病机制及治疗中的作用
Front Physiol. 2022 Mar 28;13:725919. doi: 10.3389/fphys.2022.725919. eCollection 2022.
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NADH/NAD Redox Imbalance and Diabetic Kidney Disease.NADH/NAD 氧化还原失衡与糖尿病肾病。
Biomolecules. 2021 May 14;11(5):730. doi: 10.3390/biom11050730.
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Circulating Oxidative Stress Biomarkers in Clinical Studies on Type 2 Diabetes and Its Complications.循环氧化应激生物标志物在 2 型糖尿病及其并发症的临床研究中的应用。
Oxid Med Cell Longev. 2019 May 12;2019:5953685. doi: 10.1155/2019/5953685. eCollection 2019.
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