Xu Longquan, Hiller Sylvia, Simington Stephen, Nickeleit Volker, Maeda Nobuyo, James Leighton R, Yi Xianwen
Department of Pathology and Laboratory Medicine, University of North Carolina, Chapel Hill, North Carolina, United States of America.
Division of Nephrology and Hypertension, Department of Medicine, University of Florida, Jacksonville, Florida, United States of America.
PLoS One. 2016 Oct 5;11(10):e0163208. doi: 10.1371/journal.pone.0163208. eCollection 2016.
Oxidative stress is implicated in the pathogenesis of diabetic nephropathy (DN) but outcomes of many clinical trials are controversial. To define the role of antioxidants in kidney protection during the development of diabetic nephropathy, we have generated a novel genetic antioxidant mouse model with over- or under-expression of lipoic acid synthase gene (Lias). These models have been mated with Ins2Akita/+ mice, a type I diabetic mouse model. We compare the major pathologic changes and oxidative stress status in two new strains of the mice with controls. Our results show that Ins2Akita/+ mice with under-expressed Lias gene, exhibit higher oxidative stress and more severe DN features (albuminuria, glomerular basement membrane thickening and mesangial matrix expansion). In contrast, Ins2Akita/+ mice with highly-expressed Lias gene display lower oxidative stress and less DN pathologic changes. Our study demonstrates that strengthening endogenous antioxidant capacity could be an effective strategy for prevention and treatment of DN.
氧化应激与糖尿病肾病(DN)的发病机制有关,但许多临床试验的结果存在争议。为了确定抗氧化剂在糖尿病肾病发展过程中对肾脏保护的作用,我们构建了一种新型的遗传抗氧化小鼠模型,该模型中硫辛酸合酶基因(Lias)过表达或低表达。这些模型已与I型糖尿病小鼠模型Ins2Akita/+小鼠进行杂交。我们将这两种新小鼠品系的主要病理变化和氧化应激状态与对照组进行比较。我们的结果表明,Lias基因低表达的Ins2Akita/+小鼠表现出更高的氧化应激和更严重的DN特征(蛋白尿、肾小球基底膜增厚和系膜基质扩张)。相比之下,Lias基因高表达的Ins2Akita/+小鼠氧化应激较低,DN病理变化较少。我们的研究表明,增强内源性抗氧化能力可能是预防和治疗DN的有效策略。