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Anti-inflammatory effects of C-peptide on kidney of type 1 diabetes mellitus animal model

机译:C-肽对1型糖尿病动物模型肾脏的抗炎作用

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摘要

Type 1 diabetes mellitus (T1DM) is characterized by C-peptide deficiency and elevated levels of pro-inflammatory cytokines. The aim of this study was to investigate the role of C-peptide in renal and inflammatory complications in streptozotocin (STZ)-diabetic mice model of T1DM with kidney disease. The study was performed in 8-week old male C57BL/6 mice. Two streptozotocin-diabetic groups (a T1DM animal model), after 4 weeks of diabetes, were treated with subcutaneous infusion of either vehicle (n = 12) or C-peptide (n = 11). Two non-diabetic groups (vehicle, n = 10; C-peptide, n = 9) were treated using the same protocol as described for the diabetic mice. The treatment with C-peptide in the diabetic group reduced the urinary levels of IL17 and TNF alpha, as well as IL4 and IL10 (p < 0.05). Contrary, the diabetic + C-peptide group presented higher IL10 gene expression in kidney. Besides, it displayed a reduction of TNF alpha gene expression. The data suggest that C-peptide may modulate pro- and anti-inflammatory signalling pathways, resulting in attenuation of kidney inflammation in T1DM animal model.
机译:1型糖尿病(T1DM)的特征在于C-肽缺乏和升高的促炎细胞因子。本研究的目的是探讨C-肽在链脲佐菌素(STZ) - 糖尿病与肾病中的糖尿病小鼠模型中肾癌和炎症并发症的作用。该研究在8周龄雄性C57BL / 6小鼠中进行。两种链脲佐菌素 - 糖尿病群(T1DM动物模型)在4周后糖尿病经皮(n = 12)或C-肽(n = 11)处理。使用与糖尿病小鼠所述的相同方案处理两种非糖尿病基团(载体,N = 10; C-肽,N = 9)。糖尿病组中的C-肽处理降低了IL17和TNFα的尿液水平,以及IL4和IL10(P <0.05)。相反,糖尿病+ C-肽基团呈肾脏呈现较高的IL10基因表达。此外,它显示出TNFα基因表达的减少。该数据表明C-肽可以调节促炎和抗炎信号传导途径,导致T1DM动物模型中的肾脏炎症衰减。

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