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Exogenous biological renal support ameliorates renal pathology after ischemia reperfusion injury in elderly mice

机译:外源性生物肾脏支持改善老年小鼠缺血再灌注损伤后的肾脏病理

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摘要

We established an exogenous biological renal support model through the generation of parabiotic mice. At 72 hours after ischemia reperfusion injury (IRI), the aged mice that received exogenous biological renal support showed significantly higher levels of renal cell proliferation and dedifferentiation, lower levels of renal tubular injury, improved renal function, and a lower mortality than those that did not receive exogenous biological renal support. Using the Quantibody Mouse Cytokine Antibody Array, we found that aged IRI mice that received exogenous biological renal support had an up-regulation of multiple inflammatory related cytokines compared to the group that did not receive exogenous biological renal support. We suggest that the exogenous biological renal support might promote renal tubular epithelial cell proliferation and dedifferentiation and improve the prognosis of aged IRI mice. Exogenous biological renal support may play an important role in the amelioration of renal IRI by regulating the expression of multiple cytokines.
机译:我们建立了通过共生小鼠的外源性生物肾脏支持模型。缺血再灌注损伤(IRI)后72小时,接受外源性生物肾支持的老年小鼠表现出明显更高的肾细胞增殖和去分化水平,更低水平的肾小管损伤,改善的肾功能和更低的死亡率。没有获得外源性生物肾脏支持。使用Quantibody小鼠细胞因子抗体阵列,我们发现与未接受外源性生物肾支持的组相比,接受外源性生物肾支持的老年IRI小鼠具有多种炎症相关细胞因子的上调。我们建议外源性生物肾支持可能促进肾小管上皮细胞增殖和去分化并改善老年IRI小鼠的预后。外源性生物肾脏支持可能通过调节多种细胞因子的表达在改善肾脏IRI中起重要作用。

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