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Oxidative Stress and Modification of Renal Vascular Permeability Are Associated with Acute Kidney Injury during P. berghei ANKA Infection

机译:氧化应激与肾血管通透性关联急性肾损伤技改期间伯氏疟原虫感染aNKa

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摘要

Malaria associated-acute kidney injury (AKI) is associated with 45% of mortality in adult patients hospitalized with severe form of the disease. However, the causes that lead to a framework of malaria-associated AKI are still poorly characterized. Some clinical studies speculate that oxidative stress products, a characteristic of Plasmodium infection, as well as proinflammatory response induced by the parasite are involved in its pathophysiology. Therefore, we aimed to investigate the development of malaria-associated AKI during infection by P. berghei ANKA, with special attention to the role played by the inflammatory response and the involvement of oxidative stress. For that, we took advantage of an experimental model of severe malaria that showed significant changes in the renal pathophysiology to investigate the role of malaria infection in the renal microvascular permeability and tissue injury. Therefore, BALB/c mice were infected with P. berghei ANKA. To assess renal function, creatinine, blood urea nitrogen, and ratio of proteinuria and creatininuria were evaluated. The products of oxidative stress, as well as cytokine profile were quantified in plasma and renal tissue. The change of renal microvascular permeability, tissue hypoxia and cellular apoptosis were also evaluated. Parasite infection resulted in renal dysfunction. Furthermore, we observed increased expression of adhesion molecule, proinflammatory cytokines and products of oxidative stress, associated with a decrease mRNA expression of HO-1 in kidney tissue of infected mice. The measurement of lipoprotein oxidizability also showed a significant increase in plasma of infected animals. Together, our findings support the idea that products of oxidative stress, as well as the immune response against the parasite are crucial to changes in kidney architecture and microvascular endothelial permeability of BALB/c mice infected with P. berghei ANKA.
机译:疟疾相关的急性肾损伤(AKI)与住院严重疾病的成年患者的死亡率有45%相关。但是,导致与疟疾有关的AKI框架的原因仍然不明确。一些临床研究推测,疟原虫感染的特征之一是氧化应激产物,以及由寄生虫诱导的促炎反应,都参与了其病理生理。因此,我们旨在研究伯氏疟原虫ANKA感染期间与疟疾相关的AKI的发展,尤其要注意炎症反应和氧化应激的参与。为此,我们利用了严重疟疾的实验模型,该模型显示了肾脏病理生理的显着变化,以研究疟疾感染在肾脏微血管通透性和组织损伤中的作用。因此,BALB / c小鼠感染了伯氏疟原虫ANKA。为了评估肾功能,评估了肌酐,血尿素氮以及蛋白尿和肌酐的比率。在血浆和肾组织中对氧化应激的产物以及细胞因子谱进行定量。还评估了肾脏微血管通透性,组织缺氧和细胞凋亡的变化。寄生虫感染导致肾功能不全。此外,我们观察到感染小鼠肾脏组织中黏附分子,促炎细胞因子和氧化应激产物的表达增加,与HO-1 mRNA表达的降低有关。脂蛋白氧化性的测量还显示出被感染动物血浆中的显着增加。总之,我们的发现支持以下观点:氧化应激产物以及针对寄生虫的免疫反应对于感染了伯氏疟原虫ANKA的BALB / c小鼠的肾脏结构和微血管内皮通透性的变化至关重要。

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