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Effect of Baoshenfang Formula on Podocyte Injury via Inhibiting the NOX-4/ROS/p38 Pathway in Diabetic Nephropathy

机译:保肾方方剂通过抑制糖尿病性肾病中NOX-4 / ROS / p38途径对足细胞损伤的作用

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摘要

Diabetic nephropathy (DN) is a serious kidney-related complication of type 1 and type 2 diabetes. The Chinese herbal formula Baoshenfang (BSF) shows therapeutic potential in attenuating oxidative stress and apoptosis in podocytes in DN. This study evaluated the effects of BSF on podocyte injury in vivo and in vitro and explored the possible involvement of the nicotinamide adenine dinucleotide phosphate-oxidase-4/reactive oxygen species- (NOX-4/ROS-) activated p38 pathway. In the identified compounds by mass spectrometry, some active constituents of BSF were reported to show antioxidative activity. In addition, we found that BSF significantly decreased 24-hour urinary protein, serum creatinine, and blood urea nitrogen in DN patients. BSF treatment increased the nephrin expression, alleviated oxidative cellular damage, and inhibited Bcl-2 family-associated podocyte apoptosis in high-glucose cultured podocytes and/or in diabetic rats. More importantly, BSF also decreased phospho-p38, while high glucose-mediated apoptosis was blocked by p38 mitogen-activated protein kinase inhibitor in cultured podocytes, indicating that the antiapoptotic effect of BSF is p38 pathway-dependent. High glucose-induced upexpression of NOX-4 was normalized by BSF, and NOX-4 siRNAs inhibited the phosphorylation of p38, suggesting that the activated p38 pathway is at least partially mediated by NOX-4. In conclusion, BSF can decrease proteinuria and protect podocytes from injury in DN, in part through inhibiting the NOX-4/ROS/p38 pathway.
机译:糖尿病肾病(DN)是1型和2型糖尿病的严重肾脏相关并发症。中草药配方“保神坊”(BSF)在减轻DN足细胞的氧化应激和凋亡方面显示出治疗潜力。这项研究评估了BSF在体内和体外对足细胞损伤的影响,并探讨了烟酰胺腺嘌呤二核苷酸磷酸-氧化酶4 /活性氧-(NOX-4 / ROS-)激活的p38途径的可能参与。在通过质谱鉴定的化合物中,据报道,BSF的某些活性成分具有抗氧化活性。此外,我们发现BSF可以显着降低DN患者的24小时尿蛋白,血清肌酐和血液尿素氮。在高糖培养的足细胞和/或糖尿病大鼠中,BSF处理增加了肾素的表达,减轻了氧化性细胞损伤,并抑制了Bcl-2家族相关足细胞凋亡。更重要的是,BSF还能降低磷酸化p38,而在培养的足细胞中p38丝裂原活化的蛋白激酶抑制剂阻止了高葡萄糖介导的凋亡,这表明BSF的抗凋亡作用是p38途径依赖性的。高葡萄糖诱导的NOX-4的高表达已通过BSF正常化,并且NOX-4 siRNA抑制了p38的磷酸化,表明激活的p38途径至少部分由NOX-4介导。总之,BSF可以通过抑制NOX-4 / ROS / p38途径来降低蛋白尿并保护足细胞免受DN损伤。

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