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Indoxyl sulfate, a uremic toxin, downregulates renal expression of Nrf2 through activation of NF-κB

机译:硫酸吲哚酚硫酸盐(尿毒症毒素)通过激活NF-κB来下调Nrf2的肾脏表达

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Background Indoxyl sulfate, a uremic toxin, is accumulated in the serum of chronic kidney disease (CKD) patients, accelerating the progression of CKD. In CKD rat kidney, the expressions of nuclear factor (erythroid-derived 2)-like 2 (Nrf2) and its related genes are downregulated. AST-120, an oral sorbent, reduces serum indoxyl sulfate and slows the progression of CKD. The present study aimed to determine whether indoxyl sulfate downregulates Nrf2 expression in human proximal tubular cells and rat kidneys and whether AST-120 upregulates Nrf2 expression in CKD rat kidneys. Methods Effects of indoxyl sulfate on expression of Nrf2 were determined using HK-2 cells as human proximal tubular cells and the following animals: (1) Dahl salt-resistant normotensive rats (DN), (2) Dahl salt-resistant normotensive indoxyl sulfate-administered rats (DN+IS), (3) Dahl salt-sensitive hypertensive rats (DH), and (4) Dahl salt-sensitive hypertensive indoxyl sulfate-administered rats (DH+IS). Further, AST-120 was administered to subtotally nephrectomized CKD rats to determine its effect on the expression of Nrf2. Results Indoxyl sulfate downregulated Nrf2 expression in HK-2 cells. The indoxyl sulfate-induced downregulation of Nrf2 expression was alleviated by an inhibitor of nuclear factor-κB (NF-κB) (pyrrolidine dithiocarbamate) and small interfering RNA specific to NF-κB p65. DN+IS, DH, and DH+IS rats showed decreased renal expression of Nrf2 and its downstream target genes, heme oxygenase-1 (HO-1) and NAD(P)H:quinone oxidoreductase 1 (NQO1), and increased renal expression of 8-hydroxydeoxyguanosine (8-OHdG), a marker of reactive oxygen species (ROS), compared with DN. Thus, indoxyl sulfate, as well as hypertension, downregulated renal expression of Nrf2 in rats. AST-120 upregulated renal expression of Nrf2, HO-1 and NQO1 and suppressed renal expression of 8-OHdG compared with control CKD rats. Conclusions Indoxyl sulfate downregulates renal expression of Nrf2 through activation of NF-κB, followed by downregulation of HO-1 and NQO1 and increased production of ROS. Further, AST-120 upregulates renal expression of Nrf2 in CKD rats by removing serum indoxyl sulfate, followed by upregulation of HO-1 and NQO1 and decreased production of ROS.
机译:背景技术硫酸吲哚酚硫酸盐(一种尿毒症毒素)积累在慢性肾脏病(CKD)患者的血清中,从而加速了CKD的发展。在CKD大鼠肾脏中,核因子(类胡萝卜素衍生的2)样2(Nrf2)及其相关基因的表达下调。 AST-120是一种口服吸附剂,可降低血清硫酸吲哚酚并减慢CKD的进程。本研究旨在确定硫酸吲哚酚是否下调人近端肾小管细胞和大鼠肾脏中的Nrf2表达,以及AST-120是否上调CKD大鼠肾脏中的Nrf2表达。方法以HK-2细胞为人类近端肾小管细胞,采用以下动物实验确定吲哚硫酸盐对Nrf2表达的影响:(1)Dahl耐盐性血压正常大鼠(2)给予大鼠(DN + IS),(3)达尔盐敏感性高血压硫酸吲哚酚大鼠(DH + IS)。此外,将AST-120施用于完全切除肾切除的CKD大鼠,以确定其对Nrf2表达的影响。结果硫酸吲哚酚下调HK-2细胞中Nrf2的表达。核苷因子-κB(NF-κB)(吡咯烷二硫代氨基甲酸酯)和对NF-κBp65特异的小干扰RNA抑制剂减轻了吲哚硫酸盐诱导的Nrf2表达下调。 DN + IS,DH和DH + IS大鼠显示Nrf2及其下游靶基因血红素加氧酶-1(HO-1)和NAD(P)H:醌氧化还原酶1(NQO1)的肾脏表达降低,并且肾脏表达增加与DN相比,标记了8-羟基脱氧鸟苷(8-OHdG)(一种活性氧(ROS))的标记。因此,硫酸吲哚酚和高血压下调了大鼠Nrf2的肾脏表达。与对照CKD大鼠相比,AST-120上调了Nrf2,HO-1和NQO1的肾脏表达,并抑制了8-OHdG的肾脏表达。结论硫酸吲哚酚可通过激活NF-κB来下调肾脏Nrf2的表达,进而下调HO-1和NQO1的表达并增加ROS的产生。此外,AST-120通过去除血清吲哚酚硫酸盐,然后上调HO-1和NQO1,并降低ROS的产生,来上调CKD大鼠肾脏Nrf2的表达。

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