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首页> 外文期刊>Biomedicine & pharmacotherapy =: Biomedecine & pharmacotherapie >Alpha-lipoic acid attenuates p-cresyl sulfate-induced renal tubular injury through suppression of apoptosis and autophagy in human proximal tubular epithelial cells
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Alpha-lipoic acid attenuates p-cresyl sulfate-induced renal tubular injury through suppression of apoptosis and autophagy in human proximal tubular epithelial cells

机译:α-硫辛酸通过抑制人近端管状上皮细胞中的凋亡和自噬抑制p-烯丙酯诱导的肾小管损伤

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The p-cresyl sulfate accumulates in kidney disease and may be involved in renal injury. alpha-Lipoic acid (alpha-LA) acts as an antioxidant in cell injury. We investigated the effects of alpha-LA treatment on p-cresyl sulfate-induced renal tubular injury. p-Cresyl sulfate induced cell death, and increased Bax/Bcl-2, cleaved caspase-3, Beclin-1, and LC3BII/LC3BI in human renal proximal tubular epithelial (HK-2) cells, which was counteracted by alpha-LA treatment. p-Cresyl sulfate-induced apoptosis was reduced by autophagy inhibitor 3-methyladenine, and p-cresyl sulfate induced autophagy was reduced by pan-caspase inhibitor Z-VAD-FMK. Moreover, p-cresyl sulfate treatment increased the expression of ER stress proteins and decreased the expression of baculoviral IAP repeat-containing proteins 6; these effects were prevented by alpha-LA treatment. Apoptosis and autophagy were associated with the phosphorylation of mitogen-activated protein kinase and nuclear translocation of the nuclear factor-kappa B p65 subunit. Pretreatment inhibitors of p38 and JNK, and knockdown of ATF4 gene reduced apoptosis- and autophagy-related protein expressions in p-cresyl sulfate treated HK-2 cells. These results demonstrate that alpha-lipoic acid attenuated p-cresyl sulfate-induced cell death by suppression of apoptosis and autophagy via regulation of ER stress in HK-2 cells.
机译:硫酸酯含有肾病累积,可参与肾损伤。 α-硫辛酸(Alpha-La)用作细胞损伤中的抗氧化剂。我们研究了α-LA处理对硫酸甲酚诱导的肾小管损伤的影响。硫酸酯死亡诱导的细胞死亡,并增加的Bax / Bcl-2,切割的Caspase-3,BECLIN-1和LC3BII / LC3BI在人肾近侧管状上皮(HK-2)细胞中,α-LA治疗抵消。通过自噬抑制剂3-甲基甘露苯胺降低了硫酸酯诱导的细胞凋亡,并通过PAN-Caspase抑制剂Z-VAD-FMK降低了对硫酸酯诱导的自噬。此外,硫酸酯硫酸酯处理增加了ER应激蛋白的表达,并降低了含杆病毒IAP重复蛋白6的表达;通过α-LA处理预防这些效果。细胞凋亡和自噬与偶极活性蛋白激酶磷酸化和核因子-Kappa B p65亚基的核转移有关。 P38和JNK的预处理抑制剂,以及ATF4基因的敲低降低了硫酸甲基甲基硫酸酯处理HK-2细胞的凋亡和自噬相关蛋白表达。这些结果表明,通过调节HK-2细胞中的ER应激来抑制细胞凋亡和自噬抑制α-硫辛酸衰减对番糖醛诱导的细胞死亡。

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