Alpha-lipoic acid attenuates p-cresyl sulfate-induced renal tubular injury through suppression of apoptosis and autophagy in human proximal tubular epithelial cells

被引:17
作者
Park, Jung Sun [1 ]
Choi, Hoon In [1 ]
Kim, Dong-Hyun [1 ]
Kim, Chang Seong [1 ]
Bae, Eun Hui [1 ]
Ma, Seong Kwon [1 ]
Kim, Soo Wan [1 ]
机构
[1] Chonnam Natl Univ, Dept Internal Med, Med Sch, Gwangju, South Korea
基金
新加坡国家研究基金会;
关键词
alpha-lipoic acid; p-Cresyl sulfate; Kidney proximal tubular cells; Apoptosis; Autophagy; ENDOPLASMIC-RETICULUM STRESS; UREMIC TOXINS; DUAL ROLE; PROTEIN; DEATH; CROSSTALK; MITOCHONDRIA; DYSFUNCTION; METABOLISM; MECHANISMS;
D O I
10.1016/j.biopha.2019.108679
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
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.
引用
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页数:11
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