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硫辛酸通过抑制人近端肾小管上皮细胞凋亡和自噬减轻对苯磺酸引起的肾小管损伤。

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

机构信息

Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea.

Department of Internal Medicine, Chonnam National University Medical School, Gwangju, Republic of Korea.

出版信息

Biomed Pharmacother. 2019 Apr;112:108679. doi: 10.1016/j.biopha.2019.108679. Epub 2019 Feb 21.

Abstract

The p-cresyl sulfate accumulates in kidney disease and may be involved in renal injury. α-Lipoic acid (α-LA) acts as an antioxidant in cell injury. We investigated the effects of α-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 α-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 α-LA treatment. Apoptosis and autophagy were associated with the phosphorylation of mitogen-activated protein kinase and nuclear translocation of the nuclear factor-κB 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 α-lipoic acid attenuated p-cresyl sulfate-induced cell death by suppression of apoptosis and autophagy via regulation of ER stress in HK-2 cells.

摘要

对甲酚硫酸盐在肾病中积累,可能与肾损伤有关。α-硫辛酸(α-LA)在细胞损伤中作为抗氧化剂发挥作用。我们研究了α-LA 处理对 p-对甲酚硫酸盐诱导的肾小管损伤的影响。p-对甲酚硫酸盐诱导细胞死亡,并增加人肾近端肾小管上皮(HK-2)细胞中的 Bax/Bcl-2、裂解的 caspase-3、Beclin-1 和 LC3BII/LC3BI,α-LA 处理可逆转这种情况。自噬抑制剂 3-甲基腺嘌呤可减少 p-对甲酚硫酸盐诱导的细胞凋亡,泛半胱天冬酶抑制剂 Z-VAD-FMK 可减少 p-对甲酚硫酸盐诱导的自噬。此外,p-对甲酚硫酸盐处理增加了内质网应激蛋白的表达,减少了杆状病毒 IAP 重复蛋白 6 的表达;α-LA 处理可预防这些作用。凋亡和自噬与丝裂原激活的蛋白激酶磷酸化和核因子-κB p65 亚基的核转位有关。p38 和 JNK 的预处理抑制剂和 ATF4 基因的敲低减少了 p-对甲酚硫酸盐处理的 HK-2 细胞中与凋亡和自噬相关的蛋白表达。这些结果表明,α-硫辛酸通过调节 HK-2 细胞中的内质网应激来抑制凋亡和自噬,从而减轻 p-对甲酚硫酸盐诱导的细胞死亡。

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