Pang Li, Deng Ping, Liang Yi-Dan, Qian Jing-Yu, Wu Li-Chuan, Yang Ling-Ling, Yu Zheng-Ping, Zhou Zhou
Department of Cell Biology , School of Life Sciences and School of Medicine , Guangxi University , Nanning 530004 , China . Email:
Department of Occupational Health , Third Military Medical University , Chongqing 400038 , China.
Toxicol Res (Camb). 2019 Sep 27;8(6):918-927. doi: 10.1039/c9tx00186g. eCollection 2019 Nov 1.
Paraquat (PQ) is a widely used herbicide in the agricultural field. The lack of an effective antidote is the significant cause of high mortality in PQ poisoning. Here, we investigate the antagonistic effects of alpha lipoic acid (α-LA), a naturally existing antioxidant, on PQ toxicity in human microvascular endothelial cells (HMEC-1). All the doses of 250, 500 and 1000 μM α-LA significantly inhibited 1000 μM PQ-induced cytotoxicity in HMEC-1 cells. α-LA pretreatment remarkably diminished the damage to cell migration ability, recovered the declined levels of the vasodilator factor nitric oxide (NO), elevated the expression level of endothelial nitric oxide synthases (eNOS), and inhibited the upregulated expression of vasoconstrictor factor endothelin-1 (ET-1). Moreover, α-LA pretreatment inhibited reactive oxygen species (ROS) generation, suppressed the damage to the mitochondrial membrane potential (Δ ) and mitigated the inhibition of adenosine triphosphate (ATP) production in HMEC-1 cells. These results suggested that α-LA could alleviate PQ-induced endothelial dysfunction by suppressing oxidative stress. In summary, our present study provides novel insight into the protective effects and pharmacological potential of α-LA against PQ toxicity in microvascular endothelial cells.
百草枯(PQ)是农业领域广泛使用的除草剂。缺乏有效的解毒剂是PQ中毒死亡率高的重要原因。在此,我们研究天然存在的抗氧化剂α-硫辛酸(α-LA)对人微血管内皮细胞(HMEC-1)中PQ毒性的拮抗作用。所有剂量为250、500和1000μM的α-LA均显著抑制1000μM PQ诱导的HMEC-1细胞的细胞毒性。α-LA预处理显著减轻了对细胞迁移能力的损害,恢复了血管舒张因子一氧化氮(NO)下降的水平,提高了内皮型一氧化氮合酶(eNOS)的表达水平,并抑制了血管收缩因子内皮素-1(ET-1)表达的上调。此外,α-LA预处理抑制了活性氧(ROS)的产生,抑制了对线粒体膜电位(Δ)的损害,并减轻了对HMEC-1细胞中三磷酸腺苷(ATP)产生的抑制。这些结果表明,α-LA可通过抑制氧化应激来减轻PQ诱导的内皮功能障碍。总之,我们目前的研究为α-LA对微血管内皮细胞中PQ毒性的保护作用和药理潜力提供了新的见解。