Potential Involvement of Oxidative Stress, Apoptosis and Proinflammation in Ipconazole-Induced Cytotoxicity in Human Endothelial-like Cells

被引:4
作者
Ruiz-Yance, Iris [1 ]
Siguas, Junior [2 ]
Bardales, Brandy [1 ]
Robles-Castaneda, Ingrid [1 ]
Cordova, Karen [1 ]
Ypushima, Alina [1 ]
Estela-Villar, Esteban [1 ]
Quintana-Criollo, Carlos [1 ]
Estacio, Darwin [1 ]
Rodriguez, Jose-Luis [3 ]
机构
[1] Univ Nacl Intercultural Amazonia, Agroforestry Dept, Pucallpa 25004, Peru
[2] Univ Nacl Mayor San Marcos, Anim Physiol Dept, Lima 15021, Peru
[3] Univ Complutense Madrid, Pharmacol & Toxicol Dept, Madrid 28040, Spain
关键词
cytotoxicity; EA.hy926; ipconazole fungicide; oxidative stress; proinflammation; EPOXICONAZOLE-INDUCED TOXICITY; NLRP3 INFLAMMASOME ACTIVATION; ROS GENERATION; FUNGICIDES; DEATH; PROPICONAZOLE; MITOCHONDRIA; MOUSE; ACID;
D O I
10.3390/toxics11100839
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Triazole fungicides are widely used in the world, mainly in agriculture, but their abuse and possible toxic effects are being reported in some in vivo and in vitro studies that have demonstrated their danger to human health. This in vitro study evaluated the cytotoxicity, oxidative stress and proinflammation of EA.hy926 endothelial cells in response to ipconazole exposure. Using the MTT assay, ipconazole was found to produce a dose-dependent reduction (*** p < 0.001; concentrations of 20, 50 and 100 <mu>M) of cell viability in EA.hy926 with an IC50 of 29 mu M. Also, ipconazole induced a significant increase in ROS generation (** p < 0.01), caspase 3/7 (** p < 0.01), cell death (BAX, APAF1, BNIP3, CASP3 and AKT1) and proinflammatory (NLRP3, CASP1, IL1 beta, NF kappa B, IL6 and TNF alpha) biomarkers, as well as a reduction in antioxidant (NRF2 and GPx) biomarkers. These results demonstrated that oxidative stress, proinflammatory activity and cell death could be responsible for the cytotoxic effect produced by the fungicide ipconazole, such that this triazole compound should be considered as a possible risk factor in the development of alterations in cellular homeostasis.
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页数:14
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