Comparative Mechanisms of Zearalenone and Ochratoxin A Toxicities on Cultured HepG2 cells: Is Oxidative Stress a Common Process?

被引:41
作者
Bennour, Emna El Golli [1 ]
Bouaziz, Chayma [1 ]
Ladjimi, Moncef [2 ]
Renaud, Flore [2 ]
Bacha, Hassen [1 ]
机构
[1] Fac Dent, Lab Res Biol Compatible Cpds, Monastir 5000, Tunisia
[2] Versailles St Quentin Univ, CNRS, UMR 8159, Lab Genet & Cellular Biol, F-78035 Versailles, France
关键词
zearalenone; ochratoxin A; Hsp responses; oxidative damage; CHRONIC INTERSTITIAL NEPHROPATHY; HEAT-SHOCK PROTEINS; VITAMIN-E; MAMMALIAN-CELLS; KIDNEY-CELLS; MOUSE-LIVER; DNA-DAMAGE; A EXPOSURE; VERO CELLS; RAT-LIVER;
D O I
10.1002/tox.20449
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Zearalenone (ZEN) and Ochratoxin A (OTA) are structurally diverse fungal metabolites that can contaminate feed and foodstuff and can cause serious health problems for animals as well as for humans. In this study, we get further insight of the molecular aspects of ZEN and OTA toxicities in cultured human HepG2 hepatocytes. In this context, we have monitored the effects of ZEN and OTA on (i) cell viability, (ii) heat shock protein (Hsp) 70 and Hsp 27 gene expressions as a parameter of protective and adaptive response, (iii) oxidative damage, and (iv) cell death pathways. Our results clearly showed that both ZEN and OTA inhibit cell proliferation. For ZEN, a significant induction of Hsp 70 and Hsp 27 was observed. In the same conditions, ZEN generated an important amount of reactive oxygen species (ROS). Antioxidant supplements restored the major part of cell mortality induced by ZEN. However, OTA treatment clownregulated Hsp 70 and Hsp 27 protein and mRNA levels and did not induce ROS generation. Antioxidant supplements did not have a significant effect on OTA-induced cell mortality. Using another cell system (Vero monkey kidney cells), we demonstrated that OTA downregulates three members of HSP 70 family: Hsp 70, Hsp 75, and Hsp 78. Our findings showed that oxidative damage seemed to be the predominant toxic effect for ZEN, while OTA toxicity seemed to be rather because of the absence of Hsps protective response. Furthermore, the two mycotoxins induced an apoptotic cell death. (C) 2008 Wiley Periodicals. Inc. Environ Toxicol 24: 538-548, 2009.
引用
收藏
页码:538 / 548
页数:11
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