Patulin triggers NRF2-mediated survival mechanisms in kidney cells

被引:20
|
作者
Pillay, Y. [1 ]
Phulukdaree, A. [2 ]
Nagiah, S. [1 ]
Chuturgoon, A. A. [1 ]
机构
[1] Univ KwaZulu Natal, Discipline Med Biochem, ZA-4041 Durban, South Africa
[2] Univ Pretoria, Dept Physiol, ZA-0002 Pretoria, South Africa
基金
新加坡国家研究基金会;
关键词
Patulin; Antioxidant response; NRF2; OXIDATIVE STRESS; MYCOTOXIN PATULIN; TOXICITY; TOXICOLOGY; DEFENSE;
D O I
10.1016/j.toxicon.2015.03.004
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Patulin (PAT), a mycotoxin contaminant of apples and apple products, has been implicated in nephrotoxicity. PAT depletes glutathione (GSH) and elevates reactive oxygen species (ROS). The antioxidant (AO) response is activated by Nuclear erythroid 2-related factor (NRF2) and enhanced by Silent information regulator 3 (SIRT3). The effects of PAT on these molecules have yet to be examined. We investigated the effects of PAT on AO response survival pathways in human embryonic kidney cells (HEK293). PAT cytotoxicity on HEK293 cells was evaluated (MTT assay; 24 h; [0-100 mu M]) to determine an IC50. GSH levels were measured using luminometry. Intracellular ROS was evaluated by flow cytometry. Protein expression of Keapl, NRF2, SIRT3 and PGC-1 alpha was quantified by western blotting and gene expression of SOD2, CAT and GPx was evaluated by qPCR. PAT caused a dose dependent decrease in HEK293 cell viability and a significant increase in levels of intracellular ROS (p = 0.0006). A significant increase in protein expression (p = 0.029) was observed. PAT increased gene expression of SOD2 and CAT (p = 0.0043), however, gene expression of GPx was significantly reduced (p = 0.0043). These results show the up-regulation of NRF2 mediated AO mechanisms in response to PAT toxicity. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1 / 5
页数:5
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