Effects of aflatoxin B1, fumonisin B1 and their mixture on the aryl hydrocarbon receptor and cytochrome P450 1A induction

被引:46
|
作者
Mary, Veronica S. [1 ]
Valdehita, Ana [2 ]
Navas, Jose M. [2 ]
Rubinstein, Hector R. [1 ]
Fernandez-Cruz, Maria L. [2 ]
机构
[1] Univ Nacl Cordoba, Fac Ciencias Quim, Dept Bioquim Clin, Ctr Invest Bioquim Clin & Inmunol CIBICI,CONICET, RA-5000 Cordoba, Argentina
[2] Inst Nacl Invest & Tecnol Agr & Alimentaria INIA, Dept Medio Ambiente, Madrid 28040, Spain
关键词
Aflatoxin B-1; Fumonisin B-1; Cyp1A; Ahr; Mixture; EXPERIMENTAL SUBCHRONIC MYCOTOXICOSES; HEPATOMA HEPG2 CELLS; OXIDATIVE STRESS; IN-VITRO; HEPATOCELLULAR-CARCINOMA; SIGNALING PATHWAYS; CYP1A1; INDUCTION; RAT HEPATOCYTES; PPAR-ALPHA; P450; 1A2;
D O I
10.1016/j.fct.2014.10.030
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Aflatoxin B-1 (AFB(1)) and fumonisin B-1 (FB1) are mycotoxins widely found as cereal contaminants and their co-occurrence in corn has been associated with a high incidence of liver cancer. Both toxins are immunotoxic, with AFB(1) being a procarcinogen, and its bioactivation through specific cytochrome P450 (Cyp) enzymes, such as Cyp1A, being a requirement for hepatocarcinogenic and toxic activities. This study evaluated the effects of these mycotoxins, alone or combined, on activation and expression of Cyp1A and its transcription factor aryl hydrocarbon receptor (Ahr) in hepatoma cell line H4IIE and spleen mononuclear cells of rats. The results demonstrate that in H4IIE cells, AFB(1) induced an increase in Cyp1A activity and cyp1A transcription, associated with an enhanced Ahr activity, which suggests that this toxin can act as an Ahr agonist. Moreover, FB1 caused a small rise in Cyp1A activity and cyp1A expression. Similarly in spleen cells, AFB(1) and FB1, induced overexpression of cyp1A and ahr genes. This work shows that the response potency was significantly higher for the mixture, indicating the existence of an interaction between both toxins. This study proposes the Ahr pathway activation as a toxicity mechanism of AFB(1) and FB1, and highlights that FB1 may increase AFB(1) bioactivation. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:104 / 111
页数:8
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