4.7 Article

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

期刊

FOOD AND CHEMICAL TOXICOLOGY
卷 75, 期 -, 页码 104-111

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.fct.2014.10.030

关键词

Aflatoxin B-1; Fumonisin B-1; Cyp1A; Ahr; Mixture

资金

  1. Programa Iberoamericano de Ciencia y Tecnologia para el Desarrollo (CYTED IBEROAMERICA Accion) [109AC0371]
  2. Secretaria de Ciencia y Tecnologia-Universidad Nacional de Cordoba [05/C365]
  3. Agenda Nacional de Promocion Cientifica y Tecnologica [PICT 2010-1232]
  4. Ministerio de Ciencia y Tecnologia de Cordoba [0279-005429/2006]
  5. INIA Project [RTA 2012-00053-00-00]
  6. Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET-Argentina)

向作者/读者索取更多资源

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.

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