Food, Drugs and Chemical Toxicology Group, CSIR- Indian Institute of Toxicology Research, Lucknow, India.
Academy of Scientific and Innovative Research (AcSIR) CSIR-IITR campus, Lucknow, India.
Crit Rev Food Sci Nutr. 2020;60(16):2710-2729. doi: 10.1080/10408398.2019.1655388. Epub 2019 Aug 26.
Zearalenone (ZEA) is a mycotoxin produced by the fungi of genera, which contaminates the cereals and food stuffs worldwide. mycotoxins are considered as important metabolites related to animal and human health. Evidences indicate that ZEA has been found to be present in different food stuffs from developed countries like USA, Canada, France, Germany, Japan, etc. and developing nations like Egypt, Thailand, Iran, Croatia, Philippines, etc. The toxicokinetic studies reveal that following oral exposure of ZEA, the compound is absorbed through gastrointestinal tract (GIT), gets metabolized and distributed to different body parts. ZEA has been shown to cause reproductive disorders in laboratory animals. Although the toxicity of ZEA in humans have not been conclusively established nonetheless, limited evidences indicate that ZEA can cause hyper estrogenic syndrome. Though, ZEA causes low acute toxicity, but reports are available confirming the systemic toxicity caused by ZEA. There is no review available that addresses the occurrence, systemic toxicity and the probable mechanisms of ZEA toxicity. This review shall address the world-wide occurrence and & toxicity studies of ZEA over the past 20 years. The review shall also discuss the toxicokinetics of ZEA and metabolites; illustrates the systemic toxicity and probable mechanisms of action leading to the risk associated with ZEA.
玉米赤霉烯酮(ZEA)是一种由镰刀菌属真菌产生的真菌毒素,污染了世界各地的谷物和食品。真菌毒素被认为是与动物和人类健康有关的重要代谢物。有证据表明,ZEA 已在不同的食品中被发现,这些食品来自美国、加拿大、法国、德国、日本等发达国家,以及埃及、泰国、伊朗、克罗地亚、菲律宾等发展中国家。毒代动力学研究表明,ZEA 经口服暴露后,会通过胃肠道(GIT)被吸收,发生代谢,并分布到身体的不同部位。ZEA 已被证明会导致实验动物生殖障碍。尽管 ZEA 对人类的毒性尚未得到明确证实,但有限的证据表明 ZEA 可能会引起类雌激素综合征。虽然 ZEA 的急性毒性较低,但有报道证实 ZEA 会引起全身毒性。目前还没有关于 ZEA 发生、全身毒性和可能的毒性作用机制的综述。本文将综述过去 20 年来 ZEA 在世界范围内的发生情况和毒性研究。本文还将讨论 ZEA 的毒代动力学及其代谢物;说明导致与 ZEA 相关风险的全身毒性和可能的作用机制。