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Ochratoxin A

机译:ch曲毒素A

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The Food Safety Commission of Japan (FSCJ) conducted a risk assessment on ochratoxin A (hereinafter referred to as OTA) as a self-tasking risk assessment. OTA is a mycotoxin produced by fungal species such as Aspergillus ochraceus and Penicilium verrucosum , which occur mainly in stored foods. Food contamination with OTA has been reported in various food commodities including cereal, coffee, cocoa, beer and wine. Nephrotoxicity was observed in all the animal species examined in the subacute toxicity studies. Pathological changes observed in the studies are karyomegaly and cytomegaly as well as tubular atrophy and degeneration in proximal tubules at the outer zone of renal medulla. The dose- and treatment period-dependent changes were observed in kidneys in rats and pigs. In chronic toxicity/carcinogenicity studies with oral administration, tumor induction was observed at the outer zone of renal medulla in rodents, mainly in male rats. Chromosome aberration was observed both in in vitro and in vivo genotoxicity studies, but gene point mutation was not detected. After reviewing the results of various toxicological studies, FSCJ considered that OTA is a non-genotoxic carcinogen acting indirectly on DNA, and that tolerable daily intake (TDI) is able to be specified for OTA. Regarding non-carcinogenic toxicity of OTA, the effects observed at the lowest dose in various studies were decreased ability to concentrate urine and degenerative changes in epithelial cells of the tubules observed in a 120-day subacute toxicity study in pigs. The lowest-observed-adverse-effect level (LOAEL) in these studies was set at 8?μg/kg bw/day. FSCJ specified the TDI of 16 ng/kg bw/day, applying an uncertainty factor of 500 (10 for species difference, 10 for individual difference and 5 for the use of LOAEL based on irreversible renal failure indices) to the LOAEL. Regarding carcinogenicity of OTA, FSCJ specified the TDI of 15 ng/kg bw/day, applying an uncertainty factor of 1000 (10 for species difference, 10 for individual difference and 10 for carcinogenicity) to the no-observed-adverse-effect level (NOAEL) of 15?μg/kg bw/day, which was derived from a two-year carcinogenicity study in rats (administered 5 times a week at 21?μg/kg bw) performed by the National Toxicology Program (NTP). The estimated exposure levels of OTA in Japan for average (the 50th percentile) and high risk consumers (the 95th percentile) are 0.14 ng/kg bw/day and 2.21 ng/kg bw/day, respectively. These estimations suggest the intake of OTA to be below the TDI even in the high risk consumers. Therefore, FSCJ considers that no apparent adverse effect is expected in Japan from the current risk estimate. OTA-producing fungi grow in agricultural products and food under different environmental conditions. OTA contamination in these products varies depending on environmental conditions such as climate. Therefore, the risk management organizations are encouraged to monitor OTA contamination in foods continuously. The monitoring is a key importance to consider the necessity of the regulation for OTA.
机译:日本食品安全委员会(FSCJ)对曲霉毒素A(以下称为OTA)进行了风险评估,将其作为自我执行的风险评估。 OTA是由真菌种类产生的霉菌毒素,例如曲霉和疣状青霉菌,主要存在于储藏食品中。据报道,谷物,咖啡,可可,啤酒和葡萄酒等各种食品中都含有OTA污染食品。在亚急性毒性研究中检查的所有动物物种中均观察到了肾毒性。在研究中观察到的病理变化是肾髓质外部区域的近端小管中的核细胞增生和细胞增生以及肾小管萎缩和变性。在大鼠和猪的肾脏中观察到剂量和治疗期依赖性变化。在口服口服的慢性毒性/致癌性研究中,在啮齿动物的肾髓质外部区域观察到了肿瘤诱导,主要是在雄性大鼠中。在体外和体内遗传毒性研究中均观察到染色体畸变,但未检测到基因点突变。在审查了各种毒理学研究的结果之后,FSCJ认为OTA是一种间接作用于DNA的非遗传毒性致癌物,并且可以为OTA指定可耐受的每日摄入量(TDI)。关于OTA的非致癌毒性,在各种研究中以最低剂量观察到的效果是:在120天的亚急性毒性研究中观察到的尿液浓缩能力降低以及肾小管上皮细胞的变性变化。这些研究中观察到的最低不良反应水平(LOAEL)设置为8微克/千克体重/天。 FSCJ将TDI指定为16 ng / kg bw /天,对LOAEL应用了不确定性因子500(物种差异为10,个体差异为10,个体基于不可逆肾衰竭指数使用LOAEL为5)。关于OTA的致癌性,FSCJ将TDI指定为15 ng / kg bw /天,将不确定因素1000(物种差异为10,个体差异为10,致癌性为10)应用于未观察到的不良影响水平(美国国家毒理学计划(NTP)对老鼠进行了为期两年的致癌性研究(每周以21µg / kg bw的剂量每周进行5次试验),得出的结果为15µg / kg bw /天。在日本,平均(第50个百分位)和高风险消费者(第95个百分位)的OTA估计暴露水平分别为0.14 ng / kg bw /天和2.21 ng / kg bw /天。这些估计表明,即使在高风险消费者中,OTA的摄入量也要低于TDI。因此,FSCJ认为,根据目前的风险估算,日本不会出现明显的不利影响。产生OTA的真菌会在不同的环境条件下在农产品和食品中生长。这些产品中的OTA污染取决于气候条件等环境条件而变化。因此,鼓励风险管理组织持续监控食品中的OTA污染。监控对于考虑OTA法规的必要性至关重要。

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    《Food Safety 》 |2015年第2期| 共3页
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