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Scientific opinion on the risks for animal and human health related to the presence of quinolizidine alkaloids in feed and food in particular in lupins and lupin‐derived products

机译:关于饲料和食品中特别是羽扇豆和羽扇豆制品中喹诺唑烷生物碱的存在对动物和人类健康风险的科学见解

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摘要

The European Commission asked for a scientific opinion on the risks for animal and human health related to the presence of quinolizidine alkaloids ( s) in feed and food. This risk assessment is limited to s occurring in s species/varieties relevant for animal and human consumption in Europe (i.e. L., L., L. and Sweet). Information on the toxicity of s in animals and humans is limited. Following acute exposure to sparteine (reference compound), anticholinergic effects and changes in cardiac electric conductivity are considered to be critical for human hazard characterisation. The Panel used a margin of exposure ( ) approach identifying a lowest single oral effective dose of 0.16 mg sparteine/kg body weight as reference point to characterise the risk following acute exposure. No reference point could be identified to characterise the risk of chronic exposure. Because of similar modes of action for s, the Panel used a group approach assuming dose additivity. For food, the highest mean concentration of Total s (Tot s) (i.e. the 6 most abundant s) was found in lupin seed samples classified as ‘Lupins (dry) and similar‐’. Due to the limited data on occurrence and consumption, dietary exposure was calculated for some specific scenarios and no full human health risk characterisation was possible. The calculated margin of exposures ( s) may indicate a risk for some consumers. For example, when lupin seeds are consumed without a debittering step, or as debittered lupin seeds high in content and when ‘lupin‐based meat imitates’ are consumed. For horses, companion and farm animals, other than salmonids, the available database on adverse effects was too limited to identify no‐observed‐adverse‐effect levels and/or lowest‐observed‐adverse‐effect levels and no risk characterisation was possible. For salmonids, the Panel considers the risk for adverse effects to be low.
机译:欧盟委员会要求就饲料和食品中喹喔啉生物碱的存在对动物和人类健康的风险提出科学意见。此风险评估仅限于与欧洲的动物和人类食用有关的s种/变种(例如L.,L.,L。和Sweet)。关于s在动物和人类中的毒性的信息是有限的。急性接触斯巴地丁(参考化合物)后,抗胆碱能作用和心脏电导率的变化被认为对人类危害的表征至关重要。小组采用暴露余量()方法确定最低口服单剂量有效剂量0.16 mg斯巴地丁/ kg体重作为参考点,以表征急性暴露后的风险。无法确定参考点来表征慢性暴露的风险。由于s的作用方式相似,专家组采用了假定剂量加和的小组方法。对于食品,在归类为“羽扇豆(干)和类似品”的羽扇豆种子样品中发现的最高总浓度(Tot s)(即6个最丰富的s)。由于有关发生和消费的数据有限,因此针对某些特定情况计算了饮食摄入量,无法全面描述人类健康风险。计算出的风险敞口幅度可能表明某些消费者有风险。例如,当食用羽扇豆种子时没有去苦味步骤,或者当羽扇豆种子中的去籽味含量高,并且食用了“基于羽扇豆的肉制品”时。对于马,伴侣动物和农场动物(鲑鱼除外),可用的不良反应数据库太有限,无法识别未观察到的不良反应水平和/或最低观察到的不良反应水平,因此无法进行风险表征。对于鲑鱼类,专家小组认为不良影响的风险较低。

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