首页> 外文期刊>EFSA supporting publications >In vivo toxicity and genotoxicity of beauvericin and enniatins. Combined approach to study in vivo toxicity and genotoxicity of mycotoxins beauvericin (BEA) and enniatin B (ENNB)
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In vivo toxicity and genotoxicity of beauvericin and enniatins. Combined approach to study in vivo toxicity and genotoxicity of mycotoxins beauvericin (BEA) and enniatin B (ENNB)

机译:博韦霉素和烯睾丙肽的体内毒性和遗传毒性。联合方法研究霉菌毒素博韦霉素(BEA)和Enniatin B(ENNB)的体内毒性和遗传毒性

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Beauvericin (BEA) and Enniatins (ENN) are mycotoxins produced by Fusarium fungi detected in food and feed; there are insufficient data to establish their reference values. To evaluate BEA and ENN oral toxicity, an integrated approach was applied. Among ENN, Enniatin B (ENNB) was selected as test substance. The approach is composed by: i) in vitro and acute in vivo genotoxicity tests; ii) a repeated‐dose oral toxicity study focused on genotoxic, immune, endocrine, nervous endpoints and the reproductive/developmental toxicity screening. For BEA, all the genotoxicity endpoints yielded negative results excluding Comet assay in duodenum and kidney after repeated doses. BEA immunotoxicity was observed in female mice, concentrated in number and functional activity of effector T cells in the spleen. Based on the repeated‐dose BEA study, the No Observed Adverse Effect Level (NOAEL) for female mice is 1 mg/kg b.w. per day (increased thyroid pycnotic nuclei and endometrial hyperplasia). In males, the NOAEL is 0.1 mg/kg b.w. per day (reduced colloid and altered T4 serum levels). Maternal NOAEL is 0.1 mg/kg b.w. per day (increased thymus weight), developmental NOAEL is 10 mg/kg b.w. per day. For ENNB, the results support a genotoxic effect in bone marrow and liver cells after acute treatment, but not after repeated exposure. Immunotoxic ENNB effects were observed in both genders, suggestive of a suppressive/inhibiting activity particularly evident in males. Based on the repeated‐dose ENNB study, the NOAEL for females is 0.18 mg/kg b.w. per day (histomorphometrical effects on thymus, uterus and spleen). In male mice, the NOAEL is 1.8 mg/kg b.w. per day (enterocyte vacuolization in duodenum and increased Reactive Oxygen Species and reduced Glutathione brain levels). The maternal NOAEL is 1.8 mg/kg b.w. per day (decreased white pulp area and increased red/white pulp area ratio in spleen), developmental NOAEL is 18 mg/kg b.w. per day.
机译:Beauvericin(BEA)和Enniatins(ENN)是在食物和饲料中检测到的镰刀菌真菌产生的霉菌毒素。没有足够的数据来建立其参考值。为了评估BEA和ENN的口服毒性,采用了一种综合方法。在ENN中,Enniatin B(ENNB)被选为测试物质。该方法包括:i)体外和急性体内遗传毒性试验; ii)重复剂量的口服毒性研究,重点是遗传毒性,免疫,内分泌,神经终点和生殖/发育毒性筛选。对于BEA,重复剂量后,除十二指肠和肾脏中的彗星试验外,所有遗传毒性终点均产生阴性结果。在雌性小鼠中观察到BEA免疫毒性,集中于脾脏中效应T细胞的数量和功能活性。根据重复剂量的BEA研究,雌性小鼠的未观察到的不良反应水平(NOAEL)为1 mg / kg体重。每天(甲状腺幽门核增加和子宫内膜增生)。在男性中,NOAEL为0.1 mg / kg体重。每天(减少的胶体和改变的T4血清水平)。母体NOAEL为0.1 mg / kg体重。每天(胸腺重量增加),发育NOAEL为10 mg / kg体重。每天。对于ENNB,该结果支持急性治疗后对骨髓和肝细胞的遗传毒性作用,但反复暴露后则无。男女均观察到了免疫毒性的ENNB效应,提示其抑制/抑制活性在男性中尤为明显。根据ENNB的重复剂量研究,女性的NOAEL为0.18 mg / kgb.w。每天(对胸腺,子宫和脾脏的组织形态计量学影响)。在雄性小鼠中,NOAEL为1.8 mg / kg体重。每天(十二指肠中的肠细胞空泡和增加的活性氧和减少的谷胱甘肽脑水平)。孕妇的NOAEL为1.8 mg / kg体重。每天(减少的白浆面积和增加的红色/白浆面积比例在脾脏中),发育性NOAEL为18 mg / kg体重。每天。

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