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Biological effect of PCBs, PCQs and PCDFs present in the oil causing yusho and yu-cheng.

机译:油中存在的PCBs,PCQs和PCDFs的生物效应会引起油腻味和油腻味。

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摘要

Male Sprague-Dawley rats were daily given orally for 22 days a regimen consisting of polychlorinated biphenyls (PCBs), 1 mg/day; polychlorinated quaterphenyls (PCQs), 1 mg/day; polychlorinated dibenzofurans (PCDFs), 10 micrograms/day; or a mixture of PCBs, PCQs and PCDFs (Mix-1, 1 mg + 1 mg + 10 micrograms/day). Female Cynomolgus monkeys were daily administered PCBs (5 mg), PCQs (5 mg) or a mixture (Mix-2) containing 5 mg PCBs + 20 micrograms PCDFs for 20 weeks. The PCBs, and PCDFs had the components of PCBs, PCQs and PCDFs similar to those contained in Japanese yusho oils, respectively. The PCB-treated rats and monkeys showed hepatic hypertrophy, immunosuppression and increased drug-metabolizing enzyme activities in hepatic microsomes, but were devoid of the dermal symptoms characteristic of yusho. PCQs caused an increase in drug-metabolizing enzyme activities in hepatic microsomes and immunosuppression in monkeys, but these effects were much smaller than those found with PCBs treatment. On the other hand, treatment with PCDF or Mix-1 or Mix-2 caused hypertrophy of the liver, immunosuppression, increase in drug-metabolizing enzyme activities of hepatic microsome to much greater extent than observed with PCBs, being more than 100 times as effective as PCBs. In addition PCDFs and the mixtures containing PCDFs caused weight loss and thymic atrophy. PCDFs and Mix-2-treated monkeys showed the dermal symptoms that are characteristic of yusho patients but were not observed in monkeys treated with PCBs and PCQs alone. These results suggest that PCDFs are the primary causative agent of yusho.
机译:每天口服雄性Sprague-Dawley大鼠22天,治疗方案为1 mg /天,由多氯联苯(PCBs)组成;多氯四苯基(PCQ),每天1 mg;多氯二苯并呋喃(PCDFs),每天10微克;或多氯联苯,多氯联苯和多氯二苯并呋喃的混合物(混合物1,每天1毫克+1毫克+ 10毫克)。雌性食蟹猴每天接受多氯联苯(5毫克),五氯苯酚(5毫克)或含有5毫克多氯联苯+ 20微克PCDF的混合物(Mix-2)治疗20周。多氯联苯和多氯二苯并呋喃的成分分别与日本柚子油中所含的成分相似。经多氯联苯处理的大鼠和猴子在肝微粒体中显示出肝脏肥大,免疫抑制和药物代谢酶活性增加,但没有柚子的皮肤症状。 PCQs引起肝微粒体中药物代谢酶活性的增加和猴类动物免疫抑制的增加,但这些作用远小于PCBs处理所产生的作用。另一方面,用PCDF或Mix-1或Mix-2进行治疗会引起肝脏肥大,免疫抑制,肝微粒体药物代谢酶活性的增加,其程度要比多氯联苯所观察到的大得多,是PCB的100倍以上作为PCB。另外,PCDF和含有PCDF的混合物引起体重减轻和胸腺萎缩。 PCDFs和Mix-2处理的猴子表现出了yusho患者所特有的皮肤症状,但在仅用PCBs和PCQs处理的猴子中没有观察到。这些结果表明PCDF是yusho的主要病原体。

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