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机构地区:[1]广州市卫生防疫站毒理科
出 处:《癌变.畸变.突变》1998年第2期98-101,共4页Carcinogenesis,Teratogenesis & Mutagenesis
摘 要:利用雄性SD大鼠每日经口给予有机锗(Ge-132)100、250、500mg/kg连续二十五d,发现高剂量组的肝细胞色素P450受到明显抑制(P<0.05)。对P448的标志酶乙氧基异吩口恶唑脱乙氧基酶(EROD)的抑制也近50%;动物以Ge-132500mg/kg/d预先处理20d,再分别给予苯巴比妥钠盐(PB)、3-甲基胆蒽(3-MC),发现Ge-132对PB诱导P450的抑制不明显,而对3-MC诱导EROD的抑制仍达33%。Male SD rats were fed orally with Ge-132 100, 250 and 500mg/kg each day for 25 days, Cyt P 450 of liver cell of high dose group was inhibited significantly (P<0.05), EROD activity was also inhibited about 50 percent in the group compared with the control. The animals were pretreated with Ge-132 500mg/kg/d for 20 days, then give PB and 3-MC, found that the inhibition of P 450 induced by PB was not obvious, but there was 33 percent inhibition of EROD activity induced by 3-MC.
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