Göttlicher M, Cikryt P
Carcinogenesis. 1987 Jul;8(7):1021-3. doi: 10.1093/carcin/8.7.1021.
The effect of the aromatic amines 2-acetylaminofluorene (AAF), 2-acetylaminophenanthrene (AAP) and trans-4-acetylaminostilbene (AAS) on the rat hepatic aromatic hydrocarbon (Ah) receptor level was studied. 3-Methylcholanthrene (MC), as a known receptor ligand, was used as a control. The complete liver carcinogen AAF and MC did not alter significantly the hepatic receptor concentration. In contrast, the strong liver tumor initiator AAS doubled the hepatic Ah receptor level when a dose of 20 mumol/kg was administered for 5 days. AAP increased the amount of the receptor 1.5-fold.
研究了芳香胺2-乙酰氨基芴(AAF)、2-乙酰氨基菲(AAP)和反式-4-乙酰氨基芪(AAS)对大鼠肝脏芳烃(Ah)受体水平的影响。已知的受体配体3-甲基胆蒽(MC)用作对照。完全性肝致癌物AAF和MC对肝脏受体浓度没有显著改变。相反,当以20 μmol/kg的剂量给药5天时,强效肝肿瘤引发剂AAS使肝脏Ah受体水平增加了一倍。AAP使受体量增加了1.5倍。