Arimoto S, Negishi T, Hayatsu H
Cancer Lett. 1980 Nov;11(1):29-33. doi: 10.1016/0304-3835(80)90125-1.
An inhibitory effect of hemin on mutagenicities of a range of carcinogens was found by adding hemin to the preincubation mixture of the Ames' test. Strong inhibitions were observed for benzo[alpha]pyrene, 3-methylcholanthrene, 7,10-dimethylbenz[alpha]anthracene, chrysene, 2-acetylaminofluorene, 2-nitrofluorene and aflatoxin B1. Generally, 50% inhibition was caused by an amount of hemin 1--2 equivalents to the mutagen. Excess of hemin caused complete inhibitions. Hemin did not affect the mutagenicities of 2-(2-furyl)-3-(5-nitro-2-furyl)acrylamide, 4-nitroquinoline-1-oxide, nitromin, N-methyl-N-nitrosourea, N-methyl-N'-nitro-N-nitrosoguanidine, N-nitrosodi-n-butyl-amine, quinoxaline-1,4-dioxide and carbadox. Biliverdin, bilirubin and chlorophyllin were also effective as inhibitors for the mutagenicity of benzo[alpha]pyrene.
通过在艾姆斯试验的预温育混合物中加入氯高铁血红素,发现氯高铁血红素对一系列致癌物的诱变性具有抑制作用。观察到对苯并[a]芘、3-甲基胆蒽、7,10-二甲基苯并[a]蒽、屈、2-乙酰氨基芴、2-硝基芴和黄曲霉毒素B1有强烈抑制作用。一般来说,与诱变剂1-2当量的氯高铁血红素量可导致50%的抑制。过量的氯高铁血红素会导致完全抑制。氯高铁血红素不影响2-(2-呋喃基)-3-(5-硝基-2-呋喃基)丙烯酰胺、4-硝基喹啉-1-氧化物、硝胺、N-甲基-N-亚硝基脲、N-甲基-N'-硝基-N-亚硝基胍、N-亚硝基二正丁胺、喹喔啉-1,4-二氧化物和卡巴氧的诱变性。胆绿素、胆红素和叶绿酸对苯并[a]芘的诱变性也有抑制作用。