Rashid K A, Babish J G, Mumma R O
J Environ Sci Health B. 1984 Nov-Dec;19(8-9):689-701. doi: 10.1080/03601238409372457.
Hepatic S9 preparations from Aroclor 1254 induced rats and 3-methylcholanthrene induced woodchucks were used to investigate, in vitro, the mutagenic potential of five amino acid conjugates of 2,4-Dichlorophenoxyacetic acid (alanine, aspartic acid, leucine, methionine and tryptophan). Five strains of Salmonella typhimurium (TA97, TA98, TA100, TA1535, TA1538) were utilized for this purpose. Dose-response effects producing a two-fold increase of revertants over spontaneous levels were not observed with either S9 preparation indicating that the amino acid conjugates are not promutagens in these assays.
使用来自用多氯联苯混合物1254诱导的大鼠和用3-甲基胆蒽诱导的土拨鼠的肝S9制剂,在体外研究2,4-二氯苯氧乙酸的五种氨基酸共轭物(丙氨酸、天冬氨酸、亮氨酸、蛋氨酸和色氨酸)的致突变潜力。为此使用了五株鼠伤寒沙门氏菌(TA97、TA98、TA100、TA1535、TA1538)。两种S9制剂均未观察到产生比自发水平回复突变体增加两倍的剂量反应效应,这表明在这些试验中氨基酸共轭物不是前诱变剂。