Bauer C, Leporini C, Bronzetti G, Corsi C, Nieri R, Del Carratore R, Tonarelli S
Boll Soc Ital Biol Sper. 1980 Feb 15;56(3):203-7.
Mutagenic experiments in vitro were performed on yeast (S. pombe) with styrene with metabolic activation by adding at fixed times fresh mouse microsomes to the incubation mixture. Preceding studies with a single initial addition of microsomes were negative up to the maximal dose of 100 mM styrene for 60 min (5). The addition of fresh microsomes at the times 12, 24, 36 and 48 min in the presence of EDTA 40 mM resulted in an increased toxicity of styrene in vitro, but not in increased mutagenicity. Gas chromatographic determination of styrene oxide in the incubation mixture with 50 mM styrene revealed a concentration of active metabolite not capable of acting mutagenically.
在体外对酵母(粟酒裂殖酵母)进行了诱变实验,使用苯乙烯并通过在固定时间向孵育混合物中添加新鲜小鼠微粒体来实现代谢活化。之前单次初始添加微粒体的研究在高达100 mM苯乙烯的最大剂量下孵育60分钟时结果均为阴性(5)。在存在40 mM乙二胺四乙酸(EDTA)的情况下,于12、24、36和48分钟时添加新鲜微粒体,导致苯乙烯在体外的毒性增加,但诱变活性未增加。用气相色谱法测定含50 mM苯乙烯的孵育混合物中的环氧苯乙烯,结果显示活性代谢物的浓度不足以发挥诱变作用。