Suzuki Yuta, Goto Ken, Nakayama Yoshihiro, Saratani Masatoshi, Takata Takuya, Okamoto Takezo, Okazaki Shuzo
Gotemba Laboratory, BoZo Research Center Inc., 1284 Kamado, Gotemba-shi, Shizuoka 412-0039, Japan.
Gotemba Laboratory, BoZo Research Center Inc., 1284 Kamado, Gotemba-shi, Shizuoka 412-0039, Japan.
Mutat Res Genet Toxicol Environ Mutagen. 2016 Nov 15;811:16-20. doi: 10.1016/j.mrgentox.2016.02.007. Epub 2016 Mar 17.
As a part of a collaborative study of the Pig-a assay by the Mammalian Mutagenicity Study Group of the Japanese Environmental Mutagen Society, a genotoxicity study on acetaminophen (APAP) was performed using the red blood cell (RBC) Pig-a and PIGRET assays. The dose levels were set at 0 (vehicle, 0.5% methylcellulose solution), 500, 1000, and 2000mg/kg, and APAP was administered once by oral gavage to male Sprague Dawley rats. For the positive control group, N-nitroso-N-ethylurea (ENU, 40mg/kg) was administered in the same way. The RBC Pig-a and PIGRET assays were performed using peripheral blood collected at pre-dosing and 1, 2 and 4 weeks after dosing. In both the RBC Pig-a and PIGRET assays, there were no changes in the Pig-a gene mutant frequency (MF) by the APAP treatment at any time point. The Pig-a MFs as measured by the RBC Pig-a assay for the ENU-treated group increased in a time-dependent manner with the maximum value at week 4; however, those using the PIGRET assay reached comparable values at week 1. Based on the above results, APAP was determined to have no mutagenicity under the conditions of this study, and the PIGRET assay could detect mutagenicity of ENU much earlier than the RBC Pig-a assay.
作为日本环境诱变剂学会哺乳动物诱变性研究组对Pig-a试验进行的合作研究的一部分,使用红细胞(RBC)Pig-a和PIGRET试验对乙酰氨基酚(APAP)进行了遗传毒性研究。剂量水平设定为0(赋形剂,0.5%甲基纤维素溶液)、500、1000和2000mg/kg,APAP通过口服灌胃法一次性给予雄性Sprague Dawley大鼠。对于阳性对照组,以相同方式给予N-亚硝基-N-乙基脲(ENU,40mg/kg)。使用给药前以及给药后1、2和4周采集的外周血进行RBC Pig-a和PIGRET试验。在RBC Pig-a和PIGRET试验中,在任何时间点,APAP处理均未导致Pig-a基因突变频率(MF)发生变化。ENU处理组通过RBC Pig-a试验测得的Pig-a MFs随时间呈依赖性增加,在第4周达到最大值;然而,使用PIGRET试验测得的Pig-a MFs在第1周就达到了相当的值。基于上述结果,在本研究条件下确定APAP无致突变性,并且PIGRET试验比RBC Pig-a试验能更早地检测到ENU的致突变性。