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;811:97-101. doi: 10.1016/j.mrgentox.2016.02.009. Epub 2016 May 27.
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 cisplatin was performed using red blood cell (RBC) Pig-a and PIGRET assays. The dose levels were set at 0 (vehicle, physiological saline), 0.5, 1, and 2 mg/kg, and cisplatin was administered intravenously once to male F344 rats. 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 the RBC Pig-a assay, an increase in the Pig-a mutant frequency (MF) was observed at week 4 in the high dose group. Although a significant increase in the Pig-a MF was also observed at week 2 in all cisplatin-treated groups, it was considered that this change was caused by a low MF in the vehicle control group and not to be biologically relevant. In the PIGRET assay, the Pig-a MF was increased at weeks 1, 2 and 4 in the high dose group. In addition, the means of the vehicle control group's Pig-a MFs in the PIGRET assay were lower than those in the RBC Pig-a assay. Based on the above results, cisplatin was determined to have mutagenicity under the conditions of this study, and it was demonstrated that the PIGRET assay was an appropriate tool to evaluate the in vivo mutagenicity 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试验的合作研究的一部分,使用红细胞(RBC)Pig-a试验和PIGRET试验对顺铂进行了遗传毒性研究。剂量水平设定为0(赋形剂,生理盐水)、0.5、1和2mg/kg,顺铂经静脉注射一次给予雄性F344大鼠。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试验和PIGRET试验。在RBC Pig-a试验中,高剂量组在第4周观察到Pig-a突变频率(MF)增加。虽然在所有顺铂治疗组的第2周也观察到Pig-a MF显著增加,但认为这种变化是由赋形剂对照组的低MF引起的,不具有生物学相关性。在PIGRET试验中,高剂量组在第1、2和4周时Pig-a MF增加。此外,PIGRET试验中赋形剂对照组的Pig-a MF平均值低于RBC Pig-a试验中的平均值。基于上述结果,确定顺铂在本研究条件下具有致突变性,并且证明PIGRET试验是比RBC Pig-a试验更早评估体内致突变性的合适工具。