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Evaluation of a single-dose PIGRET assay for cisplatin in rats compared with the RBC Pig-a assay
被引:2
|作者:
Suzuki, Yuta
[1
]
Goto, Ken
[1
]
Nakayama, Yoshihiro
[1
]
Saratani, Masatoshi
[1
]
Takata, Takuya
[1
]
Okamoto, Takezo
[1
]
Okazaki, Shuzo
[1
]
机构:
[1] BoZo Res Ctr Inc, Gotemba Lab, 1284 Kamado, Gotemba, Shizuoka 4120039, Japan
关键词:
Pig-a assay;
Mutagenicity;
Reticulocyte;
Genotoxicity;
GENE MUTATION ASSAY;
GENOTOXICITY;
CHEMOTHERAPY;
TRIAL;
D O I:
10.1016/j.mrgentox.2016.02.009
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
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 irrthe 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. (C) 2016 Elsevier B.V. All rights reserved.
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页码:97 / 101
页数:5
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