Kondo Y, Honda S, Nakajima M, Miyahana K, Hayashi M, Shinagawa Y, Sato S, Inoue K, Nito S, Ariyuki F
Safety Research Laboratory, Tanabe Seiyaku Co., Ltd., Osaka, Japan.
Mutat Res. 1992 Feb-Mar;278(2-3):187-91.
The induction of micronuclei in mouse peripheral blood reticulocytes (RETs) was studied with the spindle poisons vincristine sulfate (VINC) and colchicine (COL) using acridine orange (AO) supravital staining. Each chemical was studied independently in two laboratories using the same protocol. Blood samples were prepared at 0, 24, 48, and 72 h after a single intraperitoneal treatment with VINC (0.0625, 0.125, and 0.25 mg/kg) or COL (0.25, 0.5, 1.0, and 2.0 mg/kg). Both VINC and COL induced micronucleated RETs (MNRETs) significantly and dose-dependently with a peak at 48 h after treatment. Maximum frequencies of micronucleated polychromatic erythrocytes (MNPCEs) were observed 24 h after treatment with VINC; thus, the transition time from MNPCEs to MNRETs was about 24 h. Both spindle poisons gave comparable results in the paired laboratories, indicating that the present AO supravital staining method is highly reproducible.
采用吖啶橙(AO)活体染色法,使用纺锤体毒素硫酸长春新碱(VINC)和秋水仙碱(COL)研究了小鼠外周血网织红细胞(RET)中微核的诱导情况。每种化学物质在两个实验室中按照相同方案独立进行研究。在单次腹腔注射VINC(0.0625、0.125和0.25mg/kg)或COL(0.25、0.5、1.0和2.0mg/kg)后的0、24、48和72小时采集血样。VINC和COL均显著且剂量依赖性地诱导了微核网织红细胞(MNRET),在处理后48小时达到峰值。在用VINC处理后24小时观察到微核多染红细胞(MNPCE)的最高频率;因此,从MNPCE到MNRET的转变时间约为24小时。两种纺锤体毒素在配对实验室中给出了可比的结果,表明目前的AO活体染色方法具有高度可重复性。