Henderson L, Fedyk J, Windebank S, Smith M
Environmental Safety Laboratory, Unilever Research, Colworth House, Sharnbrook, Bedfordshire, UK.
Mutat Res. 1993 Feb;291(1):79-85. doi: 10.1016/0165-1161(93)90019-v.
The frequency of micronuclei was assessed in polychromatic erythrocytes of bone marrow and in polychromatic and normochromatic erythrocytes in peripheral blood of rats following exposure to azathioprine for 28 days. This was compared with the incidence of micronuclei in bone-marrow following exposure to a single dose of azathioprine. The incidence of micronuclei in bone-marrow polychromatic erythrocytes at the maximum tolerated dose (10 mg/kg) following exposure for 28 days was 29.5/1000. The incidence of micronucleated polychromatic erythrocytes in the peripheral blood at this dose was 4.4/1000. At the maximum tolerated dose in the single-dose study (40 mg/kg) the incidence obtained at 48 h post-treatment was 15.7/1000. This supports the view that the use of animals in a subchronic toxicity study is at least as sensitive for assessing in vivo clastogenic activity as an acute study and could reduce animal usage in toxicology assessments.
在大鼠暴露于硫唑嘌呤28天后,评估其骨髓多染红细胞以及外周血多染和正染红细胞中的微核频率。将此结果与单次暴露于硫唑嘌呤后骨髓中的微核发生率进行比较。暴露28天后,最大耐受剂量(10mg/kg)下骨髓多染红细胞中的微核发生率为29.5/1000。此剂量下外周血中微核化多染红细胞的发生率为4.4/1000。在单剂量研究的最大耐受剂量(40mg/kg)下,处理后48小时的发生率为15.7/1000。这支持了以下观点,即在亚慢性毒性研究中使用动物评估体内致断裂活性至少与急性研究一样敏感,并且可以减少毒理学评估中的动物使用量。