Hu Q Y, Zhu S P
Department of Radiotoxicology, Suzhou Medical College, Jiangsu, China.
Mutat Res. 1990 Jul;244(3):209-14. doi: 10.1016/0165-7992(90)90130-c.
Cytogenetic damage induced by a wide range of concentrations of uranyl fluoride injected into mouse testes was evaluated by determining the frequencies of chromosomal aberrations in spermatogonia and primary spermatocytes. Breaks, gaps and polyploids were observed in spermatogonia. The frequencies of the significant type of aberration, breaks, were induced according to the injected doses of uranyl fluoride. Primary spermatocytes were examined for fragments, univalents and multivalents. The multivalents observed in this study resulted either from chromatid interchanges or from reciprocal translocations. The reciprocal translocations were induced in spermatogonia and recorded in primary spermatocytes. For primary spermatocytes the incidence of aberrant cells largely depended on the administered dose. Sampling time after treatment could affect the frequencies of chromosomal aberrations in male mouse germ cells.
通过测定精原细胞和初级精母细胞中的染色体畸变频率,评估了注入小鼠睾丸的多种浓度氟化铀酰所诱导的细胞遗传学损伤。在精原细胞中观察到断裂、间隙和多倍体。显著类型的畸变(断裂)频率随氟化铀酰的注射剂量而诱导产生。对初级精母细胞进行了片段、单价体和多价体的检查。本研究中观察到的多价体要么源于染色单体互换,要么源于相互易位。相互易位在精原细胞中诱导产生,并在初级精母细胞中记录下来。对于初级精母细胞,异常细胞的发生率在很大程度上取决于给药剂量。处理后的采样时间会影响雄性小鼠生殖细胞中的染色体畸变频率。