Sýkora I, Gandalovicová D
Neoplasma. 1978;25(5):523-33.
Dominant-lethal assays in male mice were made with the following cytostatics: Cyclophosphamide, TS-160, Edikron, Penberol, Cytembena, Mercaptopurine, Butocin, and Damvar. The cytostatics were administered mostly for 14-day periods, with the exception of Butocin (7 days) and high doses of Cyclophosphamide and TS-160 (single administrations). From the first day of administration on, the males were mated with intact females mostly at eight one-week intervals, and the quality of pregnancy was checked. Antifertility effects were found with TS 160, Penberol (at high dosage), and Mercaptopurine. Effects on permiogenesis with genetic risk were found with Cyclophosphamide, TS-160, Mercaptopurine, and less marked ones also with Cytembena. The effects were mostly manifested by increases in the numbers of early fetal resorptions, and less frequently by preimplantation loss of ova. No genetic risk was revealed by the assay in the cytostatics Edikron, Penberol, Butocin, and Damvar.
环磷酰胺、TS - 160、依地 Kron(Edikron)、喷贝罗(Penberol)、塞替派(Cytembena)、巯嘌呤、布托辛(Butocin)和达姆瓦尔(Damvar)。除布托辛(7天)以及高剂量环磷酰胺和TS - 160(单次给药)外,细胞抑制剂大多给药14天。从给药第一天起,雄性小鼠大多每隔一周与未交配过的雌性小鼠交配一次,并检查妊娠情况。发现TS - 160、喷贝罗(高剂量时)和巯嘌呤有抗生育作用。发现环磷酰胺、TS - 160、巯嘌呤对精子发生有遗传风险影响,塞替派也有较轻微影响。这些影响大多表现为早期胎儿吸收数量增加,较少表现为植入前卵子丢失。依地 Kron、喷贝罗、布托辛和达姆瓦尔等细胞抑制剂试验未显示遗传风险。