Sýkora I
Neoplasma. 1981;28(6):739-46.
A dominant-lethal test of 6-mercaptopurine (Spofa, CSSR) was carried out in male mice with four intraperitoneal, two oral, and one subcutaneous dosage levels. Furthermore, the drug was administered either in single doses or repeatedly for 7 and 14 consecutive days. With all of the dosage levels as well as administration durations and routes a genetic risk was proved at the periods of meiotic division and late premeiotic stages of spermatogenesis, manifested by increased percentages of fetal resorptions. In relationship to the total dose administered, irrespective of the route of administration, the most marked effect increasing the frequency of resorptions within the specified period of spermatogenesis was found in the groups that had received, by repeated administrations, more than 5.5 mg of 6-mercaptopurine per one male. Fertility reduction was apparent mainly after intraperitoneal injection; the differences were significant in weeks 3--5 of the test. The prenidation loss figures brought no univocal information about the interrelationship between the genetic effect and the stages of spermatogenesis.
对6-巯基嘌呤(斯波法,CSSR)进行了显性致死试验,受试动物为雄性小鼠,设置了四种腹腔注射、两种口服和一种皮下注射的剂量水平。此外,药物以单次给药或连续7天和14天重复给药的方式给予。在所有剂量水平以及给药持续时间和途径下,均证明在减数分裂期和精子发生的减数分裂前晚期存在遗传风险,表现为胎儿吸收百分比增加。就给药的总剂量而言,无论给药途径如何,在通过重复给药每只雄性接受超过5.5毫克6-巯基嘌呤的组中,发现在特定精子发生期内增加吸收频率的最显著效果。生育力降低主要在腹腔注射后明显;在试验的第3至5周差异显著。着床前损失数字并未提供关于遗传效应与精子发生阶段之间相互关系的明确信息。