Higuchi H, Nakaoka M, Katsuda Y, Kawamura S, Kato T, Matsuo M
Environmental Health Science Laboratory, Sumitomo Chemical Co., Ltd., Osaka, Japan.
J Toxicol Sci. 1995 Aug;20(3):239-49. doi: 10.2131/jts.20.239.
As part of a collaborative project to determine optimal administration period and parameters to detect compound effects on male fertility in the rat, adult male rats were administered cyclophosphamide daily at 5, 10, 20 and 40 mg/kg for 2 weeks, or at 2.5, 5 and 10 mg/kg for 4 or 9 weeks. After the pre-pairing administration period, each male was paired with an untreated female. After mating, testes and epididymides were removed and examined for organ weights, sperm head counts, sperm morphology and histopathology. Mated females were caesarean-sectioned on Day 13 of gestation. Although atrophy of epithelia in the cauda epididymides and decreases of spermatogenic cells in the testes were observed in the higher dose groups in the 2w study, no other effects on the male reproductive system were noted in any of the studies. There were clear effects on pregnancy outcome; implantation efficiency was decreased in the highest dosage groups and postimplantation losses increased in all the dosage groups in all studies. These results suggest that a fertility study with females is needed particularly in the case of mutagenic agents, together with a detailed histopathological evaluation for reliable detection of toxicity on the male reproductive system.
作为一项合作项目的一部分,该项目旨在确定检测化合物对大鼠雄性生育能力影响的最佳给药期和参数,成年雄性大鼠每天分别按5、10、20和40mg/kg的剂量给予环磷酰胺,持续2周;或按2.5、5和10mg/kg的剂量给予4周或9周。在配对前给药期结束后,将每只雄性大鼠与未处理的雌性大鼠配对。交配后,取出睾丸和附睾,检查器官重量、精子头部计数、精子形态和组织病理学。在妊娠第13天对已交配的雌性大鼠进行剖腹产。虽然在2周研究的高剂量组中观察到附睾尾部上皮萎缩和睾丸中生精细胞减少,但在任何研究中均未发现对雄性生殖系统有其他影响。对妊娠结局有明显影响;在所有研究中,最高剂量组的着床效率降低,所有剂量组的着床后损失增加。这些结果表明,特别是对于诱变剂,需要对雌性进行生育力研究,并进行详细的组织病理学评估,以可靠地检测对雄性生殖系统的毒性。