James R W, Heywood R
Toxicol Lett. 1980 Jul;6(2):87-92. doi: 10.1016/0378-4274(80)90173-3.
A quantitative histomorphometric assessment of testicular spermatogenesis was undertaken on testes from rats which had received 1-amino-3 chloro-2 propanol hydrochloride (CL 88, 236) at oral doses of 0, 50, 250 or 500 mg/kg/day for 12 weeks. Rats which developed epididymal sperm granulomata or severe atrophy of the germinal epithelium were excluded from quantitative examination. Pathological changes in the epididymis and semininferous epithelium were not strongly correlated. CL 88, 236 administered at 50 mg/kg/day was without effect on the histomorphometry of the seminiferous epithelium, although epididymal lesions occurred at this dose. At higher doses a quantitative reduction in testicular spermatids was evident. It appears important to differentiate between the selective antifertility action of CL 88, 236 on the biochemistry of epididymal spermatozoa and the disruption of epididymal physiology, and testicular spermatogenesis found at unusually high doses.
对口服剂量为0、50、250或500mg/kg/天的1-氨基-3-氯-2-丙醇盐酸盐(CL 88,236)连续给药12周的大鼠睾丸进行了精子发生的定量组织形态学评估。出现附睾精子肉芽肿或生精上皮严重萎缩的大鼠被排除在定量检查之外。附睾和生精上皮的病理变化相关性不强。尽管在50mg/kg/天的剂量下出现了附睾病变,但该剂量的CL 88,236对生精上皮的组织形态学没有影响。在更高剂量下,睾丸精子细胞明显定量减少。区分CL 88,236对附睾精子生物化学的选择性抗生育作用与附睾生理功能的破坏以及在异常高剂量下发现的睾丸精子发生似乎很重要。