Yasuda Y, Kihara T, Tanimura T
Teratology. 1985 Aug;32(1):113-8. doi: 10.1002/tera.1420320115.
In an evaluation of the effect of ethinyl estradiol (EE) on the differentiation of fetal mouse testes, the ratio of the seminiferous tubular region to the testicular tissue region, the ratio of Sertoli cells to gonocytes in tubule cross sections, and the size of Leydig cells were determined by the Texture Analyse System (T.A.S., Leitz) in histological preparations of the testes. The testes were those of fetuses taken from dams given orally 0, 0.02, 0.2 or 2.0 mg/kg of body weight of EE in olive oil from day 11 through day 17 of gestation and killed at term. From experimental and the control testes, five sections were taken at 40-micron intervals. The areas of the seminiferous tubular region and the testicular region were determined and the Sertoli cells and gonocytes in tubule cross section were counted in each of the five sections. The diameters of 100 Leydig cells selected at random were averaged. These data were analyzed by Student's t test. The seminiferous tubular region was significantly increased in the testes treated with 0.02 mg/kg of EE and significantly decreased in those treated with 0.2 mg/kg of EE. The number of gonocytes per tubule cross section was significantly increased in the testes treated with 0.02 or 2.0 mg/kg of EE. The number of Sertoli cells per tubule cross section and the number of Sertoli cells per gonocyte were significantly decreased in the experimental testes. The size of the Leydig cells was significantly decreased in the testes treated with 0.2 mg/kg of EE. These findings suggest that prenatal exposure to EE before testicular differentiation affects tubular formation, the proliferation of fetal Sertoli cells, and Leydig cell differentiation, resulting in disturbances of spermatogenesis.
在一项关于炔雌醇(EE)对胎鼠睾丸分化影响的评估中,通过徕卡纹理分析系统(T.A.S.,Leitz)在睾丸组织学切片中测定了生精小管区域与睾丸组织区域的比例、小管横切面中支持细胞与生殖母细胞的比例以及睾丸间质细胞的大小。这些睾丸取自妊娠第11天至第17天经口给予橄榄油中0、0.02、0.2或2.0毫克/千克体重EE的母鼠所产的胎儿,并在足月时处死。从实验组和对照组睾丸中,每隔40微米取5个切片。测定生精小管区域和睾丸区域的面积,并对5个切片中的每一个切片中小管横切面中的支持细胞和生殖母细胞进行计数。随机选取100个睾丸间质细胞的直径求平均值。这些数据采用学生t检验进行分析。在给予0.02毫克/千克EE处理的睾丸中,生精小管区域显著增加,而在给予0.2毫克/千克EE处理的睾丸中显著减少。在给予0.02或2.0毫克/千克EE处理的睾丸中,每个小管横切面的生殖母细胞数量显著增加。在实验组睾丸中,每个小管横切面的支持细胞数量以及每个生殖母细胞的支持细胞数量显著减少。在给予0.2毫克/千克EE处理的睾丸中,睾丸间质细胞的大小显著减小。这些发现表明,在睾丸分化前产前暴露于EE会影响小管形成、胎儿支持细胞的增殖以及睾丸间质细胞的分化,从而导致精子发生紊乱。