Zhang R D, Wen X H, Kong L S, Deng X Z, Peng B, Huang A P, Wan Y, Yang Z W
Morphometric Research Laboratory, North Sichuan Medical College, Sichuan, China.
Reproduction. 2002 Jul;124(1):95-105. doi: 10.1530/rep.0.1240095.
The aim of this study was to examine the controversial effects of experimental unilateral cryptorchidism and subsequent orchiopexy on the number of germ cells and other morphometric characteristics of testicular and epididymal structures in adult rabbits. Unilateral cryptorchidism was induced in 11 mature male New Zealand white rabbits by returning one testis, together with the ipsilateral epididymis, to the abdominal cavity via a surgical procedure. After 3 months, testes and epididymides were removed from six animals (and from six age-matched control animals that did not undergo the surgery). Orchiopexy was performed on the five remaining animals and the testes and epididymides of these animals (and an additional six age-matched control animals) were removed 7 weeks later. A contemporary, unbiased and efficient stereological tool, the optical disector, was used to estimate the number of nuclei in the testis and epididymis using methacrylate-embedded sections of 25 micron in thickness. Cryptorchidism resulted in severe testicular atrophy and spermatogenic arrest: type A spermatogonia and Sertoli cells only were seen in the seminiferous epithelium, and the number of type A spermatogonia per testis was reduced by 84%. After orchiopexy, the testis remained atrophied and the number of type A spermatogonia returned to the near-normal range in four of five animals, but spermatogenesis was recovered only partially at the stage of early primary spermatocytes (one animal), late primary spermatocytes (two animals) or spermatids (one animal). In conclusion, cryptorchidism caused severe spermatogenic arrest that was potentially recoverable (in view of the restoration of the number of type A spermatogonia), but orchiopexy failed to induce full recovery of spermatogenesis.
本研究的目的是探讨实验性单侧隐睾症及随后的睾丸固定术对成年兔生殖细胞数量以及睾丸和附睾结构的其他形态学特征的争议性影响。通过手术将11只成熟雄性新西兰白兔的一侧睾丸连同同侧附睾回纳至腹腔,诱导形成单侧隐睾症。3个月后,从6只动物(以及6只未接受手术的年龄匹配对照动物)体内取出睾丸和附睾。对其余5只动物实施睾丸固定术,7周后取出这些动物(以及另外6只年龄匹配对照动物)的睾丸和附睾。使用一种现代、无偏且高效的体视学工具——光学分割器,通过厚度为25微米的甲基丙烯酸酯包埋切片来估计睾丸和附睾中的细胞核数量。隐睾症导致严重的睾丸萎缩和生精停滞:生精上皮中仅可见A型精原细胞和支持细胞,每个睾丸中A型精原细胞的数量减少了84%。睾丸固定术后,睾丸仍萎缩,5只动物中有4只的A型精原细胞数量恢复至接近正常范围,但仅在早期初级精母细胞阶段(1只动物)、晚期初级精母细胞阶段(2只动物)或精子细胞阶段(1只动物)部分恢复了生精过程。总之,隐睾症导致严重的生精停滞,这种停滞可能是可恢复的(鉴于A型精原细胞数量的恢复),但睾丸固定术未能诱导生精过程完全恢复。