Yang Zheng-Wei, Kong Ling-Shu, Guo Yang, Yin Jin-Qi, Mills Nathaniel
Morphometric Research Laboratory, North Sichuan Medical College, 234 Fujiang Road, Nanchong, Sichuan 637007, China.
Asian J Androl. 2006 May;8(3):289-99. doi: 10.1111/j.1745-7262.2006.00140.x.
To quantitatively study the histological changes of the testis and epididymis as a result of a drastic reduction of testosterone secretion.
Fourteen adult Sprague-Dawley rats were injected intraperitoneally with ethane dimethane sulfonate (EDS, 75 mg/kg) and the same number of animals were injected with normal saline as a control. At days 7 and 12 (after treatment), respectively, half of the animals from each group were killed. The testes and epididymides were removed and tissue blocks embedded in methacrylate resin. The cell number per testis was estimated using the stereological optical disector and some other parameters were obtained using other morphometric methods.
The EDS treatment resulted in an almost complete elimination of Leydig cells but had no effect on the numbers of Sertoli cells per testis. At day 7 after EDS treatment, many elongated spermatids were retained in the seminiferous epithelium and many round spermatids could be seen in the epididymal ducts. At day 12, a looser arrangement of spermatids and spermatocytes became evident, with apparent narrow empty spaces being formed between germ cells in an approximately radial direction towards the tubule lumen; the numbers (per testis) of non-type B spermatogonia and spermatocytes were similar to controls, whereas that of type B spermatogonia increased by 59%, and that of early round, elongating and late elongated spermatids decreased by 37%, 72% and 52%, respectively.
The primary spermatogenic lesions following EDS administration were (i) spermiation failure and (ii) detachment of spermatids and spermatocytes associated with impairment in spermiogenesis and meiosis.
定量研究睾酮分泌急剧减少对睾丸和附睾组织学变化的影响。
14只成年Sprague-Dawley大鼠腹腔注射乙烷二甲磺酸盐(EDS,75mg/kg),另14只动物注射生理盐水作为对照。分别在处理后的第7天和第12天,每组处死一半动物。取出睾丸和附睾,将组织块包埋于甲基丙烯酸树脂中。使用体视学光学分割器估计每个睾丸的细胞数量,并使用其他形态计量学方法获得一些其他参数。
EDS处理几乎完全消除了睾丸间质细胞,但对每个睾丸支持细胞的数量没有影响。在EDS处理后的第7天,许多长形精子细胞保留在生精上皮中,在附睾管中可见许多圆形精子细胞。在第12天,精子细胞和精母细胞的排列变得明显疏松,在生殖细胞之间朝着小管腔的大致径向方向形成明显狭窄的空隙;非B型精原细胞和精母细胞(每个睾丸)的数量与对照组相似,而B型精原细胞的数量增加了59%,早期圆形、伸长和晚期伸长精子细胞的数量分别减少了37%、72%和52%。
EDS给药后原发性生精损伤为:(i)精子释放失败;(ii)精子细胞和精母细胞脱离,伴有精子发生和减数分裂受损。