Syntin P, Robaire B
Department of Pharmacology and Therapeutics, McGill University, Montreal, Quebec, Canada.
J Androl. 2001 Mar-Apr;22(2):235-44.
The Brown Norway rat provides a useful model to study aging of the male reproductive tract because of the selective age-dependent pathological changes that are found in the testis, epididymis, and prostate. In the testis, there is a clear age-dependent decrease in both steroidogenesis and spermatogenesis. In the epididymis, some striking segment-specific changes occur at the histological and biochemical levels prior to the major loss of spermatogenesis. We hypothesized that formation of spermatozoa in the testis and maturation of spermatozoa in the epididymis (ie, acquisition of motility and loss of the cytoplasmic droplet) may be altered during aging. Changes in the morphology of spermatozoa were assessed by light and electron microscopy. Using computer-assisted sperm analysis, the motility parameters of spermatozoa obtained from the caput and cauda epididymidis of young and old Brown Norway rats were compared. In old animals, we also compared the motility of spermatozoa from epididymides adjacent to regressed testes with those from epididymides adjacent to nonregressed testes. There was a marked increase with age in the number of spermatozoa with abnormal flagellar midpieces; the nature of these defects did not change with age. In caput epididymidis, the percentage of motile sperm was similar in young and old rats. In contrast, the percentage of motile spermatozoa was significantly decreased in cauda epididymidis of old rats; spermatozoa from the regressed testis side had altered motility characteristics. Furthermore, in the cauda epididymidis on the regressed testis side of aged Brown Norway rats, the proportion of spermatozoa that retained their cytoplasmic droplet was markedly elevated. Some of these effects are likely due to changes taking place in spermatozoa during the process of spermatogenesis in the testis (eg, formation of the flagellum), whereas others could occur during sperm maturation in the epididymis (eg, acquisition of motility). The multiple effects of aging on sperm morphology, the acquisition of motility, and the shedding of the cytoplasmic droplet clearly indicate that the quality of spermatozoa is affected by aging.
由于在睾丸、附睾和前列腺中发现了与年龄相关的选择性病理变化,棕色挪威大鼠为研究雄性生殖道衰老提供了一个有用的模型。在睾丸中,类固醇生成和精子发生都有明显的年龄依赖性下降。在附睾中,在精子发生大量丧失之前,在组织学和生化水平上会出现一些显著的节段特异性变化。我们假设,睾丸中精子的形成和附睾中精子的成熟(即获得运动能力和失去细胞质滴)在衰老过程中可能会发生改变。通过光学显微镜和电子显微镜评估精子的形态变化。使用计算机辅助精子分析,比较了从年轻和年老棕色挪威大鼠附睾头和附睾尾获得的精子的运动参数。在老年动物中,我们还比较了来自萎缩睾丸附近附睾的精子与来自未萎缩睾丸附近附睾的精子的运动能力。随着年龄的增长,鞭毛中段异常的精子数量显著增加;这些缺陷的性质不会随年龄而改变。在附睾头,年轻和年老大鼠中活动精子的百分比相似。相比之下,老年大鼠附睾尾中活动精子的百分比显著降低;来自萎缩睾丸一侧的精子具有改变的运动特征。此外,在老年棕色挪威大鼠萎缩睾丸一侧的附睾尾中,保留细胞质滴的精子比例明显升高。其中一些影响可能是由于睾丸精子发生过程中精子发生的变化(例如鞭毛的形成),而其他影响可能发生在附睾精子成熟过程中(例如获得运动能力)。衰老对精子形态、运动能力的获得和细胞质滴的脱落的多重影响清楚地表明,精子的质量受到衰老的影响。