Kus I, Songur A, Ozogul C, Kavakli A, Zararsiz I, Sarsilmaz M
Department of Anatomy, Faculty of Medicine, Firat University, Elazig, Turkey.
Arch Androl. 2004 May-Jun;50(3):193-200. doi: 10.1080/01485010490425476.
The aim of this study was to examine effects of photoperiod on the ultrastructure of Leydig cells in rat. For this purpose, 21 male Wistar rats were used. Animals were divided into three groups: Control rats in group I were kept under 12 hrs light: 12 hrs dark conditions (12L: 12D) for 10 weeks. Animals in group II were exposed to long photoperiods (18L: 6D), while rats in group III were exposed to short photoperiods (6L:18D) for 10 weeks. At the end of the experiment, all animals were killed by decapitation and blood samples were obtained. Serum testosterone levels were determined with the use of a chemiluminescent enzyme immunoassay. The testes of all rats were removed and weighed, then processed for light and electron microscopy. For morphometric comparison, diameters of seminiferous tubules in each group were measured. In rats exposed to long photoperiods, testicular weights, diameters of seminiferous tubules and serum testosterone levels were significantly increased as compared to those in control rats, whereas exposure of rats to short photoperiods resulted in a significant decrease of testicular weights, diameters of seminiferous tubules and serum testosterone levels as compared to those in control rats and rats maintained in long photoperiods. The amount of mitochondria and cytoplasmic secretory granules were increased in the cytoplasm of Leydig cells of rats exposed to long photoperiods. Furthermore, an increase in extensiveness of rough endoplasmic reticulum in the cell cytoplasm was noticed in this group, whereas a decrease in mitochondria and cytoplasmic secretory granules of the Leydig cell cytoplasm was seen in rats exposed to short photoperiods. The results of our study indicate that testicular functions increase after exposure to long photoperiods and decrease after exposure to short photoperiods.
本研究的目的是检测光周期对大鼠睾丸间质细胞超微结构的影响。为此,选用了21只雄性Wistar大鼠。动物被分为三组:第一组的对照大鼠在12小时光照:12小时黑暗条件(12L:12D)下饲养10周。第二组的动物暴露于长光周期(18L:6D),而第三组的大鼠暴露于短光周期(6L:18D)10周。实验结束时,所有动物断头处死并采集血样。采用化学发光酶免疫分析法测定血清睾酮水平。取出所有大鼠的睾丸并称重,然后进行光镜和电镜处理。为进行形态计量学比较,测量了每组生精小管的直径。与对照大鼠相比,暴露于长光周期的大鼠睾丸重量、生精小管直径和血清睾酮水平显著增加,而与对照大鼠和处于长光周期的大鼠相比,暴露于短光周期的大鼠睾丸重量、生精小管直径和血清睾酮水平显著降低。暴露于长光周期的大鼠睾丸间质细胞胞质中线粒体和胞质分泌颗粒的数量增加。此外,该组可见细胞质中粗面内质网的扩张增加,而暴露于短光周期的大鼠睾丸间质细胞胞质中线粒体和胞质分泌颗粒减少。我们的研究结果表明,暴露于长光周期后睾丸功能增强,暴露于短光周期后睾丸功能减弱。