Department of Theriogenology, Faculty of Veterinary Medicine, Assiut University, Assiut, Egypt.
Animal Production Research Institute, Cairo, Egypt.
Sci Rep. 2022 May 12;12(1):7869. doi: 10.1038/s41598-022-11884-4.
This study determined the effects of scrotal insulation on testicular functions in bucks and evaluated the impact of exogenous gonadotropin-releasing hormone (GnRH) administration before scrotal insulation on sperm production and testicular vascular dynamics. Twelve bucks were randomly divided into three groups: scrotal-insulated animals without GnRH treatment (INS), scrotal-insulated animals treated previously with GnRH (GnRH + INS), and animals without insulation as controls (CON). Doppler ultrasonography was used to evaluate testicular vascular changes, and semen samples were collected to assess seminal parameters. Testicular samples were collected from slaughtered bucks at the end of the experiment for histological investigations and immunohistochemical analysis for caspase 3 (apoptotic marker), and a vascular endothelial growth factor (VEGF; hypoxic marker) evaluation. Sperm motility drastically decreased (33%) in the INS group on day 8 compared with those in the GnRH + INS and CON groups (58% and 85%, respectively). Testicular blood flow significantly decreased for 3 and 2 weeks in the INS and GnRH + INS groups, respectively. The pulsatility index (PI) reached pretreatment values at 5 and 4 weeks after insulation in the INS and GnRH + INS groups, respectively. The resistance index (RI) values increased in both insulated groups for the first 2 weeks and decreased to control values 4 weeks after insulation. However, the maximum velocity (VP) started to increase reaching pretreatment values by the 5th and 3rd weeks after insulation in the INS and GnRH + INS groups, respectively. Histological investigations showed a marked reduction in lipid inclusions in Sertoli cells in the GnRH + INS group compared with those in the INS group. The distributions of both caspase 3 and VEGF decreased in the GnRH + INS group compared with those in the INS group. This study showed that the administration of a single dose of GnRH delayed the negative effects of scrotal insulation on different seminal traits and revealed the pivotal role of GnRH in compensating testicular insulation in bucks.
本研究旨在确定阴囊隔热对公鹿睾丸功能的影响,并评估在阴囊隔热前给予外源性促性腺激素释放激素(GnRH)对精子生成和睾丸血管动力学的影响。12 只公鹿被随机分为三组:未给予 GnRH 治疗的阴囊隔热动物(INS)、先前给予 GnRH 治疗的阴囊隔热动物(GnRH+INS)和未隔热的对照动物(CON)。使用多普勒超声评估睾丸血管变化,收集精液样本评估精液参数。实验结束时,从屠宰的公鹿中采集睾丸组织样本进行组织学研究和免疫组织化学分析,以评估半胱氨酸天冬氨酸蛋白酶 3(凋亡标记物)和血管内皮生长因子(VEGF;缺氧标记物)。与 GnRH+INS 和 CON 组(分别为 58%和 85%)相比,INS 组在第 8 天精子活力急剧下降(33%)。INS 和 GnRH+INS 组睾丸血流分别在隔热后 3 周和 2 周显著减少。INS 和 GnRH+INS 组的搏动指数(PI)分别在隔热后 5 周和 4 周恢复到预处理值。在两个隔热组中,阻力指数(RI)值在前 2 周增加,4 周后降至对照值。然而,最大速度(VP)在 INS 和 GnRH+INS 组中分别在隔热后第 5 周和第 3 周开始增加,达到预处理值。组织学研究显示,与 INS 组相比,GnRH+INS 组的 Sertoli 细胞中的脂质包涵体明显减少。与 INS 组相比,GnRH+INS 组中半胱氨酸天冬氨酸蛋白酶 3 和血管内皮生长因子的分布减少。本研究表明,单次给予 GnRH 可延迟阴囊隔热对不同精液特性的负面影响,并揭示了 GnRH 在补偿公鹿睾丸隔热中的关键作用。