Johnston S D, Camacho F C, Carrillo L, Guy N, Govea J, Martinez O, Parãs A, Lisle A T, D'Occhio M
School of Animal Studies, The University of Queensland, Gatton, Queensland 4343, Australia.
Reprod Fertil Dev. 2008;20(5):563-9. doi: 10.1071/rd07215.
The aims of the present study were to examine the variability of testosterone secretion in the Virginia Opossum over a 24 h period and to develop a testosterone stimulation test that would provide an index of the prevailing testosterone biosynthetic capacity of the testes; the latter was used to clinically evaluate the efficacy of a gonadotrophin-releasing hormone agonist contraceptive. Sexually-mature captive opossums (n = 12) located in Africam Safari (Mexico) sampled every 12 h over 24 h consistently showed basal (<0.21 ng mL(-1)) blood testosterone concentrations. Intra-muscular injection of buserelin (2 microg mL(-1)) and human chorionic gonadotrophin (hCG; 1000 IU) resulted in an increase (P < 0.05) of plasma testosterone concentrations with maximal concentrations (3.9 ng mL(-1) and 5.8 ng mL(-1) respectively) occurring 120 min after injection. Plasma testosterone declined relatively rapidly to basal concentrations after 240 min with hCG but remained elevated after the same period of time with buserelin. Male opossums treated with (n = 6) and without (n = 6) a controlled-release deslorelin implant (Suprelorin; 4.7 mg deslorelin) were evaluated over a 10-week period for changes in testosterone secretion (hCG stimulation test) and sperm production (spermatorrhea). At the end of this period, the animals were hemi-castrated and their relative testicular quantitative histology compared. Testosterone concentration decreased over the course of the study in both treated and control animals (P < 0.0001) but there was no apparent effect of deslorelin on testosterone secretion, testicular histology (relative proportions of testicular cell types and seminiferous tubule diameter), or sperm production (presence of sperm in the cauda epididymis or urine).
本研究的目的是检测弗吉尼亚负鼠在24小时内睾酮分泌的变异性,并开发一种睾酮刺激试验,以提供睾丸当前睾酮生物合成能力的指标;后者用于临床评估促性腺激素释放激素激动剂避孕药的疗效。位于非洲野生动物园(墨西哥)的12只性成熟圈养负鼠在24小时内每12小时采样一次,结果显示基础血睾酮浓度始终低于0.21 ng/mL。肌肉注射布舍瑞林(2 μg/mL)和人绒毛膜促性腺激素(hCG;1000 IU)导致血浆睾酮浓度升高(P<0.05),注射后120分钟出现最大浓度(分别为3.9 ng/mL和5.8 ng/mL)。注射hCG后,血浆睾酮在240分钟后相对迅速下降至基础浓度,但注射布舍瑞林后相同时间内仍保持升高。对接受(n = 6)和未接受(n = 6)缓释地洛瑞林植入物(Suprelorin;4.7 mg地洛瑞林)治疗的雄性负鼠进行了为期10周的睾酮分泌变化(hCG刺激试验)和精子生成(遗精)评估。在此期间结束时,对动物进行半阉割,并比较其相对睾丸定量组织学。在研究过程中,治疗组和对照组动物的睾酮浓度均下降(P<0.0001),但地洛瑞林对睾酮分泌、睾丸组织学(睾丸细胞类型的相对比例和曲细精管直径)或精子生成(附睾尾或尿液中精子的存在)没有明显影响。