Lohiya N K, Sharma O P, Sharma R C
Contraception. 1986 Oct;34(4):417-33. doi: 10.1016/0010-7824(86)90094-6.
Administration of a combination formulation of danazol (100 mg/day; oral) plus testosterone enanthate (TE) (50 mg/15 days; i.m.) for 30 to 60 days in adult male langur monkeys resulted in the reversible suppression of testicular function without affecting the sexual potentia. Testicular weight and volume decreased significantly along with the mass atrophy of germinal epithelium and impaired morphology of Leydig and Sertoli cells. A conspicuous shrinkage of seminiferous tubules, Leydig cell nuclei and Sertoli cell nuclei was noted. Elevation of testicular cholesterol, total lipids, glycogen and phosphatases activity with the depletion of total proteins, nucleic acid, sialic acid and fructose was noteworthy. All changes were maintained during maintenance dose studies (danazol: 50 mg/day; oral plus TE: 50 mg/15 days; i.m.) for 60 days. Resumption of all measures to normal was evident following 120 days of recovery. It can be concluded that the exogenous TE substitutes the serum testosterone levels to maintain extratesticular androgen actions even after interference by danazol of Leydig cell function along with spermatogenesis inhibition.
在成年雄性叶猴中,给予达那唑(100毫克/天;口服)加庚酸睾酮(TE)(50毫克/15天;肌肉注射)的联合制剂30至60天,导致睾丸功能可逆性抑制,而不影响性能力。睾丸重量和体积显著下降,同时生精上皮出现块状萎缩,睾丸间质细胞和支持细胞形态受损。观察到曲细精管、睾丸间质细胞核和支持细胞核明显缩小。值得注意的是,睾丸胆固醇、总脂质、糖原和磷酸酶活性升高,同时总蛋白、核酸、唾液酸和果糖减少。在维持剂量研究(达那唑:50毫克/天;口服加TE:50毫克/15天;肌肉注射)60天期间,所有变化均持续存在。恢复120天后,所有指标明显恢复正常。可以得出结论,即使在达那唑干扰睾丸间质细胞功能并抑制精子发生后,外源性TE仍可替代血清睾酮水平,以维持睾丸外雄激素作用。