Yang Zhan-Jun, Ye Wei-San, Cui Guang-Hui, Guo Yan, Xue She-Pu
Department of Anatomy, Histology and Embryology, Institute of Basic Medical Science, Chinese Academy of Medical Sciences, School of Basic Medicine, Peking Union Medical College, Beijing 100005, China.
Contraception. 2004 Sep;70(3):203-11. doi: 10.1016/j.contraception.2004.02.019.
To evaluate the efficacy and feasibility of a new regimen of low-dose gossypol acetic acid (GA) combined with desogestrel/ethinylestradiol and testosterone undecanoate (DSG/E/TU) as a male contraceptive, adult male rats were fed orally with GA (12.5 mg/kg/day) and DSG (0.125 mg/kg)/E (0.025 mg/kg)/TU (100 mg/kg) daily for 8 weeks as loading dose until infertility, and a similar low dose of GA alone for infertility maintenance. Control animals were administered a single low dose of GA (12.5 mg/kg/day) or DSG (0.125 mg/kg)/E (0.025 mg/kg)/TU (100 mg/kg), and vehicle, respectively. Results demonstrated that the combined dosage regimen could damage epididymal sperm motility and density, and induce infertility within 8 weeks in rats; the infertility could be consistently sustained by giving single GA (12.5 mg/kg/day), and was reversible in about 8 weeks following withdrawal of gossypol. The regimen rendered treated male rats with spermiation failure within a period of 6-20 weeks of treatment. Also, the serum luteinizing hormone, follicle-stimulating hormone and testicular interstitial fluid testosterone levels showed a transient decrease at the end of 6 or 8 weeks, which returned to control levels after 8 weeks of recovery phase. No hypokalemia or other adverse effects in viscera were observed. These results provide a promising approach to using the new regimen for the development of an effective and reversible oral male contraceptive.
为评估低剂量醋酸棉酚(GA)联合去氧孕烯/炔雌醇和十一酸睾酮(DSG/E/TU)新方案作为男性避孕药的有效性和可行性,成年雄性大鼠每日口服GA(12.5毫克/千克/天)和DSG(0.125毫克/千克)/E(0.025毫克/千克)/TU(100毫克/千克),持续8周作为负荷剂量直至不育,然后单独给予类似低剂量的GA以维持不育状态。对照动物分别给予单一低剂量的GA(12.5毫克/千克/天)或DSG(0.125毫克/千克)/E(0.025毫克/千克)/TU(100毫克/千克)以及赋形剂。结果表明,联合给药方案可损害附睾精子活力和密度,并在8周内诱导大鼠不育;单独给予GA(12.5毫克/千克/天)可使不育状态持续,停用棉酚后约8周不育状态可逆转。该方案使治疗的雄性大鼠在治疗6至20周内出现精子发生失败。此外,血清促黄体生成素(LH)、促卵泡生成素(FSH)和睾丸间质液睾酮水平在6或8周结束时出现短暂下降,在恢复阶段8周后恢复至对照水平。未观察到低钾血症或其他内脏不良反应。这些结果为使用该新方案开发有效且可逆的口服男性避孕药提供了一种有前景的方法。