Department of Physiology and Cell Biology, University of Nevada, Reno School of Medicine, Reno, NV, USA.
NHC Key Laboratory of Male Reproduction and Genetics, Guangzhou, People's Republic of China.
Nat Commun. 2021 Feb 23;12(1):1253. doi: 10.1038/s41467-021-21517-5.
There are no non-hormonal male contraceptives currently on the market despite decades of efforts toward the development of "male pills". Here, we report that triptonide, a natural compound purified from the Chinese herb Tripterygium Wilfordii Hook F displays reversible male contraceptive effects in both mice and monkeys. Single daily oral doses of triptonide induces deformed sperm with minimal or no forward motility (close to 100% penetrance) and consequently male infertility in 3-4 and 5-6 weeks in mice and cynomolgus monkeys, respectively. Male fertility is regained in ~4-6 weeks after cessation of triptonide intake in both species. Either short- or long-term triptonide treatment causes no discernable systematic toxic side effects based on histological examination of vital organs in mice and hematological and serum biochemical analyses in monkeys. Triptonide appears to target junction plakoglobin and disrupts its interactions with SPEM1 during spermiogenesis. Our data further prove that targeting late spermiogenesis represents an effective strategy for developing non-hormonal male contraceptives.
尽管几十年来一直致力于开发“男性避孕药”,但目前市场上仍没有非激素男性避孕药。在这里,我们报告称,从中国草药雷公藤中纯化的天然化合物雷公藤红素在小鼠和猴子中均显示出可逆的男性避孕效果。单次口服雷公藤红素可导致精子畸形,几乎没有或完全没有前向运动(接近 100%的穿透率),分别在 3-4 周和 5-6 周导致小鼠和食蟹猴不育。在两种动物中,停止服用雷公藤红素后约 4-6 周即可恢复生育能力。基于对小鼠重要器官的组织学检查和猴子的血液学和血清生化分析,短期或长期的雷公藤红素治疗均不会引起明显的系统性毒性副作用。雷公藤红素似乎靶向连接桥粒斑蛋白并在精子发生过程中破坏其与 SPEM1 的相互作用。我们的数据进一步证明,靶向晚期精子发生是开发非激素男性避孕药的有效策略。