Impact of chronic sleep deprivation on male reproductive health: Insights from testicular and epididymal responses in mice

附睾 精子 睡眠剥夺 氧化应激 内科学 医学 内分泌学 组织病理学 精子活力 病态的 男科 生理学 病理 昼夜节律
作者
Zhenming Zheng,Hui Wang,Zhimin Chen,Hui Gao,Pan Gao,Jingjing Gao,Hui Jiang,Xiansheng Zhang
出处
期刊:International Journal of Andrology [Wiley]
标识
DOI:10.1111/andr.13718
摘要

Abstract Background Sleep deprivation (SD) can cause damage to the male reproductive system. However, the duration required for such damage and the specific sequence and severity of damage to the testis and epididymis remain unclear. Objective To investigate the effects of different durations of SD on different parts of the testis and epididymis caput, corpus, and cauda. Methods Adult ICR mice were randomly assigned to five groups: the SD group (SD for 18 h/day for 1, 2, 3, or 4 weeks), the SD + Vit E group (supplemented with Vit E 50 mg/kg/d during 4 weeks of SD, the SD+NS group (saline supplementation during 4 weeks of SD), the SD + RS group (5 weeks of recovery sleep after 4 weeks of SD), and a normal sleep control (Ctrl) group. Following the interventions, sperm parameters, testicular and epididymal histopathology, inflammatory response, and oxidative stress markers were compared between the groups. Results Compared to the Ctrl group, the SD group showed a decrease in sperm motility and concentration from SD 2 W and SD 3 W, respectively. Decreases in sperm concentration and motility were more pronounced in the cauda compared to the caput and corpus. Pathological damage was less severe in the epididymis caput than in the corpus and cauda. After 4 weeks of SD, inflammation and oxidative stress increased in both testes and epididymis. Both sleep recovery and vitamin E supplementation showed significant improvements, though they did not fully reach the level of the Ctrl group. Conclusion Chronic SD for more than 2 weeks causes varying degrees of damage to the testis, epididymis caput, corpus, and cauda in male mice. This damage is not fully reversible after 5 weeks of sleep recovery and antioxidant stress treatment. These findings help us to identify and prevent SD damage to the male reproduction at an early stage.
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