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

• DOI: 10.1111/andr.13718
• Publication Date: 2024-08-02T12:20:56Z
• Authors: Zhenming Zheng; Hui Wang; Zhimin Chen; Hui Gao; Pan Gao; Jingjing Gao; Hui Jiang; Xiansheng Zhang
• Keywords: 03 medical and health sciences; 0302 clinical medicine

AbstractBackgroundSleep 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.ObjectiveTo investigate the effects of different durations of SD on different parts of the testis and epididymis caput, corpus, and cauda.MethodsAdult 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.ResultsCompared 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.ConclusionChronic 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.