Li Yujing, Pei Tianjiao, Zhu Huili, Wang Ruiying, Wu Lukanxuan, Huang Xin, Li Fangyuan, Qiao Xinyu, Zhong Yuchan, Huang Wei
Department of Obstetrics and Gynecology, West China Second University Hospital of Sichuan University, Chengdu, Sichuan, China.
Key Laboratory of Birth Defects and Related Diseases of Women and Children, Ministry of Education, Sichuan University, Chengdu, Sichuan, China.
J Pineal Res. 2025 Jan;77(1):e70026. doi: 10.1111/jpi.70026.
Circadian rhythm disruption (CRD), stemming from sleep disorders and/or shift work, is a risk factor for reproductive dysfunction. CRD has been reported to disturb nocturnal melatonin signaling, which plays a crucial role in female reproduction as a circadian regulator and an antioxidant. The hypothalamic-pituitary-ovarian (HPO) axis regulates female reproduction, with luteinizing hormone (LH) pulse pattern playing a pivotal role in folliculogenesis and steroidogenesis. However, the effect of CRD on the HPO axis and the involvement of melatonin remains unclear. Female CBA/CaJ mice underwent CRD modeling, which involves alternating between standard light conditions and an 8-h advance schedule every 3 days for 8 weeks, whereas control mice were maintained under a standard 12:12-h light/dark (LD) cycle. Subsequent measurements of diurnal melatonin levels, LH pulse patterns assessments via serial tail-tip blood sampling and evaluations of ovarian function were conducted. CRD altered the circadian rhythms of wheel-running activity and melatonin secretion in mice and led to an augmented LH pulse pattern, evidenced by increased LH pulse frequency, mean LH levels, and pituitary LH beta-subunit (LHβ) expression, irregular estrous cycles, abnormal luteal function, altered endocrine function, and ovarian oxidative stress. Melatonin treatment (10 mg/kg/day for 4 weeks) significantly improved the HPO axis disorder in CRD mice, decreasing the enhanced LH pulse frequency and pituitary LHβ expression. These findings were further validated using an in vitro LβT2 cell perfusion model. Furthermore, melatonin restored ovarian function and scavenged reactive oxygen species, thereby preventing apoptosis and preserving ovarian function. This study offers new insights into the impact of CRD on the HPO axis and emphasizes the potential of melatonin supplementation in mitigating its effects on female reproduction.
昼夜节律紊乱(CRD)源于睡眠障碍和/或轮班工作,是生殖功能障碍的一个风险因素。据报道,CRD会扰乱夜间褪黑素信号,而褪黑素作为一种昼夜节律调节因子和抗氧化剂,在女性生殖中起着至关重要的作用。下丘脑-垂体-卵巢(HPO)轴调节女性生殖,黄体生成素(LH)脉冲模式在卵泡发生和类固醇生成中起关键作用。然而,CRD对HPO轴的影响以及褪黑素的作用仍不清楚。对雌性CBA/CaJ小鼠进行CRD建模,即每3天在标准光照条件和提前8小时的时间表之间交替,持续8周,而对照小鼠则维持在标准的12:12小时光照/黑暗(LD)周期下。随后进行了昼夜褪黑素水平的测量、通过连续尾尖采血评估LH脉冲模式以及卵巢功能评估。CRD改变了小鼠的昼夜节律性轮转活动和褪黑素分泌,导致LH脉冲模式增强,表现为LH脉冲频率增加、平均LH水平升高、垂体LHβ亚基(LHβ)表达增加、发情周期不规则、黄体功能异常、内分泌功能改变以及卵巢氧化应激。褪黑素治疗(10毫克/千克/天,持续4周)显著改善了CRD小鼠的HPO轴紊乱,降低了增强的LH脉冲频率和垂体LHβ表达。这些发现使用体外LβT2细胞灌注模型进一步得到验证。此外,褪黑素恢复了卵巢功能并清除了活性氧,从而防止细胞凋亡并维持卵巢功能。这项研究为CRD对HPO轴的影响提供了新的见解,并强调了补充褪黑素在减轻其对女性生殖影响方面的潜力。