Ma Tiantian, Matsuo Ryohei, Kurogi Kaito, Miyamoto Shunsuke, Morita Tatsumi, Shinozuka Marina, Taniguchi Fuka, Ikegami Keisuke, Yasuo Shinobu
Laboratory of Regulation in Metabolism and Behavior, Faculty of Agriculture, Kyushu University, 744 Motooka, Nishi-ku, Fukuoka, 819-0395, Japan.
Biol Sex Differ. 2024 Dec 5;15(1):102. doi: 10.1186/s13293-024-00679-z.
The circadian clock integrates external environmental changes into the internal physiology of organisms. Perturbed circadian clocks due to misaligned light cycles increase the risk of diseases, including metabolic disorders. However, the effects of sex differences in this context remain unclear.
Circadian misalignment was induced by a chronic jet lag (CJL) shift schedule (light-on time advanced by 6 h every 2 days) in C57BL/6N male and female mice. Core body temperature and activity rhythms were recorded using a nano tag, and the gene expression rhythms of clock and clock-controlled genes in the liver and adrenal glands were analyzed using qPCR. Glucose metabolism and insulin response were evaluated using glucose tolerance, insulin sensitivity, and glucose response assays. Castration and testosterone replacement were performed to assess the fundamental role of testosterone in male phenotypes under CJL.
Under CJL treatment, male mice exhibited increased weight gain, whereas females exhibited decreased weight gain compared to that of the respective controls. CJL treatment induced a lower robustness of circadian rhythms in core body temperature and a weaker rhythm of clock gene expression in the liver and adrenal glands in females, but not in males. Only male mice exhibited glucose intolerance under CJL conditions, without the development of insulin resistance. Castrated mice without testosterone exhibited decreased weight gain and reduced robustness of body temperature rhythm, as observed in intact females. Testosterone replacement in castrated mice recovered the CJL-induced weight gain, robustness of temperature rhythm, and glucose intolerance observed in intact males.
Significant sex-based differences were observed in circadian clock organization and metabolism under CJL. Testosterone plays a crucial role in maintaining the circadian clock and regulating CJL metabolism in males.
生物钟将外部环境变化整合到生物体的内部生理过程中。由于光周期失调导致的生物钟紊乱会增加包括代谢紊乱在内的疾病风险。然而,在这种情况下性别差异的影响仍不清楚。
通过慢性时差(CJL)转换时间表(每2天将开灯时间提前6小时)诱导C57BL/6N雄性和雌性小鼠的生物钟失调。使用纳米标签记录核心体温和活动节律,并使用qPCR分析肝脏和肾上腺中生物钟基因和生物钟控制基因的基因表达节律。使用葡萄糖耐量、胰岛素敏感性和葡萄糖反应测定法评估葡萄糖代谢和胰岛素反应。进行去势和睾酮替代以评估睾酮在CJL条件下对雄性表型的基本作用。
在CJL处理下,与各自的对照组相比,雄性小鼠体重增加,而雌性小鼠体重减轻。CJL处理导致雌性小鼠核心体温的昼夜节律稳健性降低,肝脏和肾上腺中生物钟基因表达的节律减弱,而雄性小鼠则没有。只有雄性小鼠在CJL条件下表现出葡萄糖不耐受,且未出现胰岛素抵抗。如在完整雌性小鼠中观察到的那样,去势且没有睾酮的小鼠体重增加减少,体温节律的稳健性降低。对去势小鼠进行睾酮替代可恢复CJL诱导的体重增加、体温节律的稳健性以及在完整雄性小鼠中观察到的葡萄糖不耐受。
在CJL条件下,观察到生物钟组织和代谢存在显著的性别差异。睾酮在维持雄性生物钟和调节CJL代谢中起关键作用。