Department of Pharmacology and Toxicology, Jacobs School of Medicine and Biomedical Sciences, University at Buffalo, State University of New York (SUNY), Buffalo, NY, USA.
Technology and Development Team for Mouse Phenotype Analysis, BioResource Research Center, RIKEN, Tsukuba-shi, Ibaraki, Japan.
J Pineal Res. 2021 Sep;71(2):e12748. doi: 10.1111/jpi.12748. Epub 2021 Jun 24.
The hormone melatonin is synthesized from serotonin by two enzymatic reactions (AANAT and ASMT/HIOMT) in the pineal gland following a circadian rhythm with low levels during the day and high levels at night. The robust nightly peak of melatonin secretion is an output signal of the circadian clock to the whole organism. However, so far the regulatory roles of endogenous melatonin in mammalian biological rhythms and physiology processes are poorly understood. Here, we establish congenic mouse lines (>N10 generations) that are proficient or deficient in melatonin synthesis (AH+/+ or AH-/- mice, respectively) on the C57BL/6J genetic background by crossing melatonin-proficient MSM/Ms with C57BL/6J. AH+/+ mice displayed robust nightly peak of melatonin secretion and had significantly higher levels of pineal and plasma melatonin vs AH-/- mice. Using this mice model, we investigated the role of endogenous melatonin in regulating multiple biological rhythms, physiological processes, and rhythmic behaviors. In the melatonin-proficient (AH+/+) mice, the rate of re-entrainment of wheel-running activity was accelerated following a 6-hour phase advance of dark onset when comparted with AH-/- mice, suggesting a role of endogenous melatonin in facilitating clock adjustment. Further in the AH+/+ mice, there was a significant decrease in body weight, gonadal weight and reproductive performance, and a significant increase in daily torpor (a hypothermic and hypometabolic state lasting only hours during adverse conditions). Endogenous melatonin, however, had no effect in the modulation of the diurnal rhythm of 2-[ I]-iodomelatonin receptor expression in the SCN, free-running wheel behavior in constant darkness, life span, spontaneous homecage behaviors, and various types of social-emotional behaviors. The findings also shed light on the role of endogenous melatonin in mice domestication and provide new insights into melatonin's action in reducing energy expenditure during a food shortage. In summary, the congenic mice model generated in this study offers a significant advantage toward understanding of the role of endogenous melatonin in regulating melatonin receptor-mediated rhythm behaviors and physiological functions.
褪黑素是由松果腺中的两种酶促反应(AANAT 和 ASMT/HIOMT)从血清素合成的,其合成节律受昼夜节律的控制,白天水平较低,晚上水平较高。褪黑素分泌的强烈夜间高峰是生物钟向整个机体发出的输出信号。然而,迄今为止,内源性褪黑素在哺乳动物生物节律和生理过程中的调节作用还知之甚少。在这里,我们通过将褪黑素合成能力强的 MSM/Ms 与 C57BL/6J 杂交,在 C57BL/6J 遗传背景上建立了能够合成或不能合成褪黑素(分别为 AH+/+ 或 AH-/- 小鼠)的同基因小鼠系(>N10 代)。AH+/+ 小鼠表现出强烈的夜间褪黑素分泌高峰,其松果体和血浆中的褪黑素水平明显高于 AH-/- 小鼠。使用这种小鼠模型,我们研究了内源性褪黑素在调节多种生物节律、生理过程和节律行为中的作用。在褪黑素合成能力强的(AH+/+)小鼠中,与 AH-/- 小鼠相比,当黑暗开始时提前 6 小时,其转轮活动的重新同步化速度加快,表明内源性褪黑素在促进时钟调整方面发挥作用。此外,在 AH+/+ 小鼠中,体重、性腺重量和生殖性能显著下降,每日打盹(一种在不利条件下持续数小时的低温和低代谢状态)显著增加。然而,内源性褪黑素对 SCN 中 2-[I]-碘褪黑素受体表达的昼夜节律、持续黑暗中的自由运行轮行为、寿命、自发的笼内行为以及各种类型的社交情感行为没有影响。这些发现还揭示了内源性褪黑素在小鼠驯化中的作用,并为褪黑素在食物短缺期间减少能量消耗的作用提供了新的见解。总之,本研究中生成的同基因小鼠模型为理解内源性褪黑素在调节褪黑素受体介导的节律行为和生理功能中的作用提供了重要优势。