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A Mathematical Model of the Circadian Phase-Shifting Effects of Exogenous Melatonin

机译:外源褪黑素的昼夜相移效应的数学模型

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摘要

Melatonin is endogenously produced and released in humans during nighttime darkness and is suppressed by ocular light exposure. Exogenous melatonin is used to induce circadian phase shifts and sleep. The circadian phase-shifting ability of a stimulus (e.g., melatonin or light) relative to its timing may be displayed as a phase response curve (PRC). Published PRCs to exogenous melatonin show a transition from phase advances to delays approximately 1 h after dim light melatonin onset. A previously developed mathematical model simulates endogenous production and clearance of melatonin as a function of circadian phase, light-induced suppression, and resetting of circadian phase by light. We extend this model to include the pharmacokinetics of oral exogenous melatonin and phase-shifting effects via melatonin receptors in the suprachiasmatic nucleus of the mammalian hypothalamus. Model parameters are fit using 2 data sets: (1) blood melatonin concentration following a 0.3- or 5.0-mg dose, and (2) a PRC to a 3.0-mg dose of melatonin. After fitting to the 3.0-mg PRC, the model correctly predicts that, by comparison, the 0.5-mg PRC is slightly decreased in amplitude and shifted to a later circadian phase. This model also reproduces blood concentration profiles of various melatonin preparations that differ only in absorption rate and percentage degradation by first-pass hepatic metabolism. This model can simulate experimental protocols using oral melatonin, with potential application to guide dose size and timing to optimally shift and entrain circadian rhythms.
机译:褪黑素是人类在夜间黑暗中内源性产生和释放的,并且受到眼光暴露的抑制。外源性褪黑激素用于诱导昼夜节律相移和睡眠。刺激(例如,褪黑激素或光)相对于其定时的昼夜相移能力可以显示为相位响应曲线(PRC)。在昏暗的褪黑素发作后约1小时,已发表的PRCs到外源性褪黑素显示出从相提前到延迟的过渡。先前开发的数学模型模拟了褪黑激素的内源性产生和清除与昼夜相,光诱导的抑制作用以及光使昼夜相复位的关系。我们扩展此模型,以包括口服外源性褪黑激素的药代动力学和通过哺乳动物下丘脑上视交叉核中褪黑激素受体的相移效应。使用2个数据集拟合模型参数:(1)剂量为0.3或5.0 mg的血液中褪黑激素浓度,以及(2)剂量为3.0 mg的褪黑激素的PRC。在拟合到3.0 mg PRC以后,该模型正确地预测到,相比之下,0.5 mg PRC的振幅会稍微降低,并转移到后来的昼夜节律阶段。该模型还复制了各种褪黑激素制剂的血药浓度曲线,这些制剂的吸收率和肝脏首过代谢的降解百分率仅不同。该模型可以模拟使用口服褪黑激素的实验方案,并有潜在的用途来指导剂量大小和时间安排,以最佳地转移和带动昼夜节律。

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