利用小分子药物进行昼夜节律调节的非线性模型预测控制

John H Abel, Ankush Chakrabarty, Francis J Doyle
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引用次数: 0

摘要

最近的体外研究发现,小分子药物可影响哺乳动物昼夜节律钟的剂量依赖性变化,为控制提供了一条新途径。大多数研究利用光来控制时钟,然而,药剂因其侵袭性较低而在时钟控制方面具有优势。在本文中,我们采用一个机理模型来预测哺乳动物昼夜节律振荡器在所研究药物作用下的相位动态。这些预测结果将用于为受限模型预测控制器(MPC)提供信息,以计算时钟再诱导的适当剂量。由于振荡器相位响应效应的非线性,在许多情况下是非直观的。我们通过室内实验证明,必须根据特定药物的相位响应曲线调整 MPC 参数,以实现最佳的相位控制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Nonlinear Model Predictive Control For Circadian Entrainment Using Small-Molecule Pharmaceuticals.

Nonlinear Model Predictive Control For Circadian Entrainment Using Small-Molecule Pharmaceuticals.

Nonlinear Model Predictive Control For Circadian Entrainment Using Small-Molecule Pharmaceuticals.

Nonlinear Model Predictive Control For Circadian Entrainment Using Small-Molecule Pharmaceuticals.

Recent in vitro studies have identified small-molecule pharmaceuticals effecting dose-dependent changes in the mammalian circadian clock, providing a novel avenue for control. Most studies employ light for clock control, however, pharmaceuticals are advantageous for clock manipulation through reduced invasiveness. In this paper, we employ a mechanistic model to predict the phase dynamics of the mammalian circadian oscillator under the effect of the pharmaceutical under investigation. These predictions are used to inform a constrained model predictive controller (MPC) to compute appropriate dosing for clock re-entrainment. Constraints in the formulation of the MPC problem arise from variation in the phase response curves (PRCs) describing drug effects, and are in many cases non-intuitive owing to the nonlinearity of oscillator phase response effects. We demonstrate through in-silico experiments that it is imperative to tune the MPC parameters based on the drug-specific PRC for optimal phase manipulation.

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