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本文引用的文献

1
Systems pharmacology models can be used to understand complex pharmacokinetic-pharmacodynamic behavior: an example using 5-lipoxygenase inhibitors.系统药理学模型可用于理解复杂的药代动力学-药效学行为:以 5-脂氧合酶抑制剂为例。
CPT Pharmacometrics Syst Pharmacol. 2013 Sep 11;2(9):e74. doi: 10.1038/psp.2013.49.
2
Negative modeling results: a dime a dozen or a stepping stone to scientific discovery?负面建模结果:多如牛毛还是科学发现的垫脚石?
CPT Pharmacometrics Syst Pharmacol. 2013 Jun 12;2(6):e48. doi: 10.1038/psp.2013.28.
3
Predicting nonlinear changes in bone mineral density over time using a multiscale systems pharmacology model.利用多尺度系统药理学模型预测随时间变化的骨矿物质密度的非线性变化。
CPT Pharmacometrics Syst Pharmacol. 2012 Nov 14;1(11):e14. doi: 10.1038/psp.2012.15.
4
Insulin signaling in type 2 diabetes: experimental and modeling analyses reveal mechanisms of insulin resistance in human adipocytes.2 型糖尿病中的胰岛素信号转导:实验和建模分析揭示了人脂肪细胞胰岛素抵抗的机制。
J Biol Chem. 2013 Apr 5;288(14):9867-9880. doi: 10.1074/jbc.M112.432062. Epub 2013 Feb 11.
5
Bariatric surgery and T2DM improvement mechanisms: a mathematical model.减重手术与2型糖尿病改善机制:一个数学模型
Theor Biol Med Model. 2012 May 15;9:16. doi: 10.1186/1742-4682-9-16.
6
Mechanism-based population modelling of the effects of vildagliptin on GLP-1, glucose and insulin in patients with type 2 diabetes.基于机制的群体模型研究维格列汀对 2 型糖尿病患者 GLP-1、血糖和胰岛素的作用。
Br J Clin Pharmacol. 2012 Mar;73(3):373-90. doi: 10.1111/j.1365-2125.2011.04109.x.
7
A hierarchical whole-body modeling approach elucidates the link between in Vitro insulin signaling and in Vivo glucose homeostasis.一种分层式全身建模方法阐明了体外胰岛素信号与体内葡萄糖动态平衡之间的联系。
J Biol Chem. 2011 Jul 22;286(29):26028-41. doi: 10.1074/jbc.M110.188987. Epub 2011 May 13.
8
Putting the pieces together in diabetes research: towards a hierarchical model of whole-body glucose homeostasis.整合糖尿病研究的各个方面:迈向全身葡萄糖稳态的层次模型。
Eur J Pharm Sci. 2009 Jan 31;36(1):91-104. doi: 10.1016/j.ejps.2008.10.027. Epub 2008 Nov 13.

评估系统药理学模型与评估标准药代动力学-药效学模型不同。

Evaluating systems pharmacology models is different from evaluating standard pharmacokinetic-pharmacodynamic models.

机构信息

MedImmune LLC, Clinical Pharmacology, Drug Metabolism, and Pharmacokinetics, Cambridge, UK.

出版信息

CPT Pharmacometrics Syst Pharmacol. 2014 Feb 19;3(2):e101. doi: 10.1038/psp.2013.77.

DOI:10.1038/psp.2013.77
PMID:24552986
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3944115/
Abstract

Based on the author's recent experience, there appears to be some confusion regarding the steps required to qualify a systems pharmacology model as adequate for the intended purpose. This manuscript outlines the model evaluation approach used in the author's recent publication(1) on the systems pharmacology of a 5-lipoxygenase inhibitor and is an attempt to generate discussion on this topic within the pharmacometrics and systems pharmacology community.

摘要

基于作者最近的经验,似乎对于将系统药理学模型达到预期目的所需的步骤存在一些混淆。本文概述了作者最近在关于 5-脂氧合酶抑制剂的系统药理学研究(1)中使用的模型评估方法,并试图在药物代谢动力学和系统药理学领域内就该主题展开讨论。