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J Diabetes Sci Technol. 2007 Mar;1(2):181-92. doi: 10.1177/193229680700100208.
2
Dynamic modeling of free fatty acid, glucose, and insulin: an extended "minimal model".游离脂肪酸、葡萄糖和胰岛素的动态建模:一个扩展的“最小模型”。
Diabetes Technol Ther. 2006 Dec;8(6):617-26. doi: 10.1089/dia.2006.8.617.
3
Partitioning glucose distribution/transport, disposal, and endogenous production during IVGTT.静脉葡萄糖耐量试验期间葡萄糖分布/转运、处置及内源性生成的划分
Am J Physiol Endocrinol Metab. 2002 May;282(5):E992-1007. doi: 10.1152/ajpendo.00304.2001.
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Compartment modeling.
Adv Drug Deliv Rev. 2001 Jun 11;48(2-3):249-64. doi: 10.1016/s0169-409x(01)00118-1.
5
Overestimation of minimal model glucose effectiveness in presence of insulin response is due to undermodeling.在存在胰岛素反应的情况下,最小模型葡萄糖效能的高估是由于模型构建不足。
Am J Physiol. 1998 Dec;275(6):E1031-6. doi: 10.1152/ajpendo.1998.275.6.E1031.
6
A model of the kinetics of insulin in man.人体胰岛素动力学模型。
J Clin Invest. 1974 May;53(5):1481-92. doi: 10.1172/JCI107697.
7
The kinetics of insulin metabolism in diabetes mellitus.糖尿病中胰岛素代谢的动力学
Postgrad Med J. 1973 Dec;49:Suppl 7:949-54.
8
A model of glucose-insulin homeostasis in man that incorporates the heterogeneous fast pool theory of pancreatic insulin release.一种纳入胰腺胰岛素释放异质性快速池理论的人体葡萄糖-胰岛素稳态模型。
Diabetes. 1978 Oct;27(10):1027-42. doi: 10.2337/diab.27.10.1027.

糖调节系统的药代动力学建模

Pharmacokinetic Modeling of the Glucoregulatory System.

作者信息

Farmer T G, Edgar T F, Peppas N A

机构信息

Department of Chemical, The University of Texas at Austin, 1 University Station C0400, Austin, TX 78712-0231, USA.

出版信息

J Drug Deliv Sci Technol. 2008 Nov;18(6):387-391. doi: 10.1016/s1773-2247(08)50076-1.

DOI:10.1016/s1773-2247(08)50076-1
PMID:21686031
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3113518/
Abstract

A pharmacokinetic model is proposed to describe the glucoregulatory process. The model describes the dynamics of glucose, amino acids, and fatty acids, as well as both the hormonal actions and dynamics of insulin, glucagon, epinephrine, and glucagon-like peptide-one. The model was developed assuming that the dynamics of each species occurrs in only one compartment. Several forms of the metabolic absorption and elimination rates, along with possibilities for increasing the complexity of each compartmental model are discussed. Once properly identified and validated, the novel model has the potential to be more descriptive than other models describing glucose dynamics in the body.

摘要

提出了一种药代动力学模型来描述葡萄糖调节过程。该模型描述了葡萄糖、氨基酸和脂肪酸的动态变化,以及胰岛素、胰高血糖素、肾上腺素和胰高血糖素样肽-1的激素作用和动态变化。该模型是在假设每个物种的动态变化仅发生在一个隔室的情况下开发的。讨论了几种代谢吸收和消除速率的形式,以及增加每个隔室模型复杂性的可能性。一旦经过适当识别和验证,这个新模型有可能比其他描述体内葡萄糖动态变化的模型更具描述性。