Putting the pieces together in diabetes research: Towards a hierarchical model of whole-body glucose homeostasis

被引:20
作者
Cedersund, Gunnar [1 ]
Stralfors, Peter [1 ]
机构
[1] Linkoping Univ, Dept Clin & Expt Med, Cell Biol & Diabet Res Ctr, S-58185 Linkoping, Sweden
基金
瑞典研究理事会;
关键词
Systems biology; Glucose homeostasis; PKPD; Hierarchical; Type; 2; diabetes; TRANSIENT C-13-LABELING EXPERIMENTS; COMPUTATIONAL MODEL; SKELETAL-MUSCLE; MINIMAL MODEL; INSULIN SENSITIVITY; METABOLIC FLUXES; HEPATIC CELLS; OSCILLATIONS; YEAST; IDENTIFICATION;
D O I
10.1016/j.ejps.2008.10.027
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Type 2 diabetes is one of the most widespread and rapidly spreading diseases world-wide and has been subject of extensive research efforts. However, understanding the molecular basis of the disease is increasing piecemeal and a consensus regarding the overall picture of normal metabolic regulation and malfunction in diabetes has not emerged. A systems biology approach, combining mathematical modelling with simultaneous high-throughput measurements, can be of considerable help. On the whole-body level, this has been done in pharmacokinetic and pharmacodynamic models, which recently have started to mature into more physiologically realistic organ-based models. At the other end of the spectrum, detailed models for crucial cellular processes are starting to mature into complete modules that potentially can be fitted into such whole-body organ-based models. The result of such a merge is a multi-level hierarchical model, which is a model type that has been common in technical systems. In this review, we report and exemplify some of the recent progress that has been made to achieve such a hierarchical model, and we argue why it is only through such a model that a Complete picture of diabetes mellitus can be obtained. (C) 2008 Published by Elsevier B.V.
引用
收藏
页码:91 / 104
页数:14
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