Multiscale modeling of metabolism, flows, and exchanges in heterogeneous organs

被引:8
作者
Bassingthwaighte, James B. [1 ]
Raymond, Gary M.
Butterworth, Erik
Alessio, Adam
Caldwell, James H.
机构
[1] Univ Washington, Dept Bioengn, Seattle, WA 98195 USA
来源
ANALYSIS OF CARDIAC DEVELOPMENT: FROM EMBRYO TO OLD AGE | 2010年 / 1188卷
基金
美国国家科学基金会;
关键词
multiscale modeling; cardiovascular system; myocardial blood flows; computational biology; capillary-tissue exchange; !text type='JS']JS[!/text]im simulation analysis; optimization; positron emission tomography; magnetic resonance imaging; BLOOD-TISSUE EXCHANGE; TRANSPORT;
D O I
10.1111/j.1749-6632.2009.05090.x
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Large-scale models accounting for the processes supporting metabolism and function in an organ or tissue with a marked heterogeneity of flows and metabolic rates are computationally complex and tedious to compute. Their use in the analysis of data from positron emission tomography (PET) and magnetic resonance imaging (MRI) requires model reduction since the data are composed of concentration time curves from hundreds of regions of interest (ROI) within the organ. Within each ROT, one must account for blood flow, intracapillary gradients in concentrations, transmembrane transport, and intracellular reactions. Using modular design, we configured a whole organ model, GENTEX, to allow adaptive usage for multiple reacting molecular species while omitting computation of unused components. The temporal and spatial resolution and the number of species are adaptable and the numerical accuracy and computational speed is adjustable during optimization runs, which increases accuracy and spatial resolution as convergence approaches. An application to the interpretation of PET image sequences after intravenous injection of (13)NH(3) provides functional image maps of regional myocardial blood flows.
引用
收藏
页码:111 / 120
页数:10
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