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(The FASEB Journal. 2008;22:1220.3)
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(The FASEB Journal. 2008;22:1220.3-1220.)
© 2008 FASEB


1220.3

SAPHIR: a collaborative multi-scale, multi-resolution Core Model Environment for the Physiome—with a prototype core model of blood pressure regulation and fluid homeostasis

S. Randall Thomas1, Patrick Hannaert2, Pierre Baconnier3, Julie Fontecave3, François Guillaud2, Virginie Le Rolle4, Pierre Maziere1, Fariza Tahi1, Farida Zehraoui1, Nadia Abchiche1 and Alfredo Hernandez3

1 FRE 2873 IBISC, CNRS, Evry, France
2 Université de Poitiers, INSERM E0324, Poitiers, France
3 Université Joseph Fourier (UJF), La Tronche, France
4 INSERM U642. LTSI, Rennes, France

ABSTRACT

We present the current state of the SAPHIR project, a multi-resolution core modeling environment (CME) in the spirit of the IUPS Physiome, with application to a prototype core model based on a modular implementation of the classic systems model by Guyton et al. (1972 Ann. Rev. Physiol. 34:13–44) and its extension by Ikeda et al. (1979 Annals Biomed. Engin. 7:135–166). This core model targets short- and long-term regulation of blood pressure and homeostasis of body fluids and major solutes. The aim is to provide a collaborative modeling environment enabling plug-and-play construction of integrated systems models with lumped-parameter sub-models at the organ/tissue level yet also allowing focus on cell- or molecular-level detailed models embedded in the larger core model. Thus, in silico exploration of gene-to-organ-to-organism scenarios is possible while keeping computation time manageable. The CME is built on the M2SL toolbox, a multi-scale, multi-resolution, multi-mode open source package developed in C++ by one of us (AH). Associated with the CME is an ontology-based database allowing exploration of the modules, parameter values, and equations.

In parallel with the CME implementation of the core model, we also present stand-alone implementations in Berkeley Madonna (Ikeda model) and Simulink (Guyton model).





This Article
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