[HTML][HTML] Modelling gastrointestinal bioelectric activity

A Pullan, L Cheng, R Yassi, M Buist - Progress in biophysics and molecular …, 2004 - Elsevier
A Pullan, L Cheng, R Yassi, M Buist
Progress in biophysics and molecular biology, 2004Elsevier
The development of an anatomically realistic biophysically based model of the human
gastrointestinal (GI) tract is presented. A major objective of this work is to develop a
modelling framework that can be used to integrate the physiological, anatomical and
medical knowledge of the GI system. The anatomical model was developed by fitting
derivative continuous meshes to digitised data taken from images of the visible man.
Structural information, including fibre distributions of the smooth muscle layers and the …
The development of an anatomically realistic biophysically based model of the human gastrointestinal (GI) tract is presented. A major objective of this work is to develop a modelling framework that can be used to integrate the physiological, anatomical and medical knowledge of the GI system. The anatomical model was developed by fitting derivative continuous meshes to digitised data taken from images of the visible man. Structural information, including fibre distributions of the smooth muscle layers and the arrangement of the networks of interstitial cells of Cajal, were incorporated using published information. A continuum modelling framework was used to simulate electrical activity from the single cell to the whole organ and body. Also computed was the external magnetic field generated from the GI electrical activity. The set of governing equations were solved using a combination of numerical techniques. Activity at the (continuum) cell level was solved using a high-resolution trilinear finite element procedure that had been defined from the previously fitted C1 continuous anatomical mesh. Multiple dipolar sources were created from the excitation waves which were embedded within a coupled C1 continuous torso model to produce both the cutaneous electrical field and the external magnetic field. Initial simulations were performed using a simplified geometry to test the implementation of the numerical solution procedure. The numerical procedures were shown to rapidly converge with mesh refinement. In the process of this testing, errors in a long standing analytic solution were identified and are corrected in Appendix B. Results of single cell activity were compared to published results illustrating that the key features of the slow wave activity were successfully replicated. Simulations using a two-dimensional slice through the gastric wall produced slow wave activity that agreed with the known frequency and propagation characteristics. Three-dimensional simulations were also performed using the full stomach mesh and results illustrated the slow wave propagation throughout the stomach musculature.
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