Model number
0163

  

Multiple tracer dilution estimates of D- and 2-deoxy-D-glucose uptake by the heart using a three region, 7-path, Blood-Tissue-Exchange (BTEX) model for albumin, L-Glucose, D-Glucose, and deoxy-Glucose. From Kuikka J, Levin M, Bassingthwaighte JB 1986 paper.

Reproducible project file example

Download the JSim project file which contains the model source code, data, simulation parameter sets and plot pages needed to reproduce the Kuikka et al. 1986 paper. This is an example of a package that reproduces a model published in a journal.

There are two related models that expand upon this one: Kuikka 1986 experiment, which is the same model as presented here but includes parameter fits to all data summarized in Tables 1 and 2 of Kuikka 1986 paper, and Kuikka 1986 two region BTEX, a simplified, two region model where the permeability and consumption term for the third region (myocardial cells) are replaced with just a consumption term in the second region (interstitial fluid). This model is only fit to data set found in Table 3 of the Kuikka 1986 paper.

MPC: This model was initially created using the Modular Program Constructor (MPC). For more information:

Description

  Multiple indicator dilution (MID) analysis for the estimation of capillary permeability in the heart.
 The MID principle is to analyze the cellular permeability surface area product for the target solute, 
 D-glucose, against two reference solutes, one to characterize the intravascular transport function, 
 href(t) through the intact organ ( (131)I-albumin in this case ), an extracellular one of the same 
 molecular weight as the target solute in order to characterize the combination of permeation through 
 the inter-endothelial cleft (using L-glucose), and the target solute, D-glucose that is taken up by 
 cells and metabolized.

  KUIKKA, JYRKI, MICHAEL LEVIN, AND JAMES B. BASSINGTHWAIGHTE.
 Multiple tracer dilution estimates of D- and 2-deoxy-D-glucose uptake by the heart. Am. J. Physiol. 250
 (Heart Circ. Physiol. 19): H29-H42, 1986.-Permeability-surface area products of the capillary wall, PSc, 
 and the myocyte sarcolemma, PSpc, for D-glucose and 2-deoxy-D-glucose were estimated via the multiple 
 indicator-dilution technique in isolated blood-perfused dog and Tyrode-perfused rabbit hearts. Aortic 
 bolus injections contained I(131)-albumin (intravascular reference), two of three glucoses: L-glucose 
 (an extracellular reference solute), D-glucose, and 2-deoxy-D-glucose. Outflow dilution curves were 
 sampled for l-2.5 min without recirculation. The long duration sampling allowed accurate evaluation 
 of PS, by fitting the dilution curves with a multiregional axially distributed capillary-interstitial 
 fluid-cell model accounting for the heterogeneity of regional flows (measured using microspheres and 
 total heart sectioning). With average blood flow of 1.3 ml/(g*min), in the dog hearts the PSc, for
 D-glucose was 0.72 +- 0.17 ml/(g*min) (mean t SD; n = ll), and PSpc, was 0.57 t 0.15 ml/(g*min). 
 In the rabbit hearts with perfusate flow of 2.0 ml/(g*min)(n = 6), PSc, was 1.2 * 0.1 and PSpc, was 
 0.4 & 0.1 ml/(g*min). PSc, for 2-deoxy-Dglucose was about 4% higher than for D-glucose and L-glucose 
 in both preparations. Relative to L-glucose, there was no measurable transendothelial transport of 
 either dextroglucose, indicating that transcapillary transport was by passive diffusion, presumably 
 via the clefts between cells. The technique allows repeated measurements of D-glucose uptake at intervals 
 of a few minutes; it may therefore be used to assess changes in transport rates occurring over intervals 
 of several minutes.

fig 1

Figure: Model representation of BTEX in the heart. (Top): Single capillary exchange into the ISF and Cellular region (parenchymal cell = pc). (Middle): Multi-path diagram of lung from injector to outlflow collector. (Bottom): Mathematical, linear system representation of the multi-path model.

Kuikka MID Data

The MID glucose datasets published in the Kuikka et al. 1986 paper are available on the Physionet web site. At the Physionet web site search for 'Cardiac Physiome Kuikka glucose' in the PhysioNetWorks area (you will need a free, personal account to access it).

Equations

The equations for this model may be viewed by running the JSim model applet and clicking on the Source tab at the bottom left of JSim's Run Time graphical user interface. The equations are written in JSim's Mathematical Modeling Language (MML). See the Introduction to MML and the MML Reference Manual. Additional documentation for MML can be found by using the search option at the Physiome home page.

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References

  

(Primary) Kuikka J., Levin M., Bassingthwaighte J. B., Multiple tracer dilution estimates 
 of D- and 2-deoxy-D-glucose uptake by the heart, Am. J. Physiol. Heart Circ. Physiol.,
 250, (H29-H42}, 1986
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Key terms
isolated heart preparation
coronary transport function
MPC
Reproducible
myocardial transsarcolemmal flux
L-glucose
dogs
rabbits
Data
Publication
PMID3510568
Acknowledgements

Please cite https://www.imagwiki.nibib.nih.gov/physiome in any publication for which this software is used and send one reprint to the address given below:
The National Simulation Resource, Director J. B. Bassingthwaighte, Department of Bioengineering, University of Washington, Seattle WA 98195-5061.

Model development and archiving support at https://www.imagwiki.nibib.nih.gov/physiome provided by the following grants: NIH U01HL122199 Analyzing the Cardiac Power Grid, 09/15/2015 - 05/31/2020, NIH/NIBIB BE08407 Software Integration, JSim and SBW 6/1/09-5/31/13; NIH/NHLBI T15 HL88516-01 Modeling for Heart, Lung and Blood: From Cell to Organ, 4/1/07-3/31/11; NSF BES-0506477 Adaptive Multi-Scale Model Simulation, 8/15/05-7/31/08; NIH/NHLBI R01 HL073598 Core 3: 3D Imaging and Computer Modeling of the Respiratory Tract, 9/1/04-8/31/09; as well as prior support from NIH/NCRR P41 RR01243 Simulation Resource in Circulatory Mass Transport and Exchange, 12/1/1980-11/30/01 and NIH/NIBIB R01 EB001973 JSim: A Simulation Analysis Platform, 3/1/02-2/28/07.