Transmural heterogeneity of myocardium in norm and pathology
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Transmural heterogeneity of myocardium in norm and pathology
Anastasia Vasilyeva1,2, Nathalie Vikulova1, Olga Solovyova1,2, Vladimir S. Markhasin1,2
1Institute of Immunology and Physiology, Ural Branch of Russian Academy of Sciences2Ural Federal University, Yekaterinburg, Russia
Workshop MMMBM, October 29-31, 2014
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Heterogeneity – an attribute of normal myocardium
Anatomy of the heart wall
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Functional heterogeneity of myocardium
HETEROGENEITY – an ATTRIBUTE of NORMAL MYOCARDIUM
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Temporal gradients of activation
A sequence of activation of ventricular regions from the endocardium to the epicardium, and from the apex to the base.
Mechanical gradients
These include transmural and apex-base gradients of passive and active mechanical properties, with tension increasing from epicardium to endocardium, and from apex to base
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Wan X, Bryant S et al., 2003
Experimental data on isolated cells
Laurita K, et al., 2003
ENDO, EPI and MID- myocytes of LV wall differ in their electrophysiological and mechanical properties
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Ischemia
Ischemia – is a restriction in blood supply to tissues, causing a shortage of oxygen and glucose needed for cellular metabolism.
Ischemic heart disease is the most common cause of death in most Western countries and a major cause of hospital admissions.
Subendocardial ischemiaSubepicardial ischemia
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Experimental data on isolated cells
Qi X. et al., 2000
Experimental data on isolated tissue
Lukas A. et al., 1993
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Left figure from Bers D. Cardiac excitation–contraction coupling,2002
Sulman T. et al. Bulletin of mathematical biology. 2008
The CellML-model representation can be found at the repository at http://models.cellml.org/e/b9/
Solovyova O. et al. Inter J Bifurcation & Chaos. 2003
Ekaterinburg - Oxford modelRheological scheme of
cardiomyocyte
CE – contractile element
(sarcomere)
PE, SE – parallel and series elastic
elements
XSE – external series elastic element
VS – parallel viscous element
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Electrical block of the model
Solovyova O. et al. Inter J Bifurcation & Chaos. 2003
Membrane potential
Noble D. 1998
Vm – membrane potential Cm – membrane capacity
ii – ionic current
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Ionic currents:
gx – channel conductivityEx – reversal potential[X]o и [X]i –extracellular and intracellular ion concentration
Noble D. 1998
Electrical block of the model
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Mechanical block of the model
Sulman et al., Bulletin of mathematical biology. 2008
l1 - deviation of SE from slack length,l2 - deviation of PE from slack length,l3 - deviation of XSE from slack length
FXSE = FPE+FCE+FVS
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Rheological scheme of cardiomyocyte
CE – contractile element
(sarcomere)
PE, SE – parallel and series elastic
elements
XSE – external series elastic element
VS – parallel viscous element
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Cooperative Mechanisms
Type A. Affinity of TnC for Ca2+ increases with [Ca-TnC] (A=[Ca-TnC], aoff depends on
A).
Type B. Affinity of TnC for Ca2+ increases with mean concentration of strongly bound XBr (N) about each Ca-TnC complex (aoff depends on N/A).
Type C. Fraction of active sites on the thin filament in the overlap zone increases cooperatively due to tropomyosin end-to-end interaction.
From A. M. Gordon, M. Regnier, and E. Homsher. Skeletal and Cardiac Muscle Contractile Activation: Tropomyosin “Rocks and Rolls”. News Physiol. Sci. 16:49 –55, 2001
Nk-N)-(1(A,...)k dt
dN
A)
K
A(1
1)
A
N(a-CaA)-(1a
dt
dA
offon
moffon
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Heterogeneity in ENDO and EPI model parameters and modeled cell activity
Vasilyeva A., Solovyova О. CinC. 2012.
Vasilyeva A., Solovyova О. Biophysics. 2012.
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Weiss et al., 1991
t,min [ATP],mM [K+]0,mM
0 6.8 4.05 6.1 5.6
10 4.8 7.815 3.4 9.4
Simulation of cell responses to the acute ischemia
Input model parameters of time-dependent changes in [ATP]i and in [K+]o during 5, 10, and 15 minutes of the acute ischemia.
Experimental data
Model parameters
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gK(ATP) - is the maximum conductance at [ATP]i = 0 mM;PATP - is the open probability of the KATP channel at a given ATP concentration which increases with decreasing [ATP]i;n – model parameter;Vm - membrane potential;EK - K+ reversal potential.
Equations are adapted from Rudy et al., 1997
k0.5 – is the [ATP]i at which 50% of the KATP channels are open (half-maximal saturation point);
h – Hill coefficient characterizing the steepness of relationship
Simulation of cell responses to the acute ischemiaModeling ATP-sensitive potassium current IK(ATP)
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Experimental data from Furukawa et al., 1991
ENDO EPI
k0.5, µM 23.6 97.6
h 2.09 1.59
Simulation of cell responses to the acute ischemia
Model parameters
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Ischemia effects on the electrical activity of single ENDO and EPI cells
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Ischemia effects on the mechanical activity of single ENDO and EPI cells
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Continuous model of cardiac muscle fiber
Vikulova N. et al. Russ J Numer Anal Math Modelling. 2014. 18
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Continuous model of cardiac muscle fiber
l1(x,t) – sarcomere deformation
l (x,t) – cell deformation
Global parameters Local parameters
ˆ( )( )
l t xl x t
x
Micro- and macro mechanics coupling
- deviation of XSE from slack length
ˆ( )l x t - deviation of cell x from ref. position
)(tlex
Isometric mode of contraction:ˆ( ) ( )F exl x t l t const
3 3(exp( ) 1)x x xPE VS CE ex exF F F F l
Isotonic mode of contraction:𝐹𝑥 = 𝐹𝑒𝑥 = 𝐹ത.
Local deformation of the fiber at point x in the macrospace is equal to the relative deformation of cell x in the microspace. 19
1 point = 1 cell (microlevel)
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Boundary conditions Left border: Right border:
( )0FV x t
x
Initial conditions
( 0) restV x V
0,0 xI stim s] 25[0.06;0.06t3
,0
whennAI
x
stim
V(0,t) = VODE(t).
),()(
1
)),(1(
),()),(1(
3
'2
2
txixCtxl
x
Vtxltxl
x
V
Dt
Vion
m
x
Continuous model of cardiac muscle fiberMicro- and macro electrical coupling
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Effects of ischemia in 1D tissue model
Control Ischemia 15 min
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Conclusions:1. Modeling results suggest a significant increase in the transmural
heterogeneity of the electrical and mechanical activity between EPI and ENDO cells under ischemia, which is consistent with experimental data.
2. Models suggest that distinguishing ATP-sensitivity of IK(ATP) currents in ENDO and EPI cells may contribute to greater electrical effects of ischemia on EPI cells. Models also predict greater mechanical effects of ischemia on EPI cells as compared to ENDO cells.
3. In the tissue model, ischemia causes an increase in the electrical heterogeneity between coupled cells and an increase in dispersion of repolarization as substrate for arrhythmia.
4. Unexpectedly, effects of ischemia on tissue mechanics were less pronounced then that in isolated cells suggesting a compensation mechanism of interaction between the coupled cells.
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Acknowledgements
Institute of Immunology and Physiology:
Laboratory of mathematical physiology
Ural Federal University
This work was supported by The Russian Science Foundation (#14-35-00005).
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