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Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

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Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook. Joint work with Pei Ye, Emilia Entcheva and Scott A. Smolka. Background. Excitable cells Neuron Cardiac Cells Different concentrations of ions inside and outside of cells form: - PowerPoint PPT Presentation
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Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook Joint work with Pei Ye, Emilia Entcheva and Scott A. Smolka
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Page 1: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Efficient Modeling of Excitable Cells Using Hybrid Automata

Radu GrosuSUNY at Stony Brook

Joint work with Pei Ye, Emilia Entcheva and Scott A. Smolka

Page 2: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Background

• Excitable cells– Neuron– Cardiac Cells

• Different concentrations of ions inside and outside of cells form:– Trans-membrane potential– Ion currents through channels across the cell

membrane

Page 3: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

channel

Ions and Channels of Excitable Cells

Na+

Na+

Na+

Na+

Na+

Na+

Na+

K+

Ca2+

K+

K+

K+

K+

Ca2+

Ca2+

Ca2+

Cell

Cell

Page 4: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Action Potential (AP)

• Caused by positive ions moving in and then out of the cell membrane.

• 5 stages– Resting– Upstroke– Early Repolarization– Plateau– Final Repolarization

Page 5: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Restitution Property

• Excitable cells respond to different frequency stimuli.

• Each cycle is composed of:

– Action Potential Duration (APD)

– Diastolic Interval (DI)

• Longer DI, longer APD

Page 6: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Restitution Property

Page 7: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Mathematical Models

• Hodgkin-Huxley (HH) model – Membrane potential for squid giant axon – Developed in 1952– Framework for the following models

• Luo-Rudy (LRd) model– Model for cardiac cells of guinea pig– Developed in 1991

• Neo-Natal Rat (NNR) model– Being developed in Stony Brook University by Emilia

Entcheva et al.

Page 8: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Hodgkin-Huxley Model

• C: Cell capacitance• V: Trans-membrane voltage

• gna, gk, gL: Maximum channel conductance

• Ena, Ek, EL: Reversal potential

• m, n, h: Ion channel gate variables

• Ist: Stimulation current

Page 9: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Circuit for Hodgkin-Huxley Model

V

ELEna

C

EK

gLgKgna

Page 10: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Hybrid Automata (HA)

• Variables• Control Graph

– Modes– Switches

• Init, Inv and flow• Jumps and Actions• Events

Page 11: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Two Ways of Abstraction

• Rational method: derive the flow functions from the differential equations in the original model

• Empirical method: use curve-fitting techniques to get the flow functions with the form chosen (here we use the form ).

Page 12: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

General HA Template

• 4 control modes:– Resting and Final repolarization (FR)– Stimulated– Upstroke– Early repolarization (ER) and Plateau

• Threshold voltage monitoring mode switches– Vo, VT and VR

• Event VS represents the presence of stimulus

Page 13: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

HA for HH Model

Page 14: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Simulation of HH Model

Page 15: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

New Features of HA for LRd and NNR Model

• Adding vz to enrich modeling ability

• Using vn to remember the current voltage when the next stimulus is coming.

– Define , , determines the time cell stays in mode ER and plateau

– Thus, APD will change with DI

• For NNR model, define and , thus the threshold voltages are

also influenced by DI.

Page 16: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

HA for LRd Model

Page 17: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

HA for NNR Model

Page 18: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Simulation for LRd Model

Page 19: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Simulation for NNR Model

Single cell, single AP 3 APs on a 2*2 cell array

Page 20: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Large-scale Spatial Simulation for NNR Model

Re-entry on a 400*400 cell array

Page 21: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Performance Comparison

Page 22: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Future Work

• Using Optimization techniques to derive the parameters for HA model automatically.

• Develop simpler spatial model to further improve efficiency.

Page 23: Efficient Modeling of Excitable Cells Using Hybrid Automata Radu Grosu SUNY at Stony Brook

Thank you

04/05/2005


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