1 / 33

PHYSIOLOGICAL MODELING

PHYSIOLOGICAL MODELING. OBJECTIVES. Describe the process used to build a mathematical physiological model. Explain the concept of a compartment. Analyze a physiological system using compartmental analysis. Solve a nonlinear compartmental model. Qualitatively describe a saccadic eye movement.

teegan-tran
Télécharger la présentation

PHYSIOLOGICAL MODELING

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. PHYSIOLOGICAL MODELING

  2. OBJECTIVES • Describe the process used to build a mathematical physiological model. • Explain the concept of a compartment. • Analyze a physiological system using compartmental analysis. • Solve a nonlinear compartmental model. • Qualitatively describe a saccadic eye movement. • Describe the saccadic eye movement system with a second-order model. • Explain the importance of the pulse-step saccadic control signal. • Explain how a muscle operates using a nonlinear and linear muscle model. • Simulate a saccade with a fourth-order saccadic eye movement model. Estimate the parameters of a model using system identification.

  3. INTRODUCTION Physiology – the science of the functioning of living organisms and of their component parts. 2 Types of physiological model: • A quantitative physiological model is a mathematical representation that approximates the behavior of an actual physiological system. • A qualitative physiological model describes the actual physiological system without the use of mathematics.

  4. Flow Chart for physiological modeling

  5. Deterministic and Stochastic Models • A deterministic model is one that has an exact solution that relates the independent variables of the model to each other and to the dependent variable. For a given set of initial conditions, a deterministic model yields the same solution each and every time. • A stochastic model involves random variables that are functions of time and include probabilistic considerations. For a given set of initial conditions, a stochastic model yields a different solution each and every time.

  6. Solutions • A closed-form solution exists for models that can be solved by analytic techniques such as solving a differential equation using the classical technique or by using Laplace transforms. example: • A numerical or simulation solution exists for models that have no closed-form solution. example:

  7. COMPARTMENTAL MODELING • Compartmental modeling is analyzing systems of the body characterized by a transfer of solute from one compartment to another, such as the respiratory and circulatory systems. • It is concerned with maintaining correct chemical levels in the body and their correct fluid volumes. • Some readily identifiable compartments are: • Cell volume that is separated from the extracellular space by the cell membrane • Interstitial volume that is separated from the plasma volume by the capillary walls that contain the fluid that bathes the cells • Plasma volume contained in the circulatory system that consists of the fluid that bathes blood cells

  8. Transfer of Substances Between Two Compartments Separated by a Thin Membrane Fick’s law of diffusion: Where: q = quantity of solute A = membrane surface area c = concentration D = diffusion coefficient dx = membrane thickness

  9. Compartmental Modeling Basics • Compartmental modeling involves describing a system with a finite number of compartments, each connected with a flow of solute from one compartment to another. • Compartmental analysis predicts the concentrations of solutes under consideration in each compartment as a function of time using conservation of mass: accumulation equals input minus output. • The following assumptions are made when describing the transfer of a solute by diffusion between any two compartments: 1. The volume of each compartment remains constant. 2. Any solute q entering a compartment is instantaneously mixed throughout the entire compartment. 3. The rate of loss of a solute from a compartment is proportional to the amount of solute in the compartment times the transfer rate, K, given by Kq.

  10. Multi-compartmental Models • Real models of the body involve many more compartments such as cell volume, interstitial volume, and plasma volume. Each of these volumes can be further compartmentalized. • For the case of N compartments, there are N equations of the general form Where qi is the quantity of solute in compartment i. For a linear system, the transfer rates are constants.

  11. Modified Compartmental Modeling • Many systems are not appropriately described by the compartmental analysis because the transfer rates are not constant. • Compartmental analysis, now termed modified compartmental analysis, can still be applied to these systems by incorporating the nonlinearities in the model. Because of the non linearity, solution of the differential equation is usually not possible analytically, but can be easily simulated. • Another method of handling the nonlinearity is to linearize the nonlinearity or invoke pseudostationary conditions.

  12. Transfer of Solutes Between Physiological Compartments by Fluid Flow • Uses a modified compartmental model to consider the transfer of solutes between compartments by fluid flow. Compartmental model for the transfer of solutes between compartments by fluid flow

  13. Dye Dilution Model • Dye dilution studies are used to determine cardiac output, cardiac function, perfusion of organs, and the functional state of the vascular system. • Usually the dye is injected at one site in the cardiovascular system and observed at one or more sites as a function of time.

  14. AN OVERVIEW OF THE FAST EYE MOVEMENT SYSTEM • A fast eye movement is usually referred to as a saccade and involves quickly moving the eye from one image to another image. • The saccade system is part of the oculomotor system that controls all movements of the eyes due to any stimuli. • Each eye can be moved within the orbit in three directions: vertically, horizontally, and torsionally, due to three pairs of agonist–antagonist muscles. • Fast eye movements are used to locate or acquire targets.

  15. TYPES OF EYE MOVEMENTS • Smooth pursuit - used to track or follow a target • Vestibular ocular - used to maintain the eyes on the target during head movements • Vergence - used to track near and far targets • Optokinetic – used when moving through a target-filled environment or to maintain the eyes on target during continuous head rotation • Visual – used for head and body movements

  16. Saccade Characteristics • Saccadic eye movements, among the fastest voluntary muscle movements the human is capable of producing, are characterized by a rapid shift of gaze from one point of fixation to another. • Saccadic eye movements are conjugate and ballistic, with a typical duration of 30–100ms and a latency of 100–300ms.

  17. WESTHEIMER SACCADIC EYE MOVEMENT MODEL The first quantitative saccadic horizontal eye movement model, was published by Westheimer in 1954. Westheimer proposed a second-order model equation

  18. THE SACCADE CONTROLLER • One of the challenges in modeling physiological systems is the lack of data or information about the input to the system. Recording the signal would involve invasive surgery and instrumentation • In 1964, Robinson attempted to measure the input to the eyeballs during a saccade by fixing one eye using a suction contact lens, while the other eye performed a saccade from target to target. He proposed that muscle tension driving the eyeballs during a saccade is a pulse plus a step, or simply, a pulse-step input .

  19. THE SACCADE CONTROLLER • Microelectrode studies have been carried out to record the electrical activity in oculomotor neurons: micropipet used to record the activity in the oculomotor nucleus, an important neuron population responsible for driving a saccade

  20. THE SACCADE CONTROLLER • Collins and his coworkers reported using a miniature ‘‘C’’-gauge force transducer to measure muscle tension in vivo at the muscle tendon during unrestrained human eye movements.

  21. DEVELOPMENT OF AN OCULOMOTOR MUSCLE MODEL • An accurate model of muscle is essential in the development of a model of the horizontal fast eye movement system. • The model elements consist of an active-state tension generator (input), elastic elements, and viscous elements. Each element is introduced separately and the muscle model is incremented in each subsection.

  22. Passive Elasticity • Involves recording of the tension observed in an eye rectus muscle. • The tension required to stretch a muscle is a nonlinear function of distance.

  23. Active-State Tension Generator • In general, a muscle produces a force in proportion to the amount of stimulation. The element responsible for the creation of force is the active-state tension generator. • The relationship between tension, T, active-state tension, F, and elasticity is given by

  24. Elasticity Series Elastic Element • Experiments carried out by Levin and Wyman in 1927, and Collins in 1975 indicated the need for a series elasticity element Length–Tension Elastic Element • Given the inequality between Kse and K, another elastic element, called the length–tension elastic element, Klt, is placed in parallel with the active-state tension element

  25. Force–Velocity Relationship • Early experiments indicated that muscle had elastic as well as viscous properties. • Muscle was tested under isotonic (constant force) experimental conditions to investigate muscle viscosity.

  26. LINEAR MUSCLE MODEL • Examines the static and dynamic properties of muscle in the development of a linear model of oculomotor muscle. • B- viscosity • K- elasticity • F- tension generator

  27. A LINEAR HOMEOMORPHIC SACCADIC EYE MOVEMENT MODEL • In 1980, Bahill and coworkers presented a linear fourth-order model of the horizontal oculomotor plant that provides an excellent match between model predictions and horizontal eye movement data. This model eliminates the differences seen between velocity and acceleration predictions of the Westheimer and Robinson models and the data.

  28. A LINEAR HOMEOMORPHIC SACCADIC EYE MOVEMENT MODEL

  29. A TRUER LINEAR HOMEOMORPHIC SACCADIC EYE MOVEMENT MODEL

  30. SYSTEM IDENTIFICATION • In modeling physiological systems, GOAL: not to design a system, but to identify the parameters and structure of the system Ideally: • Input and output is known • Information on the Internal dynamics is available

  31. SYSTEM IDENTIFICATION • System identification is the process of creating a model of a system and estimating the parameters of the model. 2 concepts of S.I.: a. Time domain b. Frequency domain • Before S.I. begins, understanding the characteristics of the input and output signals is important (e.g. voltage and frequency range,type of signal whether it is deterministic or stochastic and if coding is involved.)

  32. SYSTEM IDENTIFICATION The simplest and most direct method of system identification is sinusoidal analysis. Source of sinusoidal excitation consists: a. sine wave generator b. a measurement transducer c. recorder to gather frequency response data(can be obtained using the oscilloscope)

  33. SYSTEM IDENTIFICATION Another type of identification technique either for a • first-order system or • a second-order system is by using a time-domain approach.

More Related