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Comparing ordinary and delay differential equations models for human gastric acid secretion : Comparing ordinary and delay differential equations models for human gastric acid secretion Denise Kirschner, PhD
Department of Microbiology and Immunology
University of Michigan Medical School
Ann Arbor, Michigan USA
Outline of lecture : Outline of lecture Context of problem- H. pylori
Review relevant gastric physiology
Present ODE model
Present delay and DDE model
Compare results of both
Discussion
Helicobacter pylori (identified in 1982) : Helicobacter pylori (identified in 1982) Gram negative, spiral-shaped, motile bacteria
Strict human pathogen- colonizes the stomach
Different disease trajectories
Colonization/persistence – superficial gastritis (most common outcome)- acts like IM
Peptic ulcer disease (75% correlated)
Duodenal ulcers (95% correlated)
Lymphomas/ carcinomas
pH-dependent growth, virulence is adherence and motility
Some countries 100% infected, USA:50%, Italy:80%
Treatment: antibiotics for 6 weeks
How does this pathogen survive in the hostile environment of the stomach?
pH, shedding of mucus, sloughing of cells, peristalsis
Introduction to gastric acid secretion : Introduction to gastric acid secretion Gastric acid is important for two reasons:
Activation pepsin
Sterilization of the stomach
Maintenance of pH homeostasis is critical for proper function and protection of the stomach.
Gastric acid secretion is diurnal.
Goals : Goals Study how Helicobacter pylori, a strict human stomach pathogen, affects the gastric acid secretion system to allow its infection and persistence
* Develop a virtual human model of gastric acid secretion
*Incorporate a delay to reduce system
The stomach: corpus and antrum regions : The stomach: corpus and antrum regions Corpus Antrum
Gastric glands : Gastric glands mucosa mucus gland Taken from H.F. Helander (1992)
Key cell types in the gastric system : Antrum
G cells – secrete Gastrin (+)
D cells – secrete Somatostatin (-)
Corpus
D cells
ECL cells – secrete histamine (+)
Parietal cells – secrete acid
Key cell types in the gastric system
Development of antrum and corpus cells : Development of antrum and corpus cells Antrum Corpus
Gastric acid secretion regulation by gastric cells : Gastric acid secretion regulation by gastric cells
Gastro-protective mechanisms: bicarbonate secretion : Gastro-protective mechanisms: bicarbonate secretion
Methods for ODE model system : Methods for ODE model system Developed a system of ordinary differential equations.
Estimated parameters
estimated numbers for each cell population
acquired parameter values from literature with preference given to estimates from human studies
studied the effect of these parameters using sensitivity and uncertainty analyses (latin hypercube sampling/partial rank correlation)
Analyzed the system of differential equations using three approaches: Matlab, Mathematica and code we wrote based on a finite differencing schemes.
Compared simulations results with published experimental data
Performed virtual deletion experiments
Food function profile F(t) : Food function profile F(t) Breakfast: 7:00h
Lunch: 13:00h
Dinner: 19:00h The daily food function profile is representative of the volume of food eaten during each meal. (1 liter maximal volume)
Neural stimulation equations : Neural stimulation equations
Cell dynamics: stasis in the short-term : Cell dynamics: stasis in the short-term
Hormonal dynamics: gastrin, an inducer of gastric acid secretion : Hormonal dynamics: gastrin, an inducer of gastric acid secretion Taken from Smith et al., 1990.
Slide21 : Hormonal dynamics: somatostatin, an inhibitor of
gastric acid secretion Taken from Burhol et al., 1984
Slide22 : Acid dynamics: gastric acid Taken from Feldman and Richardson, 1986.
Slide23 : Hormonal dynamics: histamine, an inducer of
gastric acid secretion- no data available
Slide24 : Ion dynamics: bicarbonate, a gastro-protective
mechanism
Partial reciprocity of gastrin and somatostatin: positive and negative regulators of gastric acid secretion : Partial reciprocity of gastrin and somatostatin: positive and negative regulators of gastric acid secretion Taken from Zavros et al, 1999 Negative Feedback
Stability: attracting limit cycles : Stability: attracting limit cycles
A stable period 3- cycle is observed which is a function of food intake
Results of virtual deletion studies : Results of virtual deletion studies Virtual gastrin deletion study
basal and stimulated acid concentrations are lower than controls during deletion simulations and qualitatively compare with literature (e.g. Wada et al, 1997).
Virtual histamine deletion study
Basal acid concentrations remain normal but stimulated acid levels are drastically reduced during deletion simulations when compared to controls. This results is demonstrated by Kobayashi et al (2000).
Virtual total somatostatin deletion study
Both basal and stimulated gastrin, histamine, and acid levels are increased during deletion simulations when compared to controls. Martinez et al (1998) demonstrate this in studies done in somatostatin deficient mice.
Findings : Findings The system is robust
Cellular and physiological homeostasis observed
Simulation results correlate with experimental data
pH homeostasis is maintained during the course of the virtual experiments
We will now extend the model to assess the interaction dynamics between H. pylori and the virtual host.
Our findings may provide more insight into how H. pylori alters the gastric physiological environment to favor its persistence within its human host.
Discussion : Discussion Gastrin is the key regulator of gastric acid secretion
Model is complex, can we reduce?
18 non-linear ODEs, 1 forcing function
A delay exists between the signals received in the corpus region, and the transference of information to the antrum.
Can we introduce a continuous delay in the system and still capture the qualitative behavior?
Review: stomach anatomy : Review: stomach anatomy
Continuous Delay functions : Continuous Delay functions **The total amount of antral gastrin produced in the past minutes;
The average amount of antral gastrin produced in the past minutes;
The percentage of the total amount of antral gastrin produced in the past minutes (p1+p2=1) We explored three different delay functions:
Delay physiology : Delay physiology
. Amount of gastrin released by G cells in the antrum diffuses gradually into the corpus and is then available to the D and parietal cells only after a certain time period
Thus, the total amount of gastrin released in the previous minutes that is already located in the corpus region is effectively inducing the secretion of somatostatin and acid
This is physiologically relevant as it in part describes the Hill kinetics (i.e., a critical concentration of gastrin is required before a “surge” of its affect is observed)
Figure 2: DDE diagram : Figure 2: DDE diagram
Figure 3: ODE vs DDE baseline : Figure 3: ODE vs DDE baseline
Figure 4: phase portraits ODE vs DDE : Figure 4: phase portraits ODE vs DDE
Figure 5: phase portraits DDE with different delays : Figure 5: phase portraits DDE with different delays
Figure 6: Antral Somatostatin depletion : Figure 6: Antral Somatostatin depletion
Figure 7: Corpal Somatostatin depletion : Figure 7: Corpal Somatostatin depletion
Figure 9: Antral Gastrin depletion : Figure 9: Antral Gastrin depletion
Conclusions: : Conclusions: the temporal behavior of the DDE model closely reproduces that of the ODE model
the stability of the ODE system is also observed in the DDE model at a delay length of tau= 30 minutes
virtual depletion experiments further validate that the DDE model replicates the behavior of the ODE system
Acknowledgments : Acknowledgments The Kirschner Lab
Brian M. Murphy, PhD
David Gammack, PhD
Simeone Marino, PhD
Suman Ganguli, PhD
Ping Ye, MS
Seema Bajaria, MS
Ian Joseph
Benjamin H. Singer
Stewart Chang
Karyn Sutton
Jim Zakowski
Christian Ray
Vanessa Pherigo $$ from NIH and The Whitaker Foundation
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