• Register
X
Forgot Password

If you have forgotten your password you can enter your email here and get a temporary password sent to your email.

X

Leaving Community

Are you sure you want to leave this community? Leaving the community will revoke any permissions you have been granted in this community.

No
Yes

A mathematical model of metabolic insulin signaling pathways.

We develop a mathematical model that explicitly represents many of the known signaling components mediating translocation of the insulin-responsive glucose transporter GLUT4 to gain insight into the complexities of metabolic insulin signaling pathways. A novel mechanistic model of postreceptor events including phosphorylation of insulin receptor substrate-1, activation of phosphatidylinositol 3-kinase, and subsequent activation of downstream kinases Akt and protein kinase C-zeta is coupled with previously validated subsystem models of insulin receptor binding, receptor recycling, and GLUT4 translocation. A system of differential equations is defined by the structure of the model. Rate constants and model parameters are constrained by published experimental data. Model simulations of insulin dose-response experiments agree with published experimental data and also generate expected qualitative behaviors such as sequential signal amplification and increased sensitivity of downstream components. We examined the consequences of incorporating feedback pathways as well as representing pathological conditions, such as increased levels of protein tyrosine phosphatases, to illustrate the utility of our model for exploring molecular mechanisms. We conclude that mathematical modeling of signal transduction pathways is a useful approach for gaining insight into the complexities of metabolic insulin signaling.

Pubmed ID: 12376338

Authors

  • Sedaghat AR
  • Sherman A
  • Quon MJ

Journal

American journal of physiology. Endocrinology and metabolism

Publication Data

November 11, 2002

Associated Grants

None

Mesh Terms

  • Animals
  • Dose-Response Relationship, Drug
  • Feedback, Physiological
  • Glucose Transporter Type 4
  • Humans
  • Insulin
  • Insulin Resistance
  • Models, Biological
  • Monosaccharide Transport Proteins
  • Muscle Proteins
  • Protein Tyrosine Phosphatases
  • Signal Transduction