Knowledge of the shape of the dose-response curve must extend to levels at which humans are typically? exposed if we are to accurately assess the risks of adverse effects on the public health from exposures to? environmental chemicals. Health effects data are usually sparse at environmental levels of exposure and? computational models are being used to estimate both chemical disposition (i.e., pharmacokinetics) and? tissue responses (i.e., pharmacodynamics). While current pharmacokinetic models incorporate physiological? and anatomical information to provide accurate estimates of target tissue doses, the pharmacodynamic? relationship between a chemical at its target site and the ultimate biological effect is usually described? empirically or semi-empirically. Molecular level descriptions of pharmacodynamic mechanisms would? provide a better understanding of dose-response curves and would reduce uncertainty in safety and risk? assessments. The mission of this Core will be to provide the skills and resources needed to develop? computational models of biochemical pathways and to thereby provide insight into the adverse health effects? of TCDD and related chemicals. Since development of computational models is an iterative process, with? model development and laboratory experiments proceeding hand-in-hand, the work in this Core will be? collaborative with the work in the Research Projects that the Core supports. The? overall approach to be used for development of computational models is defined by 4 Specific Aims:? SA1. Develop initial descriptions of biochemical pathways where the nodes of the pathway and the? interactions between nodes are linked to biomedical databases.? SA2. Develop a directed graph by curating the pathway description obtained under SA1.? SA3. Develop computational models based on the network structures described by directed graphs.? SA4. Determine if a stochastic or Boolean model is preferable to an ODE-based model for understanding? the dynamic behavior of a particular biochemical network.? This Core will also seek to train postdoctoral fellows and other staff from the Research Projects in the use of? software for development of pathway maps and for computational modeling of the pathways.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Hazardous Substances Basic Research Grants Program (NIEHS) (P42)
Project #
5P42ES004911-19
Application #
7599131
Study Section
Special Emphasis Panel (ZES1)
Project Start
Project End
Budget Start
2008-04-01
Budget End
2009-03-31
Support Year
19
Fiscal Year
2008
Total Cost
$222,319
Indirect Cost
Name
Michigan State University
Department
Type
DUNS #
193247145
City
East Lansing
State
MI
Country
United States
Zip Code
48824
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