Skip Navigation
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Your Environment. Your Health.

Michigan State University

Superfund Research Program

Non-Additive Ah Receptor Ligand Interactions

Project Leader: Timothy R. Zacharewski
Grant Number: P42ES004911
Funding Period: 2006-2020

Learn More About the Grantee

Visit the grantee's eNewsletter page Visit the grantee's eNewsletter page

Project Summary (2006-2013)

Although human exposure to toxicants occurs as a complex mixture, risk assessments are typically based on single chemical studies conducted in rodent models. Limitations associated with current approaches are increasingly being questioned due to the potential for significant health, societal and economic consequences. In order to improve the quantitative risk assessment of chronic and subchronic exposure to synthetic and natural chemicals and their complex mixtures, uncertainties within the source-to-outcome continuum must be minimized in the context of the whole organisms, and its genome. In this project, 2,3,7,8-tetrachlrodibenzo-p-dioxin (TCDD), 3,3',4,4',5-pentachlorobiphenyl (PCB126), and 2,2',4,4',5,5'- hexachlorobiphenyl (PCB153) as well as a reconstituted mixture that reflects environmental levels of these contaminants is being systematically examined to elucidate the mechanisms of action of additive, antagonistic and synergistic interactions that occur at molecular and physiological levels. Ray designs and modeling approaches are being used to minimize full factorial studies in order to investigate the hypothesis that a mixture of TCDD, PCB126 and PCB153 at environmentally relevant levels elicit non-additive hepatotoxic effects. Dose- and time-dependent hepatic gene expression and fatty liver effects are being assessed using a mouse cDNA array enriched with dioxin responsive genes and complementary histopathology approaches. Microarray data is being computationally integrated with histopathology and clinical chemistry to identify associations between changes in gene expression and physiological/toxic outcomes that facilitates the elucidation the mechanisms of action of dioxin-mediated fatty liver toxicity. The mixture is then examined to detect and characterize the additive, synergistic and antagonistic interactions that affect the fatty liver response using response surface models for genes associated with fatty liver. This project does not only develop innovative and credible statistical strategies to rigorously assess interactions induced by mixtures containing chemicals that use a common mechanism of action, but also further elucidates mechanisms of toxicity associated with TCDD-induced fatty liver response.

Back
to Top