Mechanisms of Perfluorooctanesulfonamide- Induced Oxidative Stress in Female Rats

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Project Period: 
2007
Project Investigator(s): 
W. Xie, H. Lehmler, Department of Occupational and Environmental Health, The University of Iowa
D. Spitz, Department of Radiation Oncology, The University of Iowa
Abstract: 

Perfluorinated compounds such as perfluorooctanesulfonamides (PFOSAs) are emerging as an important class of environmentally persistent chemicals. Our knowledge of their mechanisms of toxicity is very limited. Exposure to these chemicals has been associated with developmental toxicity in several animal models. Based on the observation that PFOSAs are peroxisome proliferators and cause mitochondrial dysfunction we hypothesize that oral exposure to a typical PFOSA such as N-EtFOSE (N-ethyl perfluorooctanesulfonamidoethanol) may cause oxidative stress in vivo. We will test this hypothesis by measuring markers of oxidative stress and the activity of enzyme in selected organs. This pilot study will answer important questions regarding the toxicity of PFOSAs and allow us to design further investigations of the mechanisms of their toxicity.

Publications: 

Xie W, Ludewig G, Wang K, Lehmler HJ; Model and cell membrane partitioning of perfluorooctanesulfonate is independent of the lipid chain length; Colloids Surf B Biointerfaces 2010 Mar1;76(1): 128-36.

Xie W, Bothun GD, Lehmler HJ; Partitioning of perfluorooctanoate into phosphatidylcholine bilayers is chain length-independent; J Chem Phys Lipids 2010 Mar; 163(3): 300-8.

Xie W, Kania-Korwel I, Tharappel JC, Telu S, Coleman MC, Glauert HP, Kannan K, Mariappan SVS, Spitz DR, Weydert J, Lehmler HJ; Subacute exposure to N-ethyl perfluorooctanesulfonamidoethanol results in the formation of perfluorooctanesulfonate and alters superoxide dismutase activity in female rats; Arch Toxicol 2009; 83:909-924.