It is well established that there are a number of important copper-dependent enzyme systems that are intimately involved in immunologic and inflammatory responses. Even though overt copper deficiency is rare and the copper requirement is small (1.5-3.0 mg/day), the intake of copper is often near or below the recommended U.S. Estimated Safe and Adequate Daily Dietary Intakes suggesting that marginal copper deficiency may be relatively common. Hopkins and Failla have shown that marginal copper intake reduces neutrophil function under conditions where the usual conventional indicators of copper are not markedly affected. Charges in neutrophil function may be even more consequential in some populations such as premature infants where copper deficiency is common. Yet, despite the importance of copper and the potential of even marginal copper deficiency to present a health hazard, the mechanisms by which copper modulates inflammatory reactions and the level of copper deficiency necessary to induce such effects are not known. The proposed research will focus on mechanisms underlying the relationship between dietary copper and the mobilization of leukocytes during injury or infectious stimuli in the microcirculation. Our previous research identified the endothelium as one of the major tissues affected by dietary copper deficiency. Since circulating leukocytes must interact with the endothelium prior to transmigration to sites of infection or injury, we will determine how marginal and deficient copper intake affect endothelial interactions with leukocytes. The studies will demonstrate how minimal decreases in dietary copper intake can significantly influence the response to inflammatory stimuli.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Project (R01)
Project #
1R01DK055030-01A1
Application #
2908137
Study Section
Nutrition Study Section (NTN)
Program Officer
May, Michael K
Project Start
1999-08-01
Project End
2003-07-31
Budget Start
1999-08-01
Budget End
2000-07-31
Support Year
1
Fiscal Year
1999
Total Cost
Indirect Cost
Name
University of Louisville
Department
Type
Schools of Medicine
DUNS #
City
Louisville
State
KY
Country
United States
Zip Code
40292
Wei, Xiaoli; Song, Ming; Yin, Xinmin et al. (2015) Effects of Dietary Different Doses of Copper and High Fructose Feeding on Rat Fecal Metabolome. J Proteome Res 14:4050-8
Song, Ming; Schuschke, Dale A; Zhou, Zhanxiang et al. (2015) Kupffer cell depletion protects against the steatosis, but not the liver damage, induced by marginal-copper, high-fructose diet in male rats. Am J Physiol Gastrointest Liver Physiol 308:G934-45
Song, Ming; Schuschke, Dale A; Zhou, Zhanxiang et al. (2013) Modest fructose beverage intake causes liver injury and fat accumulation in marginal copper deficient rats. Obesity (Silver Spring) 21:1669-75
Song, Ming; Schuschke, Dale A; Zhou, Zhanxiang et al. (2012) High fructose feeding induces copper deficiency in Sprague-Dawley rats: a novel mechanism for obesity related fatty liver. J Hepatol 56:433-40
Sakai, Nozomu; Shin, Thomas; Schuster, Rebecca et al. (2011) Marginal copper deficiency increases liver neutrophil accumulation after ischemia/reperfusion in rats. Biol Trace Elem Res 142:47-54
Schuschke, Dale A; Adeagbo, Ayotunde S O; Patibandla, Phani K et al. (2009) Cyclooxygenase-2 is upregulated in copper-deficient rats. Inflammation 32:333-9
Falcone, Jeff C; Lominadze, David; Johnson, W Thomas et al. (2008) Endothelial cell-derived nitric oxide mobilization is attenuated in copper-deficient rats. Appl Physiol Nutr Metab 33:1073-8
Saari, Jack T; Wold, Loren E; Duan, Jinhong et al. (2007) Cardiac nitric oxide synthases are elevated in dietary copper deficiency. J Nutr Biochem 18:443-8
Gordon, Sharon A; Lominadze, David; Saari, Jack T et al. (2005) Impaired deformability of copper-deficient neutrophils. Exp Biol Med (Maywood) 230:543-8
Lominadze, David; Saari, Jack T; Percival, Susan S et al. (2004) Proinflammatory effects of copper deficiency on neutrophils and lung endothelial cells. Immunol Cell Biol 82:231-8

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