This subproject is one of many research subprojects utilizing theresources provided by a Center grant funded by NIH/NCRR. The subproject andinvestigator (PI) may have received primary funding from another NIH source,and thus could be represented in other CRISP entries. The institution listed isfor the Center, which is not necessarily the institution for the investigator.This proposal will examine the central hypothesis that: AA supplementation will acutely potentiate cytokine activation and oxidative stress produced by intravenous Fe by increasing NTBI concentrations in hemodialysis (HD) patients.
Specific Aims1) To determine the effect of AA in the presence of NTBI on cytokine activation, DNA, lipid, and protein oxidation.2) To study the relationship between AA and magnitude of NTBI apparance.3) To evaluate clinically-revelant predictors and AA and Fe-induced oxidative stress and inflammation in HD patients.
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