4.7 Article

Impacts of antioxidants on hydroxyl radical production from individual and mixed transition metals in a surrogate lung fluid

期刊

ATMOSPHERIC ENVIRONMENT
卷 45, 期 40, 页码 7555-7562

出版社

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.atmosenv.2010.12.021

关键词

Reactive oxygen species (ROS); Particulate matter (PM); Oxidative stress; Iron; Copper; Fenton reaction

资金

  1. National Institute of Environmental Health Sciences [P42ES004699]
  2. California Agricultural Experiment Station [CA-D*-LAW-6403-RR]
  3. University of California through the Atmospheric Aerosols and Health Lead Campus

向作者/读者索取更多资源

Inhalation of ambient particulate matter causes morbidity and mortality in humans. One hypothesized mechanism of toxicity is the particle-induced formation of reactive oxygen species (ROS) - including the highly damaging hydroxyl radical ((OH)-O-center dot) followed by inflammation and a variety of diseases. While past studies have found correlations between ROS formation and a variety of metals, there are no quantitative measurements of (OH)-O-center dot formation from transition metals at concentrations relevant to 24-hour ambient particulate exposure. This research reports specific and quantitative measurements of (OH)-O-center dot formation from 10 individual transition metals (and several mixtures) in a cell-free surrogate lung fluid (SLF) with four antioxidants: ascorbate, citrate, glutathione, and uric acid. We find that Fe and Cu can produce (OH)-O-center dot under all antioxidant conditions as long as ascorbate is present and that mixtures of the two metals synergistically increase (OH)-O-center dot production. Manganese and vanadium can also produce (OH)-O-center dot under some conditions, but given that their ambient levels are typically very low, these metals are not likely to chemically produce significant levels of (OH)-O-center dot in the lung fluid. Cobalt, chromium, nickel, zinc, lead, and cadmium do not produce (OH)-O-center dot under any of our experimental conditions. The antioxidant composition of our SLF significantly affects (OH)-O-center dot production from Fe and Cu: ascorbate is required for (OH)-O-center dot formation, citrate increases (OH)-O-center dot production from Fe, and both citrate and glutathione suppress (OH)-O-center dot production from Cu. MINTEQ ligand speciation modeling indicates that citrate and glutathione affect (OH)-O-center dot production by changing metal speciation, altering the reactivity of the metals. In the most realistic SLF (i.e., with all four antioxidants), Fe generates approximately six times more (OH)-O-center dot than does the equivalent amount of Cu. Since levels of soluble Fe in PM are typically higher than those of Cu, our results suggest that Fe dominates the chemical generation of (OH)-O-center dot from deposited particles in the lungs. (C) 2010 Elsevier Ltd. All rights reserved.

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