N-acetylcysteine dual and antagonistic effect on cadmium cytotoxicity in human leukemia cells
Language English Country Netherlands Media print-electronic
Document type Journal Article
PubMed
31288199
DOI
10.1016/j.etap.2019.103213
PII: S1382-6689(19)30084-5
Knihovny.cz E-resources
- Keywords
- Cadmium chelation, Cadmium cytotoxicity, K562 cells, N-acetylcysteine, Reactive oxygen species, U937 cells,
- MeSH
- Acetylcysteine pharmacology MeSH
- K562 Cells MeSH
- Chelating Agents pharmacology MeSH
- Cadmium toxicity MeSH
- Environmental Pollutants toxicity MeSH
- Humans MeSH
- Reactive Oxygen Species metabolism MeSH
- U937 Cells MeSH
- Cell Survival drug effects MeSH
- Dose-Response Relationship, Drug MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Names of Substances
- Acetylcysteine MeSH
- Chelating Agents MeSH
- Cadmium MeSH
- Environmental Pollutants MeSH
- Reactive Oxygen Species MeSH
Although cadmium (Cd2+) is unable to form reactive oxygen species (ROS) directly, many of its adverse effects are connected to increased ROS generation resulting in cell death. In support of this supposition, a large number of studies have shown protective effects of antioxidants such as N-acetylcysteine (NAC) against cadmium induced cytotoxicity. Here, we describe the cytotoxic effects of Cd2+ on human leukemia U937 and K562 cells that were not mediated by oxidative stress. Surprisingly, we observed that addition of low concentrations of NAC can drastically potentiate cadmium cytotoxicity solely via ROS production. However, all adverse effects of the metal were prevented by NAC at high concentrations. Detailed analysis indicated that the protective effect of NAC was mediated by its ability to form stable complex with cadmium [Cd(NAC)2]. In conclusion, NAC exhibits dual and antagonistic effects on Cd2+ cytotoxicity in human leukemia cells.
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