Low concentration platinum nanoparticles effectively scavenge reactive oxygen species in rat skeletal L6 cells

Hidekazu Nakanishi, Takeki Hamasaki, Tomoya Kinjo, Hanxu Yan, Noboru Nakamichi, Shigeru Kabayama, Kiichiro Teruya, Sanetaka Shirahata

Research output: Contribution to journalArticle

4 Citations (Scopus)

Abstract

Prolonged exposure to excessive reactive oxygen species (ROS) increases risk factorsfor many diseases. Therefore, elimination of ROS as well as prevention of its production becomes critically important. In the present study, we evaluated the levels of cytotoxicity and ROS scavenging activity induced by synthetic platinum nanoparticles (PtNPs). Average size of synthesized PtNPs was 2.2 nm. Synthetic PtNPs were found to scavenge both induced and endogenous H2O2 significantly in L6 rat skeletal muscle cells at a very low concentration (10-2 mg/l). To investigate the mechanism of action, the hierarchical oxidative stress model was used as an experimental model. To evaluate this possibility, we assessedglutathione concentration and gene levels of several antioxidant enzymes in PtNPs-treated(10-3-10 mg/l) L6 cells. Reduced glutathione (GSH) was increased in the range of 10-3-1 mg/l, but not in the 10 mg/l PtNP-treated cells. The GSH/GSSG ratio increased significantly at 1 mg/l and decreased in the 10 mg/l PtNPtreated cells. Most of the gene transcripts for oxidative stress inducible heme oxygenase-1 (HO-1), glutathione reductase (GR), copper-zinc superoxide dismutase (CuZn-SOD), manganese superoxide dismutase (Mn-SOD), glutathione peroxidase (GPx), and catalase were increased significantly by PtNPs at 10-1-10 mg/l.Such upregulatory effects induced by synthetic PtNPs at high concentrations (1-10 mg/l) in L6 cells can be explained by the hierarchical oxidative stress model. However, the cellular responses induced by low levels (10-3-10-2 mg/l) of PtNPs could not be fully explained by this model.

Original languageEnglish
Pages (from-to)76-85
Number of pages10
JournalNano Biomedicine and Engineering
Volume5
Issue number2
DOIs
Publication statusPublished - Jul 11 2013

All Science Journal Classification (ASJC) codes

  • Biomedical Engineering

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