Urethane increases reactive oxygen species and activates extracellular signal-regulated kinase in RAW 264.7 macrophages and A549 lung epithelial cells
Archives of Pharmacal Research, ISSN: 0253-6269, Vol: 36, Issue: 6, Page: 775-782
2013
- 22Citations
- 9Captures
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Example: if you select the 1-year option for an article published in 2019 and a metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019. If you select the 3-year option for the same article published in 2019 and the metric category shows 90%, that means that the article or review is performing better than 90% of the other articles/reviews published in that journal in 2019, 2018 and 2017.
Citation Benchmarking is provided by Scopus and SciVal and is different from the metrics context provided by PlumX Metrics.
Metrics Details
- Citations22
- Citation Indexes22
- 22
- CrossRef7
- Captures9
- Readers9
Article Description
Urethane, which is used as an anesthetic for animal experiments, causes inflammation and cancer in the lung. BALB/c mice received 1 mg/g of urethane once a week for four consecutive weeks via intraperitoneal injections developed interstitial infiltration of inflammatory cells and tumors in the lung. However, the intracellular signaling events which urethane causes inflammation and cancer are largely unknown. Here we show that urethane caused overproduction of reactive oxygen species (ROS) in RAW 264.7 macrophages and A549 lung epithelial cells. Pretreatment of these cells with the antioxidant N-acetylcysteine attenuated the urethane-induced ROS production. Urethane increased heme oxygenase-1 expression to protect these cells from cytotoxicity caused by overproduced ROS. In addition, urethane activated extracellular signal-regulated kinase (ERK) in both cell types. Overall, our data imply that urethane stimulates ROS production and ERK activation in macrophages and lung epithelial cells, and the overproduced ROS and activated ERK may promote tumor formation in the lung. © 2013 The Pharmaceutical Society of Korea.
Bibliographic Details
http://www.scopus.com/inward/record.url?partnerID=HzOxMe3b&scp=84878965702&origin=inward; http://dx.doi.org/10.1007/s12272-013-0104-8; http://www.ncbi.nlm.nih.gov/pubmed/23543651; http://link.springer.com/10.1007/s12272-013-0104-8; https://dx.doi.org/10.1007/s12272-013-0104-8; https://link.springer.com/article/10.1007/s12272-013-0104-8
Springer Science and Business Media LLC
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