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Effect of cerium oxide nanoparticles to inflammation and oxidative DNA damages in H9c2 cells
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  • Effect of cerium oxide nanoparticles to inflammation and oxidative DNA damages in H9c2 cells
  • Effect of cerium oxide nanoparticles to inflammation and oxidative DNA damages in H9c2 cells
저자명
Rim. Kyung Taek,Kim. Soo Jin,Song. Se Wook,Park. Jung Sun
간행물명
Molecular & cellular toxicology
권/호정보
2012년|8권 3호|pp.271-280 (10 pages)
발행정보
대한독성유전단백체학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

Occupational heart disease have occurred continuously, making social problems, and increasing the needs for its effective prevention. As natural antioxidants, selenium ($Na_2SeO_3$) and cerium oxide ($CeO_2$) nanoparticles, we verified the effect with suspected cardiotoxic chemicals, 1,1,1-trichloroethane (TCEtn) based on the myocardial cell line due to inflammation and oxidative DNA damage, and reliable anti-cardiotoxic effects of selenium and $CeO_2$ nanoparticles. We measured the changes of gene expression with real-time RT-PCR, and oxidative DNA damage with Fragment Length Analysis with Restriction Enzyme (FLARE) assay in H9c2 cell line, and discuss their molecular mechanism from these data. In the result, it has anticytotoxic effect with $CeO_2$ nanoparticles below 100 ${mu}M$ which the particles dispersed well. The early expression of COX2 mRNA is increased with TCEtn but decreased with $Na_2SeO_3$, $CeO_2$ nanoparticles, has some anti-inflammatory effect. The PPAR${gamma}$ is much increased with all of TCEtn, $Na_2SeO_3$, $CeO_2$ nanoparticles in 36 hour pretreat, are evaluated their activation to cytokines, transcription factors related to overcome and decrease the cardiotoxic effects of test chemical. With the oxidative DNA damage, the $CeO_2$ nanoparticles have more active anti-oxidative effect to selenium.