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Acta Pharmacologica Sinica 2008 November; 29 (11): 1319-1326; doi: 10.1111/j.1745-7254.2008.00878.x |
| Original Article | [
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| Protective effect of esculetin against oxidative stress-induced cell damage via scavenging reactive oxygen species |
So-hyung KIM1, Kyoung-ah KANG1, Rui ZHANG1, Mei-jing PIAO1, Dong-ok KO1, Zhi-hong WANG1, Sung-wook CHAE2, Sam-sik KANG3, Keun-hwa LEE1, Hee-kyoung KANG1, Hyun-wook KANG1, Jin-won HYUN1, 4 1School of Medicine and Institute of Medical Science, Cheju National University, Jeju-si, Republic of Korea; 2Department of Herbal Resources Research, Korea Institute of Oriental Medicine, Daejeon, Republic of Korea; 3Natural Products Research Institute and College of Pharmacy,
Seoul National University, Seoul, Republic of Korea |
Methods: The radical scavenging activity was assessed by 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical, hydroxyl radical, and intracellular reactive oxygen species (ROS). In addition, lipid peroxidation was assayed by the measure of related substances which react with thiobarbituric acid. The amount of carbonyl formation in protein was determined using a protein carbonyl ELISA kit. As well, cellular DNA damage was detected by Western blot and immuno-fluorescence image. Cell viability was assessed by 3-(4,5-dimethylthiazole-2-yl)-2,5-diphenyltetrazolium bromide assay. Results: Esculetin exhibited DPPH radical scavenging, hydroxyl radical scavenging, and intracellular ROS scavenging activities. The radical scavenging activity of esculetin resulted in the protection of cells from lipid peroxidation, protein carbonyl, and DNA damage induced by H2O2. Therefore, esculetin recovered cell viability exposed to H2O2.
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