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Non-thermal dielectric-barrier discharge plasma damages human keratinocytes by inducing oxidative stress.
Kim, Ki Cheon; Piao, Mei Jing; Madduma Hewage, Susara Ruwan Kumara; Han, Xia; Kang, Kyoung Ah; Jo, Jin Oh; Mok, Young Sun; Shin, Jennifer H; Park, Yeunsoo; Yoo, Suk Jae; Hyun, Jin Won.
Affiliation
  • Kim KC; School of Medicine and Institute for Nuclear Science and Technology, Jeju National University, Jeju 63243, Republic of Korea.
  • Piao MJ; School of Medicine and Institute for Nuclear Science and Technology, Jeju National University, Jeju 63243, Republic of Korea.
  • Madduma Hewage SR; School of Medicine and Institute for Nuclear Science and Technology, Jeju National University, Jeju 63243, Republic of Korea.
  • Han X; School of Medicine and Institute for Nuclear Science and Technology, Jeju National University, Jeju 63243, Republic of Korea.
  • Kang KA; School of Medicine and Institute for Nuclear Science and Technology, Jeju National University, Jeju 63243, Republic of Korea.
  • Jo JO; Department of Chemical and Biological Engineering, Jeju National University, Jeju 63243, Republic of Korea.
  • Mok YS; Department of Chemical and Biological Engineering, Jeju National University, Jeju 63243, Republic of Korea.
  • Shin JH; Department of Mechanical Engineering and Graduate School of Medical Science and Engineering, KAIST, Daejeon 34141, Republic of Korea.
  • Park Y; National Fusion Research Institute, Plasma Technology Research Center, Gunsan 54004, Republic of Korea.
  • Yoo SJ; National Fusion Research Institute, Plasma Technology Research Center, Gunsan 54004, Republic of Korea.
  • Hyun JW; School of Medicine and Institute for Nuclear Science and Technology, Jeju National University, Jeju 63243, Republic of Korea.
Int J Mol Med ; 37(1): 29-38, 2016 Jan.
Article in En | MEDLINE | ID: mdl-26573561
ABSTRACT
The aim of this study was to identify the mechanisms through which dielectric-barrier discharge plasma damages human keratinocytes (HaCaT cells) through the induction of oxidative stress. For this purpose, the cells were exposed to surface dielectric-barrier discharge plasma in 70% oxygen and 30% argon. We noted that cell viability was decreased following exposure of the cells to plasma in a time-dependent manner, as shown by 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. The levels of intracellular reactive oxygen species (ROS) were determined using 2',7'-dichlorodihydrofluorescein diacetate and dihydroethidium was used to monitor superoxide anion production. Plasma induced the generation of ROS, including superoxide anions, hydrogen peroxide and hydroxyl radicals. N-acetyl cysteine, which is an antioxidant, prevented the decrease in cell viability caused by exposure to plasma. ROS generated by exposure to plasma resulted in damage to various cellular components, including lipid membrane peroxidation, DNA breaks and protein carbonylation, which was detected by measuring the levels of 8-isoprostane and diphenyl-1-pyrenylphosphine assay, comet assay and protein carbonyl formation. These results suggest that plasma exerts cytotoxic effects by causing oxidative stress-induced damage to cellular components.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen / Argon / Keratinocytes / Oxidative Stress / Plasma Gases Limits: Humans Language: En Journal: Int J Mol Med Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2016 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Oxygen / Argon / Keratinocytes / Oxidative Stress / Plasma Gases Limits: Humans Language: En Journal: Int J Mol Med Journal subject: BIOLOGIA MOLECULAR / GENETICA MEDICA Year: 2016 Document type: Article