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Esculetin Prevents the Induction of Matrix Metalloproteinase-1 by Hydrogen Peroxide in Skin Keratinocytes.
Zhen, Ao Xuan; Piao, Mei Jing; Kang, Kyoung Ah; Fernando, Pincha Devage Sameera Madushan; Kang, Hee Kyoung; Koh, Young Sang; Hyun, Jin Won.
Affiliation
  • Zhen AX; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Piao MJ; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Kang KA; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Fernando PDSM; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Kang HK; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Koh YS; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
  • Hyun JW; Department of Biochemistry, Jeju National University School of Medicine, Jeju, Korea.
J Cancer Prev ; 24(2): 123-128, 2019 Jun.
Article in En | MEDLINE | ID: mdl-31360691
ABSTRACT

BACKGROUND:

Reactive oxygen species (ROS) are involved in various cellular diseases. Excessive ROS can cause intracellular oxidative stress, resulting in a calcium imbalance and even aging. In this study, we evaluated the protective effect of esculetin on oxidative stress-induced aging in human HaCaT keratinocytes.

METHODS:

Human keratinocytes were pretreated with esculetin for 30 minutes and treated with H2O2. Then, the protective effects on oxidative stress-induced matrix metalloproteinase (MMP)-1 were detected by Flou-4-AM staining, reverse transcription-PCR, Western blotting, and quantitative fluorescence assay.

RESULTS:

Esculetin prevented H2O2-induced aging by inhibiting MMP-1 mRNA, protein, and activity levels. In addition, esculetin decreased abnormal levels of phospho-MEK1, phospho-ERK1/2, phospho-SEK1, phospho-JNK1/2, c-Fos, and phospho-c-Jun and inhibited activator protein 1 binding activity.

CONCLUSIONS:

Esculetin prevented excessive levels of intracellular calcium and reduced the expression levels of aging-related proteins.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Cancer Prev Year: 2019 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: J Cancer Prev Year: 2019 Document type: Article