Eruca sativa and its flavonoid components, quercetin and isorhamnetin, improveskin barrier function by activation of peroxisome proliferator-activated receptor (PPAR)-α and suppression of inflammatory cytokines

Bora Kim, Yoon-E Choi, Hyun Soo Kim

Research output: Contribution to journalArticle

27 Citations (Scopus)

Abstract

Atopic dermatitis,which is related to dermatologic disorders and is associatedwith skin barrier dysfunction, represents an epidemic problem demanding effective therapeutic strategies. In the present study, we showed that the treatment with Eruca sativa extract resulted in a significant increase in the transactivation activity of peroxisome proliferator-activated receptor (PPAR) response element such as PPAR-α and suppression in the expression of inflammatory cytokine and antimicrobial peptides. In addition, E. sativa extract promotes the expression of filaggrin related to skin barrier protection. Quercetin and isorhamnetin, flavonoids' constituents of E. sativa, also promoted PPAR-α activity. These results indicate that E. sativa extract may be an appropriate material for improving skin barrier function as a skin therapeutic agent for atopic dermatitis.

Original languageEnglish
Pages (from-to)1359-1366
Number of pages8
JournalPhytotherapy Research
Volume28
Issue number9
DOIs
Publication statusPublished - 2014 Sep 1
Externally publishedYes

Fingerprint

Peroxisome Proliferator-Activated Receptors
Quercetin
Flavonoids
Cytokines
Skin
Atopic Dermatitis
Response Elements
Transcriptional Activation
Peptides
3-methylquercetin
Therapeutics

Keywords

  • Anti-inflammation
  • Eruca sativa extract
  • Filaggrin
  • Flavonoid
  • Peroxisome proliferators-activated receptors

ASJC Scopus subject areas

  • Pharmacology

Cite this

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abstract = "Atopic dermatitis,which is related to dermatologic disorders and is associatedwith skin barrier dysfunction, represents an epidemic problem demanding effective therapeutic strategies. In the present study, we showed that the treatment with Eruca sativa extract resulted in a significant increase in the transactivation activity of peroxisome proliferator-activated receptor (PPAR) response element such as PPAR-α and suppression in the expression of inflammatory cytokine and antimicrobial peptides. In addition, E. sativa extract promotes the expression of filaggrin related to skin barrier protection. Quercetin and isorhamnetin, flavonoids' constituents of E. sativa, also promoted PPAR-α activity. These results indicate that E. sativa extract may be an appropriate material for improving skin barrier function as a skin therapeutic agent for atopic dermatitis.",
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AB - Atopic dermatitis,which is related to dermatologic disorders and is associatedwith skin barrier dysfunction, represents an epidemic problem demanding effective therapeutic strategies. In the present study, we showed that the treatment with Eruca sativa extract resulted in a significant increase in the transactivation activity of peroxisome proliferator-activated receptor (PPAR) response element such as PPAR-α and suppression in the expression of inflammatory cytokine and antimicrobial peptides. In addition, E. sativa extract promotes the expression of filaggrin related to skin barrier protection. Quercetin and isorhamnetin, flavonoids' constituents of E. sativa, also promoted PPAR-α activity. These results indicate that E. sativa extract may be an appropriate material for improving skin barrier function as a skin therapeutic agent for atopic dermatitis.

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