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Inhibition of Poly(I:C)-Induced Inflammation by Salvianolic Acid A in Skin Keratinocytes.

Authors :
Zhang QL
Jiang RH
Li XM
Ko JW
Kim CD
Zhu MJ
Lee JH
Source :
Annals of dermatology [Ann Dermatol] 2019 Jun; Vol. 31 (3), pp. 279-285. Date of Electronic Publication: 2019 May 01.
Publication Year :
2019

Abstract

Background: Skin keratinocytes participate actively in inducing immune responses when external pathogens are introduced, thereby contributing to elimination of pathogens. However, in condition where the excessive inflammation is occurred, chronic skin disease such as psoriasis can be provoked.<br />Objective: We tried to screen the putative therapeutics for inflammatory skin disease, and found that salvianolic acid A (SAA) has an inhibitory effect on keratinocyte inflammatory reaction. The aim of this study is to demonstrate the effects of SAA in poly(I:C)-induced inflammatory reaction in skin keratinocytes.<br />Methods: We pre-treated keratinocytes with SAA then stimulated with poly(I:C). Inflammatory reaction of keratinocytes was verified using real-time polymerase chain reaction, enzyme-linked immunosorbent assay and Western blot.<br />Results: When skin keratinocytes were pre-treated with SAA, it significantly inhibited poly (I:C)-induced expression of inflammatory cytokines including interleukin (IL)-1β, IL-6, IL-8, tumor necrosis factor-α, and CCL20. SAA inhibited poly(I:C)-induced activation of nuclear factor-κB signaling. And SAA also inhibited inflammasome activation, evidenced by decrease of IL-1β secretion. Finally, SAA markedly inhibited poly(I:C)-induced NLRP3 expression.<br />Conclusion: These results demonstrate that SAA has an inhibitory effect on poly(I:C)-induced inflammatory reaction of keratinocytes, suggesting that SAA can be developed for the treatment of inflammatory skin diseases such as psoriasis.<br />Competing Interests: CONFLICTS OF INTEREST: The authors have nothing to disclose.<br /> (Copyright © 2019 The Korean Dermatological Association and The Korean Society for Investigative Dermatology.)

Details

Language :
English
ISSN :
2005-3894
Volume :
31
Issue :
3
Database :
MEDLINE
Journal :
Annals of dermatology
Publication Type :
Academic Journal
Accession number :
33911592
Full Text :
https://doi.org/10.5021/ad.2019.31.3.279