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Cited 22 time in webofscience Cited 25 time in scopus
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Oleanolic Acid Alleviates Atopic Dermatitis-like Responses In Vivo and In Vitroopen access

Authors
Kang, Yun-MiKim, Hye-MinLee, MinhoAn, Hyo-Jin
Issue Date
Nov-2021
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
oleanolic acid; atopic dermatitis; 2,4-dinitrochlorobenzene; keratinocyte; NF-kappa B; STAT1
Citation
International Journal of Molecular Sciences, v.22, no.21
Indexed
SCIE
SCOPUS
Journal Title
International Journal of Molecular Sciences
Volume
22
Number
21
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/4246
DOI
10.3390/ijms222112000
ISSN
1661-6596
1422-0067
Abstract
Oleanolic acid (OA) is a pentacyclic triterpenoid, abundantly found in plants of the Oleaceae family, and is well known for its beneficial pharmacological activities. Previously, we reported the inhibitory effect of OA on mast cell-mediated allergic inflammation. In this study, we investigated the effects of OA on atopic dermatitis (AD)-like skin lesions and its underlying mechanism of action. We evaluated the inhibitory effect of OA on AD-like responses and the possible mechanisms using a 1-chloro-2,4-dinitrochlorobenzene (DNCB)-induced AD animal model and tumor necrosis factor (TNF)-alpha/interferon (IFN)-gamma-stimulated HaCaT keratinocytes. We found that OA has anti-atopic effects, including histological alterations, on DNCB-induced AD-like lesions in mice. Moreover, it suppressed the expression of Th2 type cytokines and chemokines in the AD mouse model and TNF-alpha/IFN-gamma-induced HaCaT keratinocytes by blocking the activation of serine-threonine kinase Akt, nuclear factor-kappa B, and the signal transducer and activator of transcription 1. The results demonstrate that OA inhibits AD-like symptoms and regulates the inflammatory mediators; therefore, it may be used as an effective and attractive therapeutic agent for allergic disorders, such as AD. Moreover, the findings of this study provide novel insights into the potential pharmacological targets of OA for treating AD.
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