Red ginseng extracts attenuate skin inflammation in atopic dermatitis through p70 ribosomal protein S6 kinase activation

被引:29
作者
Osada-Oka, Mayuko [1 ]
Hirai, Sayaka [1 ]
Izumi, Yasukatsu [2 ]
Misumi, Kazuhiro [1 ]
Samukawa, Keiichi [2 ]
Tomita, Shuhei [2 ]
Miura, Katsuyuki [3 ]
Minamiyama, Yukiko [1 ]
Iwao, Hiroshi [4 ]
机构
[1] Kyoto Prefectural Univ, Grad Sch Life & Environm Sci, Div Appl Life Sci, Food Hyg & Environm Hlth, Kyoto, Japan
[2] Osaka City Univ, Med Sch, Dept Pharmacol, Osaka, Japan
[3] Osaka City Univ, Med Sch, Appl Pharmacol & Therapeut, Osaka, Japan
[4] Shitennoji Univ, Dept Educ, Habikino, Japan
关键词
p70 ribosomal protein S6 kinase; Red ginseng; Atopic dermatitis; Basophil; Keratinocyte; CHRONIC ALLERGIC INFLAMMATION; AFFINITY IGE RECEPTOR; MAST-CELL; HUMAN KERATINOCYTES; TYROSINE KINASE; T-CELLS; INHIBITORS; BASOPHILS; CYTOKINES; DISEASES;
D O I
10.1016/j.jphs.2017.11.002
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
Atopic dermatitis (AD) is a chronic and relapsing inflammatory skin disease with increased immunoglobulin E (IgE) levels. Activation of the mammalian target of rapamycin (mTOR)/p70 ribosomal protein S6 kinase (p70S6K) signaling is known to occur in the inflammatory regions of AD skin. We previously demonstrated that red ginseng extract (RGE), as an anti-inflammatory agent, had potential for treating AD. However, it is still unclear whether RGE inhibits mTOR/p70S6K signaling. Thus, we examined the anti-inflammatory effects of RGE on IgE or interferon-gamma (IFN-gamma) induced signaling pathways. In KU812 human basophils, activation of Fce receptor type Ia (FCeRI), also known as the high affinity IgE receptor, induced phosphorylation of both mTOR and p70S6K. Moreover, levels of phosphorylated p70S6K (pp70S6K), but not p-mTOR, were decreased by RGE. RGE also decreased p-p70S6K levels in IFN-gamma-stimulated human keratinocytes, suppressing the IFN-gamma induced increase in levels of C-C chemokine ligand 2 mRNA. Interestingly, the increased p70S6K phosphorylation in skin lesions of AD model mice was attenuated by RGE treatment. In conclusion, RGE is a potential therapy against inflammatory responses involving the p70S6K signaling pathway. (C) 2018 The Authors. Production and hosting by Elsevier B. V. on behalf of Japanese Pharmacological Society. This is an open access article under the CC BY-NC-ND license.
引用
收藏
页码:9 / 15
页数:7
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