4.6 Article

Inhibition of aryl hydrocarbon receptor signaling and induction of NRF2-mediated antioxidant activity by cinnamaldehyde in human keratinocytes

期刊

JOURNAL OF DERMATOLOGICAL SCIENCE
卷 85, 期 1, 页码 36-43

出版社

ELSEVIER IRELAND LTD
DOI: 10.1016/j.jdermsci.2016.10.003

关键词

Cinnamaldehyde; Keratinocytes; Aryl hydrocarbon receptor; Nrf2; Keishibukuryogan

资金

  1. Ministry of Health, Labour and Welfare, Japan [15K09770]
  2. Research on Development of New Drugs from Japan Agency for Medical Research and Development (AMED)
  3. Leading Advanced Projects for Medical Innovation (LEAP)
  4. Grants-in-Aid for Scientific Research [15K09770] Funding Source: KAKEN

向作者/读者索取更多资源

Background: Dioxins and other environmental pollutants are toxic and remain in biological tissues for a long time leading to various levels of oxidative stress. Although the toxicity of these agents has been linked to activation of the aryl hydrocarbon receptor (AHR), no effective treatment has been developed. Objective: To explore novel phytochemicals that inhibit AHR activation in keratinocytes. Methods: Keratinocytes were used in this study because the skin is one of the organs most affected by dioxin and other environmental pollutants. HaCaT cells, which are a human keratinocyte cell line, and normal human epidermal keratinocytes were stimulated with benzo[a]pyrene to induce AHR activation, and the effects of traditional Japanese Kampo herbal formulae were analyzed. Quantification of mRNA, western blotting, immunofluorescence localization of molecules, siRNA silencing, and visualization of oxidative stress were performed. Results: Cinnamomum cassia extract and its major constituent cinnamaldehyde significantly inhibited the activation of AHR. Cinnamaldehyde also activated the NRF2/HO1 pathway and significantly alleviated the production of reactive oxygen species in keratinocytes. The inhibition of AHR signaling and the activation of antioxidant activity by cinnamaldehyde operated in a mutually independent manner as assessed by siRNA methods In addition, AHR signaling was effectively inhibited by traditional Kampo formulae containing C cassia. Conclusion: Cinnamaldehyde has two independent biological activities; namely, an inhibitory action on AHR activation and an antioxidant effect mediated by NRF2/HO1 signaling. Through these dual functions, cinnamaldehyde may be beneficial for the treatment of disorders related to oxidative stress such as dioxin intoxication, acne, and vitiligo. (C) 2016 Japanese Society for Investigative Dermatology. Published by Elsevier Ireland Ltd. All rights reserved.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.6
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据