Fermented Angelicae tenussimae with Aspergillus oryzae Improves Skin Barrier Properties, Moisturizing, and Anti-Inflammatory Responses

Int J Mol Sci. 2022 Oct 11;23(20):12072. doi: 10.3390/ijms232012072.

Abstract

Angelicae tenussimae root has been used as a traditional medicine in Asia. Recently, anti-melanogenic and anti-photogenic effects of fermented A. tenuissima root (FAT) were identified. However, information about the anti-atopic dermatitis action of FAT is limited. Thus, the purpose of this study is to determine the applicability of FAT to AD by identifying the efficacy of FAT on the skin barrier and inflammatory response, which are the main pathogenesis of AD. Expression levels of skin barrier components and the production of inflammatory mediators in human keratinocyte and mouse macrophage cells were measured by quantitative RT-PCR or ELISA. FAT upregulated the expression of skin barrier components (filaggrin, involucrin, loricurin, SPTLC1) and inhibited the secretion of an inflammatory chemokine TARC in HaCaT cells. Furthermore, it suppressed pro-inflammatory cytokines (IL-6, TNF-α) and nitric oxide production in LPS-induced RAW264.7 cells. In addition, ligustilide increased filaggrin and SPTLC1, and also lowered pro-inflammatory mediators that increased in atopic environments, such as in FAT results. This means that ligustilide, one of the active ingredients derived from FAT, can ameliorate AD, at least in part, by promoting skin barrier formation and downregulating inflammatory mediators. These results suggest that FAT is a potential functional cosmetic material for the care and management of AD.

Keywords: Angelicae tenussimae; atopic dermatitis; inflammation; ligustilide; moisturizing; skin barrier.

MeSH terms

  • Animals
  • Anti-Inflammatory Agents / metabolism
  • Anti-Inflammatory Agents / pharmacology
  • Aspergillus oryzae*
  • Chemokines / metabolism
  • Cytokines / metabolism
  • Humans
  • Inflammation Mediators / metabolism
  • Interleukin-6 / metabolism
  • Lipopolysaccharides / pharmacology
  • Mice
  • Nitric Oxide / metabolism
  • Plant Extracts / pharmacology
  • Skin / metabolism
  • Tumor Necrosis Factor-alpha* / metabolism

Substances

  • Tumor Necrosis Factor-alpha
  • Lipopolysaccharides
  • Interleukin-6
  • Nitric Oxide
  • ligustilide
  • Plant Extracts
  • Chemokines
  • Cytokines
  • Inflammation Mediators
  • Anti-Inflammatory Agents