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Effects of Cymbidium Root Ethanol Extract on Atopic Dermatitis.
Kim, Wan-Joong; Cha, Hae-Sim; Lee, Myung-Hun; Kim, Sun-Young; Kim, Seo Ho; Kim, Tack-Joong.
Afiliación
  • Kim WJ; Division of Biological Science and Technology, Yonsei-Fraunhofer Medical Device Laboratory, College of Science and Technology, Yonsei University, Wonju 220-710, Republic of Korea.
  • Cha HS; Division of Biological Science and Technology, Yonsei-Fraunhofer Medical Device Laboratory, College of Science and Technology, Yonsei University, Wonju 220-710, Republic of Korea.
  • Lee MH; Division of Biological Science and Technology, Yonsei-Fraunhofer Medical Device Laboratory, College of Science and Technology, Yonsei University, Wonju 220-710, Republic of Korea.
  • Kim SY; Division of Biological Science and Technology, Yonsei-Fraunhofer Medical Device Laboratory, College of Science and Technology, Yonsei University, Wonju 220-710, Republic of Korea.
  • Kim SH; Division of Biological Science and Technology, Yonsei-Fraunhofer Medical Device Laboratory, College of Science and Technology, Yonsei University, Wonju 220-710, Republic of Korea.
  • Kim TJ; Division of Biological Science and Technology, Yonsei-Fraunhofer Medical Device Laboratory, College of Science and Technology, Yonsei University, Wonju 220-710, Republic of Korea.
Article en En | MEDLINE | ID: mdl-26981139
ABSTRACT
Cymbidium has known antibacterial and antiedema activity and has been used as an ingredient in cosmetics and fragrances. The effects of Cymbidium ethanol extract (CYM) on allergic response and the underlying mechanisms of action have not been reported. Therefore, the purpose of this study was to determine the effect of CYM on allergic responses. Topical application of CYM was effective against immunoglobulin E (IgE)/dinitrophenyl-conjugated bovine serum albumin- (DNP-BSA-) induced degranulation of RBL-2H3 cells and anaphylaxis in ICR mice. An allergic dermatitis-like mouse model was used to evaluate the therapeutic potential of CYM in vivo. Continuous application of 2,4-dinitrochlorobenzene (DNCB) not only induced dermatitis in ICR mice but also aggravated the skin lesioning. However, the application of CYM decreased skin lesion severity, scratching behavior, and IgE levels. In addition, CYM downregulated the expression of the proinflammatory cytokines interleukin- (IL-) 4, IL-13, and tumor necrosis factor- (TNF-) α. Studies of signal transduction pathways showed that CYM suppressed the phosphorylation of spleen tyrosine kinase (Syk), an upstream molecule. It also inhibited the phosphorylation of Akt, phospholipase C- (PLC-) γ, and mitogen-activated protein kinase kinase kinase (MEKK). These results indicate that CYM may be effective in preventing and reducing allergic response and may have therapeutic potential as an antiallergic agent in disorders such as atopic dermatitis.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Evid Based Complement Alternat Med Año: 2016 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: Evid Based Complement Alternat Med Año: 2016 Tipo del documento: Article
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