Oral Administration of SSC201, a Medicinal Herbal Formula, Suppresses Atopic Dermatitis-Like Skin Lesions

Atopic dermatitis (AD) is a chronic inflammatory skin disease, which requires safe and effective treatment. In this study, we evaluated the effects of SSC201, a herbal formulation consisting of Stemonae Radix, Spirodelae Herba, and Cnidii Fructus, on the development of AD induced by 2,4-dinitrochlor...

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Veröffentlicht in:Journal of medicinal food 2014, 17(4), , pp.496-504
Hauptverfasser: Park, Bo-Kyung, Park, Yang-Chun, Jung, In Chul, Kim, Seung-Hyung, Choi, Jung-Eun, Park, Sunyoung, Choi, Jeong June, Jin, Mirim
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Sprache:eng
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Zusammenfassung:Atopic dermatitis (AD) is a chronic inflammatory skin disease, which requires safe and effective treatment. In this study, we evaluated the effects of SSC201, a herbal formulation consisting of Stemonae Radix, Spirodelae Herba, and Cnidii Fructus, on the development of AD induced by 2,4-dinitrochlorobenzene in the NC/Nga murine model. Oral administration of SSC201 significantly reduced the severity of dermatitis and the tendency of mice to scratch their lesions. SSC201 significantly reduced the thickening of the epidermis/dermis and the infiltration of T cells, eosinophils, and mast cells into the dermis. These results were supported by findings of reduced numbers of CD4⁺, CCR3⁺, and CD117⁺FcɛRIα⁺ cells in the skin. Furthermore, SSC201 significantly decreased the number of CD4⁺, CD8⁺, and CD3⁺CD69⁺ T cells in lymph nodes. SSC201 not only decreased the plasma levels of immunoglobulin E (IgE) and the numbers of IgE-producing B cells (B220⁺CD23⁺), but also reduced the number of eosinophils and the levels of eotaxin as well as concentrations of thymus and activation-regulated chemokine in the periphery. Splenic levels of Th2 cytokines, including interleukin (IL)-4, IL-5, and IL-13, were reduced, whereas the levels of IL-12, a Th1 cytokine, were increased. Taken together, our data suggest that SSC201 may be an effective therapeutic agent for the treatment of AD.
ISSN:1557-7600
1096-620X
1557-7600
DOI:10.1089/jmf.2013.2941