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논문 기본 정보

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학술저널
저자정보
이병웅 (대전대학교) 김선빈 (대전대학교) 송향희 (벽성대학) 지중구 (중부대학교) 박지원 (대전대학교) 김동희 (대전대학교)
저널정보
한의병리학회 동의생리병리학회지 동의생리병리학회지 제26권 제4호
발행연도
2012.8
수록면
446 - 454 (9page)

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In order to evaluate the efficacy of SHT against atopic dermatitis (AD), various immune related cytokines as well as histological comparison were performed in animal models, and the results are described. Clinical skin index of the SHT treated group decreased significantly in weeks 11 and 13, compared to the control group. Also, CD4+ immune cell ratio in the dorsal skin was significantly decreased to 69%, and both epidermal and dermal skin thickness was decreased. Serum IL-4, IL-5, IL-6, IL-13, and TNF-α, which are all important markers of inflammation, were decreased to 64%, 44%, 87%, 48%, and 45%, respectively. The expression of histamine, a chemical transmitter increasingly released during the progression of inflammation, was significantly decreased to 47%. The production of IgE immunoglobulin was significantly decreased to 16% compared to the control group. In conclusion, SHT pacifies the activation of T cells, leading to suppression of both Th2 cytokine overexpression and infiltration of immune cells into skin. As a result, relative thinning of both epidermis and dermis were observed. With the results obtained from in vitro studies, the immune modulatory effect of SHT in AD animal models was experimentally demonstrated. This study should provide solid information to construct EBM and for clinical practice.

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UCI(KEPA) : I410-ECN-0101-2015-510-001222148