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Dracocephalum moldavica L. seed oil ameliorates DNCB-induced atopic
            dermatitis-like symptoms in mice model

            Jaeyoung Choi 1 , Eunsu Song 1 , Kyo-Yeon Lee 2 , Sung-Gil Choi 2 , Su Kang Kim 3 , Hui Jin 4 , Yun Hee Chang 1 , Jinah Hwang 1
            1 Food and Nutrition, Myongji University, Yongin,  Republic of Korea,  2 Food Science and Technology, Gyeongsang National University, Jinju, Republic of Korea,  3 Department of Biomedical
            Laboratory Science, Catholic Kwandong University, Gangneung, Republic of Korea,  4  Center of Nutraceutical and Pharmaceutical Materials, Myongji University, Yongin, Republic of Korea
                              BACKGROUND                                                  AIM

    Dracocephalum moldavica L. (DM) has unique nutritional characteristics in terms of  This study was conducted to
    lipid profile and various polyphenols. Due to its features, DM has been used for  determine anti-atopic effect
    dermal problem in North America and Eastern Europe. According to previous study,  of DMS by supercritical fluid
    there were various phytochemicals which may improve atopic dermatitis. However,  extraction in vivo.
    there is no report regarding anti-atopic effect of DM seed oil (DMS) in animal model.


                                                METHODS












     Figure 1. Experimental scheme of DM seed oil by supercritical CO 2 extraction
                                                RESULTS

    After 4 weeks treatment with DMS (2.5-10% v/v) in DNCB-
    induced atopic mice model, increase in epidermal layer and
    hyperkeratosis was observed in atopy-induced group (DNCB
    only). However, DMS treatment showed decrease in epidermal
    layer in a dose-dependent manner compared to vehicle control
    group. In addition, significantly decrease in skin TEWL was
                                                2
    observed with 2.5-10% DMS (48.96-59.42 g/m /h) compared
    with vehicle control (115.52 g/m /h). In terms of SCORAD index,
                                2
    10% DMS-treated group decreased the indexes by 78% in
    edema and by 60% in pruritus and dry skin compared to vehicle
    group.
   (A)                        (B)











    Figure 2. Water content of stratum corneum (TEWL) and the severity of clinical  Figure 3. Treatment of DMS efficiently attenuates severe
    symptoms of the skin lesions (SCORAD Index) were reduced after DMS  symptoms of experimental atopic dermatitis in DNCB-
    treatment for 4 weeks. SCORAD Index was expressed for the following four  induced BALB/c mice model after 4 weeks. (A) Cross
    symptoms: erythema/ edema/ pruritus/ lichenification. (A) Transepidermal  images of dorsal area lesions on the mice. (B) H&E–
    water loss (TEWL) index. (B) SCORAD Index.                  stained images of dorsal skin.

          CONCLUSION                        REFERENCES                   ACKNOWLEDGEMENTS

                                     •    Lee et al., Disease-specific primed  This work was supported under the
    DMS       treatment    showed    human   adult  stem  cells  effectively  framework  of   international
    improvement of atopic dermatitis-  ameliorate  experimental  atopic  cooperation program managed by
    like symptoms through indexes of                                     the National Research Foundation
    TEWL, SCORAD, optical images     dermatitis in mice, Theranostics 2019,  of Korea (2017R1A2B4010140).
    and  H&E   staining  in  DNCB-   9(12):3608-3621
    induced mice models. Therefore,  •    Motoyama  et  al.,  Anti-allergic
    It is expected that DMS can be                                      CONTACT INFORMATION
    used as a functional cosmetic and  effects of novel sulfated polysaccharide
    pharmaceutical ingredient through  sacran on mouse model of 2,4-Dinitro-1-
    further research related to the  fluorobenzene-induced atopic dermatitis,  Jaeyoung Choi: n_jyoung92@naver.com
    improvement of atopic dermatitis  International  Journal  of  Biological  Jinah Hwang*: jhwang@mju.ac.kr
    symptoms.                        Macromolecules 2018, 108, 112-118
                                                                          *corresponding author
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