Evaluation of Anti-atopic Dermatitis Activity of Hypsizigus marmoreus Extract

被引:14
作者
Kim, TaeHo [1 ]
Park, KiMoon [1 ]
Jung, Hye Sun [1 ]
Kong, Won-Sik [2 ]
Jeon, DaeHoon [3 ]
Lee, Seung Ho [4 ]
机构
[1] Sungkyunkwan Univ, Dept Food Sci & Biotechnol, Seoul, South Korea
[2] Rural Dev Adm, Natl Inst Hort & Herbal Sci, Mushroom Res Div, Eumseong 368873, South Korea
[3] Gyeonggi Do Agr Res & Extens Serv, Mushroom Res Stn, Gyeonggi Do, South Korea
[4] Incheon Natl Univ, Inchon 406772, South Korea
关键词
Hypsizigus marmoreus; atopic dermatitis; inflammation; cytokines; nitric oxide; RIBOSOME-INACTIVATING PROTEIN; NF-KAPPA-B; GENE-EXPRESSION; HUMAN MONOCYTES; NC/NGA MICE; MUSHROOM; IL-4; INTERLEUKIN-4; INHIBITION; MECHANISMS;
D O I
10.1002/ptr.5164
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Hypsizigus marmoreus is an edible mushroom that is cultivated worldwide. In this study, we investigated antiinflammatory activities of H.marmoreus extract on atopic dermatitis (AD)-like symptoms. Ethanol extract of H.marmoreus (HMEE) was administrated in powder to BALB/c mice in which AD was induced by 1-chloro 2, 4, 6-trinitrobenzene [picryl-chloride, (PCL)]. The dermatitis severity score and the thickness of the epidermis were significantly decreased following daily intake of HMEE powder (1g/kg/day) for 5weeks compared with a PCL-treated group. The mRNA expression of proinflammatory cytokines, such as interleukin-1 beta (IL-1) and interferon-gamma (IFN-), was significantly attenuated in the dorsal skin of the HMEE-fed mouse group compared with the PCL-treated mouse group. In addition, in concanavalin A-stimulated and lipopolysaccharide-stimulated mouse splenocytes and macrophages, levels of IL-1 and IFN- production were attenuated following the addition of HMEE. Interestingly, the administration of HMEE to mouse splenocytes stimulated the production of an antiinflammatory cytokine, IL-4. However, increases in the levels of proinflammatory cytokines and nitric oxide were attenuated by treating the mouse splenocytes, mouse macrophages, and Raw 264.7 cell line with HMEE. These results strongly suggest that HMEE exhibits anti-AD activity via the regulation of inflammatory responses. Copyright (c) 2014 John Wiley & Sons, Ltd.
引用
收藏
页码:1539 / 1546
页数:8
相关论文
共 28 条
  • [1] Molecular Properties of Water-Unextractable Proteoglycans from Hypsizygus marmoreus and Their in Vitro Immunomodulatory Activities
    Bao, Hong Hui
    Tarbasa, Mehdi
    Chae, Hee Mun
    You, Sang Guan
    [J]. MOLECULES, 2012, 17 (01): : 207 - 226
  • [2] Allergen-specific immunotherapy: current concepts and future directions
    Bieber, T.
    Simon, H-U
    [J]. ALLERGY, 2011, 66 (06) : 709 - 712
  • [3] Mechanisms of disease: Atopic dermatitis
    Bieber, Thomas
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 2008, 358 (14) : 1483 - 1494
  • [4] Brown MA, 1997, CRIT REV IMMUNOL, V17, P1
  • [5] Proinflammatory cytokines
    Dinarello, CA
    [J]. CHEST, 2000, 118 (02) : 503 - 508
  • [6] Corticosteroid-induced adverse events in adults - Frequency, screening and prevention
    Fardet, Laurence
    Kassar, Abdulrhaman
    Cabane, Jean
    Flahault, Antoine
    [J]. DRUG SAFETY, 2007, 30 (10) : 861 - 881
  • [7] A role for Th1 and Th2 cells in the immunopathogenesis of atopic dermatitis
    Grewe, M
    Bruijnzeel-Koomen, CAFM
    Schöpf, E
    Thepen, T
    Langeveld-Wildschut, AG
    Ruzicka, T
    Krutmann, J
    [J]. IMMUNOLOGY TODAY, 1998, 19 (08): : 359 - 361
  • [8] DIFFERENTIAL IN-SITU CYTOKINE GENE-EXPRESSION IN ACUTE VERSUS CHRONIC ATONIC DERMATITIS
    HAMID, Q
    BOGUNIEWICZ, M
    LEUNG, DYM
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 1994, 94 (02) : 870 - 876
  • [9] Anti-inflammatory activity of edible oyster mushroom is mediated through the inhibition of NF-κB and AP-1 signaling
    Jedinak, Andrej
    Dudhgaonkar, Shailesh
    Wu, Qing-li
    Simon, James
    Sliva, Daniel
    [J]. NUTRITION JOURNAL, 2011, 10
  • [10] Animal Models of Atopic Dermatitis
    Jin, Haoli
    He, Rui
    Oyoshi, Michiko
    Geha, Raif S.
    [J]. JOURNAL OF INVESTIGATIVE DERMATOLOGY, 2009, 129 (01) : 31 - 40