Basidiomycetes-X, an edible mushroom, alleviates the development of atopic dermatitis in NC/Nga mouse model

被引:3
|
作者
Watanabe, Kenichi [1 ,2 ]
Karuppagounder, Vengadeshprabhu [2 ,3 ]
Sreedhar, Remya [2 ]
Kandasamy, Geetha [4 ]
Harima, Meilei [2 ,5 ]
Velayutham, Ravichandiran [6 ]
Arumugam, Somasundaram [2 ,6 ]
机构
[1] Niigata Univ, Sch Med & Dent Sci, Dept Lab Med & Clin Epidemiol Prevent Noncommunic, Chuo Ku, 757 Ichibancho, Niigata 9518510, Japan
[2] Niigata Univ Pharm & Appl Life Sci, Fac Pharmaceut Sci, Dept Clin Pharmacol, Akiha Ku, 265-1 Higashijima, Niigata 9568603, Japan
[3] Penn State Coll Med, Dept Orthoped & Rehabil, 500 Univ Dr, Hershey, PA 17033 USA
[4] King Khalid Univ, Coll Pharm, Dept Clin Pharm, Abha, Saudi Arabia
[5] Niigata Univ Rehabil, Fac Allied Hlth Sci, 2-16 Kaminoyama, Niigata 9580053, Japan
[6] Natl Inst Pharmaceut Educ & Res, 168 Manicktala Main Rd, Kolkata 700054, W Bengal, India
关键词
Basidiomycetes-X; Tumor necrosis factor; Cytokine; Atopic dermatitis; Inflammation; Interferon; SKIN INFLAMMATION; EXTRACT; PATHWAY; MICE;
D O I
10.1016/j.yexmp.2018.10.005
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Basidiomycetes-X (BDM-X) is a novel edible mushroom recently identified as a new fungi species and is effective against oxidative stress and anti-inflammation associated with immune response. However the effect of BDM-X on atopic dermatitis (AD) has not been elucidated. In this study, we have investigated the effect of BDM-X on AD skin lesions in NC/Nga mouse model. AD-like lesion was induced by the application of house dust mite extract (DfE) to the dorsal skin of NC/Nga mouse. After AD induction, BDM-X was administered once daily for 2 weeks. We have analyzed the effects of BDM-X on dermatitis severity, histopathological changes and changes in inflammatory and proinflammatory proteins expressions in DfE induced AD mice skin. Treatment with BDM-X attenuated the development of AD-like clinical symptoms and effectively inhibited hyperkeratosis, parakeratosis, acanthosis and mast cells in AD mice skin. Furthermore, BDM-X treatment inhibited DIE induced tumor necrosis factor (TNF)alpha, high mobility group protein (HMG)B1, nuclear factor kappa (NF kappa)B and inflammatory cytokines. These results indicate that BDM-X inhibits AD through modulating nil and Th2 responses and diminishing the mast cells infiltration in the skin lesions in NC/Nga mice.
引用
收藏
页码:322 / 327
页数:6
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