Inhibitory effect of galangin on atopic dermatitis-like skin lesions

被引:61
作者
Choi, Jin Kyeong [1 ]
Kim, Sang-Hyun [1 ]
机构
[1] Kyungpook Natl Univ, Sch Med, Dept Pharmacol, BK21 Plus KNU Biomed Convergence Program, Taegu 700422, South Korea
基金
新加坡国家研究基金会;
关键词
Atopic dermatitis; Keratinocyte; Galangin; Mast cells; MEDIATED ALLERGIC INFLAMMATION; CONTACT-DERMATITIS; PROPOLIS EXTRACT; SUPPRESSES; INDUCTION; CELLS; ANTIHISTAMINES; KERATINOCYTES; ACTIVATION; MECHANISMS;
D O I
10.1016/j.fct.2014.03.021
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Galangin is a member of the flavonol class of flavonoids having anti-inflammatory and anti-oxidative potential. Previously we reported the inhibitory effect of galangin on the mast cell-mediated allergic inflammation. For incremental research, we investigated the effects of galangin on atopic dermatitis (AD)-like skin lesions and underlying mechanisms of action. We established an atopic dermatitis model in BALB/c mice by repeated local exposure of house dust mite (Dermatophagoides farinae) extract (DFE) and 2,4-dinitrochlorobenzene (DNCB) to the ears. Repeated alternative treatment of DFE/DNCB caused AD-like skin lesions. Topical application of galangin reduced AD symptoms based on ear thickness and histopathological analysis, in addition to serum IgE and IgG2a levels. Galangin inhibited mast cell infiltration into the ear and serum histamine level. Galangin suppressed DFE/DNCB-induced expression of interleukin (IL)-4, IL-5, IL-13, IL-31, IL-32, and interferon (IFN)-gamma in the ear tissue. To define the underlying mechanisms of action, tumor necrosis factor-alpha/IFN-gamma-activated human keratinocytes (HaCaT) model was used. Galangin significantly inhibited the expression of cytokines and chemokine by the down-regulation of nuclear factor-KB and mitogen-activated protein kinases in HaCaT cells. Taken together, the results demonstrate that galangin inhibited AD-like symptoms, suggesting that galangin might be a candidate for the treatment of AD. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:135 / 141
页数:7
相关论文
共 43 条
[1]   Mitogen-activated protein kinases [J].
Arbabi, S ;
Maier, RV .
CRITICAL CARE MEDICINE, 2002, 30 (01) :S74-S79
[2]   Chrysin suppresses mast cell-mediated allergic inflammation: Involvement of calcium, caspase-1 and nuclear factor-κB [J].
Bae, Yunju ;
Lee, Soyoung ;
Kim, Sang-Hyun .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2011, 254 (01) :56-64
[3]   Atopic Dermatitis [J].
Bieber, Thomas .
ANNALS OF DERMATOLOGY, 2010, 22 (02) :125-137
[4]   Phytochemical compounds involved in the anti-inflammatory effect of propolis extract [J].
Borrelli, F ;
Maffia, P ;
Pinto, L ;
Ianaro, A ;
Russo, A ;
Capasso, F ;
Ialenti, A .
FITOTERAPIA, 2002, 73 :S53-S63
[5]  
Brandt EB, 2011, J CLIN CELL IMMUNOL, V2
[6]   Suppression of dust mite extract and 2,4-dinitrochlorobenzene-induced atopic dermatitis by the water extract of Lindera obtusiloba [J].
Choi, Eun-Ju ;
Lee, Soyoung ;
Kim, Hui-Hun ;
Singh, Thoudam S. K. ;
Choi, Jin Kyeong ;
Choi, Hyun Gyu ;
Suh, Won Mo ;
Lee, Seung-Ho ;
Kim, Sang-Hyun .
JOURNAL OF ETHNOPHARMACOLOGY, 2011, 137 (01) :802-807
[7]   Oleanolic acid acetate inhibits atopic dermatitis and allergic contact dermatitis in a murine model [J].
Choi, Jin Kyeong ;
Oh, Hyun-Mee ;
Lee, Soyoung ;
Park, Jin-Woo ;
Khang, Dongwoo ;
Lee, Seung Woong ;
Lee, Woo Song ;
Rho, Mun-Chual ;
Kim, Sang-Hyun .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 2013, 269 (01) :72-80
[8]   Assessment of the antibacterial activity of galangin against 4-quinolone resistant strains of Staphylococcus aureus [J].
Cushnie, TPT ;
Lamb, A .
PHYTOMEDICINE, 2006, 13 (03) :187-191
[9]   Mite allergen is a danger signal for the skin via activation of inflammasome in keratinocytes [J].
Dai, Xiuju ;
Sayama, Koji ;
Tohyama, Mikiko ;
Shirakata, Yuji ;
Hanakawa, Yasushi ;
Tokumaru, Sho ;
Yang, Lujun ;
Hirakawa, Satoshi ;
Hashimoto, Koji .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2011, 127 (03) :806-U486
[10]   The immune system and atopic dermatitis [J].
Dokmeci, Elif ;
Herrick, Christina A. .
SEMINARS IN CUTANEOUS MEDICINE AND SURGERY, 2008, 27 (02) :138-143