Paeoniflorin attenuates allergic inflammation in asthmatic mice

被引:22
作者
Sun, Jing [1 ]
Wu, Jinfeng [2 ]
Xu, Changqing [3 ]
Luo, Qingli [1 ]
Li, Bei [1 ]
Dong, Jingcheng [1 ]
机构
[1] Fudan Univ, Huashan Hosp, Dept Integrat Med, Shanghai 200040, Peoples R China
[2] Fudan Univ, Huashan Hosp, Dept Dermatol, Shanghai 200040, Peoples R China
[3] Hangzhou Normal Univ, Affiliated Hosp, Dept Respirat, Hangzhou 310015, Zhejiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Paeoniflorin; Asthma; IL-5; IL-13; IL-17; MAPK; PROTEIN-KINASE PATHWAYS; AIRWAY HYPERRESPONSIVENESS; TARGETING EOSINOPHILS; PAEONIA-LACTIFLORA; CHINESE HERBS; DISEASE; IL-13; LUNG; CYTOKINE;
D O I
10.1016/j.intimp.2014.11.016
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Paeoniflorin (PF), one of the major active ingredients of Chinese peony, has demonstrated anti-inflammatory and immunoregulatory effects. However, it has remained unclear whether PF treatment can inhibit allergic inflammation in asthma. In this study, we evaluated the effects of PF on pulmonary function and airway inflammation in asthmatic mice. The allergic asthma models were established in BALB/c mice. The mice were sensitized and challenged with ovalbumin. Airway hyperresponsiveness was detected by direct airway resistance analysis. Lung tissues were examined for inflammatory cell infiltration. IL-5, IL-13, IL-17, and eotaxin in bronchoalveolar lavage fluid (BALF) and their mRNA expression in lung tissue were examined by ELISA and realtime PCR, respectively. The total IgE level in serum was measured by ELISA. The protein expression of p-ERK and p-JNK was detected by western blot. Our data showed that PF oral administration significantly reduced airway hyperresponsiveness to aerosolized methacholine and decreased IL-5, IL-13, IL-17 and eotaxin levels in the BALF, and decreased IgE level in the serum. Histological studies showed that PF administration markedly decreased inflammatory infiltration. Similarly, treatment with PF significantly inhibited IL-5, IL-13, IL-17 and eotaxin mRNA expression in lung tissues. The protein expression levels of p-ERK and p-JNK were substantially decreased after oral administration of PF. In summary, PF displayed anti-inflammatory effects in the OVA-induced asthmatic model by decreasing the expression of IL-5, IL-13, IL-17 and eotaxin. These effects were mediated at least partially by inhibiting the activation of MAPK pathway. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:88 / 94
页数:7
相关论文
共 35 条
[1]
Temporal correlation of measurements of airway hyperresponsiveness in ovalbumin-sensitized mice [J].
Albertine, KH ;
Wang, L ;
Watanabe, S ;
Marathe, GK ;
Zimmerman, GA ;
McIntyre, TM .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2002, 283 (01) :L219-L233
[2]
Pathophysiology of allergic inflammation [J].
Barnes, Peter J. .
IMMUNOLOGICAL REVIEWS, 2011, 242 :31-50
[3]
Bergeron Celine, 2009, Proc Am Thorac Soc, V6, P301, DOI 10.1513/pats.200808-089RM
[4]
Complementary and alternative interventions in asthma, allergy, and immunology [J].
Bielory, L .
ANNALS OF ALLERGY ASTHMA & IMMUNOLOGY, 2004, 93 (02) :S45-S54
[5]
Treatment of allergic inflammation and hyperresponsiveness by a simple compound, Bavachinin, isolated from Chinese herbs [J].
Chen, Xi ;
Wen, Ti ;
Wei, Jun ;
Wu, Zhenzhou ;
Wang, Puyue ;
Hong, Zhangyong ;
Zhao, Liqing ;
Wang, Bin ;
Flavell, Richard ;
Gao, Shumei ;
Wang, Min ;
Yin, Zhinan .
CELLULAR & MOLECULAR IMMUNOLOGY, 2013, 10 (06) :497-505
[6]
p38 Mitogen-Activated Protein Kinase Pathways in Asthma and COPD [J].
Chung, Kian Fan .
CHEST, 2011, 139 (06) :1470-1479
[7]
Eotaxin and the attraction of eosinophils to the asthmatic lung [J].
Conroy, DM ;
Williams, TJ .
RESPIRATORY RESEARCH, 2001, 2 (03) :150-156
[8]
Corren J, 2012, DISCOV MED, V13, P305
[9]
Targeting mitogen-activated protein kinases for asthma [J].
Duan, Wei ;
Wong, W. S. Fred .
CURRENT DRUG TARGETS, 2006, 7 (06) :691-698
[10]
Anti-IL-5 treatment reduces deposition of ECM proteins in the bronchial subepithelial basement membrane of mild atopic asthmatics [J].
Flood-Page, P ;
Menzies-Gow, A ;
Phipps, S ;
Ying, S ;
Wangoo, A ;
Ludwig, MS ;
Barnes, N ;
Robinson, D ;
Kay, AB .
JOURNAL OF CLINICAL INVESTIGATION, 2003, 112 (07) :1029-1036