Prime-O-glucosylcimifugin attenuates lipopolysaccharide-induced acute lung injury in mice

被引:54
作者
Chen, Na [1 ]
Wu, Qianchao [1 ]
Chi, Gefu [2 ]
Soromou, Lanan Wassy [3 ]
Hou, Jinli [4 ]
Deng, Yanhong [1 ]
Feng, Haihua [1 ]
机构
[1] Jilin Univ, Coll Anim Sci & Vet Med, Changchun 130062, Peoples R China
[2] Inner Mongolia Univ Nationalities, Affiliated Hosp, Dept Outpatient Clin, Tongliao 028000, Peoples R China
[3] Inst Super Sci & Med Vet ISSMV Dalaba, Dept Vet Med, Dalaba, Guinea
[4] Jilin Univ, Inst Zoonosis, Minist Educ, Key Lab Zoonosis, Changchun 130062, Peoples R China
基金
中国博士后科学基金;
关键词
Prime-O-glucosylcimifugin; Lipopolysaccharide; Acute lung injury; NITRIC-OXIDE SYNTHASE; TUMOR-NECROSIS-FACTOR; CYTOKINES; INSIGHTS; RELEASE; CELLS; BRONCHOALVEOLAR; IDENTIFICATION; APOPTOSIS; PATHOLOGY;
D O I
10.1016/j.intimp.2013.04.014
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Prime-O-glucosylcimifugin is an active chromone isolated from Saposhnikovia root which has been reported to have various activities, such as anti-convulsant, anticancer, anti-inflammatory properties. The purpose of this study was to evaluate the effect of prime-O-glucosylcimifugin on acute lung injury (ALI) induced by lipopolysaccharide in mice. BALB/c mice received intraperitoneal injection of Prime-O-glucosylcimifugin 1 h before intranasal instillation (i.n.) of lipopolysaccharide (LPS). Concentrations of tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta and interleukin (IL)-6 in bronchoalveolar lavage fluid (BALF) were measured by enzyme-linked immunosorbent assay (ELISA). Pulmonary histological changes were evaluated by hematoxylineosin, myeloperoxidase (MPO) activity in the lung tissue and lung wet/dry weight ratios were observed. Furthermore, the mitogen-activated protein kinases (MAPK) signaling pathway activation and the phosphorylation of I kappa B alpha protein were determined by Western blot analysis. Prime-O-glucosylcimifugin showed promising anti-inflammatory effect by inhibiting the activation of MAPK and NF-kappa B signaling pathway. (c) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:139 / 147
页数:9
相关论文
共 45 条
[1]   Neutrophils and acute lung injury [J].
Abraham, E .
CRITICAL CARE MEDICINE, 2003, 31 (04) :S195-S199
[2]  
BABA K, 1987, Shoyakugaku Zasshi, V41, P189
[3]   Suppression of proinflammatory cytokine production by specific metabolites of Lactobacillus plantarum 10hk2 via inhibiting NF-κB and p38 MAPK expressions [J].
Chon, Heeson ;
Choi, Byungryul ;
Jeong, Gajin ;
Lee, Eungyo ;
Lee, Seunghui .
COMPARATIVE IMMUNOLOGY MICROBIOLOGY AND INFECTIOUS DISEASES, 2010, 33 (06) :E41-E49
[4]   Ceftiofur attenuates lipopolysaccharide-induced acute lung injury [J].
Chu, Xiao ;
Song, Keji ;
Xu, Kan ;
Zhang, Xiaozhe ;
Zhang, Xuemei ;
Song, Yu ;
Wang, Dacheng ;
Liu, Songcai ;
Deng, Xuming .
INTERNATIONAL IMMUNOPHARMACOLOGY, 2010, 10 (05) :600-604
[5]   Different Effects of Farrerol on an OVA-Induced Allergic Asthma and LPS-induced Acute Lung Injury [J].
Ci, Xinxin ;
Chu, Xiao ;
Wei, Miaomiao ;
Yang, Xiaofeng ;
Cai, Qinren ;
Deng, Xuming .
PLOS ONE, 2012, 7 (04)
[6]  
Cochran FR, 1996, MED RES REV, V16, P547, DOI 10.1002/(SICI)1098-1128(199611)16:6<547::AID-MED3>3.3.CO
[7]  
2-W
[8]   Stem cells in sepsis and acute lung injury [J].
Cribbs, Sushma K. ;
Matthay, Michael A. ;
Martin, Greg S. .
CRITICAL CARE MEDICINE, 2010, 38 (12) :2379-2385
[9]   Therapeutic strategies for severe acute lung injury [J].
Diaz, Janet V. ;
Brower, Roy ;
Calfee, Carolyn S. ;
Matthay, Michael A. .
CRITICAL CARE MEDICINE, 2010, 38 (08) :1644-1650
[10]   Targeting mitogen-activated protein kinases for asthma [J].
Duan, Wei ;
Wong, W. S. Fred .
CURRENT DRUG TARGETS, 2006, 7 (06) :691-698