NEMO-Binding Domain Peptide Attenuates Lipopolysaccharide-Induced Acute Lung Injury by Inhibiting the NF-κB Signaling Pathway

被引:23
作者
Huang, Jianhua [1 ,2 ]
Li, Li [1 ]
Yuan, Weifeng [1 ]
Zheng, Linxin [1 ]
Guo, Zhenhui [3 ,4 ]
Huang, Wenjie [1 ,4 ]
机构
[1] Gen Hosp Guangzhou Mil Command PLA, Dept Resp Med, Guangzhou, Guangdong, Peoples R China
[2] Chenzhou 1 Peoples Hosp, Dept Pulm Med, Chenzhou, Hunan, Peoples R China
[3] Gen Hosp Guangzhou Mil Command PLA, Dept Med Intens Care Unit, Guangzhou, Guangdong, Peoples R China
[4] Guangdong Prov Key Lab Geriatr Infect & Organ Fun, Guangzhou, Guangdong, Peoples R China
关键词
ALVEOLAR-CAPILLARY BARRIER; INNATE IMMUNITY; INVOLVEMENT; CHEMOKINES; ACTIVATION; OUTCOMES; MODEL; MAPK;
D O I
10.1155/2016/7349603
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The aim of the present study is to investigate the protective effects and relevant mechanisms exerted by NEMO-binding domain peptide (NBD) against lipopolysaccharide- (LPS-) induced acute lung injury (ALI) in mice. The ALI model was induced by intratracheally administered atomized LPS (5 mg/kg) to BABL/c mice. Half an hour before LPS administration, we treated the mice with increasing concentrations of intratracheally administered NBD or saline aerosol. Two hours after LPS administration, each group of mice was sacrificed. We observed that NBD pretreatment significantly attenuated LPS-induced lung histopathological injury in a dose-dependent manner. Western blotting established that NBD pretreatment obviously attenuated LPS-induced I kappa B-alpha and NF-kappa Bp65 activation and NOX1, NOX2, and NOX4 overexpression. Furthermore, NBD pretreatment increased SOD and T-AOC activity and decreased MDA levels in lung tissue. In addition, NBD also inhibited TNF-alpha and IL-1 beta secretion in BALF after LPS challenge. In conclusion, NBD protects against LPS-induced ALI in mice.
引用
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页数:11
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共 37 条
[11]   Regulation of NF-κB by TNF family cytokines [J].
Hayden, Matthew S. ;
Ghosh, Sankar .
SEMINARS IN IMMUNOLOGY, 2014, 26 (03) :253-266
[12]   Oxygen free radical involvement in acute lung injury induced by H5N1 virus in mice [J].
He, Guimei ;
Dong, Changgui ;
Luan, Zhihua ;
McAllan, Bronwyn M. ;
Xu, Tong ;
Zhao, Lihong ;
Qiao, Jian .
INFLUENZA AND OTHER RESPIRATORY VIRUSES, 2013, 7 (06) :945-953
[13]   Novel concepts of acute lung injury and alveolar-capillary barrier dysfunction [J].
Herold, Susanne ;
Gabrielli, Nieves M. ;
Vadasz, Istvan .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2013, 305 (10) :L665-L681
[14]   Protective effects of luteolin against lipopolysaccharide-induced acute lung injury involves inhibition of MEK/ERK and PI3K/Akt pathways in neutrophils [J].
Lee, Jen-pei ;
Li, Yi-ching ;
Chen, Hung-yi ;
Lin, Ruey-hseng ;
Huang, Shiang-suo ;
Chen, Hui-ling ;
Kuan, Pai-chuan ;
Liao, Mao-fang ;
Chen, Chun-jung ;
Kuan, Yu-hsiang .
ACTA PHARMACOLOGICA SINICA, 2010, 31 (07) :831-838
[15]  
Liu C., 2016, SCI REPORTS, V6
[16]   P38MAPK inhibition attenuates LPS-induced acute lung injury involvement of NF-κB pathway [J].
Liu, Su ;
Feng, Guang ;
Wang, Guang-lei ;
Liu, Gong-jian .
EUROPEAN JOURNAL OF PHARMACOLOGY, 2008, 584 (01) :159-165
[17]   Isovitexin Exerts Anti-Inflammatory and Anti-Oxidant Activities on Lipopolysaccharide-Induced Acute Lung Injury by Inhibiting MAPK and NF-κB and Activating HO-1/Nrf2 Pathways [J].
Lv, Hongming ;
Yu, Zhenxiang ;
Zheng, Yuwei ;
Wang, Lidong ;
Qin, Xiaofeng ;
Cheng, Genhong ;
Ci, Xinxin .
INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2016, 12 (01) :72-86
[18]   The acute respiratory distress syndrome [J].
Matthay, Michael A. ;
Ware, Lorraine B. ;
Zimmerman, Guy A. .
JOURNAL OF CLINICAL INVESTIGATION, 2012, 122 (08) :2731-2740
[19]   Animal models of acute lung injury [J].
Matute-Bello, Gustavo ;
Frevert, Charles W. ;
Martin, Thomas R. .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2008, 295 (03) :L379-L399
[20]   Selective inhibition of NF-κB activation by a peptide that blocks the interaction of NEMO with the IκB kinase complex [J].
May, MJ ;
D'Acquisto, F ;
Madge, LA ;
Glöckner, J ;
Pober, JS ;
Ghosh, S .
SCIENCE, 2000, 289 (5484) :1550-1554