Protective effect of florfenicol on acute lung injury induced by lipopolysaccharide in mice

被引:89
作者
Zhang, Xuemei [1 ,2 ]
Song, Keji [1 ]
Xiong, Huanzhang [2 ]
Li, Hongyu [1 ]
Chu, Xiao [1 ]
Deng, Xuming [1 ]
机构
[1] Jilin Univ, Coll Anim Sci & Vet Med, Dept Vet Pharmacol, Changchun 130062, Jilin, Peoples R China
[2] Yanbian Univ, Coll Agr, Dept Anim Med, Longjing 133400, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
Florfenicol; LPS; Acute lung injury; RESPIRATORY-DISTRESS-SYNDROME; BOVINE; EFFICACY; INFLAMMATION; ENDOTOXIN; RESPONSES;
D O I
10.1016/j.intimp.2009.09.007
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Florfenicol, an antibiotic used to treat infection, has previously been shown to modulate early cytokine responses and increase mouse survival in endotoxemia. In the present study, we investigated in vivo the effect of florfenicol on acute lung injury (ALI) induced by lipopolysaccharide (LIPS). In the mouse model of LPS-induced inflammatory lung injury, we found that pretreatment with a single 100 mg/kg dose of florfenicol significantly decreases the W/D ratio of lungs and protein concentration in the bronchoalveolar lavage fluid (BALF) and significantly reduces the number of total cells, neutrophils and macrophages in the BALF at 24 h after LPS challenge. In addition, histopathological examination indicates that florfenicol significantly attenuates tissue injury of the lungs in LPS-induced ALI. Furthermore, florfenicol also inhibits the production of several inflammatory cytokines, including tumor necrosis factor-alpha (TNF-alpha) at 6 and 12 h. interleukin-6 (IL-6) at 12 and 24 h, and interleukin-1 beta (IL-1 beta) at 12 h, in the BALF after LIPS challenge. These results suggest that florfenicol protects against LPS-induced ALI in mice. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:1525 / 1529
页数:5
相关论文
共 25 条
[1]   Neutrophils and acute lung injury [J].
Abraham, E .
CRITICAL CARE MEDICINE, 2003, 31 (04) :S195-S199
[2]   Efficacy of florfenicol for treatment of naturally occurring infectious bovine keratoconjunctivitis [J].
Angelos, JA ;
Dueger, EL ;
George, LW ;
Carrier, TK ;
Mihalyi, JE ;
Cosgrove, SB ;
Johnson, JC .
JOURNAL OF THE AMERICAN VETERINARY MEDICAL ASSOCIATION, 2000, 216 (01) :62-64
[3]   Clinical efficacy of florfenicol in the treatment of calf respiratory tract infections [J].
Aslan, V ;
Maden, M ;
Erganis, O ;
Birdane, FM ;
Corlu, M .
VETERINARY QUARTERLY, 2002, 24 (01) :35-39
[4]   AN INVIVO HAMSTER BIOASSAY TO ASSESS THE TOXICITY OF PARTICULATES FOR THE LUNGS [J].
BECK, BD ;
BRAIN, JD ;
BOHANNON, DE .
TOXICOLOGY AND APPLIED PHARMACOLOGY, 1982, 66 (01) :9-29
[5]   Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome [J].
Bhatia, M ;
Moochhala, S .
JOURNAL OF PATHOLOGY, 2004, 202 (02) :145-156
[6]   Acute respiratory distress syndrome: update on the latest developments in basic and clinical research [J].
Bosma, Karen ;
Fanelli, Vito ;
Ranieri, V. Marco .
CURRENT OPINION IN ANESTHESIOLOGY, 2005, 18 (02) :137-145
[7]  
Cepkova Magda, 2006, J Intensive Care Med, V21, P119, DOI 10.1177/0885066606287045
[8]   Transcriptional mechanisms of acute lung injury [J].
Fan, J ;
Ye, RD ;
Malik, AB .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 2001, 281 (05) :L1037-L1050
[9]   Local stimulation of α7 cholinergic receptors inhibits LPS-induced TNF-α release in the mouse lung [J].
Giebelen, Ida A. J. ;
van Westerloo, David J. ;
LaRosa, Gregory J. ;
de Vos, Alex F. ;
van der Poll, Tom .
SHOCK, 2007, 28 (06) :700-703
[10]   Cytokine-mediated inflammation in acute lung injury [J].
Goodman, RB ;
Pugin, J ;
Lee, JS ;
Matthay, MA .
CYTOKINE & GROWTH FACTOR REVIEWS, 2003, 14 (06) :523-535