Ceftiofur attenuates lipopolysaccharide-induced acute lung injury

被引:28
作者
Chu, Xiao [1 ]
Song, Keji [2 ]
Xu, Kan [1 ]
Zhang, Xiaozhe [1 ]
Zhang, Xuemei [1 ]
Song, Yu [1 ]
Wang, Dacheng [1 ]
Liu, Songcai [1 ]
Deng, Xuming [1 ]
机构
[1] Jilin Univ, Dept Vet Pharmacol, Coll Anim Sci & Vet Med, Changchun 130062, Jilin, Peoples R China
[2] Heilongjiang Bayi Agr Univ, Dept Vet Pharmacol, Coll Anim Sci & Technol, Daqing 163319, Heilongjiang, Peoples R China
基金
中国国家自然科学基金;
关键词
Ceftiofur; Lipopolysaccharide (LPS); Acute lung injury (ALI); Cytokine; TNF-ALPHA; INTERLEUKIN-8; APOPTOSIS; CYTOKINES; EFFICACY; STRESS;
D O I
10.1016/j.intimp.2010.02.010
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Ceftiofur is a new broad-spectrum, third-generation cephalosporin antibiotic for veterinary use. Our laboratory has previously been reported that ceftiofur can modulate early cytokine responses and increase mouse survival in endotoxemia. In the present study, we investigated the effect of ceftiofur on acute lung injury (ALL) induced by lipopolysaccharide (LPS) in vivo. Mice were pretreated with ceftiofur 1 h before challenge with a dose of 0.5 mg/kg LPS. Mice treated with LPS alone showed marked increased TNF-alpha, IL-6, and IL-8 levels in the bronchoalveolar lavage fluid (BALF). When pretreated with 30 mg/kg of ceftiofur, the TNF-alpha, IL-6, and IL-8 levels were significantly decreased. In addition, the W/D ratio of the lung tissue and the number of total cells, neutrophils and macrophages in the BALF significantly decreased at 8 h after pretreatment with ceftiofur. Furthermore, ceftiofur markedly attenuated the LPS-induced histological alteration. These studies indicate that ceftiofur significantly decreases the inflammation in a murine model of LPS-mediated ALL and may represent a novel prevention strategy for nonspecific inflammation in the lungs. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:600 / 604
页数:5
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