Ceftiofur Regulates LPS-Induced Production of Cytokines and Improves LPS-Induced Survival Rate in Mice

被引:11
作者
Ci, Xinxin [1 ]
Li, Hongyu [1 ]
Song, Yu [1 ]
An, Na [1 ]
Yu, Qinlei [1 ]
Zeng, Fanqin [1 ]
Deng, Xuming [1 ]
机构
[1] Jilin Univ, Coll Anim Sci & Vet Med, Dept Vet Pharmacol, Changchun 130062, Jilin, Peoples R China
基金
中国国家自然科学基金;
关键词
ceftiofur; LPS; cytokines; survival rate; mice;
D O I
10.1007/s10753-008-9094-y
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The influence of ceftiofur on immune responses has been suggested by results of in vitro studies. This effect was studied using a murine model that measured mortality and early cytokine responses after challenge with endotoxin. To investigate the treatment of endotoxic mice with ceftiofur, mice were pretreated with ceftiofur at different times before and after challenge with a lethal dose of 30 mg/kg lipopolysaccharide (LPS). We found that 20 mg/kg ceftiofur had a significant protective effect and reduced the mortality of mice at early stages. To further understand the mechanism of action of ceftiofur, we examined plasma cytokine levels. Mice treated with LPS alone showed markedly increased plasma levels of TNF-alpha, IL-1 beta, IL-6 and IL-10, whereas mice pretreated with 20 mg/kg ceftiofur showed significantly decreased plasma levels of TNF-alpha, IL-1 beta and IL-6, but increased plasma levels of IL-10. These results support the idea that ceftiofur has a beneficial effect on LPS-induced endotoxemia caused by LPS through its modulation of cytokine levels. This confirms the effect of ceftiofur for the treatment of endotoxemia, which is caused by a Gram-negative bacterial infection.
引用
收藏
页码:422 / 427
页数:6
相关论文
共 20 条
[11]  
Karzai W, 1997, INT J CLIN PRACT, V51, P232
[12]  
Labro M. T., 1998, Journal of Antimicrobial Chemotherapy, V41, P37, DOI 10.1093/jac/41.suppl_2.37
[13]   ADJUNCTIVE THERAPY FOR SEPTIC SHOCK - A REVIEW OF EXPERIMENTAL APPROACHES [J].
LYNN, WA ;
COHEN, J .
CLINICAL INFECTIOUS DISEASES, 1995, 20 (01) :143-158
[14]  
MAHRT CR, 1992, AM J VET RES, V53, P2201
[15]   CEFODIZIME MODULATES IN-VITRO TUMOR-NECROSIS-FACTOR-ALPHA, INTERLEUKIN-6 AND INTERLEUKIN-8 RELEASE FROM HUMAN PERIPHERAL MONOCYTES [J].
MELONI, F ;
BALLABIO, P ;
BIANCHI, L ;
GRASSI, FA ;
GRASSI, GG .
CHEMOTHERAPY, 1995, 41 (04) :289-295
[16]   INTERLEUKIN-12, INTERFERON-GAMMA, AND TUMOR-NECROSIS-FACTOR-ALPHA ARE THE KEY CYTOKINES OF THE GENERALIZED SHWARTZMAN REACTION [J].
OZMEN, L ;
PERICIN, M ;
HAKIMI, J ;
CHIZZONITE, RA ;
WYSOCKA, M ;
TRINCHIERI, G ;
GATELY, M ;
GAROTTA, G .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (03) :907-915
[17]   SEPTIC SHOCK IN HUMANS - ADVANCES IN THE UNDERSTANDING OF PATHOGENESIS, CARDIOVASCULAR DYSFUNCTION, AND THERAPY [J].
PARRILLO, JE ;
PARKER, MM ;
NATANSON, C ;
SUFFREDINI, AF ;
DANNER, RL ;
CUNNION, RE ;
OGNIBENE, FP .
ANNALS OF INTERNAL MEDICINE, 1990, 113 (03) :227-242
[18]  
Rotimi VO, 2000, J CHEMOTHERAPY, V12, P40
[19]   The effects of macrolides on inflammatory cells [J].
Tamaoki, J .
CHEST, 2004, 125 (02) :41S-51S
[20]   ANTI-CACHECTIN TNF MONOCLONAL-ANTIBODIES PREVENT SEPTIC SHOCK DURING LETHAL BACTEREMIA [J].
TRACEY, KJ ;
FONG, Y ;
HESSE, DG ;
MANOGUE, KR ;
LEE, AT ;
KUO, GC ;
LOWRY, SF ;
CERAMI, A .
NATURE, 1987, 330 (6149) :662-664