Olprinone decreases elevated concentrations of cytokine-induced neutrophil chemoattractant-1 in septic rats

被引:10
作者
Miyakawa, Hiroshi [1 ]
Kira, Shinichiro [1 ]
Okuda, Kentaro [1 ]
Takeshima, Naozumi [1 ]
Mori, Masakazu [1 ]
Noguchi, Takayuki [1 ]
机构
[1] Oita Univ, Dept Anesthesiol, Fac Med, Oita 8795593, Japan
关键词
abdominal sepsis; cytokine-induced neutrophil chemoattractant-1; phosphodiesterase inhibitor;
D O I
10.1007/s00540-007-0572-4
中图分类号
R614 [麻醉学];
学科分类号
100217 [麻醉学];
摘要
Purpose. The diaphragm is one of the organs directly affected by abdominal sepsis. Evidence suggests that sepsis induces diaphragmatic fatigability and that activated neutrophils play a crucial role in the development of diaphragmatic fatigability. In the present study, we investigated whether olprinone, a phosphodiesterase inhibitor, influenced the kinetics of cytokine-induced neutrophil chemoattractant-1 (CINC-1) in the diaphragm under abdominal septic conditions. Methods. Male Wistar rats were randomly assigned to a sham group, a cecal ligation and perforation group, and a phosphodiesterase inhibitor-pretreated group. To measure serial changes in CINC-1 concentrations, the right hemidiaphragm was removed at 4, 8, and 16 h after the surgical procedure in each group. Result. In the cecal ligation and perforation group, CINC-1 concentrations in the diaphragm were significantly elevated compared with those in the sham group at both 4 and 8 h after the cecal ligation and perforation procedure. In the phosphodiesterase inhibitor-pretreated group, olprinone significantly attenuated the elevated CINC-1 concentrations at both 4 and 8 h after the surgical procedure. However, we observed no statistically significant differences in CINC-1 concentrations between the cecal ligation and perforation group and the phosphodiesterase inhibitor-pretreated groups at 16 h after the surgical procedure. Conclusion. Olprinone decreases elevated CINC-1 concentration in the diaphragm under septic conditions. This suggests that olprinone may inhibit neutrophil recruitment to the diaphragm.
引用
收藏
页码:27 / 31
页数:5
相关论文
共 23 条
[1]
Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care [J].
Angus, DC ;
Linde-Zwirble, WT ;
Lidicker, J ;
Clermont, G ;
Carcillo, J ;
Pinsky, MR .
CRITICAL CARE MEDICINE, 2001, 29 (07) :1303-1310
[2]
BAKER RA, 2004, DIS MON, V50, P168
[3]
CINC-1 is identified as an acute-phase protein induced by focal brain injury causing leukocyte mobilization and liver injury [J].
Campbell, SJ ;
Hughes, PM ;
Iredale, JP ;
Wilcockson, DC ;
Waters, S ;
Docagne, F ;
Perry, VH ;
Anthony, DC .
FASEB JOURNAL, 2003, 17 (06) :1168-+
[4]
CHANANI NK, 2002, CIRCULATION S1, V106, P284
[5]
Phosphodiesterase inhibition decreases nuclear factor-κB activation and shifts the cytokine response toward anti-inflammatory activity in acute endotoxemia [J].
Coimbra, R ;
Melbostad, H ;
Loomis, W ;
Tobar, M ;
Hoyt, DB .
JOURNAL OF TRAUMA-INJURY INFECTION AND CRITICAL CARE, 2005, 59 (03) :575-582
[6]
Mitochondrial dysfunction in septic shock and multiple organ dysfunction syndrome [J].
Crouser, ED .
MITOCHONDRION, 2004, 4 (5-6) :729-741
[7]
Impact of IL-10 on diaphragmatic cytokine expression and contractility during Pseudomonas infection [J].
Divangahi, Maziar ;
Demoule, Alexandre ;
Danialou, Gawiyou ;
Yahiaoui, Linda ;
Bao, Weisheng ;
Xing, Zhou ;
Petrof, Basil J. .
AMERICAN JOURNAL OF RESPIRATORY CELL AND MOLECULAR BIOLOGY, 2007, 36 (04) :504-512
[8]
Effect of free radical scavengers on diaphragmatic contractility in septic peritonitis [J].
Fujimura, N ;
Sumita, S ;
Aimono, M ;
Masuda, Y ;
Shichinohe, Y ;
Narimatsu, E ;
Namiki, A .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2000, 162 (06) :2159-2165
[9]
Alteration in diaphragmatic contractility during septic peritonitis in rats: Effect of polyethylene glycol-absorbed superoxide dismutase [J].
Fujimura, N ;
Sumita, S ;
Narimatsu, E .
CRITICAL CARE MEDICINE, 2000, 28 (07) :2406-2414
[10]
Incidence of acute lung injury in the United States [J].
Goss, CH ;
Brower, RG ;
Hudson, LD ;
Rubenfeld, GD .
CRITICAL CARE MEDICINE, 2003, 31 (06) :1607-1611