Sickness behavior of rats with abdominal sepsis can be improved by antibiotic and G-CSF prophylaxis in clinic modeling randomized trials

被引:12
作者
Bauhofer, A
Schwarting, RKW
Köster, M
Schmitt, A
Lorenz, W
Pawlak, CR
机构
[1] Univ Marburg, Inst Theoret Surg, D-35033 Marburg, Germany
[2] Univ Marburg, D-35032 Marburg, Germany
关键词
sickness behavior; social interaction; open field; elevated plus-maze; quality of life; granulocyte-colony stimulating factor (G-CSF); sepsis; clinic modeling randomized trial (CMRT);
D O I
10.1007/s00011-004-1314-9
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Background and aim: In clinical sepsis research nearly all immune-modulators have demonstrated no benefit in regard to the 28-day mortality rate. Other endpoints such as quality of life have become more attractive, but clinically relevant animal models analyzing an equivalent to quality of life by measurement of sickness behavior are extremely rare. The concept of clinic modeling randomized trials was used in an animal trial to model clinical complexity and conditions of a randomized clinical trial. Methods: 80 adult male Wistar rats were randomly assigned to (1) control: anesthesia and sham operation, (2) sepsis: laparotomy and peritoneal infection with human stool bacteria, (3) sepsis with antibiotic prophylaxis: cefuroxime/metronidazole and (4) sepsis with antibiotic plus a cytokine prophylaxis with granulocyte-colony stimulating factor (G-CSF). Endpoints were physiological and behavioral parameters. Results: The combination of antibiotics plus G-CSF was most effective in reducing mortality. All infected animals showed reduced open field activity acutely after infection, and recovery was improved during the 9 day follow-up in rats with prophylactic treatments. In the social interaction test, but not in the elevated plus-maze anxiety test, prophylaxis was also efficient, especially with antibiotics and G-CSE Conclusions: The results show that improving sickness behavior in septic rats with G-CSF plus antibiotics may be a promising approach.
引用
收藏
页码:697 / 705
页数:9
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