Colon ascendens stent peritonitis -: A model of sepsis adopted to the rat:: Physiological, microcirculatory and laboratory changes

被引:70
作者
Lustig, Martina Katja
Bac, Vo Hoai
Pavlovic, Dragan
Maier, Stefan
Gruendling, Matthias
Grisk, Olaf
Wendt, Michael
Heidecke, Claus-Dieter
Lehmann, Christian
机构
[1] Univ Greifswald, Chirurg Klin, Greifswald, Germany
[2] Univ Greifswald, Klin Anasthesiol & Intens Med, Greifswald, Germany
[3] Univ Greifswald, Inst Physiol, Greifswald, Germany
来源
SHOCK | 2007年 / 28卷 / 01期
关键词
peritonitis; sepsis; intravital microscopy; microcirculation; cytokines;
D O I
10.1097/SHK.0b013e31802e454f
中图分类号
R4 [临床医学];
学科分类号
1002 [临床医学]; 100602 [中西医结合临床];
摘要
The colon ascenclens stent peritonitis (CASP) procedure creates an intestinal leakage of feces, resulting in diffuse peritonitis and polymicrobial sepsis. Mouse models of CASP have been used to study sepsis experimentally. The aim of the present study was to establish CASP sepsis in rats and to provide basic functional characteristics of this model. In analogy to the mouse model, 3 degrees of severity of CASP sepsis, 2 sublethal and 1 lethal, were established depending on the stent diameter. Radio-telemetric recordings in a sublethal model showed that the nonsurvivors remained hemodynamically stable until approximately 1 h before death, when heart rate and blood pressure fell rapidly. Intestinal microcirculatory changes were analyzed 3, 6, 12, and 18 h after CASP surgery using intravital microscopy in a sublethal model. After 18 h, the numbers of the leukocytes firmly adhering to the endothelium and of the ones temporarily interacting were significantly increased. The levels of IL-6 and IL-1 beta increased continuously during the CASP experiments while remaining unchanged in the sham group. TNF-alpha and IL-10 levels of CASP animals reached a maximum after 12 h. In conclusion, a rat model of CASP sepsis has been established and characterized with regard to alterations in cardiovascular and microcirculatory function as well as plasma cytokine levels. In experimental settings where genetically engineered animals are not required, it will facilitate detailed examination of dynamic changes in integrated organ function during the course of sepsis and the investigation of treatment strategies.
引用
收藏
页码:59 / 64
页数:6
相关论文
共 24 条
[1]
BARTELS H, 1991, KLIN WOCHENSCHR, V69, P53
[2]
PREPARATION OF RAT INTESTINAL MUSCLE AND MUCOSA FOR QUANTITATIVE MICROCIRCULATORY STUDIES [J].
BOHLEN, HG ;
GORE, RW .
MICROVASCULAR RESEARCH, 1976, 11 (01) :103-110
[3]
Intravenous glycine after cecal ligation and puncture has no effect on impaired hepatic microperfusion, leukocyte adhesion, and mortality in septic rats [J].
Croner, RS ;
Kulu, Y ;
Hoerer, E ;
Peters, V ;
Schmidt-Mader, B ;
Schemmer, P ;
Herfarth, C ;
Klar, E .
MICROVASCULAR RESEARCH, 2005, 69 (1-2) :71-78
[4]
Decreased capillary density in vivo in bowel mucosa of rats with normotensive sepsis [J].
Farquhar, I ;
Martin, CM ;
Lam, C ;
Potter, R ;
Ellis, CG ;
Sibbald, WJ .
JOURNAL OF SURGICAL RESEARCH, 1996, 61 (01) :190-196
[5]
IL-1 is an important mediator for microcirculatory changes in endotoxin-induced intestinal mucosal damage [J].
Fukumura, D ;
Miura, S ;
Kurose, I ;
Higuchi, H ;
Suzuki, H ;
Ebinuma, H ;
Han, JY ;
Watanabe, N ;
Wakabayashi, G ;
Kitajima, M ;
Ishii, H .
DIGESTIVE DISEASES AND SCIENCES, 1996, 41 (12) :2482-2492
[6]
Analysis of arterial pressure regulating systems in renal post-transplantation hypertension [J].
Grisk, O ;
Heukäufer, M ;
Steinbach, A ;
Gruska, S ;
Rettig, R .
JOURNAL OF HYPERTENSION, 2004, 22 (01) :199-207
[7]
Long-term arterial pressure in spontaneously hypertensive rats is set by the kidney [J].
Grisk, O ;
Klöting, I ;
Exner, J ;
Spiess, S ;
Schmidt, R ;
Junghans, D ;
Lorenz, G ;
Rettig, R .
JOURNAL OF HYPERTENSION, 2002, 20 (01) :131-138
[8]
Evaluation of protein C and other biomarkers as predictors of mortality in a rat cecal ligation and puncture model of sepsis [J].
Heuer, JG ;
Sharma, GR ;
Gerlitz, B ;
Zhang, TH ;
Bailey, DL ;
Ding, CJ ;
Berg, DT ;
Perkins, D ;
Stephens, EJ ;
Holmes, KC ;
Grubbs, RL ;
Fynboe, KA ;
Chen, YF ;
Grinnell, B ;
Jakubowski, JA .
CRITICAL CARE MEDICINE, 2004, 32 (07) :1570-1578
[9]
Cecal ligation and puncture [J].
Hubbard, WJ ;
Choudhry, M ;
Schwacha, MG ;
Kerby, JD ;
Rue, LW ;
Bland, KI ;
Chaudry, IH .
SHOCK, 2005, 24 :52-57
[10]
Cecal ligation and puncture versus colon ascendens stent peritonitis:: Two distinct animal models for polymicrobial sepsis [J].
Maier, S ;
Traeger, T ;
Entleutner, M ;
Westerholt, A ;
Kleist, B ;
Hüser, N ;
Holzmann, B ;
Stier, A ;
Pfeffer, K ;
Heidecke, CD .
SHOCK, 2004, 21 (06) :505-511