Evaluation of lung injury and respiratory mechanics in a rat model of acute pancreatitis complicated with endotoxin

被引:30
作者
Elder, Alison S. F. [1 ]
Saccone, Gino T. P. [2 ]
Bersten, Andrew D. [1 ]
Dixon, Dani-Louise [1 ]
机构
[1] Flinders Univ S Australia, Dept Crit Care Med, Adelaide, SA 5001, Australia
[2] Flinders Univ S Australia, Flinders Med Ctr, Adelaide, SA 5001, Australia
关键词
Acute lung injury; Ventilation; Pancreatitis; Endotoxin; GLYCATION END-PRODUCTS; NEUTROPHIL CHEMOATTRACTANT CINC; CERULEIN-INDUCED PANCREATITIS; INFLAMMATORY MEDIATORS; SOLUBLE RECEPTOR; LIPOPOLYSACCHARIDE; EXPRESSION; FAILURE; PATHOPHYSIOLOGY; PATHOGENESIS;
D O I
10.1016/j.pan.2012.03.001
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
Background: Acute lung injury (ALI) is a common complication of acute pancreatitis (AP) and contributes to the majority of AP-associated deaths, particularly in the setting of secondary infection. This 'two-hit' model mimics clinical cases where the presentation of AP is associated with mild lung injury that, following a secondary direct lung infection, can result in respiratory dysfunction and death. We therefore aimed to characterize lung injury in a clinically-relevant 'two-hit' rat model of caerulein-induced AP combined with intratracheal endotoxin. Methods: Rats received 7 hourly intraperitoneal injections of caerulein (50 mu g/kg). Twenty four hours following the first caerulein injection, rats were anaesthetised and LPS (15 mg/kg) was instilled intratracheally. Following LPS instillation, rats were ventilated for a total of 2 h. Results: In the present study, AP results in mild pulmonary injury indicated by increased lung myeloperoxidase (MPO) activity and edema, but with no alteration of respiratory function, while intratracheal instillation of LPS results in more substantial pulmonary injury. The induction of AP challenged with secondary intratracheal LPS results in an exacerbation of lung damage indicated by further increased lung edema, plasma and bronchoalveolar (BAL) CINC-1 concentration, lung damage histology score, and lung tissue resistance and elastance, compared with LPS alone. Conclusions: In conclusion, the addition of instilled LPS acted as a "second-hit" and exacerbated caerulein-induced AP, compared with the induction of AP alone or the instillation of LPS alone. Given its clinical relevance, this model could prove useful for examination of therapeutic interventions for ALI following secondary infection. Copyright (C) 2012, LAP and EPC. Published by Elsevier India, a division of Reed Elsevier India Pvt. Ltd. All rights reserved.
引用
收藏
页码:240 / 247
页数:8
相关论文
共 49 条
[1]
EFFECT OF N-ACETYLCYSTEINE ON THE PULMONARY RESPONSE TO ENDOTOXIN IN THE AWAKE SHEEP AND UPON INVITRO GRANULOCYTE FUNCTION [J].
BERNARD, GR ;
LUCHT, WD ;
NIEDERMEYER, ME ;
SNAPPER, JR ;
OGLETREE, ML ;
BRIGHAM, KL .
JOURNAL OF CLINICAL INVESTIGATION, 1984, 73 (06) :1772-1784
[2]
Bhatia M, 2000, J PATHOL, V190, P117
[3]
Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome [J].
Bhatia, M ;
Moochhala, S .
JOURNAL OF PATHOLOGY, 2004, 202 (02) :145-156
[4]
Treatment with neutralising antibody against cytokine induced neutrophil chemoattractant (CINC) protects rats against acute pancreatitis associated lung injury [J].
Bhatia, M ;
Brady, M ;
Zagorski, J ;
Christmas, SE ;
Campbell, F ;
Neoptolemos, JP ;
Slavin, J .
GUT, 2000, 47 (06) :838-844
[5]
Pathophysiology of pulmonary complications of acute pancreatitis [J].
Browne, George W. ;
Pitchumoni, C. S. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2006, 12 (44) :7087-7096
[6]
Plasma receptor for advanced glycation end products and clinical outcomes in acute lung injury [J].
Calfee, C. S. ;
Ware, L. B. ;
Eisner, M. D. ;
Parsons, P. E. ;
Thompson, B. T. ;
Wickersham, N. ;
Matthay, M. A. .
THORAX, 2008, 63 (12) :1083-1089
[7]
Blockade of interleukin 6 accelerates acinar cell apoptosis and attenuates experimental acute pancreatitis in vivo [J].
Chao, KC ;
Chao, KF ;
Chuang, CC ;
Liu, SH .
BRITISH JOURNAL OF SURGERY, 2006, 93 (03) :332-338
[8]
Chen YP, 2009, HEPATOB PANCREAT DIS, V8, P535
[9]
Acute pancreatitis and bacterial translocation [J].
Cicalese, L ;
Sahai, A ;
Sileri, P ;
Rastellini, C ;
Subbotin, V ;
Ford, H ;
Lee, K .
DIGESTIVE DISEASES AND SCIENCES, 2001, 46 (05) :1127-1132
[10]
Endotoxin induces respiratory failure and increases surfactant turnover and respiration independent of alveolocapillary injury in rats [J].
Davidson, KG ;
Bersten, AD ;
Barr, HA ;
Dowling, KD ;
Nicholas, TE ;
Doyle, IR .
AMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2002, 165 (11) :1516-1525