CO2 abdominal insufflation decreases local and systemic inflammatory response in experimental acute pancreatitis

Pancreas

Volumn 39, Issue 2, 2010, Pages 175-181

  MacHado, Marcel Cerqueira Cesar ^a   Coelho, Ana Maria Mendonça ^a   Martins, Joilson O ^a   Sampietre, Sandra N ^a   Molan, Nilza A T ^a   Patzina, Rosely A ^a   MacHado, Marcel Autran Cesar ^a   Jancar, Sonia ^a  

^a UNIVERSITY OF SÃO PAULO   (Brazil)

Author keywords

Acute experimental pancreatitis; Carbon dioxide; Inflammation; Pneumoperitoneum; SIRS

Indexed keywords

AMYLASE; CARBON DIOXIDE; CYCLOOXYGENASE 2; INDUCIBLE NITRIC OXIDE SYNTHASE; INTERLEUKIN 10; INTERLEUKIN 6; MYELOPEROXIDASE; TUMOR NECROSIS FACTOR ALPHA;

ABDOMEN; ACINAR CELL; ACUTE PANCREATITIS; AERATION; AMYLASE BLOOD LEVEL; ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; ARTICLE; CELL COUNT; CONTROLLED STUDY; ENZYME ACTIVITY; FAT NECROSIS; LIVER MITOCHONDRION; MALE; NONHUMAN; PERITONEAL CAVITY; PNEUMOPERITONEUM; PRIORITY JOURNAL; PROTEIN BLOOD LEVEL; PROTEIN EXPRESSION; RAT;

AMYLASES; ANIMALS; ASCITES; CARBON DIOXIDE; CYCLOOXYGENASE 2; DISEASE MODELS, ANIMAL; INFLAMMATION MEDIATORS; INSUFFLATION; INTERLEUKIN-10; INTERLEUKIN-6; LUNG; MALE; MITOCHONDRIA, LIVER; NITRIC OXIDE SYNTHASE TYPE II; OXIDATION-REDUCTION; OXIDATIVE PHOSPHORYLATION; PANCREAS; PANCREATITIS; PEROXIDASE; PNEUMOPERITONEUM, ARTIFICIAL; RATS; RATS, WISTAR; SYSTEMIC INFLAMMATORY RESPONSE SYNDROME; TAUROCHOLIC ACID; TIME FACTORS; TUMOR NECROSIS FACTOR-ALPHA;

EID: 77649252651     PISSN: 08853177     EISSN: None     Source Type: Journal    
DOI: 10.1097/MPA.0b013e3181bd651a     Document Type: Article

References (38)

1. Jacobs ML, Dagget WM, Civetta DM, et al. Acute pancreatitis: analysis of factors influencing survival. Ann Surg. 1977;185:43-51.
2. Banks P. Predictors of severity in acute pancreatitis. Pancreas. 1991;6:S7-S12.
3. de Beaux AC, Goldie AS, Ross JA, et al. Serum concentrations of inflammatory mediators related to organ failure in patients with acute pancreatitis. Br J Surg. 1996;83:349-353.
4. Carey L. Extra-abdominal manifestations of acute pancreatitis. Surgery. 1979;86:337-342.
5. Ranson JH, Spencer FC. The role of peritoneal lavage in severe acute pancreatitis. Ann Surg. 1978;187:565-575.
6. Coticchia JM, Lessler MA, Carey LC, et al. Peritoneal fluid in human acute pancreatitis blocks hepatic mitochondrial respiration. Surgery. 1986;100:850-856.
7. Bielecki JW, Dlugosz J, Pawlicka E, et al. The effect of pancreatitis associated ascitic fluid on some functions of rat liver mitochondria. A possible mechanism of the damage to the liver in acute pancreatitis. Int J Pancreatol. 1989;5:145-156.
8. Satake K, Kanazawa G, Hiura A, et al. Renal function in experimentally induced acute pancreatitis in dogs: how it is affected by the nephrotoxic substance in pancreatic exudate from ascetic fluid. Jpn J Surg. 1991;21:88-95.
9. Heath DI,Wilson C, Gudgeon AM, et al. Trypsinogen activation peptide (TAP) concentration in the peritoneal fluid of patients with acute pancreatitis and their relation to the presence of histologically confirmed pancreatic necrosis. Gut. 1994;35:1311-1315.
10. Tracey KJ, Cerami A. Tumor necrosis factor: an updated review of its biology. Crit Care Med. 1993;21:S415-S422.
11. Sameshima N, Kei S, Mori K, et al. The role of tumor necrosis factor > in the aggravation of cerulein-induced pancreatitis in rats. Int J Pancreatol. 1993;14:107-115. (Pubitemid 23326229)
12. Lundberg AH, Eubanks JW, Henry J, et al. Trypsin stimulates production of cytokine from peritoneal macrophages in vitro and in vivo. Pancreas. 2000;21:41-51.
13. Mikami Y, Takeda K, Shibuya K, et al. Do peritoneal macrophages play an essential role in the progression of acute pancreatitis in rats? Surgery. 2002;132:86-92.
14. West MA, Baker J, Bellingham J. Kinetics of decreased LPS stimulated-cytokine release by macrophages exposed to CO2. J Surg Res. 1996;63:269-274.
15. Fuentes JM, Hanly EJ, Aurora AR, et al. CO2 abdominal insufflation pretreatment increases survival after a lipopolysaccharide-contaminated laparotomy. J Gastrointest Surg. 2006;10:32-38.
16. Misawa T, Shiba H, Usuba T, et al. Systemic inflammatory response syndrome after hand-assisted laparoscopic distal pancreatectomy. Surg Endosc. 2007;21:1446-1449.
17. Lankisch PG, Winckler K, Bokermann M, et al. The influence of glucagon on acute pancreatitis in the rat. Scand J Gastroenterol. 1974;9:725-729.
18. Storck G. Fat necrosis in acute pancreatitis. Morphological and chemical studies in the rat. Acta Chir Scand. 1971;137:1-36.
19. Jamieson AD, Pruit KM, Calwell RC. An improved amylase assay. J Dental Res. 1969;48:483.
20. Goldblum SE, Wu KM, Jay M. Lung myeloperoxidase as a measure of pulmonary leukostasis in rabbits. J Appl Physiol. 1985;59: 1978-1985.
21. Warren JS, Yabroff KR, Mandel DM, et al. Role of O2 j in the neutrophil recruitment into site of dermal and pulmonary vasculitis. Free Radic Biol Med. 1990;8:163-172.
22. Coelho AM, Machado MC, Sampietre SN, et al. Hepatic damage during acute pancreatitis in the rat. Braz J Med Biol Res. 1997;30:947-953.
23. Estabrook RW. Mitochondrial respiratory control and the polarographic measurement of ADP/O ratios. In: Estabrook RW, Pullman ME, eds. Methods in Enzymology. New York, NY: Academic Press; 1967: 41-47.
24. Chance B, Willians GR. A simple and rapid assay of oxidative phosphorylation. Nature. 1955;175:1120-1121.
25. Lowry OH, Rosebrough NJ, Farr AL, et al. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:263-275.
26. Schmidt J, Rattner DW, Lewandrowski K, et al. A better model of acute pancreatitis of evaluating therapy. Ann Surg. 1992;215:44-56.
27. Norman J, Franz M, Messina J, et al. Interleukin-1 receptor antagonist decreases severity of experimental acute pancreatitis. Surgery. 1995;117:648-655.
28. Heath DI, Cruickshank DH, Gudgeon M, et al. Role of interleukin-6 in mediating the acute phase protein response and potential as an early means of severity assessment in acute pancreatitis. Gut. 1993;34:41-45.
29. Dijskstra CD, Döpp EA, Joling P, et al. The heterogeneity of mononuclear phagocytes in lymphoid organs: distinct macrophage subpopulations in the rat recognized by monoclonal antibodies ED1, ED2 and ED3. Immunology. 1985;54:589-599.
30. Nishikawa J, Takeyama Y, Ueda T, et al. Induction of apoptotic cell death by pancreatitis-associated ascitic fluid in Mardin-Darby canine kidney cells. FEBS Lett. 1995;373:19-22.
31. Are C, Talamini MA, Murata K, et al. Carbon dioxide pneumoperitoneum alters acute-phase response induced by lipopolysaccharide. Surg Endosc. 2002;16:1464-1467.
32. Hanly EJ, Bachman SL, Marohn MR, et al. Carbon dioxide pneumoperitoneum-mediated attenuation of the inflammatory response is independent of systemic acidosis. Surgery. 2005;137:559-566.
33. Schietroma M, Carlei F, Franchi L, et al. A comparison of serum interleukin-6 concentrations in patients treated by cholecystectomy via laparotomy or laparoscopy. Hepatogastroenterology. 2004;51: 1595-1599.
34. Hirota M, Nozawa F, Okabe A, et al. Relationship between plasma cytokine concentration and multiple organ failure in patients with acute pancreatitis. Pancreas. 2000;21:141-146.
35. Leindler L, Morschl E, László F, et al. Importance of cytokines, nitric oxide and apoptosis in the pathological process of necrotizing pancreatitis in rats. Pancreas. 2004;29:157-161.
36. Souza LJ, Shio MT, Molan NA, et al. Acute pancreatitis affects non-parenchymal liver cells by a mechanism dependent on platelet-activating factor. Pancreatology. 2007;7:67-73.
37. Strobel O, Wachter D, Werner J, et al. Effect of a pneumoperitoneum on systemic cytokine levels, bacterial translocation, and organ complication in a rat model of severe acute pancreatitis with infected necrosis. Surg Endosc. 2006;20:1897-1903.
38. Yol S, Bostanci EB, Ozogul Y, et al. Effect of carbon dioxide pneumoperitoneum and the severity of acute pancreatitis. Surg Endosc. 2004;18:1747-1751.