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Year 2004, Volume: 5 Issue: 2, 11 - 14, 01.08.2004

Abstract

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References

  • 1. Steer ML. Etiology and pathophysiology of acute pantreatitis. In: Go VLV, Dimango EP, Gardner JD, Lebenthal E, Rober HA. Scheele GA (eds). The pancreas:biology, pathobiology, and disease. NewYork Raven, 1993: 581-92.
  • 2. Renner I, Savage W, Pantoja J, et al. Death due to acute pancreatitis: a retrospective analysis of 405 autopsy cases. Dig Dis Sci 1985; 30: 1005-18.
  • 3. Lankrisch PG, Burchard-Reckert S, Petersen M, et al.. Morbidity and mortality in 602 patients with aute pancreatitis seen between the years 1980-1994. Z Gastroenterol 1996; 34: 371-7.
  • 4. Ostrovsky L, Woodman RC, Payne D.Antithrombin III prevents and rapidly reverses leukocyte recruitment in ischemia/reperfusion. Circulation 1997; 96: 2302-10.
  • 5. Harada N, Okajima K, Kushimoto S, et al. Antithrombin reduces ischemia/reperfusion injury of rat liver by increasing the hepatic level of prostacyclin. Blood Coagul Fibrinol 1999; 93: 157-64.
  • 6. Özden A, Sarýoglu A, Demirkan NÇ, et al. Antithrombin reduces renal ischemia-reperfusion injury in rats. Res Exp Med (Berl) 2001; 200: 195-203.
  • 7. Özden A, Tetik C, Bilgihan A. Antithrombin III prevents 60 min warm intestinal ischemia reperfusion injury in rats. Res Exp Med (Berl) 1999; 198: 237-46.
  • 8. Woodman RC, Ostrovsky L, Teoh D.Antithrombin and ischemia/reperfusion. Blood Coagul Fibrinol 1998; 9: 7-15.
  • 9. Koike K, Moore E, Moore F, et al. Gut ischemia/reperfusion produces lung injury independent of endotoxin. Crit Care Med 1994; 22: 1438-44.
  • 10. Zyromski N, Murr MM. Evolving consepts in the pathophysiology of acute pancreatitis. Surgery 2003; 133: 235-7.
  • 11. Kusske AM, Rongione AJ, Reber HA. Cytokines and acute pancreatitis. Gastroenterology 1996; 110: 639- 42.
  • 12. Gukovskaya AS, Gukuvsky I, Zaninovic V, et al. Pancreatic acinar cells produce, release, and respond to tumor necrosis factor-alpha. Role in regulating cell death and pancreatitis. J Clin Invest 1997; 100: 1853- 62.
  • 13. Mikami Y, Takeda KT, Shibuya K, et al. Peritoneal inflammatory cells in acute pancreatitis: Relationship of infiltration dynamics and cytokine production with severity of illness. Surgery 2002; 132: 86-92.
  • 14. Frossard JL, Saluja A, Bhagat L, et al. The role of intercellular adhesion molecule-1 and neutrophils in acute pancreatitis and pancreatitis-associated lung injury. Gastroenterology 1999; 116: 694-701.
  • 15. Bhatia M, Moochhala S. Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome. J Pathol 2004; 202: 145-56.
  • 16. Pastor CM, Matthay MA, Frossard JL. Pancreatitisassociated acute lung injury: new insights. Chest 2003; 124: 2341-51.
  • 17. McMillen MA, Huribal M, Sumpio B. Common pathway of endothelial-leukocyte interaction in shock, ischemia, and reperfusion. Am J Surg 1993; 166: 557- 62.
  • 18. Serafini FM, Rosemurgy AS. Adhesion molecules: Clinical implications. Surgery 2000; 127: 481-3.
  • 19. Zimmerman GA, McIntyre TM, Prescott SM. Trombin stimulate the adherence of neutrophils to human endothelial cell in vitro. J Clin Invest 1985; 76: 2235- 46.
  • 20. Jaffray C, Yang J, Carter G, et al. Pancreatic elastase activates pulmonary nuclear factor kappa B and inhibitory kappa B, mimicking pancreatitis-associated adult respiratory distress syndrome. Surgery 2000; 128: 225-31.
  • 21. Schmelling DJ, Caty MG, Oldham KT, et al. Evidence for neutrophil-related acute lung injury after intestinal ischemia-reperfusion. Surgery 1989; 106: 195-7.
  • 22. Dowdall JF, Winter DC, Bouchier-Hayes DJ. Inosine modulates gut barrier dysfunction and end organ damage in a model of ischemia-reperfusion injury. J Surg Res 2002; 108: 61-8.
  • 23. Koike K, Yamamoto Y, Hori Y, et al. Group II phospholipase A2 mediates lung injury in intestinal ischemia-reperfusion.Ann Surg 2000; 232: 90-7.
  • 24. Tavaf-Motamen H, Miner TJ, Starnes BW, et al. Nitric oxide mediates acute lung injury by lation of inflammation. J Surg Res 1998; 78: 137-43.
  • 25. Kruse P, Hage E., Lasson A., Proteases and protease inhibitors in taurocholate-induced acute pancreatitis in rats. Int J Pancreatol 1999; 25: 113-21.
  • 26. Lasson A, Ohisson.K. Comsumptive coagulopathy, fibrinolysis and protease-anthiprotease interactions during acute human pancreatitis. Thromb Res 1986; 41: 167-83.
  • 27. Warren BL, Eid A, Singer P, et al. Caring for the critically ill patient. High-dose antithrombin III in severe sepsis: a randomized controlled trial. JAMA 2001; 286:1869-78.

The effects of Antitrombin III on Lung Injury in a Model of Experimental aCute Pancreatitis

Year 2004, Volume: 5 Issue: 2, 11 - 14, 01.08.2004

Abstract

Background: Acute pancreatitis, especially in the severe form, is a well-known disease causing both local intra- abdominal and remote organ disturbances, including lungs. As a natural inhibitor of serine proteases, antithrombin was previously shown to attenuate the tissue damage after ischemia-reperfusion, sepsis, and shock in several organ systems. Here, we examined the effects of antithrombin on pulmonary injury in a rat acute pancreatitis model. Methods: Thirty male Wistar-Albino rats underwent median laparotomy and randomized into three groups: group I (control) bilio-pancreatic duct was dissected but not ligated (n=10), group II (acute pancreatitis group) bilio-pancreatic duct was ligated (n=10), and group III (AT treated group) AT III 250 U/Kg was injected following bilio-pancreatic duct ligation (n=10). After observation time (48 hours) animals were sacrificed and myeloperoxidase activity together with tissue wet/dry ratio in the lung parenchyma were assessed and compared. Results: There was a statistically significant increase in the quantity of myeloperoxidase activity and tissue wet/dry ratio of lungs in the acute pancreatitis group when compared to the control group. Treatment of animals with antithrombin partly reduced the pulmonary injury characterized by increased tissue wet/dry ratio and myeloperoxidase activity. But this reduction was not found to be statistically significant. Conclusion: Beneficial effects of AT in preventing pulmonary injury following experimental models of sepsis and ischemia-reperfusion have been reported previously. In our model of experimental acute pancreatitis, AT showed some attenuating effect on pulmonary injury despite it was limited when compared to that of ischemia- reperfusion and sepsis models. This result suggests that some other confounding factors may be involved in the mechanisms of pulmonary injury related to acute pancreatitis. We believe that further detailed studies are needed to elucidate the exact mechanisms of that injury.

References

  • 1. Steer ML. Etiology and pathophysiology of acute pantreatitis. In: Go VLV, Dimango EP, Gardner JD, Lebenthal E, Rober HA. Scheele GA (eds). The pancreas:biology, pathobiology, and disease. NewYork Raven, 1993: 581-92.
  • 2. Renner I, Savage W, Pantoja J, et al. Death due to acute pancreatitis: a retrospective analysis of 405 autopsy cases. Dig Dis Sci 1985; 30: 1005-18.
  • 3. Lankrisch PG, Burchard-Reckert S, Petersen M, et al.. Morbidity and mortality in 602 patients with aute pancreatitis seen between the years 1980-1994. Z Gastroenterol 1996; 34: 371-7.
  • 4. Ostrovsky L, Woodman RC, Payne D.Antithrombin III prevents and rapidly reverses leukocyte recruitment in ischemia/reperfusion. Circulation 1997; 96: 2302-10.
  • 5. Harada N, Okajima K, Kushimoto S, et al. Antithrombin reduces ischemia/reperfusion injury of rat liver by increasing the hepatic level of prostacyclin. Blood Coagul Fibrinol 1999; 93: 157-64.
  • 6. Özden A, Sarýoglu A, Demirkan NÇ, et al. Antithrombin reduces renal ischemia-reperfusion injury in rats. Res Exp Med (Berl) 2001; 200: 195-203.
  • 7. Özden A, Tetik C, Bilgihan A. Antithrombin III prevents 60 min warm intestinal ischemia reperfusion injury in rats. Res Exp Med (Berl) 1999; 198: 237-46.
  • 8. Woodman RC, Ostrovsky L, Teoh D.Antithrombin and ischemia/reperfusion. Blood Coagul Fibrinol 1998; 9: 7-15.
  • 9. Koike K, Moore E, Moore F, et al. Gut ischemia/reperfusion produces lung injury independent of endotoxin. Crit Care Med 1994; 22: 1438-44.
  • 10. Zyromski N, Murr MM. Evolving consepts in the pathophysiology of acute pancreatitis. Surgery 2003; 133: 235-7.
  • 11. Kusske AM, Rongione AJ, Reber HA. Cytokines and acute pancreatitis. Gastroenterology 1996; 110: 639- 42.
  • 12. Gukovskaya AS, Gukuvsky I, Zaninovic V, et al. Pancreatic acinar cells produce, release, and respond to tumor necrosis factor-alpha. Role in regulating cell death and pancreatitis. J Clin Invest 1997; 100: 1853- 62.
  • 13. Mikami Y, Takeda KT, Shibuya K, et al. Peritoneal inflammatory cells in acute pancreatitis: Relationship of infiltration dynamics and cytokine production with severity of illness. Surgery 2002; 132: 86-92.
  • 14. Frossard JL, Saluja A, Bhagat L, et al. The role of intercellular adhesion molecule-1 and neutrophils in acute pancreatitis and pancreatitis-associated lung injury. Gastroenterology 1999; 116: 694-701.
  • 15. Bhatia M, Moochhala S. Role of inflammatory mediators in the pathophysiology of acute respiratory distress syndrome. J Pathol 2004; 202: 145-56.
  • 16. Pastor CM, Matthay MA, Frossard JL. Pancreatitisassociated acute lung injury: new insights. Chest 2003; 124: 2341-51.
  • 17. McMillen MA, Huribal M, Sumpio B. Common pathway of endothelial-leukocyte interaction in shock, ischemia, and reperfusion. Am J Surg 1993; 166: 557- 62.
  • 18. Serafini FM, Rosemurgy AS. Adhesion molecules: Clinical implications. Surgery 2000; 127: 481-3.
  • 19. Zimmerman GA, McIntyre TM, Prescott SM. Trombin stimulate the adherence of neutrophils to human endothelial cell in vitro. J Clin Invest 1985; 76: 2235- 46.
  • 20. Jaffray C, Yang J, Carter G, et al. Pancreatic elastase activates pulmonary nuclear factor kappa B and inhibitory kappa B, mimicking pancreatitis-associated adult respiratory distress syndrome. Surgery 2000; 128: 225-31.
  • 21. Schmelling DJ, Caty MG, Oldham KT, et al. Evidence for neutrophil-related acute lung injury after intestinal ischemia-reperfusion. Surgery 1989; 106: 195-7.
  • 22. Dowdall JF, Winter DC, Bouchier-Hayes DJ. Inosine modulates gut barrier dysfunction and end organ damage in a model of ischemia-reperfusion injury. J Surg Res 2002; 108: 61-8.
  • 23. Koike K, Yamamoto Y, Hori Y, et al. Group II phospholipase A2 mediates lung injury in intestinal ischemia-reperfusion.Ann Surg 2000; 232: 90-7.
  • 24. Tavaf-Motamen H, Miner TJ, Starnes BW, et al. Nitric oxide mediates acute lung injury by lation of inflammation. J Surg Res 1998; 78: 137-43.
  • 25. Kruse P, Hage E., Lasson A., Proteases and protease inhibitors in taurocholate-induced acute pancreatitis in rats. Int J Pancreatol 1999; 25: 113-21.
  • 26. Lasson A, Ohisson.K. Comsumptive coagulopathy, fibrinolysis and protease-anthiprotease interactions during acute human pancreatitis. Thromb Res 1986; 41: 167-83.
  • 27. Warren BL, Eid A, Singer P, et al. Caring for the critically ill patient. High-dose antithrombin III in severe sepsis: a randomized controlled trial. JAMA 2001; 286:1869-78.
There are 27 citations in total.

Details

Other ID JA72BZ22VE
Journal Section Research Article
Authors

Faruk Önder Aytekin This is me

Koray Tekin This is me

Burhan Kabay This is me

Mehmet Tekin This is me

Atilla Özer This is me

Yıldız Güney This is me

Akın Özden This is me

Publication Date August 1, 2004
Published in Issue Year 2004 Volume: 5 Issue: 2

Cite

EndNote Aytekin FÖ, Tekin K, Kabay B, Tekin M, Özer A, Güney Y, Özden A (August 1, 2004) The effects of Antitrombin III on Lung Injury in a Model of Experimental aCute Pancreatitis. Meandros Medical And Dental Journal 5 2 11–14.