Background/Aim: The pancreas is an organ highly susceptible to ischemic damage. This discussion reviews the role of ischemia as an etiologic factor in acute pancreatitis. Methods: Literature review. Results: The susceptibility of the pancreas to ischemia/reperfusion injury has been demonstrated in experimental studies and in clinical settings such as cardiopulmonary bypass, hemorrhagic shock, and transplantation of the pancreas. Oxygen free radicals, activation of polymorphonuclear leukocytes, failure of microvascular perfusion, cellular acidosis, and disturbance of intracellular homeostasis appear to be important factors/mechanisms in the pathogenesis of ischemia/reperfusion-induced acute pancreatitis. In clinical practice, the diagnosis of ischemic pancreatitis is difficult and often delayed, especially during the postoperative period after cardiac or major vascular surgery. Conclusions: Ischemia appears to be one important factor in acute pancreatitis. The management of ischemic pancreatitis is similar to that of acute pancreatitis of any etiology.

1.
Menger MD, Sack FU, Barker JH, Feifel G, Messmer K: Quantitative analysis of microcirculatory disorders after prolonged ischemia in skeletal muscles: Therapeutic effects of prophylactic isovolemic hemodilution. Res Exp Med (Berl) 1988;188:151–165.
2.
Gotoh O, Asano T, Koide T, Takakura K: Ischemic brain edema following occlusion of the middle cerebral artery in the rat. I. The time courses of the brain water, sodium and potassium contents and blood-brain barrier permeability to 125I-albumin. Stroke 1985;16:101–109.
3.
Kloner RA, Braunwald E: Observations on experimental myocardial ischemia. Cardiovasc Res 1980;14:371–395.
4.
Hannson R, Jonsson O, Lundstam S, Petterson S: Effects of free radical scavengers on renal circulation after ischemia in the rabbit. Clin Sci 1983;65:605–610.
5.
Rauen U, Viebahn R, Lauchart W, de Croot H: The potential role of oxygen species in liver ischemia/reperfusion injury following liver surgery. Hepatogastroenterology 1994;41:333–336.
6.
Perry MA, Wadhwa SS: Gradual reintroduction of oxygen reduces reperfusion injury in cat stomach. Am J Physiol 1988;254:G366–G372.
7.
Gross V, Arndt H, Andus T, Palitzsch KD, Scholmerich J: Free radicals in inflammatory bowel diseases: Pathophysiology and therapeutic implications. Hepatogastroenterology 1994;41:320–327.
8.
Messmer K, Sack FU, Menger MD: White cell-endothelium interaction during postischemic reperfusion of skin and skeletal muscle. Adv Exp Med Biol 1988;242:95–98.
9.
Panum P: Experimentelle Beiträge zur Lehre von der Embolie. V Arch Pathol Anat Physiol Klin Med 1886;25:303–338.
10.
Popper HL, Necheles H, Russekk KC: Transition of pancreatic edema into pancreatic necrosis. Surg Gynecol Obstet 1948;87:79–83.
11.
Fernandez-del Castillo C, Harringer W, Warshaw AL, Vlahakes GJ, Koski G, Zaskavsky AM, Rattner DW: Risk factors for pancreatic cellular injury after cardiopulmonary bypass. N Engl J Med 1991;325:382–387.
12.
Warshaw AL, O’Hara PJ: Susceptibility of the pancreas to ischemic injury in shock. Ann Surg 1978;188:197–201.
13.
Fernandez-Cruz L, Sabater L, Gilbert R, Ricart MJ, Saenz A, Astudillo E: Native and graft pancreatitis following combined pancreas-renal transplantation. Br J Surg 1993;80:1429–1432.
14.
Klar E, Messmer K, Warshaw AL, Herfarth C: Pancreatic ischemia in experimental acute pancreatitis: Mechanisms, significance and therapy. Br J Surg 1990:77:1205–1210.
15.
Sokolowski A, Spormann H, Urbahn H, Letko G: Contribution of pancreatic edema and short-term ischemia to experimental acute pancreatitis in the rat. II. Behaviour of serum parameters. Z Exp Chir Transplant Künstliche Organe 1986;19:331–339.
16.
Spormann H, Sokolowski A, Birkigt H-G, Letko G: Contribution of pancreatic edema and short-term ischemia to experimental acute pancreatitis in the rat. I. Procedure and pathomorphological investigations. Z Exp Chir Transplant Künstliche Organe 1986;19:323–330.
17.
Haas GS, Warshaw AL, Daggett WM, Aretz HT: Acute pancreatitis after cardiopulmonary bypass. Am J Surg 1985;149:508–515.
18.
Rattner DW, Gu ZY, Vlahakis GJ, Warshaw AL: Hyperamylasemia after cardiac surgery: Incidence, significance and management. Ann Surg 1989;209:279–283.
19.
Spormann H, Sokolowski A, Letko G: Effect of temporary ischemia upon the development and histological pattern of acute pancreatitis in the rat. Pathol Res Pract 1989;184:507–513.
20.
Kyogoku T, Manabe T, Tobe T: Role of ischemia in acute pancreatitis: Hemorrhagic shock converts edematous pancreatitis to hemorrhagic pancreatitis in rats. Dig Dis Sci 1992;37:1409–1417.
21.
Svensson LG, Decker G, Kinsley RB: A prospective study of hyperamylasemia and pancreatitis after cardiopulmonary bypass. Ann Thorac Surg 1985;39:409–411.
22.
Rose DM, Ranson JHC, Cunningham JN: Patterns of severe pancreatic injury following cardiopulmonary bypass. Ann Surg 1984;199:168–172.
23.
Feiner H: Pancreatitis after cardiac surgery: A morphologic study. Am J Surg 1976;131:684–688.
24.
Gmaz-Nikulin E, Nikulin A, Plemnac P: Pancreatic lesions in shock and their significance. J Pathol 1981;135:223–236.
25.
Pfeffer RB, Lazarini-Robertson A, Safadi D: Gradations of pancreatitis, edematous, through hemorrhagic, experimentally produced by controlled injection of microspheres into blood vessels in dogs. Surgery 1962;51:764–769.
26.
Redha F, Uhlschmid G, Ammann RW, Freiburghaus AU: Injection of microspheres into pancreatic arteries causes acute hemorrhagic pancreatitis in the rat: A new animal model. Pancreas 1990;5:188–193.
27.
Takahashi T, Yaginuma N: Ischemic injury of the human pancreas: Its basic patterns correlated with the pancreatic microvasculature. Pathol Res Pract 1985;179:645–651.
28.
Tsiotos GG, Mullany CJ, Zietlow S, Van Heerden JA: Abdominal complications following cardiac surgery. Am J Surg 1994;167:553–557.
29.
Kusterer K, Poschmann T, Friedemann A, Enghofer M, Zeandler S, Usadel KH: Arterial constriction, ischemia-reperfusion, and leukocyte adherence in acute pancreatitis. Am J Physiol 1993;265:G165–G171.
30.
Broe PJ, Zuidema GD, Cameron JL: The role of ischemia in acute pancreatitis: Studies with an isolated perfused canine pancreas. Surgery 1982;91:377–382.
31.
Fleischer GM, Herden P, Spormann H: Tierexperimentelle Untersuchungen zur Rolle der Ischämie in the Pathogenese der akuten Pankreatitis. Z Exp Chir Transplant Künstliche Organe 1984;17:179–187.
32.
Kloppel G, Dreyer T, Willemer S, Kern HF, Adler C: Human acute pancreatitis: Its pathogenesis in the light of immunocytochemical and ultrastructural findings in acinar cells. Virchows Arch A Pathol Anat Histopathol 1986;409:791–803.
33.
Busing M, Hopt UT, Quarken M, Becker HD, Morgenroth K: Morphological studies of graft pancreatitis following pancreas transplantation. Br J Surg 1993;80:1170–1173.
34.
Lerch MM, Saluja AK, Dawra R, Ramarao P, Saluja M, Steer ML: Acute necrotizing pancreatitis in the oppossum: Earliest morphological changes involve acinar cells. Gastroenterology 1992;103:205–213.
35.
Schmidt J, Rattner DW, Lewandrowski K, Compton CC, Mandavilli U, Knoefel WT, Warshaw AL: A better model of acute pancreatitis for evaluating therapy. Ann Surg 1992;215:44–56.
36.
Hoffmann TF, Leiderer R, Harris AG, Messmer K: Ischemia and reperfusion of the pancreas. Microsc Res Tech 1997;37:557–571.
37.
Gilsdorf RB, Long D, Moderg A: Central nervous system influence on experimentally induced pancreatitis. JAMA 1965;192:394–397.
38.
Goodhead B, Wright PW: The effect of postganglionic sympathectomy on the development of hemorrhagic pancreatitis in the dog. Ann Surg 1969;170:951–960.
39.
Schmidt J, Fernandez-del Castillo C, Rattner DW: Hyperoncotic ultrahigh molecular weight dextran solutions reduce trypsinogen activation, prevent acinar necrosis and lower mortality in rodent pancreatitis. Am J Surg 1993;165:40–45.
40.
Klar E, Mall G, Messmer K: Improvement of impaired pancreatic microcirculation by isovolemic hemodilution protects pancreatic morphology in acute biliary pancreatitis. Surg Gynecol Obset 1993;176:144–150.
41.
Probstein JG, Joshi RA, Blumenthal HT: Atheromatous embolization: An etiology of acute pancreatitis. Arch Surg 1957;75:566–572.
42.
Hochachka PW: Defence strategies against hypoxia and hypothermia. Science 1986;231:234–241.
43.
McCord JM: Oxygen-derived free radicals in postischemic tissue injury. N Engl J Med 1985;312:159–163.
44.
Batelli MG, Della Corte E, Stirpe F: Xanthine oxidase type D (dehydrogenase) in the intestine and other organs of the rat. Biochem J 1972;126:747–749.
45.
Nordback IH, Cameron JL: The mechanism of conversion of xanthine dehydrogenase to xanthine oxidase in acute pancreatitis in the canine isolated pancreas preparation. Surgery 1993;113:90–97.
46.
Cunningham SK, Keaveny TV: Splanchnic organ adenine nucleotides and their metabolites in hemorrhagic shock. Ir J Med Sci 1977;146:136–143.
47.
Becker H, Vinten-Johansen J, Buckberg GD, Bugyi HI: Correlation of pancreatic blood flow and high-energy phosphates during experimental pancreatitis. Eur Surg Res 1982;14:203–210.
48.
Zimmerman BJ, Grangler DN: Oxygen free radicals and the gastrointestinal tract: Role in ischemia-reperfusion injury. Hepatogastroenterology 1994;41:337–342.
49.
Parks DA, Granger DN: Ischemia induced vascular changes: Role of xanthine oxidase and hydroxyl radicals. Am J Physiol 1983;245:G285–G289.
50.
Warshaw AL: Ischemia- and reperfusion-related injury in pancreatitis. Dig Dis Sci 1996;41:821–822.
51.
Menger MD, Bonkhoff H, Vollmar B: Ischemia-reperfusion induced pancreatic microvascular injury: An intravital fluorescence microscopic study in rats. Dig Dis Sci 1996;41:823–830.
52.
Parks D, Grangler N: Xanthine oxidase: Biochemistry, distribution and physiology. Acta Physiol Scand 1986;(suppl 548):87–99.
53.
Schoenberg MH, Büchler M, Berger HG: Oxygen radicals in experimental acute pancreatitis. Hepatogastroenterology 1994;41:313–319.
54.
Tanjoh K, Shima A, Aida M, Tomita R, Munakata K, Kurosu Y: Nitric oxide (NO) and active oxygen intermediates in severe pancreatitis (abstract). 14th World Congr Coll Int Chir Dig, Los Angeles, 1994, pp 539–543.
55.
Sanfey H, Bulkley G, Cameron J: The role of oxygen derived free radicals in the pathogenesis of acute pancreatitis. Ann Surg 1984;200:405–413.
56.
Sanfey H, Bulkley G, Cameron J: The pathogenesis of acute pancreatitis: The source and role of oxygen derived free radicals in three different experimental models. Ann Surg 1985;201:633–639.
57.
DeGroot H: Reactive oxygen species in tissue injury. Hepatogastroenterology 1994;41:328–332.
58.
Kirschner RE, Fantini GA: Role of iron and oxygen-derived free radicals in ischemia-reperfusion injury. Am J Surg 1994;179:103–117.
59.
Majno G, Joris I: Apoptosis, oncosis and necrosis: An overview of cell death. Am J Pathol 1995;146:3–15.
60.
Formela LJ, Galloway SW, Kingsnorth AN: Inflammatory mediators in acute pancreatitis. Br J Surg 1995;82:6–13.
61.
Braganza JM: Experimental acute pancreatitis. Curr Opin Gastroenterol 1990;6:763–768.
62.
Braganza J, Rinderknecht H: Free radicals and acute pancreatitis. Gastroenterology 1988;94:1111–1112.
63.
Schoenberg MH, Büchler M, Gaspar M: Oxygen free radicals in acute pancreatitis or the rat. Gut 1990;31:1138–1143.
64.
Dabrowski A, Gabryelewicz U, Wereszczynska S, Chyczewski L: Oxygen derived free radicals in caerulein-induced acute pancreatitis. Scand J Gastroenterol 1989;23:1245–1249.
65.
Granger DN, Benoit JN, Suzuki M, Grisham MB: Leukocyte adherence to venular endothelium during ischemia-reperfusion. Am J Physiol 1989;257:G683–G688.
66.
Lehr HA, Guhlmann A, Nolte D, Keppler D, Messmer K: Leukotrienes as mediators in ischemia-reperfusion injury in a microcirculation model in the hamster. J Clin Invest 1991;87:2036–2042.
67.
Springer TA: Traffic signals for lymphocyte recirculation and leukocyte emigration: The multistep paradigm. Cell 1994;76:301–314.
68.
Springer TA: Adhesion receptors of the immune system. Nature 1990;346:425–434.
69.
Adams DH, Shaw S: Leukocyte-endothelial interactions and regulation of leukocyte migration. Lancet 1994;343:831–836.
70.
Granger DN, Kubes P: The microcirculation and inflammation: Modulation of leukoyte-endothelial cell adhesion. J Leukoc Biol 1994;55:662–675.
71.
Rosales C, Juliano RL: Signal transduction by cell adhesion receptors in leukocytes. J Leukoc Biol 1995;57:189–198.
72.
McEver RP: Selectins: Novel receptors that mediate leukocyte adhesion during inflammation. Thromb Haemost 1991;65:223–228.
73.
Granger DN, Kvietus PR, Perry MA: Leukocyte endothelial cell adhesion induced by ischemia and reperfusion. Can J Physiol Pharmacol 1993;71:67–75.
74.
Kishimoto TK, Anderson DC: The role of integrins in inflammation; in Gallin JI, Goldstein IM, Snydermann R (eds): Inflammation: Basic Principles and Clinical Correlates. New York, Raven Press, 1992, pp 353–406.
75.
Menger MD, Vollmar B, Glasz J, Post S, Messmer K: Microcirculatory manifestations of hepatic ischemia/reperfusion injury. Prog Appl Microcirc 1993;19:106–124.
76.
Weiss SJ: Tissue destruction by neutrophils. N Engl J Med 1989;320:365–376.
77.
Harlan JM: Leukocyte-endothelial interactions. Blood 1985;65:513–525.
78.
Ley K, Gaehtgens P: Endothelial, nonhemodynamic differences are responsible for preferential leukocyte rolling in rat mesenteric venules. Circ Res 1991;69:1034–1041.
79.
Raud J, Lidbom L, Dahlen SE, Heqvist P: Periarteriolar localization of mast cells promotes oriented interstitial migration of leukocytes in the hamster cheek pouch. Am J Pathol 1989;134:161–169.
80.
Patel KD, Zimmernal GA, Prescott SM, McEver RP, McIntyre TM: Oxygen radicals induce human endothelial cells to express GMP-140 and bind neutrophils. J Cell Biol 1991;112:749–759.
81.
Uhl W, Büchler M, Malfertheiner P, Martini M, Beger HG: PMN-elastase in comparison with CRP, antiproteases and LDH as indicators of necrosis in human acute pancreatitis. Pancreas 1991;6:253–259.
82.
Gross V, Scholmerich J, Leser HG: Granulocyte elastase in assessment of severity of acute pancreatitis: Comparison with acute-phase proteins C-reactive protein, alpha 1-antitrypsin, and protease inhibitor alpha 2-macroglobulin. Dig Dis Sci 1990;35:97–105.
83.
Dominguez-Munoz JE, Carballo F, Garcia MJ: Clinical usefulness of polymorphonuclear elastase in predicting the severity of acute pancreatitis: Results of a multicentre study. Br J Surg 1991;78:1230–1234.
84.
Uhl W, Büchler M, Malfertheiner P, Martini M, Beger HG: PMN elastase: A new serum marker for the staging of acute pancreatitis. Digestion 1989;43:176–177.
85.
Rinderknecht H: Fatal pancreatitis: A consequence of excessive leukocyte stimulation? Int J Pancreatol 1988;3:105–112.
86.
Vollmar B, Waldner H, Schmand J, Conzen PF, Goetz AE, Habazettl H, Schweiberer L, Brendel W: Release of arachidonic acid metabolites during acute pancreatitis in pigs. Scand J Gastroenterol 1989;24:1253–1264.
87.
Nonaka A, Manabe T, Tamura K, Asano N, Imanishi K, Tobe T: Changes of xanthine oxidase, lipid peroxide and superoxide dismutase in mouse acute pancreatitis. Digestion 1989;43:41–46.
88.
Bassi D, Kollias N, Fernandez-del Castillo C, Foitzik T, Warshaw AL, Rattner DW: Impairment of pancreatic microcirculation correlates with the severity of acute experimental pancreatitis. J Am Coll Surg 1994;179:257–263.
89.
Menger MD, Pelikan S, Steiner D, Messmer K: Microvascular ischemia/reperfusion injury in striated muscle: Significance of ‘reflow-paradox’. Am J Physiol 1992;263:H1901–H1906.
90.
Kusterer K, Enghofer M, Zendler S, Blöchle C, Usadel KH: Microcirculatory changes in sodium taurocholate-induced pancreatitis in rats. Am J Physiol 1991;260:G346–G351.
91.
Hoffmann TF, Leiderer R, Waldner H, Messmer K: Ischemia/reperfusion of the pancreas: A new in vivo model for acute pancreatitis in rats. Res Exp Med (Berl) 1995;195:125–144.
92.
Klar E, Endrich B, Messmer K: Microcirculation of the pancreas: A quantitative study of physiology and changes in pancreatitis. Int J Microcirc Clin Exp 1990;12:985–1101.
93.
Knoefel WT, Kollias N, Warshaw AL, Waldner H, Nishioka NS, Rattner DW: Pancreatic microcirculatory changes in experimental pancreatitis of graded severity in the rat. Surgery 1994;116:904–913.
94.
Ames A, Wright RL, Kowada M, Thurston JM, Majno G: Cerebral ischemia. II. The no-reflow phenomenon. Am J Pathol 1968;52:437–452.
95.
Quinones-Baldrich WJ, Chervu A, Hernandez JJ, Colburn M, Moore WS: Skeletal muscle function after ischemia: ‘Non-reflow’ versus reperfusion injury. J Surg Res 1991;51:5–12.
96.
Harris AG, Skalak TC: Leukocyte cytoskeletal structure determines capillary plugging and network resistance. Am J Physiol 1993;265:H1670–H1675.
97.
Messmer K, Lewis D, Sunder-Plassmann L, Klovekorn W, Mendler N, Holper K: Acute normovolemic hemodilution; Changes of central hemodynamics and microcirculatory flow in skeletal muscle. Eur Surg Res 1972;4:55–70.
98.
Kloner RA, Ganote CE, Jennings RB: The ‘non-reflow’ phenomenon after temporary coronary occlusion in the dog. J Clin Invest 1975;54:1496–1508.
99.
Jerome SN, Smith CW, Korthuis RJ: CD18-dependent adherence reactions play an important role in the development of the no-reflow phenomenon. Am J Physiol 1993;264:H479–H483.
100.
Kwaan HC, Anderson MC, Gramatica LA: A study of pancreatic enzyme as a factor in the pathogenesis of disseminated intravascular coagulation during acute pancreatitis. Surgery 1971;69:663–672.
101.
Bockman DE, Schiller WR, Suriyapa C, Mutschler JHW, Anderson MC: Fine structure of early experimental acute pancreatitis in dogs. Lab Invest 1973;22:584–592.
102.
Anderson MC: Venous stasis in the transition of edematous pancreatitis to pancreatic necrosis. JAMA 1963;183:534–537.
103.
Anderson MC, Schiller WR: Microcirculatory dynamics in the normal and inflammed pancreas. Am J Surg 1968;115:118–127.
104.
Anderson MC, Schoenfeldt FB, Iams WB, Suwa M: Circulatory changes in acute pancreatitis. Surg Clin North Am 1967;47:127–132.
105.
Farber JL, Kenneth RC, Mittnacht S: The pathogenesis of irreversible cell injury in ischemia. Am J Pathol 1981;102:271–281.
106.
Rinderknecht H: Activation of pancreatic zymogens: Normal activation, premature intrapancreatic activation, protective mechanisms against inappropriate activation. Dig Dis Sci 1986;31:314–321.
107.
Steer ML, Meldolesi J: The cell biology of experimental pancreatitis. N Engl J Med 1987;316:144–150.
108.
Mithofer K, Fernandez-del Castillo C, Frick TW, Foitzik T, Bassi DG, Lewandrowski KB, Rattner DW, Warshaw AL: Increased intrapancreatic trypsinogen activation in ischemia-induced experimental pancreatitis. Ann Surg 1995;221:364–371.
109.
Lefer AM, Barenholz Y: Pancreatic hydrolases and the formation of a myocardial depressant factor in shock. Am J Physiol 1972;223:1103–1109.
110.
Steer ML, Meldolesi J, Figarella C: Pancreatitis: The role of lysosomes. Dig Dis Sci 1984;29:934–938.
111.
La Manna JC: Hypoxia/ischemia and the pH paradox. Adv Exp Med Biol 1996;388:283–292.
112.
Cheung JY, Bonventre JV, Malis CD: Calcium and ischemic injury. N Engl J Med 1986;314:1670–1676.
113.
Chien KR, Abrams J, Serroni A, Martin JT, Farber JL: Accelerated phospholipid degradation and associated membrane dysfunction in irreversible, ischemic liver cell injury. J Biol Chem 1978;253:4809–4817.
114.
Frick TW, Fernandez-del Castillo C, Mithofer K: Calcium accelerates trypsinogen activation (abstract). Gastroenterology 1994;106(suppl):292.
115.
Ellison EC, Pappas TN, Johnson JA, Fabri PJ, Carey LC: Demonstration and characterization of the hemoconcentrating effect of ascitic fluid that accumulates during hemorrhagic pancreatitis. J Surg Res 1981;30:241–248.
116.
Shimizu I, Wada S, Okahisa T, Kamamura M, Yano M, Kodaira T: Radioimmunoreactive plasma bradykinin levels and histological changes during the course of cerulein-induced pancreatitis in rats. Pancreas 1993;8:220–225.
117.
Vollmar B, Waldner H, Schmand J, Conzen P, Goetz A, Habazettl H: Oleic acid induced pancreatitis in pigs. J Surg Res 1991;50:196–204.
118.
Griesbacher T, Lemberk F: Effects of the bradykinin antagonist, HOE 140, in experimental acute pancreatitis. Br J Pharmacol 1992;107:356–360.
119.
Iwatsuki K, Homma T, Malik KU: Permissive role of prostaglandins in the action of bradykinin on the pancreas of anesthetized dogs. J Pharmacol Exp Ther 1985;233:700–706.
120.
Ryan JW, Moffat JG, Thompson AG: Role of bradykinin in the development of acute pancreatitis. Nature 1964;204:1212–1213.
121.
Yotsumoto F, Manabe T, Oshio G: Bradykinin involvement in the aggravation of acute pancreatitis in rabbits. Digestion 1993;54:224–230.
122.
Bhoola KD, Figueroa CD, Worthy K: Bioregulation of kinins: Kallikrein, kininogens and kininases. Pharmacol Rev 1992;44:1–80.
123.
Cahill M, Fishman JB, Polgar P: Effect of des arginine9-bradykinin and other bradykinin fragments on the synthesis of prostacyclin and the binding of bradykinin by vascular cells in culture. Agents Actions 1988;24:224–231.
124.
D’Orleans-Juste P, de Nucci G, Vane JR: Kinins act on B1 or B2 receptor to release conjointly endothelium-derived relaxing factor and prostacyclin from bovine aortic endothelial cells. Br J Pharmacol 1989;96:920–926.
125.
Dahlen SE, Björk J, Hedqvist P, Arfors KE, Hammarström S, Lindgren JA, Samuelson B: Leukotrienes promote plasma leakage and leukocyte adhesion in postcapillary venules: In vivo effects with relevance to the acute inflammatory response. Proc Natl Acad Sci USA 1981;78:3887–3891.
126.
Lehr HA, Huebner C, Nolte D, Kohlschütter A, Messmer K: Dietary fish oil blocks the microcirculatory manifestations of ischemia-reperfusion injury in striated muscle in hamsters. Proc Natl Acad Sci USA 1991;88:6726–6730.
127.
Figueroa CD, Henderson LM, Kaufmann J, De la Cadena RA, Colman RW, Müller-Esterl W, Bhoola KD: Immunovisualization of high (HK) and low (LK) molecular weight kininogens on isolated human neutrophils. Blood 1992;79:754–759.
128.
Figueroa CD, Maciver AG, Bhoola KD: Identification of a tissue kallikrein in human polymorphonuclear leukocytes. Br J Haematol 1989;72:321–328.
129.
Mullins RJ, Hudgens RW: Increased skin lymph protein clearance after a 6-h arterial bradykinin infusion. Am J Physiol 1987;253:H1462–H1469.
130.
Yotsumoto F, Manabe T, Oshio G, Imanishi K, Ando K, Kyogoku T, Hirano T, Tobe T: Role of pancreatic blood flow and vasoactive substances in the development of canine acute pancreatitis. J Surg Res 1993;55:531–536.
131.
Munn JS, Prinz RA, Castelli M, Dobrin P, Marks WH, Djuricin G: Does ischemia cause pancreatitis? Int J Pancreatol 1990;5:299–313.
132.
Binder PS, Heiskell CA, Adams JR, Cerra FB, Eilert JB, Bergan JJ: Pancreatic function after normothermic ischemia. I. In vivo ischemia. Am J Surg 1970;120:687–692.
133.
Slater DN, Bardsley D, Magnall Y, Smythe A, Fox M: Pancreatic ischemia: Sensitivity and reversibility of the changes. Br J Exp Pathol 1975;56:530–536.
134.
Mithofer K, Fernandez-del Castillo C, Bassi DG, Lewandrowski KB, Rattner DW, Warshaw AL: Role of hypercalcemia and ischemia in pancreatic injury. Pancreas 1993;8:765–766.
135.
Furukawa M, Kimura T, Yamaguchi H, Kinjoh M, Nawata H: Role of oxygen-derived free radicals in hemorrhagic pancreatitis induced by stress and cerulein in rats. Pancreas 1994;9:67–72.
136.
Siech M, Weber H, Letko G, Dummler W, Schroenber MH, Beger HG: Similar morphological and intracellular biochemical changes in alcoholic acute pancreatitis and ischemic acute pancreatitis in rats. Pancreas 1997;14:32–38.
137.
Fernandez-del Castillo C, Rattner DW, Warshaw AL: Acute pancreatitis. Lancet 1993;342:475–479.
138.
Grewal HP, Garland L, Novak K, Gaber L, Tolley EA, Gaber AO: Risk factors for postimplantation pancreatitis and pancreatic thrombosis in pancreas transplant recipients. Transplantation 1993;56:609–612.
139.
Fernandez-Cruz L, Sabater L, Gilabert R, Ricart R, Ricart MJ, Saenz A, Astudillo E: Native and graft pancreatitis following combined pancreas-renal transplantation. Br J Surg 1993;80:1429–1432.
140.
Huddy SPJ, Joyce WP, Pepper JR: Gastrointestinal complications in 4,473 patients who underwent cardiopulmonary bypass surgery. Br J Surg 1991;78:293–296.
141.
Lawhorne TW Jr, Davis JL, Smith GW: General surgical complications after cardiac surgery. Am J Surg 1976;136:254–256.
142.
Tikanoja T, Rautianinen P, Leijala M, Svens E, Tikanoja S: Hyperamylasemia after cardiac surgery in infants and children. Intensive Care Med 1996;22:959–963.
143.
Foitzik T, Bassi DG, Fernandez-del Castillo C, Warshaw AL, Rattner DW: Intravenous contrast medium impairs oxygenation of the pancreas in acute necrotizing pancreatitis in the rat. Arch Surg 1994;129:706–711.
144.
Kaiser AM, Grady T, Gerdes D, Saluja M, Steer ML: Intravenous contrast medium does not increase the severity of acute necrotizing pancreatitis in the opossum. Dig Dis Sci 1995;40:1547–1553.
145.
Tsiotos GG, Luque-de Leon E, Soreide JA, Bannon MP, Zietlow SP, Baerga-Varela Y, Sarr MG: Management of necrotizing pancreatitis by repeated operative necrosectomy using a zipper technique. Am J Surg 1998;175:91–98.
146.
Gullo L, Cavicci L, Tomassetti P, Spagnolo C, Freyrie A, D’Addato M: Effects of ischemia on the human pancreas. Gastroenterology 1996;111:1033–1038.
147.
Ohri SK, Bjarnason I, Pathi V, Somassundaram S, Bowles CT, Keogh BE, Khaghani A, Menzies I, Yacoub MH, Taylor KM: Cardiopulmonary bypass impairs small intestinal transport and increases gut permeability. Ann Thorac Surg 1993;55:1080–1086.
148.
Ott MJ, Buchman TG, Baumgartner WA: Postoperative abdominal complications in cardiopulmonary bypass patients: A case-controlled study. Ann Thorac Surg 1995;59:1210–1213.
149.
Taniguchi N: Clinical significance of superoxide dismutases: Changes in aging, diabetes, ischemia and cancer. Adv Clin Chem 1992;29:1–59.
150.
Marber MS, Latchman DS, Walker JM, Yellon DM: Cardiac stress protein elevation 24 hours after brief ischemia or heat stress is associated with resistance to myocardial infarction. Circulation 1993;88:1264–1272.
151.
Simovic MO, Bonham MJD, Abu-Zidan FM, Windsor JA: Manganese superoxide dismutase: A marker of ischemia-reperfusion injury in acute pancreatitis? Pancreas 1997;15:78–82.
152.
McKay CJ, Curran F, Sharples C, Baxter JN, Imrie CW: Prospective placebo-controlled trial of lexipafant in predicted severe acute pancreatitis. Br J Surg 1997;84:1239–1243.
Copyright / Drug Dosage / Disclaimer
Copyright: All rights reserved. No part of this publication may be translated into other languages, reproduced or utilized in any form or by any means, electronic or mechanical, including photocopying, recording, microcopying, or by any information storage and retrieval system, without permission in writing from the publisher.
Drug Dosage: The authors and the publisher have exerted every effort to ensure that drug selection and dosage set forth in this text are in accord with current recommendations and practice at the time of publication. However, in view of ongoing research, changes in government regulations, and the constant flow of information relating to drug therapy and drug reactions, the reader is urged to check the package insert for each drug for any changes in indications and dosage and for added warnings and precautions. This is particularly important when the recommended agent is a new and/or infrequently employed drug.
Disclaimer: The statements, opinions and data contained in this publication are solely those of the individual authors and contributors and not of the publishers and the editor(s). The appearance of advertisements or/and product references in the publication is not a warranty, endorsement, or approval of the products or services advertised or of their effectiveness, quality or safety. The publisher and the editor(s) disclaim responsibility for any injury to persons or property resulting from any ideas, methods, instructions or products referred to in the content or advertisements.
You do not currently have access to this content.