Significance of Reperfusion Injury after Venous Strangulation Obstruction of Equine Jejunum

References

• MacDonald M H, Pascoe J R, Stover S M, Meagher D M. Survival after small intestinal resection and anastomosis in horses. Vet Surg. 1989; 18: 415–423
   PubMed Web of Science ®Google Scholar
• White N A, Moore J N, Cowgil L M, Brown J. Epizootiology and risk factors in equine colic at University hospitals. Proceedings. Vet Sem Univ Georgia 1986; 2: 26–29
   Google Scholar
• Freeman D E, Cimprich R E, Richardson D W, et al. Early mucosal healing and chronic changes in pony jejunum after various types of strangulation obstruction. Am J Ver Res. 1988; 49: 810–818
   PubMedGoogle Scholar
• Shah S D, Anderson C A. Prediction of small bowel viability using Doppler ultrasound. Ann Surg. 1981; 194: 97–99
   PubMedGoogle Scholar
• Boley S J, Kaleya R N, Brandt L J. Mesenteric venous thrombosis. Surg Clin N Am. 1992; 72: 183–199
   PubMed Web of Science ®Google Scholar
• Parks D A, Granger D N. Contributions of ischemia and reperfusion to mucosal lesion formation. Am J Physiol. 1986; 250: G749–G753
   PubMed Web of Science ®Google Scholar
• Granger D N. Role of xanthine oxidase and granulocytes in ischemia-reperfusion injury. Am J Physiol. 1988; 255: H1269–H1275
   PubMed Web of Science ®Google Scholar
• Nilsson U A, Lundgren E H, Haglind E, Bylund-Fellenius A-C. Radical production during in vivo intestinal ischemia and reperfusion in the cat. Am J Physiol. 1989; 257: G409–G414
   Google Scholar
• Kurtel H, Tso P, Granger D N. Granulocyte accumulation in postischemic intestine: role of leukocyte adhesion glycoprotein CD11/CD18. Am J Physiol. 1992; 262: G878–G882
   Google Scholar
• Kubes P, Hunter J, Granger N D. Ischemia/reperfusion-induced feline intestine dysfunction: importance of granulocyte recruitment. Gastroentereology 1992; 103: 807–812
   PubMed Web of Science ®Google Scholar
• Kubes P, Arfors K E, Granger D N. Platelet-activating factor-induced mucosal dysfunction: role of oxidants and granulocytes. Am J Physiol 1991; 260: G965–G971
   Google Scholar
• Zimmerman B J, Guillory D J, Grisham M B, Gaginella T S, Granger D N. Role of leukotriene B, in granulocyte infiltration into the postischemic feline intestine. Gastroenterology 1990; 99: 1358–1363
   PubMed Web of Science ®Google Scholar
• Park P O, Hnglund U, Bulkley G B, Falt K. The sequence of development of intestinal tissue injury after strangulation ischemia and reperfusion. Surgery. 1990; 107: 574–580
   PubMed Web of Science ®Google Scholar
• Otamiri T, Tagesson C. Role of phospholipase A2 and oxygenated free radicals in mucosal damage after small intestinal ischemia and reperfusion. Am J Surg. 1989; 107: 562–566
   Google Scholar
• Simpson R, Alon R, Kohzik L, Valeri C R, Shepro D, Hechtman H B. Neutrophil and nonneutrophil-mediated injury in intestinal ischemia-reperfusion. Ann Surg. 1993; 218: 444–454
   PubMed Web of Science ®Google Scholar
• Arden W A, Slocombe R F, Stick J A, Parks A H. Morphologic and ultrastructural evaluation of effect of ischemia and dimethyl sulfoxide on equine jejunum. Am J Vet Res. 1990; 31: 1784–1791
   Google Scholar
• Ohkawa H, Ohishi N, Yagi K. Assay for lipid peroxides in animal tissues by thiobarbituric acid reaction. Anal Biochem. 1979; 95: 351–358
   PubMed Web of Science ®Google Scholar
• Slater T F. Overview of methods used for detecting lipid peroxidation. Methods in Enzymology: Oxygen Radicals in Biological Systems, L Packer. Academic, New York 1984; 283–293
   Google Scholar
• Grisham M B, Benoit J N, Granger D N. Assessment of leukocyte involvement during ischemia and reperfusion of intestine. Methods in Enzymology: Oxygen Radicals in Biologic Systems, L. Packer, A N Glazer. Academic, New York 1990; 729–742
   Google Scholar
• Chiu C-J, McArdle A H, Brown R, Scott H J, Curd F N. Intestinal mucosal lesion in low-flow states. Arch Surg. 1970; 101: 478–483
   PubMedGoogle Scholar
• Metcalf J A, Gallin J I, Nauseef W M, Root R K. Laboratory Manual of Neutrophil Function. Raven, New York 1986; 150–151
   Google Scholar
• Winer B J. Statistical Principles in Experimental Design,ed 2. McGraw-Hill, New York 1971; 514–603
   Google Scholar
• Mortillaro N A, Taylor A E. Interaction of capillary and tissue forces in the cat small intestine. Circ Res. 1976; 39: 348–358
   PubMed Web of Science ®Google Scholar
• Prichard M, Ducharme N G, Wilkins P A, Erb H N, Butt M. Xanthine oxidase formation during experimental ischemia of the equine small intestine. Can J Vet Res. 1991; 55: 310–314
   PubMedGoogle Scholar
• Johnston J K, Freeman D E, Gillette D, Soma L R. Effects of superoxide dismutase on injury induced by anoxia and reoxygenation in equine small intestine in vitro. Am J Vet Res. 1991; 52: 2050–2054
   PubMedGoogle Scholar
• Freeman D E, Johnston J K, Laws E G. Failure of superoxide dismutase to mitigate changes caused by ischemia and reperfusion in horse intestine. Vet Surg. 1992; 21: 389, Abstract
   Google Scholar
• Leung F W, Su K C, Passaro E, Guth P H. Regional differences in gut blood flow and mucosal damage in response to ischemia and reperfusion. Am J Physiol. 1992; 263: G301–G305
   Google Scholar
• Henry T D, Archer S L, Nelson D, Weir E K, From H L. Postischemic oxygen radical production varies with duration of ischemia. Am J Physiol. 1993; 264: H1478–H1484
   PubMedGoogle Scholar
• Linas S L, Whittenburg D, Repine J E. O, metabolites cause reperfusion injury after short but not prolonged renal ischemia. Am J Physiol. 1987; 253: F685–F691
   Google Scholar
• Sussman M S, Bulkley G B. Oxygen-derived free radicals in reperfusion injury. Methods in Enzymology: Oxygen Radicals in Biological Systems, L Packer, A N Glazer. Academic, New York 1990; 711–723
   Google Scholar