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Experimental pancreatitis in the rat. Changes in pulmonary phospholipids during sodium taurocholate-induced acute pancreatitis

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Research in Experimental Medicine

Summary

Acute haemorrhagic pancreatitis was induced in rats by injecting aqueous solution of sodium taurocholate into the common biliopancreatic duct. Lecithin and lysolecithin were separated from pulmonary homogenate by thin layer chromatography and quantified by phosphorus determination. The ratio of lysolecithin to lecithin increased after the sodium taurocholate injection as well as after i.v. administration of porcine pancreatic phospholipase A2. It was concluded that phospholipase A2, released from pancreatic acinar cells into blood, may convert pulmonary lecithin into lysolecithin during acute pancreatitis. Destruction of pulmonary surfactant may contribute to the development of the adult respiratory distress syndrome as seen in patients suffering from severe acute pancreatitis.

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References

  • Aho HJ, Koskensalo S M-L, Nevalainen TJ (1980a) Experimental pancreatitis in the rat. Sodium taurocholate-induced acute haemorrhagic pancreatitis. Scand J Gastroenterol 15:411–416

    PubMed  Google Scholar 

  • Aho HJ, Nevalainen TJ, Lindberg RLP, Aho AJ (1980b) Experimental pancreatitis in the rat. The role of phospholipase A in sodium taurocholate-induced acute haemorrhagic pancreatitis. Scand J Gastroenterol 15:1027–1031

    PubMed  Google Scholar 

  • Bartlett GR (1959) Phosphorus assay in column chromatography. J Biol Chem 234:466–468

    PubMed  Google Scholar 

  • Bolooki H, Minkowitz S, Giammona ST, Jude JR (1971) Respiratory failure in acute pancreatitis. I. The biophysical characteristics of lungs in experimental pancreatitis. J Surg Oncol 3:31–42

    PubMed  Google Scholar 

  • Bolooki H, Mobin-Uddin K, Lombardo CR, Jude JR, Smith ME (1968) Biophysical characteristics of lungs in acute pancreatitis. Surg Forum 19:371–373

    PubMed  Google Scholar 

  • Cotran RS, Majno G (1964) A light- and electron-microscopic analysis of vascular injury. Ann NY Acad Sci 116:750–764

    PubMed  Google Scholar 

  • Dougall AM, Brennan MM, Wong C-Y, Harding PGR, Possmayer F, Ahmad D, Enhorning G, Passi RB (1977) Effect of experimental hemorrhagic pancreatitis on respiratory function and pulmonary phospholipids. Surg Forum 28:189–191

    PubMed  Google Scholar 

  • Enquist IF, Gliedman ML (1958) Gross autopsy findings in cases of fatal acute pancreatitis. Arch Surg 77:985–991

    Google Scholar 

  • Giacobino JP, Simon GT (1971) Experimental glomerulonephritis induced by minimal doses of trypsin. Arch Pathol 21:193–200

    Google Scholar 

  • van Golde LMG (1976) Metabolism of phospholipids in the lung. Am Rev Resp Dis 114:977–999

    PubMed  Google Scholar 

  • de Haas GH, Postema NM, Nieuwenhuizen W, van Deenen LLM (1968) Purification and properties of an anionic zymogen of phospholipase A from porcine pancreas. Biochim Biophys Acta 159:118–129

    PubMed  Google Scholar 

  • Hatao M (1969) On etiology and pathophysiology of acute pancreatitis with special reference to participation of phospholipase A. Arch Jpn Chir 38:76–106

    Google Scholar 

  • Heinle FJ, Levine G, Webster MW (1978) Pulmonary and skeletal capillary permeability to albumin in experimental acute hemorrhagic pancreatitis. J Surg Res 25:119–121

    PubMed  Google Scholar 

  • Helenius A, Simons K (1975) Solubilization of membranes by detergents. Biochim Biophys Acta 415:43–51

    Google Scholar 

  • Jacobs ML, Daggett WM, Civetta JM, Vasu MA, Lawson DW, Warshaw AL, Nardi GL, Bartlett MK (1977) Acute pancreatitis: Analysis of factors influencing survival. Ann Surg 185:43–51

    PubMed  Google Scholar 

  • Kimura T, Toung JK, Margolis S, Bell WR, Cameron JL (1980) Repiratory failure in acute pancreatitis: the role of free fatty acids. Surgery 87:509–513

    PubMed  Google Scholar 

  • Kumar R, Hegde KS, Krishna B, Sharma RS (1980) Combined effect of hypoxia and cold on the phospholipid composition of lung surfactant in rats. Aviat Space Environ Med 51:459–462

    PubMed  Google Scholar 

  • Lee BC, Malik AB, Barie PS, Minnear FL (1981) Effect of acute pancreatitis on pulmonary transvascular fluid and protein exchange. Am Rev Resp Dis 123:618–621

    PubMed  Google Scholar 

  • Maciver AG, Metcalfe IL, Possmayer F, Harding PGR, Passi RB (1977) Alteration of surfactant chemistry in experimental hemorrhagic pancreatitis. J Surg Res 23:311–314

    PubMed  Google Scholar 

  • Morgan AP, Jenny ME, Haessler H (1968) Phospholipids, acute pancreatitis and the lungs: Effect of lecithinase infusion on pulmonary surface activity in dogs. Ann Surg 167:329–335

    PubMed  Google Scholar 

  • Petty TL, Ashbaugh DG (1971) The adult respiratory distress syndrome. Clinical features, factors influencing prognosis and principles of management. Chest 60:233–239

    PubMed  Google Scholar 

  • Ranson JHC, Turner JW, Roses DF, Rifkind KM, Spencer FC (1974) Respiratory complications in acute pancreatitis. Ann Surg 179:557–566

    PubMed  Google Scholar 

  • Schröder T, Kivilaakso E, Kinnunen PKJ, Lempinen M (1980) Serum phospholipase A2 in human acute pancreatitis. Scand J Gastroenterol 15:633–636

    PubMed  Google Scholar 

  • Zieve L, Vogel WC (1961) Measurement of lecithinase A in serum and other body fluids. J Lab Clin Med 57:586–599

    PubMed  Google Scholar 

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Supported by grants from the Sigrid Jusélius, Paulo and Hoechst Fennica Foundations

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Aho, H.J., Ahola, R.A., Tolvanen, A.M. et al. Experimental pancreatitis in the rat. Changes in pulmonary phospholipids during sodium taurocholate-induced acute pancreatitis. Res. Exp. Med. 182, 79–84 (1983). https://doi.org/10.1007/BF01852290

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  • DOI: https://doi.org/10.1007/BF01852290

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