Literature DB >> 3817332

Pathways of enzyme transfer in sodium taurocholate-induced acute hemorrhagic pancreatitis.

J F Lange, P J Beyaert, H van Vugt, G N Tytgat, J van Gool.   

Abstract

The pathways of enzyme transfer from the pancreas into the systemic circulation were analyzed in sodium taurocholate-induced acute hemorrhagic pancreatitis in the rat by estimating lipase concentrations in blood, lymph and ascites. During the first few hours of pancreatitis high enzyme levels were observed in thoracic duct lymph. However, cannulation of the thoracic duct did not prevent a significant increase in the lipase concentration in peripheral blood. The portal vein lipase concentration was found to exceed the peripheral values by approximately 10%. Extremely high concentrations of lipase were measured in the ascites collected during pancreatitis. When the ascites was transferred to the peritoneal space of healthy rats, a significant increase in the lipase concentration in peripheral blood was measured. This increase could not be prevented by transection of the parasternal lymphatics. It was concluded that the hematogenous rather than the lymphatic transport of lipase from the pancreas and the peritoneal surface is the most important pathway. In this respect, this study does not support thoracic duct drainage but advocates peritoneal lavage as a logical therapeutic measure to reduce the concentration of circulating toxic substances from the pancreas in acute pancreatitis.

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Year:  1986        PMID: 3817332     DOI: 10.1159/000199373

Source DB:  PubMed          Journal:  Digestion        ISSN: 0012-2823            Impact factor:   3.216


  11 in total

1.  Pathophysiological role of secretory type I and II phospholipase A2 in acute pancreatitis: an experimental study in rats.

Authors:  W Uhl; H J Schrag; N Schmitter; T J Nevalainen; J Aufenanger; A M Wheatley; M W Büchler
Journal:  Gut       Date:  1997-03       Impact factor: 23.059

2.  The resorption of FITC-dextran 10,000 from the peritoneum in different modifications of bile-induced acute pancreatitis and in bacterial peritonitis.

Authors:  E Tarpila; P O Nyström; I Ihse
Journal:  Int J Pancreatol       Date:  1991 Nov-Dec

3.  Increased peritoneal permeability in acute experimental pancreatitis.

Authors:  C Svensson; R Sjödahl; C Tagesson; I Ihse
Journal:  Int J Pancreatol       Date:  1989-02

4.  Specific pancreatic enzymes activate macrophages to produce tumor necrosis factor-alpha: role of nuclear factor kappa B and inhibitory kappa B proteins.

Authors:  C Jaffray; C Mendez; W Denham; G Carter; J Norman
Journal:  J Gastrointest Surg       Date:  2000 Jul-Aug       Impact factor: 3.452

5.  Effect of peritoneal lavage and lymph ligature on systemic complications of experimental acute pancreatitis.

Authors:  E Folch; D Closa; E Gelpí; J Roselló-Catafau
Journal:  Dig Dis Sci       Date:  2000-05       Impact factor: 3.199

6.  Ascites of severe acute pancreatitis in rats transcriptionally up-regulates expression of interleukin-6 and -8 in vascular endothelium and mononuclear leukocytes.

Authors:  A Masamune; T Shimosegawa; M Fujita; A Satoh; M Koizumi; T Toyota
Journal:  Dig Dis Sci       Date:  2000-02       Impact factor: 3.199

7.  The role of ascites and phospholipase A2 on peritoneal permeability changes in acute experimental pancreatitis.

Authors:  C Svensson; R Sjödahl; I Lilja; I Ihse
Journal:  Int J Pancreatol       Date:  1990-01

Review 8.  Microvasculature of the pancreas. Relation to pancreatitis.

Authors:  D E Bockman
Journal:  Int J Pancreatol       Date:  1992-08

9.  Peritoneal absorption of pancreatic enzymes in dogs.

Authors:  T Hayakawa; T Kondo; T Shibata; S Naruse
Journal:  Gastroenterol Jpn       Date:  1992-04

10.  Pancreatic phospholipase A2 in cerulein-induced acute pancreatitis in the rat.

Authors:  A J Hietaranta; H J Aho; T J Nevalainen
Journal:  Int J Pancreatol       Date:  1993-12
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