The role of ascites and phospholipase a2 on peritoneal permeability changes in acute experimental pancreatitis

1990 ◽  
Vol 6 (1) ◽  
pp. 71-79
Author(s):  
Conny Svensson ◽  
Rune Sjödahl ◽  
Ingela Lilja ◽  
Ingemar Ihse
1981 ◽  
Vol 37 (5) ◽  
pp. 531-532
Author(s):  
P. D. Broulík ◽  
J. Škrha ◽  
V. Pacovský

Cell Research ◽  
2010 ◽  
Vol 20 (5) ◽  
pp. 599-602 ◽  
Author(s):  
Ina A Weber ◽  
Igor Buchwalow ◽  
Daniela Hahn ◽  
Wolfram Domschke ◽  
Markus M Lerch ◽  
...  

Pancreatology ◽  
2015 ◽  
Vol 15 (3) ◽  
pp. S9
Author(s):  
Balázs Kui ◽  
Zsolt Balla ◽  
Eszter S. Kormányos ◽  
Béla Iványi ◽  
Péter Hegyi ◽  
...  

2006 ◽  
Vol 327 (3) ◽  
pp. 485-492 ◽  
Author(s):  
Dirk Uhlmann ◽  
Heike Lauer ◽  
Frederik Serr ◽  
Stefan Ludwig ◽  
Andrea Tannapfel ◽  
...  

1989 ◽  
Vol 4 (1) ◽  
pp. 91-98 ◽  
Author(s):  
Conny Svensson ◽  
Rune Sjödahl ◽  
Christer Tagesson ◽  
Ingemar Ihse

2005 ◽  
Vol 25 (3_suppl) ◽  
pp. 11-14 ◽  
Author(s):  
Jie Ni ◽  
Yvette Cnops ◽  
Rachel M. McLoughlin ◽  
Nicholas Topley ◽  
Olivier Devuyst

Acute peritonitis is the most frequent complication of peritoneal dialysis. Previous studies have suggested a major role for nitric oxide (NO) in the permeability changes and loss of ultrafiltration induced by acute peritonitis. In this study, we further investigated the potential role of NO in a mouse model of peritonitis induced by Escherichia coli lipopolysaccharide (LPS). A 2-hour peritoneal equilibration test was performed in control and LPS-treated mice using 7% glucose dialysate supplemented or not with the NO synthase inhibitor NG-nitro-L-arginine methyl ester (L-NAME). The levels of NO metabolites in the dialysate were maximal 18 hours after LPS injection. At that time, acute peritonitis induced by LPS was reflected by an increased recruitment of leukocytes, an increased intraperitoneal release of interleukin-6, a significant increase in the peritoneal permeability for small solutes, a loss of sodium sieving, and a loss of ultrafiltration in comparison with controls. Addition of L-NAME in LPS-treated mice significantly reversed permeability modifications and prevented the release of NO metabolites into the dialysate. These results confirm that increased NO mediates permeability modifications during acute peritonitis, and illustrate the potential of mouse models to investigate the molecular mechanisms regulating peritoneal permeability.


Pancreas ◽  
2006 ◽  
Vol 33 (4) ◽  
pp. 493
Author(s):  
M. Ruthenb??rger ◽  
J. Mayerle ◽  
B. Brandt-Nedelev ◽  
I. Jaroscakova ◽  
T. Wartmann ◽  
...  

1986 ◽  
Vol 41 (4) ◽  
pp. 362-366 ◽  
Author(s):  
O.Juhani Rämö ◽  
Tom Schröder ◽  
Timo Kuusi ◽  
Pauli Puolakkainen ◽  
Anu Mäkelä ◽  
...  

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