|
|
||||||||
Bench Science |
Departments of 1 Nephrology,2 Animal Laboratory,3 Pathology, 4 and Biochemistry, Dokuz Eylül University Medical School, Izmir, Turkey
Correspondence to: R. Ersoy, Department of Nephrology, Dokuz Eylül
University Medical School, 155. sok. No. 43/10 Hatay, Izmir,
Turkey.
uzmanersoy{at}yahoo.com
Background: Bacterial peritonitis episodes may disturb the
functional and histological integrity of the peritoneum in peritoneal dialysis
patients. The renin-angiotensin-aldosterone system may have fibrotic effects
on the peritoneum.
Objective: To study the effects of an angiotensin II
receptor antagonist (irbesartan) and an aldosterone antagonist
(spironolactone) in the prevention of peritoneal fibrosis in a rat model of
bacterial peritonitis.
Methods: 40 Wistar rats were randomized into 5 groups:
bacteria (B), bacteria-irbesartan (BI), bacteria-spironolactone (BS),
bacteria-irbesartan-spironolactone (BIS), and control (C) groups. The C group
received only dextran beads (Cytodex; Sigma Chemicals, St Louis, Missouri,
USA); the others were given bacteria and dextran beads intraperitoneally.
Irbesartan and/or spironolactone were given to 3 groups: BI, BS, and BIS. On
the eighth day, the rats were sacrificed, peritoneal adhesion was quantified,
and peritoneal tissue sections were evaluated histologically.
Results: The peritoneal total adhesion score was
significantly higher in the B group than in the BI, BIS, and C groups
(p < 0.01). Mean peritoneal thickness, mean inflammation score,
and mean fibrosis score were significantly higher in the B group in comparison
to the C group (p < 0.05). Mean peritoneal thickness of all
treatment groups was significantly lower than the B group (p <
0.05). Serum transforming growth factor beta-1 level was significantly higher
in the B group than in the BI, BS, and C groups (p < 0.05).
Conclusion: Irbesartan and spironolactone seem to decrease
the extent of peritoneal injury caused by bacterial peritonitis.
KEY WORDS: Peritonitis; peritoneal fibrosis; irbesartan; spironolactone; TGF-ß1.
Received 7 March 2006; accepted 20 March 2007.
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |