The ace inhibitor, quinapril, ameliorates peritoneal fibrosis in an encapsulating peritoneal sclerosis model in mice

被引:39
作者
Sawada, T [1 ]
Ishii, Y [1 ]
Tojimbara, T [1 ]
Nakajima, I [1 ]
Fuchinoue, S [1 ]
Teraoka, S [1 ]
机构
[1] Tokyo Womens Med Univ, Kidney Ctr, Dept Surg, Shinjuku Ku, Tokyo 1628666, Japan
关键词
angiotensin-converting enzyme; peritoneal dialysis; EPS; quinapril;
D O I
10.1016/S1043661802002281
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Encapsulating peritoneal sclerosis (EPS) is a serious complication of patients on continuous ambulatory peritoneal dialysis. In the present study, the inhibitory effect of angiotensin-converting enzyme inhibitor, quinapril, on the peritoneal fibrosis was examined in an experimental EPS model in mice. C57BL/6 mice were divided into three groups. Group 1 (n = 20) mice received daily intraperitoneal injection of 0.3 ml of SH solution which consists of 0.1% chlorhexidine gluconate and 15% ethanol dissolved in saline. Group 2 (n = 20) and group 3 (n = 20) mice received SH solution by the same manner of group 1 mice, and were given orally 1 or 3 mg kg(-1) of quinapril, respectively, on daily basis. Five mice from each group were sacrificed on day 3, 7, 21, and 56, and evaluated macroscopically and histologically. Macroscopic examination revealed that fibrotic change in parietal peritoneum in group 1 was more severe than in group 2 and 3, accompanied with statistical significance. Histological examination demonstrated that peritoneal thickening in group 2 and 3 were markedly ameliorated than in group 1. Semi-quantitative analysis showed that histological fibrotic score was significantly higher in group 1 than in group 2 and 3. These results suggest that quinapril ameliorate the fibrotic change in parietal peritoneum in experimental EPS model in mice, and may have a clinical utility for the prevention of EPS. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:505 / 510
页数:6
相关论文
共 22 条
[1]   Effect of maximal reduction of angiotensin in renal fibrosis: Bad news-good news from a pediatric mouse - Discussion [J].
Border, WA ;
Noble, NA .
AMERICAN JOURNAL OF KIDNEY DISEASES, 2000, 35 (04) :773-775
[2]  
BORDER WA, 1994, NEW ENGL J MED, V331, P1286
[3]  
BORDER WA, 1993, GROWTH FACTORS, V8, P1
[4]   SPECTROPHOTOMETRIC ASSAY AND PROPERTIES OF ANGIOTENSIN-CONVERTING ENZYME OF RABBIT LUNG [J].
CUSHMAN, DW ;
CHEUNG, HS .
BIOCHEMICAL PHARMACOLOGY, 1971, 20 (07) :1637-+
[5]  
DENIS J, 1980, ANN INTERN MED, V93, P508
[6]  
DOBBIE JW, 1992, PERITON DIALYSIS INT, V12, P14
[7]   Reduced angiotensinogen expression attenuates renal interstitial fibrosis in obstructive nephropathy in mice [J].
Fern, RJ ;
Yesko, CM ;
Thornhill, BA ;
Kim, HS ;
Smithies, O ;
Chevalier, RL .
JOURNAL OF CLINICAL INVESTIGATION, 1999, 103 (01) :39-46
[8]   SCLEROTIC THICKENING OF THE PERITONEAL MEMBRANE IN MAINTENANCE PERITONEAL-DIALYSIS PATIENTS [J].
GANDHI, VC ;
HUMAYUN, HM ;
ING, TS ;
DAUGIRDAS, JT ;
JABLOKOW, VR ;
IWATSUKI, S ;
GEIS, WP ;
HANO, JE .
ARCHIVES OF INTERNAL MEDICINE, 1980, 140 (09) :1201-1203
[9]   VASCULAR SMOOTH-MUSCLE CELL HYPERTROPHY VS HYPERPLASIA - AUTOCRINE TRANSFORMING GROWTH FACTOR-BETA-1 EXPRESSION DETERMINES GROWTH-RESPONSE TO ANGIOTENSIN-II [J].
GIBBONS, GH ;
PRATT, RE ;
DZAU, VJ .
JOURNAL OF CLINICAL INVESTIGATION, 1992, 90 (02) :456-461
[10]  
HOLMES CJ, 1990, CONTRIB NEPHROL, V86, P73