Korean J Pathol.  1998 Dec;32(12):1058-1065.

The Effects of Angiotensin Converting Enzyme Inhibitor on Progressive Glomerular Sclerosis

Affiliations
  • 1Department of Pathology, School of Medicine, Catholic University of Taegu-Hyosung, Taegu, Korea.
  • 2Genetic Resources Center, Korea Research Institute of Bioscience & Biotechnology, Korea Institute of Science and Technology, Taejon, Korea.
  • 3Department of Pathology, School of Medicine, Kyungpook National University, Taegu, Korea.

Abstract

Almost all advanced glomerular diseases have glomerular sclerotic changes to varying degrees whatever causes their primary glomerular disease are. Pathogenesis of these sclerosis has been thought of as the hyperfiltration in the primary glomerulosclerosis due to development of glomerular hypertension in each insulted glomeruli. This background gave the theoretical bases for antihypertensive therapies for supporting chronic renal insufficient patients. Angiotensin converting enzyme (ACE) inhibitor, one of the antihypertensive drugs, has received attention recently for its effectiveness. The aims of this study determined the effects and mechanism of the ACE inhibitor, enalapril, on the glomerulosclerosis in FGS/NgaKist mice, which was an animal model of chronic renal failure by generating spontaneously heavy proteinuria and progressive glomerulosclerosis. Five-week-old FGS/NgaKist mice (n=38) were assigned to four groups. Group 1a (n=6) and group 2a (n=8) fed with a vehicle, were sacrificed at the end of 10 weeks and 15 weeks, respectively. Group 1b (n=12) and 2b (n=12) received enalapril (100 mg/L) in drinking water for 5 weeks and 10 weeks from 6th week of age respectively, and were sacrified on the same day as the control groups. Doses of enanapril were maintained to 2 mg/kg/day by measuring the amount of water consumption. In enalapril groups 1b and 2b, systemic blood pressure (74.7 14.0 mm Hg, 74.3 15.9 mmHg) were significantly lower than control group 2a (116.1 4.6 mmHg, P<0.001). Similarly, degree of proteinuria lowered in enalapril group 2b versus control group 2a (0% and 50.0%, P<0.001). Glomerulosclerosis percentage significantly decreased (P<0.001) (group 1b and 2b; 1.9 6.5, 5.6 7.0 vs control 1a and 2a; 32.8 15.5, 31.4 13.8). Glomerulosclerosis score also decreased (P<0.001) (group 1b and 2b; 0.02 0.08 vs control 1a and 2a; 0.48 0.12, 0.30 0.14). The immunofluorescent staining of enalapril groups showed negative for mesangial deposition of IgG, IgA, IgM, and C3 which were positive in control groups. Immunohistochemical staining with TGF-beta1 was negative in enalapril groups and sclerotic glomeruli both enalapril groups and control groups. These results support that the ACE inhibitor has a renoprotective effect on glomerulosclerosis not only by decreasing the blood pressure but also by suppressing the immune deposits on glomeruli.

Keyword

Glomerulosclerosis; Angiotensin converting enzyme inhibitor; Enalapril; TGF-beta1

MeSH Terms

Angiotensins*
Animals
Antihypertensive Agents
Blood Pressure
Drinking
Drinking Water
Enalapril
Humans
Hypertension
Immunoglobulin A
Immunoglobulin G
Immunoglobulin M
Kidney Failure, Chronic
Mice
Models, Animal
Peptidyl-Dipeptidase A*
Proteinuria
Sclerosis*
Transforming Growth Factor beta1
Angiotensins
Antihypertensive Agents
Drinking Water
Enalapril
Immunoglobulin A
Immunoglobulin G
Immunoglobulin M
Peptidyl-Dipeptidase A
Transforming Growth Factor beta1
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