Addition of the antioxidant probucol to angiotensin II type I receptor antagonist arrests progressive mesangioproliferative glomerulonephritis in the rat

被引:38
作者
Kondo, Shuji
Shimizu, Maki
Urushihara, Maki
Tsuchiya, Koichiro
Yoshizumi, Masanori
Tamaki, Toshiaki
Nishiyama, Akira
Kawachi, Hiroshi
Shimizu, Fujio
Quinn, Mark T.
Lambeth, David J.
Kagami, Shoji
机构
[1] Univ Tokushima, Grad Sch, Inst Hlth Biosci, Dept Pediat, Tokushima 7708503, Japan
[2] Univ Tokushima, Grad Sch, Inst Hlth Biosci, Dept Pharmacol, Tokushima, Japan
[3] Kagawa Med Univ, Dept Pharmacol, Kagawa, Japan
[4] Niigata Univ, Sch Med, Inst Nephrol, Dept Cell Biol, Niigata, Japan
[5] Montana State Univ, Dept Vet Mol Biol, Bozeman, MT 59717 USA
[6] Emory Univ, Dept Pathol & Lab Med, Atlanta, GA 30322 USA
来源
JOURNAL OF THE AMERICAN SOCIETY OF NEPHROLOGY | 2006年 / 17卷 / 03期
关键词
D O I
10.1681/ASN.2005050519
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
Angiotensin II (Ang II) and reactive oxidative species (ROS) that are produced by NADPH oxidase have been implicated in the progression of glomerulonephritis (GN). This study examined the effect of simultaneously interrupting Ang 11 and ROS with an Ang II receptor blocker (ARB), candesartan, and a free radical scavenger, probucol, in a model of progressive mesangioproliferative GN induced by the injection of anti-Thy-1 antibody into uninephrectomized rats. Nephritic rats were divided into four groups and given daily oral doses of the following: Vehicle, 1% probucol diet, 70 mg/L candesartan in drinking water, and probucol plus candesartan. These treatments lasted until day 56. Vehicle-treated nephritic rats developed progressively elevated proteinuria and glomerulosclerosis. Candesartan kept proteinuria significantly lower than vehicle or probucol. The addition of probucol to candesartan normalized urinary protein excretion. Increases in BP in nephritic rats were lowered by these treatments, except with probucol. It is interesting that both glomerular cell number and glomerulosclerosis were significantly decreased by candesartan and normalized by the addition of probucol. Immunohistochemical studies for TGF-beta 1, collagen type I, and fibronectin revealed that the combined treatment abolished glomerular fibrotic findings compared with candesartan. In addition, glomerular expression of NADPH oxidase components and superoxide production suggested that the combined treatment completely eliminated NADPH oxidase-associated ROS production. In conclusion, our study provides the first evidence that the antioxidant probucol, when added to an Ang II receptor blockade, fully arrests proteinuria and disease progression in GN. Furthermore, the data suggest that NADPH oxidase-associated ROS production may play a pivotal role in the progression of GN. The combination of probucol and candesartan may represent a novel route of therapy for patients with progressive GN.
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收藏
页码:783 / 794
页数:12
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