Additive antifibrotic effects of pioglitazone and candesartan on experimental renal fibrosis in mice

被引:34
作者
Higashi, Keishi [1 ]
Oda, Takashi [1 ]
Kushiyama, Taketoshi [1 ]
Hyodo, Toshitake [1 ]
Yamada, Muneharu [1 ]
Suzuki, Shigenobu [1 ]
Sakurai, Yutaka [2 ]
Miura, Soichiro [1 ]
Kumagai, Hiroo [1 ]
机构
[1] Natl Def Med Coll, Dept Nephrol, Tokorozawa, Saitama 3598513, Japan
[2] Natl Def Med Coll, Dept Prevent Med & Publ Hlth, Tokorozawa, Saitama 3598513, Japan
关键词
angiotensin II type 1 receptor blockers; fibrosis; plasminogen activator inhibitor-1; peroxisome proliferator-activated receptor-gamma; ureteral obstruction; PLASMINOGEN-ACTIVATOR INHIBITOR-1; ANGIOTENSIN INHIBITION; KIDNEY; DEFICIENCY; INJURY; GLOMERULOSCLEROSIS; ROSIGLITAZONE; INFLAMMATION; REGRESSION; PROTECTS;
D O I
10.1111/j.1440-1797.2009.01253.x
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
100201 [内科学]; 100221 [泌尿外科学];
摘要
Aim: To examine the additive protective effects of the peroxisome proliferator-activated receptor-gamma agonist pioglitazone (Pio) and the angiotensin II receptor blocker candesartan (Cand) in a murine model of renal fibrosis: mice with unilateral ureteral obstruction (UUO). Methods: Mice were randomly assigned into four groups that after UUO received i.p. injections of either Pio (10 mg/kg/day), Cand (1 mg/kg/day), Cand + Pio or vehicle for 10 days. Physiological parameters, the degree of renal fibrosis and molecules related to renal fibrosis were analysed, and sham-operated mice were used as controls. Results: Total collagen assay showed prominent renal fibrosis in the vehicle-treated mice, significantly attenuated renal fibrosis in the Cand-treated and the Pio-treated mice, and further attenuated renal fibrosis in the (Cand + Pio)-treated mice. Real-time reverse transcription polymerase chain reaction revealed that this attenuation pattern was also evident in the expression of the mRNA for transforming growth factor-beta, collagens I and III, and plasminogen activator inhibitor-1. Conclusion: Pioglitazone and candesartan have additive protective effects on renal fibrosis due to UUO in mice, suggesting that their use in combination would be an effective treatment for chronic kidney disease.
引用
收藏
页码:327 / 335
页数:9
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