Absence of Gelatinase (MMP-9) or Collagenase (MMP-13) Attenuates Adriamycin-Induced Albuminuria and Glomerulosclerosis

被引:20
|
作者
Sakamaki, Yusuke
Sasamura, Hiroyuki [1 ]
Hayashi, Kaori
Ishiguro, Kimiko
Takaishi, Hironari [2 ]
Okada, Yasunori [3 ]
D'Armiento, Jeanine M. [4 ]
Saruta, Takao
Itoh, Hiroshi
机构
[1] Keio Univ, Sch Med, Dept Internal Med, Shinjuku Ku, Tokyo 1608582, Japan
[2] Keio Univ, Sch Med, Dept Orthoped Surg, Tokyo 1608582, Japan
[3] Keio Univ, Sch Med, Dept Pathol, Tokyo 1608582, Japan
[4] Columbia Univ, Coll Phys & Surg, Dept Med, New York, NY USA
来源
NEPHRON EXPERIMENTAL NEPHROLOGY | 2010年 / 115卷 / 02期
关键词
Matrix metalloproteinase; Adriamycin; Glomerulosclerosis; MATRIX METALLOPROTEINASES; MATRIX-METALLOPROTEINASE-9; MICE; SUSCEPTIBILITY; NEPHROPATHY; INHIBITORS;
D O I
10.1159/000312883
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
Background/Aims: The role of matrix metalloproteinases (MMPs) in the pathogenesis of glomerular injury appears to be complex. To investigate the role of individual MMPs, we examined the course of Adriamycin-induced albuminuria and glomerulosclerosis in mice lacking either a gelatinase (MMP-9) or a collagenase (MMP-13). Methods: Adriamycin was administered to MMP-9 or MMP-13 knockout (KO) mice. Glomerular injury was assessed by the quantification of albuminuria, the glomerular injury score and type IV collagen immunostaining. Results: Treatment of mice with Adriamycin (18 mg/kg i.v.) resulted in marked albuminuria and glomerulosclerosis reaching a peak at 4-8 weeks. The albuminuria and glomerulosclerosis were significantly (p < 0.05) attenuated in both the MMP-9 KO and MMP-13 KO mice compared to controls. In contrast, treatment of wild-type mice with the broad-spectrum MMP inhibitor doxycycline did not have a beneficial effect on the albuminuria and glomerulosclerosis. Conclusion: These results support a role for both gelatinase (MMP-9) and collagenase (MMP-13) in the pathogenesis of glomerular injury in the Adriamycin-induced glomerulosclerosis model. MMP inhibitors with high specificity towards MMP-9 and/or MMP-13 may be potential future candidates to provide more effective therapies to inhibit the development of glomerulosclerosis. Copyright (C) 2010 S. Karger AG, Basel
引用
收藏
页码:E22 / E32
页数:11
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