Enhanced gene expression of myocardial matrix metalloproteinases 2 and 9 after acute treatment with doxorubicin in mice

被引:46
作者
Kizaki, K
Ito, R
Okada, M
Yoshioka, K
Uchide, T
Temma, K
Mutoh, K
Uechi, M
Hara, Y
机构
[1] Kitasato Univ, Sch Vet Med & Anim Sci, Dept Vet Pharmacol, Towada, Aomori 0348628, Japan
[2] Kitasato Univ, Sch Vet Med & Anim Sci, Dept Vet Anat, Towada, Aomori 0348628, Japan
[3] Kitasato Univ, Sch Vet Med & Anim Sci, Dept Toxicol, Towada, Aomori 0348628, Japan
[4] Kitasato Univ, Vet Teaching Hosp, Sch Vet Med & Anim Sci, Towada, Aomori 0348628, Japan
关键词
doxorubicin (DOX); matrix metalloproteinase (MMP); cardiotoxicity;
D O I
10.1016/j.phrs.2006.01.001
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
We investigated the expression of the genes for matrix metalloproteinases (MMP)-2 and MMP-9 in the ventricle for 1, 2 and 4 days after acute treatment with doxorubicin (DOX) to induce cardiomyopathy in mice, at a single dose of 25 mg kg(-1). Ventricle weights, ventricle weight-to-tail length ratios, and left ventricular systolic and diastolic internal dimensions all decreased time-dependently. Histology showed increased vacuolisation of cardiomyocytes in the DOX-treated mice on day 4 compared with controls. Northern blot hybridisation revealed that MMP-2 and MMP-9 gene transcripts increased in the ventricle of DOX-treated mice on day 2. MMP-2 mRNA approximately doubled in the DOX-treated mice on days 1 and 2, measured using quantitative real-time reverse transcription polymerase chain reaction. By contrast, MMP-9 mRNA expression did not differ in either group on day 1, whereas it increased significantly to 2.9-fold and 2.1-fold in the DOX-treated mice on days 2 and 4, respectively. Consequently, MMP-2 and MMP-9 gene expressions are induced in the ventricle after treatment with DOX, indicating that they might play an important role in the development of DOX-induced cardiotoxicity. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:341 / 346
页数:6
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