Blood pressure-independent cardiac hypertrophy induced by locally activated renin-angiotensin system

被引:165
作者
Mazzolai, L
Nussberger, J
Aubert, JF
Brunner, DB
Gabbiani, G
Brunner, HR
Pedrazzini, T [1 ]
机构
[1] Univ Lausanne, Sch Med, Div Hypertens & Vasc Med, CH-1011 Lausanne, Switzerland
[2] Univ Geneva, Sch Med, Dept Pathol, CH-1211 Geneva, Switzerland
关键词
heart; hypertrophy; renin; angiotensinogen; mice; transgenic;
D O I
10.1161/01.HYP.31.6.1324
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Cardiac hypertrophy is frequent in chronic hypertension. The renin-angiotensin system, via its effector angiotensin II (Ang II), regulates blood pressure and participates in sustaining hypertension. In addition, a growing body of evidence indicates that Ang II acts also as a growth factor. However, it is still a matter of debate whether the trophic effect of Ang II can trigger cardiac hypertrophy in the absence of elevated blood pressure. To address this question, transgenic mice overexpressing the rat angiotensinogen gene, specifically in the heart, were generated to increase the local activity of the renin-angiotensin system and therefore Ang II production. These mice develop myocardial hypertrophy without signs of fibrosis independently from the presence of hypertension, demonstrating that local Ang II production is important in mediating the hypertrophic response in vivo.
引用
收藏
页码:1324 / 1330
页数:7
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