Myocardial Infarction and Cardiac Remodelling in Mice

Fang Yang(Henry Ford Hospital), Yunhe Liu(Henry Ford Hospital), Xiaoping Yang(Henry Ford Hospital), Jiang Xu(Henry Ford Hospital), Alissa Kapke(Henry Ford Hospital), Oscar A. Carretero(Henry Ford Hospital)
Experimental Physiology
September 1, 2002
Cited by 189Open Access
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Abstract

We established a mouse model of cardiac dysfunction due to myocardial infarction (MI). For this we ligated the left anterior descending coronary artery in male C57BL/6J mice and assessed healing and left ventricular (LV) remodelling at 1, 2 and 4 days and 1, 2 and 4 weeks after MI. Echocardiography was performed at 1 and 2 weeks and 1, 2, 4 and 6 months after MI. We found that neutrophil infiltration of the infarct border was noticeable at 1-2 days. Marked macrophage infiltration occurred at day 4, while lymphocyte infiltration was apparent at 7-14 days. Massive proliferation of fibroblasts and collagen accumulation began by day 7-14, and scar formation was completed by day 21. LV diastolic dimension increased markedly at 2 weeks and remained at the same level thereafter. LV shortening fraction decreased significantly at 2 weeks and then slowly decreased. In non-infarcted areas of the LV, myocyte cross-sectional area and interstitial collagen fraction increased progressively, reaching a maximum at 4 months. This study provides important qualitative and quantitative information about the natural history of cardiac remodelling after MI in mice.


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