Serial MRI evaluation of cardiac structure and function in mice after reperfused myocardial infarction

Antwone J. Ross, Zequan Yang, Stuart S. Berr, Wesley D. Gilson, William C. Petersen, John N. Oshinski, Brent A. French

Research output: Contribution to journalArticlepeer-review


This study evaluated the utility of cardiac MRI for assessing the impact of myocardial infarction (MI) on cardiac structure and function in mice following reperfused 1- or 2-hr occlusions of the left anterior descending coronary artery (LAD). When assessed 1 day after MI, the left ventricular ejection fraction (LVEF) had declined by more than half, and remained depressed for the duration of the study. Furthermore, MI initiated dramatic increases in both LV end-systolic volume (LVESV) and end-diastolic volume (LVEDV), with a greater than threefold increase in LVESV and a twofold increase in LVEDV by 4 weeks post-MI. Transmural LV wall thickening (WTh) analysis revealed that noninfarcted myocardium in the remote septal region exhibited an early deficit in contractile function after MI that transiently resolved by day 7, only to be followed by a late phase of dysfunction that became fully manifest by day 28 post-MI. In conclusion, MRI allows the serial assessment of cardiac structure and function after MI in mice, with a resolution adequate to document both regional and temporal changes. The application of these imaging techniques in transgenic and knock-out mice will greatly expedite research aimed at defining the functional roles of individual genes in the pathophysiology of LV remodeling (LVR) after reperfused MI.

Original languageEnglish (US)
Pages (from-to)1158-1168
Number of pages11
JournalMagnetic Resonance in Medicine
Issue number6
StatePublished - 2002
Externally publishedYes


  • Cardiac MRI
  • LV remodeling
  • Mice
  • Myocardial infarction

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging
  • Radiological and Ultrasound Technology

Fingerprint Dive into the research topics of 'Serial MRI evaluation of cardiac structure and function in mice after reperfused myocardial infarction'. Together they form a unique fingerprint.

Cite this