Assessment of infarct size and myocardial function in mice using transesophageal echocardiography

J Am Soc Echocardiogr. 2004 Jun;17(6):649-53. doi: 10.1016/j.echo.2004.02.019.

Abstract

Background: Because transthoracic echocardiography (TTE) has significant limitations in assessing changes consequent to myocardial infarction (MI) in mice, we studied two novel methods to characterize such infarcts.

Methods: Large MIs were produced by proximal left coronary artery ligation, and small MIs by distal left coronary artery ligation. Serum cardiac troponin I levels were measured 24 hours postoperatively. At 2 weeks, mice underwent transesophageal echocardiography (TEE) and TTE. Infarct sizes were determined histologically.

Results: Surviving mice were classified according to infarct size. TEE identified all histologically proven large infarcts, and 4 of 5 small infarcts. TTE identified 4 of 5 large infarcts, but only 1 of 5 small infarcts. TEE-derived fractional area change, but not TTE-estimated left ventricular fractional shortening, was significantly different among large, small, and sham infarcts. Cardiac troponin I showed excellent correlation with infarct size and mortality.

Conclusions: Cardiac troponin I was found to predict infarct size and mortality, whereas TEE proved superior to TTE in determining infarct size and/or myocardial function in a murine MI model. These tools should provide more accurate assessments in preclinical studies of ischemic cardiomyopathy.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Analysis of Variance
  • Animals
  • Coronary Vessels
  • Disease Models, Animal
  • Echocardiography
  • Echocardiography, Transesophageal*
  • Female
  • Forecasting
  • Ligation
  • Linear Models
  • Male
  • Mice
  • Mice, Inbred C57BL
  • Mice, Inbred Strains
  • Myocardial Contraction / physiology
  • Myocardial Infarction / blood
  • Myocardial Infarction / diagnostic imaging*
  • Myocardial Infarction / pathology
  • Survival Rate
  • Time Factors
  • Troponin I / blood
  • Ventricular Function, Left / physiology

Substances

  • Troponin I