Novel rat model of ischemic cardiomyopathy induced by repetitive myocardial ischemia/reperfusion injury while conscious

Circ J. 2007 May;71(5):788-95. doi: 10.1253/circj.71.788.

Abstract

Background: A rodent model of ischemic cardiomyopathy (ICM) induced by repetitive brief ischemia/reperfusion (I/R) injury while conscious has not been previously established.

Methods and results: A newly developed coronary occluder was implanted in male Wistar rats. A repetitive I/R protocol (20 s, 2 min, followed by main 30 min--ischemia, every 48 h, for 4 weeks) was introduced while the animals were conscious. The I/R protocol did not induce transmural scar formation but induced (1) residual myocytes with scattered infiltration of fibrosis (Masson trichrome stain), (2) coronary hypoperfusion ((201)Tl-Cl autoradiogram), (3) reduced coronary microvascular volume fraction (microCT), and (4) gradually progressive left ventricular (LV) dilation (echocardiography). These parameters of ICM showed interindividual variation; however, the percent increase in LV diastolic area on day 3 was significantly correlated with LV dilation (r=0.91, p<0.0001), fibrosis (r=0.77, p=0.0034), and reduction in microvessels (r=0.67, p=0.040) at week 4. The LV dilatory response on day 3 also correlated with inducible nitric oxide synthase expression (immunohistochemistry, day 3) in the LV (r=0.92, p=0.028).

Conclusions: A novel rat model of ICM induced by repetitive I/R while conscious showed interindividual variation in the severity of ICM in the advanced stage, but this was predictable non-invasively (by LV dilatory response) during the initial stage of repetitive I/R.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Consciousness
  • Coronary Circulation
  • Disease Models, Animal*
  • Fibrosis
  • Imaging, Three-Dimensional
  • Immunohistochemistry
  • Male
  • Microcirculation
  • Myocardial Ischemia / diagnostic imaging
  • Myocardial Ischemia / etiology*
  • Myocardial Ischemia / pathology
  • Myocardial Ischemia / physiopathology
  • Myocardial Reperfusion Injury / complications*
  • Myocardium / enzymology
  • Myocardium / pathology
  • Nitric Oxide Synthase Type II / metabolism
  • Rats*
  • Rats, Wistar
  • Recurrence
  • Time Factors
  • Tomography, X-Ray Computed
  • Ventricular Function, Left

Substances

  • Nitric Oxide Synthase Type II