| Myocardial
Infarction in the Mouse
Dr.
Wang in the laboratory has developed an in vivo open chest
model of myocardial infarction(MI) in the mouse that closely
mimics the human syndrome of acute MI. Briefly, the chest
is opened through a thoracotomy and a major branch of the
left anterior descending coronary artery (LAD) is occluded
for 30 minutes. The occlusion is then removed, the chest closed,
and the vasculature and heart allowed to reperfuse for 24
hours. The animal is then sacrificed and the heart is excised
and perfused with triphenyltetrazolium chloride (TTC) to facilitate
determination of the live (appears red) verses dead (appears
white) myocardial tissue. The LAD is then reoccluded in the
same place as before and the heart perfused with phthalo blue
dye. This process leaves regions of the myocardium not rendered
ischemic by the occlusion stained blue. In this regard, infarct
size is characterized as a percentage of the region that was
ischemic (region at risk) during occlusion. We use this model
on a regular basis to examine the role of known or suspected
cardiac protective proteins in the development or prevention
of MI.

Cultured
Neonatal Mouse Cardiomyocytes
We commonly employ a model of isolated adult mouse and rabbit
cardiomyocytes. These cells are analyzed using a battery of
biochemical and molecular biological approaches, notably adenoviral-mediated
gene transfer.
Cultured
Neonatal Mouse Cardiomyocytes
Also developed by Dr. Wang, while working for Dr. Y. James
Kang at the University of Louisville, is a model of cultured
neonatal mouse cardiomyocytes (this was the first such model
in the world). Briefly, one to three day old mice are euthanized,
the hearts excised and the ventricles retained for cell isolation.
Ventricles are washed, minced into small fragments and the
cells enzymatically separated. Non-muscle and muscle cells
are then separated and muscle cells plated in tissue culture
dishes for experimentation. These cells are analyzed using
various biochemical and molecular biological assays.
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