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Arben Santo, M.D., Ph.D.
Professor, Discipline Chair of Pathology
Edward Via Virginia College of Osteopathic Medicine
2265 Kraft Drive, Blacksburg, VA 24060
Tele: 540-231-4867
Fax: 540-231-5252
Email: asanto@vcom.vt.edu

Discipline: Pathology
Education:
1973 University of Tirana School of Medicine, Albania M.D.
1984 University of Tirana, Albania Ph.D.
Currently Teaching: Pathology
Current Research
Interests :
Histological diagnosis of early period of myocardial infarction
Sudden coronary death
Experimental atherosclerosis
Acute myocardial infarction kills many people every year in the industrialized countries. To 25% of these death comes suddenly, usually within one hour of the first clinical symptoms. There is no time to establish a firm clinical diagnosis for these sudden coronary deaths; the last chance to find out what really happened is post-mortem examination. Stated in terms of general pathology, the problem is to recognize an infarct that has occurred within a very short time, of the order of one hour.

In a preliminary research study, we have examined the myofibrils of control and ischemic myocardial cells in a Jennings and Wartman model of myocardial infarction. We occluded the left circumflex coronary artery beneath the left auricular appendage in 25 open-chest, anesthetized dogs. Animals were sacrificed after 40 and 60 minutes of coronary artery occlusion: the heart was arrested by intravenous KCl injection and rapidly excised. Anterior (control) and posterior (ischemic) papillary muscles of the left ventricle were immersed in buffered 10% formaldehyde solution after the completion of rigor mortis. Paraffin sections of longitudinally oriented papillary muscles were stained with H&E and myocardial cell myofibrils were examined in polarized light microscope. Sarcomere length was calculated using a calibrated micrometer.

Control papillary muscles demonstrated uniformly contracted myocardial cells, with sarcomeres 1.3 to 1.5 micrometers long. Myocardial cells of the ischemic papillary muscles demonstrated elongated sarcomeres, of the order of 1.9 to 2.04 micrometers. The stretching of myocardial cells was observed regularly in all the ischemic samples, and is due to a loss of ability of irreversibly injured myocardial cells to develop rigor mortis. This is a very sensitive stigma of irreversible ischemic injury and allowed us to recognize the ischemic cells from the moment of their biological death. With this approach, the histological identification of myocardial infarction becomes very easy; it can be done after at least 40 minutes of coronary artery occlusion in dogs.

The examination of myofibrils by polarized light microscopy offers an accurate, very sensitive and especially simple method to identify the earliest stages of myocardial ischemia and infarction.

It is very interesting to pursue the research by examining forensic cases of autopsies of sudden coronary death. The identification of the nature of myocardial changes would elucidate the pathogenesis of this syndrome, whose mechanisms remain still poorly understood.


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