Author/Authors :
Ernst R. Schwartz، نويسنده , , Jutt Schaper، نويسنده , , Juergen vom Dahl، نويسنده , , Carsten Altehoefer، نويسنده , , Beate Grohmann، نويسنده , , Friedrich Schoendube، نويسنده , , Florence H. Sheehan، نويسنده , , Rainer Uebis، نويسنده , , Udalrich Buell، نويسنده , , Bruno J. Messmer، نويسنده , , Wolfgang Schaper، نويسنده , , Peter Hanrath، نويسنده ,
Abstract :
Objectives. The aim of this study was to analyze the morphologic characteristics of myocyte degeneration leading to replacement fibrosis in hibernating myocardium by use of electron microscopy and immunohistochemical techniques.
Background. Dat on the ultrastructure and the cytoskeleton of cardiomyocytes in myocardial hibernation are scare. Incomplete or delayed functional recovery might be due to variable degree of cardiomyocyte degeneration in hibernating myocardium.
Methods. In 24 patients, regional wall motion abnormalities were analyzed by use of the centerline method before and 6 ± 1 months after coronary artery bypass surgery. Preoperative technetium-99m sestamibi uptake was measured by single-photon emission computed tomography for assessing regional perfusion. Fluorine-18 fluorodeoxyglucose uptake was measured by positron emission tomograph to assess glucose metabolism. Transmural biopsy specimens were taken during coronary artery bypass surgery from the center of the hypocontractile are of the anterior wall.
Results. The myocytes showed varying signs of mild-to-severe degenerative changes and an increased degree of fibrosis. Immunohistochemical analysis demonstrated disruption of the cytoskeletal proteins titin and alpha-actinin. Electron microscopy of the cell organelles and immunohistochemical analysis of the cytoskeleton showed similarity in the degree of degenerative alterations. Group 1 (n = 11) represented patients with only minor structural alterations, whereas group 2 (n = 13) showed severe morphologic degenerative improvements, and nuclear imaging revealed perfusion-metabolism mismatch without significant differences between the groups.
Conclusions. Long-term hypoperfusion causes different degrees of morphologic alterations leading to degeneration. Preoperative analysis of regional contractility and perfusion-metabolism imaging does not distingush the severity of morphologic alterations nor the functional outcome after revascularization. The insufficient act of self-preservation in hibernating myocardium may lead to progressive structural degeneration with an incomplete and delayed recovery of function after restoration of blood flow.
