Literature DB >> 2458117

Alterations of the myocardial skeletal framework in acute myocardial infarction with and without ventricular rupture. A preliminary report.

S M Factor1, T F Robinson, R Dominitz, S H Cho.   

Abstract

Thinning and dilatation (expansion) of the infarct region and complete rupture of the ventricular wall are significant complications of acute transmural myocardial infarction associated with increased morbidity and mortality. The pathogenesis of these related events is unknown. Recent studies of myocardial connective tissue have delineated an extensive array of intercellular and pericellular structures which serve as a skeletal framework and which may modulate contractile activity. We have employed a modified silver impregnation method to visualize the connective tissue components by light microscopy. To explore whether the skeletal framework is altered in acute myocardial infarction with and without ventricular rupture, we studied 9 human hearts at autopsy, and 4 canine infarcts of known duration. The human infarctions included 4 nonruptured cases with infarcts 1-5 days old, and 5 ruptured cases with infarcts 3-10 days old. Sections from normal, lateral, and central infarct or ventricular rupture sites were stained with silver. The normal tissue from each heart served as a control. Silver staining was moderately decreased in the lateral infarct zones, and markedly decreased in the central non-ruptured infarct zones. In the 5 ventricular rupture cases, the rupture site had no silver staining. A similar pattern was observed in the 4 canine infarcts. Thus, we conclude that the skeletal framework is markedly altered in the central zone of acute myocardial infarction. The acute changes of silver stained connective tissue may contribute significantly to the development of infarct expansion or ventricular wall rupture.

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Year:  1987        PMID: 2458117

Source DB:  PubMed          Journal:  Am J Cardiovasc Pathol        ISSN: 0887-8005


  17 in total

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Journal:  J Mol Med (Berl)       Date:  2005-03-16       Impact factor: 4.599

4.  Myocardial matrix metalloproteinase(s): localization and activation.

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8.  Hyperoxia and transforming growth factor β1 signaling in the post-ischemic mouse heart.

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9.  Right ventricular collagen and fibronectin levels in patients with pulmonary atresia and ventricular septal defect.

Authors:  Theodorus H F Peters; Peter L de Jong; Lennart Klompe; Rolf M F Berger; Pramod R Saxena; Hari S Sharma; Ad J J C Bogers
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Review 10.  Extracellular matrix-mediated cellular communication in the heart.

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Journal:  J Mol Cell Cardiol       Date:  2016-01-14       Impact factor: 5.000

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