Document Detail


Role of intramural platelet thrombus in the pathogenesis of wall rupture and intra-ventricular thrombosis following acute myocardial infarction.
MedLine Citation:
PMID:  21057698     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
Left ventricular thrombus (LVT) and rupture are important mechanical complications following myocardial infarction (MI) and are believed to be due to unrelated mechanisms. We studied whether, in fact, wall rupture and LVT are closely related in their pathogenesis with intramural platelet thrombus (IMT) playing a pivotal role. Male 129sv and C57Bl/6 mice underwent operation to induce MI, and autopsy was performed to confirm rupture deaths. Haemodynamic features of rupture events were monitored by telemetry in conscious mice. Detailed histological examination was conducted with special attention to the presence of IMT in relation to rupture location and LVT formation. IMT was detected in infarcted hearts of 129sv (82%) and C57Bl/6 (39%) mice with rupture in the form of a narrow streak spanning the wall or an occupying mass dissecting the infarcted myofibers apart. IMT often contained dense inflammatory cells and blood clot, indicating a dynamic process of thrombus formation and destruction. Notably, IMT was found extending into the cavity to form LVT. Haemodynamic monitoring by telemetry revealed that rupture occurred either as a single event or recurrent episodes. Importantly, the anti-platelet drug clopidogrel, but not aspirin, reduced the prevalence of rupture (10% vs. 45%) and IMT, and suppressed the degree of inflammation. Thus, IMT is a key pathological element in the infarcted heart closely associated with the complications of rupture and LVT. IMT could be either triggered by a wall tear or act as initiator of rupture. IMT may propagate towards the ventricular chamber to trigger LVT.
Authors:
Xiao-Jun Du; Leonard Shan; Xiao-Ming Gao; Helen Kiriazis; Yang Liu; Abhirup Lobo; Geoffrey A Head; Anthony M Dart
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Publication Detail:
Type:  Comparative Study; Journal Article; Research Support, Non-U.S. Gov't     Date:  2010-11-05
Journal Detail:
Title:  Thrombosis and haemostasis     Volume:  105     ISSN:  0340-6245     ISO Abbreviation:  Thromb. Haemost.     Publication Date:  2011 Feb 
Date Detail:
Created Date:  2011-02-02     Completed Date:  2011-05-31     Revised Date:  2012-01-10    
Medline Journal Info:
Nlm Unique ID:  7608063     Medline TA:  Thromb Haemost     Country:  Germany    
Other Details:
Languages:  eng     Pagination:  356-64     Citation Subset:  IM    
Affiliation:
Baker IDI Heart and Diabetes Institute, St Kilda Road Central, Melbourne, Victoria 8008, Australia. xiao-jun.du@bakeridi.edu.au
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MeSH Terms
Descriptor/Qualifier:
Animals
Aspirin / pharmacology
Blood Platelets / drug effects,  pathology*
Disease Models, Animal
Hemodynamics
Inflammation / etiology,  pathology
Male
Mice
Mice, 129 Strain
Mice, Inbred C57BL
Myocardial Infarction / blood,  complications*,  drug therapy,  pathology,  physiopathology
Platelet Aggregation Inhibitors / pharmacology
Telemetry
Thrombosis / blood,  etiology*,  pathology,  physiopathology,  prevention & control
Ticlopidine / analogs & derivatives,  pharmacology
Time Factors
Ventricular Septal Rupture / blood,  etiology*,  pathology,  physiopathology,  prevention & control
Chemical
Reg. No./Substance:
0/Platelet Aggregation Inhibitors; 50-78-2/Aspirin; 55142-85-3/Ticlopidine; 90055-48-4/clopidogrel

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


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