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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Herdrich, Benjamin J. Danzer, Enrico Davey, Marcus G. Allukian, Myron Englefield, Virginia Gorman, Joseph H. Gorman, Robert C. Liechty, Kenneth W. |
| Description | Country affiliation: United States Author Affiliation: Herdrich BJ ( The University of Pennsylvania School of Medicine, Philadelphia, PA, USA. benjamin.herdrich@uphs.upenn.edu) |
| Abstract | OBJECTIVES: The adult response to myocardial infarction results in inflammation, scar formation, left ventricular dilatation, and loss of regional and global function. Regenerative scarless healing has been demonstrated in foetal dermis and tendon and is associated with diminished inflammation. We hypothesised that following foetal myocardial infarction, there would be minimal inflammation, regenerative healing, and preservation of function. METHODS: Anteroapical myocardial infarction encompassing 20% of the left ventricle was created in adult or early gestation foetal sheep. Myocardial function was serially assessed using quantitative echocardiography. Infarct architecture was examined histologically for evidence of scar formation. Cellular inflammation, cellular proliferation, and apoptosis were assessed using immunohistochemistry. RESULTS: In the adult sheep 4 weeks following myocardial infarction, there was a significant decline in ejection fraction (EF) (41±7.4% to 26±7.4%, p<0.05), and the akinetic myocardial segment increased in size (6.9±0.8 cm to 7.9±1.1 cm, p<0.05). By contrast, there was no decline in the foetal EF (53±8.1% to 55±8.8%) and no akinetic foetal myocardial segment 4 weeks post-infarction. The foetal infarcts lacked an inflammatory cell infiltrate and healed with minimal fibrosis, compared with the adults. Foetal infarcts also demonstrated 5-bromo-2'-deoxyuridine (BrdU)+ proliferating cells, including cardiomyocytes, within the infarct. CONCLUSIONS: These data demonstrate that the foetal response to myocardial infarction is dramatically different from the adult and is characterised by minimal inflammation, lack of fibrosis, myocardial proliferation and restoration of cardiac function. Diminished inflammation is associated with foetal regenerative cardiac healing following injury. Understanding the mechanisms involved in foetal myocardial regeneration may lead to applications to alter the adult response following myocardial infarction. |
| File Format | HTM / HTML |
| ISSN | 10107940 |
| e-ISSN | 1873734X |
| DOI | 10.1016/j.ejcts.2010.03.049 |
| Journal | European Journal of Cardio-Thoracic Surgery |
| Issue Number | 6 |
| Volume Number | 38 |
| Language | English |
| Publisher | Oxford University Press |
| Publisher Date | 2010-12-01 |
| Publisher Place | Germany |
| Access Restriction | Open |
| Subject Keyword | Discipline Cardiology__semicolon__surgery Fetal Diseases Physiopathology Fetal Heart Physiology Myocardial Infarction Regeneration Animals Apoptosis Cicatrix Pathology Disease Models, Animal Ultrasonography Ventricular Remodeling Research Support, N.i.h., Extramural Research Support, Non-u.s. Gov't |
| Content Type | Text |
| Resource Type | Article |
| Subject | Pulmonary and Respiratory Medicine Surgery Cardiology and Cardiovascular Medicine |
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