Chronic hibernating myocardium: interstitial changes
- PMID: 7494552
- DOI: 10.1007/BF00944781
Chronic hibernating myocardium: interstitial changes
Abstract
Chronic left ventricular dysfunctional but viable myocardium of patients with chronic hibernation is characterized by structural changes, which consist of depletion of contractile elements, accumulation of glycogen, nuclear chromatin dispersion, depletion of sarcoplasmic reticulum and mitochondrial shape changes. These alterations are not reminiscent of degeneration but are interpreted as de-differentiation of the cardiomyocytes. The above mentioned changes are accompanied by a marked increase in the interstitial space. The present study describes qualitative and quantitative changes in the cellular and non-cellular compartments of the interstitial space. In chronic hibernating myocardial segments the increased extracellular matrix is filled with large amounts of type I collagen, type III collagen and fibronectin. An increase in the number of vimentin-positive cells (endothelial cells and fibroblasts) compared with normal myocardium is seen throughout the extracellular matrix. The increase in interstitial tissue is considered as one of the main determinants responsible for the lack of immediate recovery of contractile function after restoration of the blood flow to the affected myocardial segments of patients with chronic left ventricular dysfunction.
Similar articles
-
The extracellular matrix in hibernating myocardium--a significant factor causing structural defects and cardiac dysfunction.Mol Cell Biochem. 1998 Sep;186(1-2):147-58. Mol Cell Biochem. 1998. PMID: 9774196
-
The extracellular matrix in human cardiac tissue. Part II: Vimentin, laminin, and fibronectin.Cardioscience. 1992 Mar;3(1):41-9. Cardioscience. 1992. PMID: 1554870
-
Dedifferentiated cardiomyocytes from chronic hibernating myocardium are ischemia-tolerant.Mol Cell Biochem. 1998 Sep;186(1-2):159-68. Mol Cell Biochem. 1998. PMID: 9774197
-
Hibernating myocardium: a review.J Mol Cell Cardiol. 1996 Dec;28(12):2359-72. doi: 10.1006/jmcc.1996.0229. J Mol Cell Cardiol. 1996. PMID: 9004153 Review.
-
[The basis of chronic ischemic reversible left ventricular dysfunction (hibernating myocardium)].Cesk Fysiol. 1999 Feb;48(1):4-8. Cesk Fysiol. 1999. PMID: 10377599 Review. Czech.
Cited by
-
Efficacy of coronary angioplasty for the treatment of hibernating myocardium.Heart. 1999 Aug;82(2):210-6. doi: 10.1136/hrt.82.2.210. Heart. 1999. PMID: 10409538 Free PMC article.
-
Hibernating myocardium in post-ischaemic heart failure: pathophysiology, identification and revascularisation.Ann R Coll Surg Engl. 2000 Jul;82(4):236-42. Ann R Coll Surg Engl. 2000. PMID: 10932656 Free PMC article. Clinical Trial. No abstract available.
-
Origins of cardiac fibroblasts.Circ Res. 2010 Nov 26;107(11):1304-12. doi: 10.1161/CIRCRESAHA.110.231910. Circ Res. 2010. PMID: 21106947 Free PMC article. Review.
-
Hibernating myocardium: morphological correlates of inotropic stimulation and glucose uptake.Heart. 2000 Apr;83(4):456-61. doi: 10.1136/heart.83.4.456. Heart. 2000. PMID: 10722551 Free PMC article.
-
Development of murine ischemic cardiomyopathy is associated with a transient inflammatory reaction and depends on reactive oxygen species.Proc Natl Acad Sci U S A. 2003 Mar 4;100(5):2700-5. doi: 10.1073/pnas.0438035100. Epub 2003 Feb 13. Proc Natl Acad Sci U S A. 2003. PMID: 12586861 Free PMC article.