Matrix metalloprotease activity is enhanced in the compensated but not in the decompensated phase of pressure overload hypertrophy
- PMID: 17531925
- DOI: 10.1016/j.amjhyper.2007.01.016
Matrix metalloprotease activity is enhanced in the compensated but not in the decompensated phase of pressure overload hypertrophy
Abstract
Background: During the transition of pressure overload hypertrophy (POH) to heart failure (HF) there is intense interstitial cardiac remodeling, characterized by a complex balance between collagen deposition and degradation by matrix metalloproteases (MMPs). This study was aimed at investigating the process of cardiac remodeling during the different phases of the transition of POH to HF.
Methods: Guinea pigs underwent thoracic descending aortic banding or sham operation. Twelve weeks after surgery, left-ventricular (LV) end-diastolic internal dimension and ventricular systolic pressure were measured by combined M-mode echocardiography and micromanometer cathetherization. The MMP activity, tissue-specific MMP inhibitors (TIMPs), and collagen fraction were evaluated in LV tissue samples by zymography, ELISA, and computer-aided analysis, respectively.
Results: Banded animals were divided by lung weight values into either compensated left-ventricular hypertrophy (LVH) or HF groups, as compared with sham-operated controls. All HF animals exhibited a restrictive pattern of Doppler transmitral inflow, indicative of diastolic dysfunction, and developed lung congestion. Compensated LVH was associated with increased MMP-2 activity, which was blunted after transition to HF, at a time when TIMP-2 levels and collagen deposition were increased.
Conclusions: The cardiac remodeling process that accompanies the development of POH is a phase-dependent process associated with progressive deterioration of cardiac function.
Similar articles
-
Matrix metalloproteinases and their tissue inhibitors in pressure-overloaded human myocardium during heart failure progression.J Am Coll Cardiol. 2004 Oct 19;44(8):1609-18. doi: 10.1016/j.jacc.2004.07.023. J Am Coll Cardiol. 2004. PMID: 15489093
-
Matrix metalloproteinases/tissue inhibitors of metalloproteinases: relationship between changes in proteolytic determinants of matrix composition and structural, functional, and clinical manifestations of hypertensive heart disease.Circulation. 2006 May 2;113(17):2089-96. doi: 10.1161/CIRCULATIONAHA.105.573865. Epub 2006 Apr 24. Circulation. 2006. PMID: 16636176
-
Concentric left ventricular remodeling in endothelial nitric oxide synthase knockout mice by chronic pressure overload.Cardiovasc Res. 2005 Jun 1;66(3):444-53. doi: 10.1016/j.cardiores.2005.01.021. Epub 2005 Feb 24. Cardiovasc Res. 2005. PMID: 15914109
-
Cardiac mast cell regulation of matrix metalloproteinase-related ventricular remodeling in chronic pressure or volume overload.Cardiovasc Res. 2006 Feb 15;69(3):657-65. doi: 10.1016/j.cardiores.2005.10.020. Epub 2005 Dec 22. Cardiovasc Res. 2006. PMID: 16376324 Review.
-
Contribution of systolic and diastolic abnormalities to heart failure with a normal and a reduced ejection fraction.Prog Cardiovasc Dis. 2007 Jan-Feb;49(4):229-40. doi: 10.1016/j.pcad.2006.08.009. Prog Cardiovasc Dis. 2007. PMID: 17185111 Review.
Cited by
-
Pathogenesis of target organ damage in hypertension: role of mitochondrial oxidative stress.Int J Mol Sci. 2014 Dec 31;16(1):823-39. doi: 10.3390/ijms16010823. Int J Mol Sci. 2014. PMID: 25561233 Free PMC article. Review.
-
Lobe-specific heterogeneity in asymmetric dimethylarginine and matrix metalloproteinase levels in a rat model of obstructive cholestasis.Biomed Res Int. 2014;2014:327537. doi: 10.1155/2014/327537. Epub 2014 Jun 12. Biomed Res Int. 2014. PMID: 25013773 Free PMC article.
-
Matrix Metalloproteinases and Tissue Inhibitors of Metalloproteinases in Extracellular Matrix Remodeling during Left Ventricular Diastolic Dysfunction and Heart Failure with Preserved Ejection Fraction: A Systematic Review and Meta-Analysis.Int J Mol Sci. 2020 Sep 14;21(18):6742. doi: 10.3390/ijms21186742. Int J Mol Sci. 2020. PMID: 32937927 Free PMC article.
-
Lung matrix metalloproteinase activation following partial hepatic ischemia/reperfusion injury in rats.ScientificWorldJournal. 2014 Jan 23;2014:867548. doi: 10.1155/2014/867548. eCollection 2014. ScientificWorldJournal. 2014. PMID: 24592193 Free PMC article.
-
Animal Models of Steatosis (NAFLD) and Steatohepatitis (NASH) Exhibit Hepatic Lobe-Specific Gelatinases Activity and Oxidative Stress.Can J Gastroenterol Hepatol. 2019 Feb 3;2019:5413461. doi: 10.1155/2019/5413461. eCollection 2019. Can J Gastroenterol Hepatol. 2019. PMID: 30854350 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Research Materials
Miscellaneous