Molecular Mechanisms of Myocardial Remodeling
- 1 January 1999
- journal article
- research article
- Published by American Physiological Society in Physiological Reviews
- Vol. 79 (1) , 215-262
- https://doi.org/10.1152/physrev.1999.79.1.215
Abstract
Swynghedauw, Bernard. Molecular Mechanisms of Myocardial Remodeling. Physiol. Rev. 79: 215–262, 1999. — “Remodeling” implies changes that result in rearrangement of normally existing structures. This review focuses only on permanent modifications in relation to clinical dysfunction in cardiac remodeling (CR) secondary to myocardial infarction (MI) and/or arterial hypertension and includes a special section on the senescent heart, since CR is mainly a disease of the elderly. From a biological point of view, CR is determined by 1 ) the general process of adaptation which allows both the myocyte and the collagen network to adapt to new working conditions; 2) ventricular fibrosis, i.e., increased collagen concentration, which is multifactorial and caused by senescence, ischemia, various hormones, and/or inflammatory processes; 3) cell death, a parameter linked to fibrosis, which is usually due to necrosis and apoptosis and occurs in nearly all models of CR. The process of adaptation is associated with various changes in genetic expression, including a general activation that causes hypertrophy, isogenic shifts which result in the appearance of a slow isomyosin, and a new Na+-K+-ATPase with a low affinity for sodium, reactivation of genes encoding for atrial natriuretic fator and the renin-angiotensin system, and a diminished concentration of sarcoplasmic reticulum Ca2+-ATPase, β-adrenergic receptors, and the potassium channel responsible for transient outward current. From a clinical point of view, fibrosis is for the moment a major marker for cardiac failure and a crucial determinant of myocardial heterogeneity, increasing diastolic stiffness, and the propensity for reentry arrhythmias. In addition, systolic dysfunction is facilitated by slowing of the calcium transient and the downregulation of the entire adrenergic system. Modifications of intracellular calcium movements are the main determinants of the triggered activity and automaticity that cause arrhythmias and alterations in relaxation.Keywords
This publication has 426 references indexed in Scilit:
- Increased cardiac expression of endothelin-1 mRNA in ischemic heart failure in ratsCardiovascular Research, 1997
- β-Adrenergic and Muscarinic Receptor Expression are Regulated in Opposite Ways During Senescence in Rat Left VentricleJournal of Molecular and Cellular Cardiology, 1997
- Reemergence of the Fetal Pattern of L-Type Calcium Channel Gene Expression in Noninfarcted Myocardium during Left Ventricular RemodelingBiochemical and Biophysical Research Communications, 1995
- Interstitial Collagen is Increased in the Non-infarcted Human Myocardium After Myocardial InfarctionJournal of Molecular and Cellular Cardiology, 1993
- Myocardial myoglobin deficiency in various animal models of congestive heart failureJournal of Molecular and Cellular Cardiology, 1992
- Risk of ventricular arrhythmias in left ventricular hypertrophy: The Framingham Heart StudyThe American Journal of Cardiology, 1987
- Morphometric analysis of collagen network and plasma perfused capillary bed in the myocardium of rats during evolution of cardiac hypertrophyBasic Research in Cardiology, 1986
- Alterations in cardiovascular structure and function with advancing ageThe American Journal of Cardiology, 1986
- Myosin heavy chain and actin fractional rates of synthesis in normal and overload rat heart ventriclesJournal of Molecular and Cellular Cardiology, 1984
- Infarct expansion versus extension: Two different complications of acute myocardial infarctionThe American Journal of Cardiology, 1978