Bioenergetic Consequences of Left Ventricular Remodeling
- 15 August 1995
- journal article
- research article
- Published by Wolters Kluwer Health in Circulation
- Vol. 92 (4) , 1011-1019
- https://doi.org/10.1161/01.cir.92.4.1011
Abstract
Background Left ventricular (LV) remodeling is associated with LV dysfunction and decrease of coronary flow reserve. The underlying mechanisms responsible for these alterations are unclear. Changes in myocardial high-energy phosphate levels may be associated with these alterations. Methods and Results Twelve dogs with LV remodeling secondary to discrete necrosis produced by transmyocardial DC shock were compared with 8 normal dogs. LV mass and end-diastolic volume were measured by magnetic resonance imaging 7 days before and 12.9±1.3 months after DC shock. Transmurally localized 31 P nuclear magnetic resonance spectra from five layers across the LV wall were obtained simultaneously with transmural blood flow measurements (microspheres) under basal conditions and during pacing at 200 and 240 beats per minute. LV mass and end-diastolic volume were significantly increased after DC shock (33% and 26%, respectively, each P <.01). Under basal conditions, the subendocardial creatine phosphate (CP)/ATP ratio was significantly lower in remodeled LV compared with the control group (1.71±0.09 versus 2.04±0.09, P <.05). The subendocardial CP/ATP ratio was inversely correlated with both the increase in LV mass and LV end-diastolic volume ( r =−.77 and r =−.70, P <.01 and P <.05, respectively). In remodeled myocardium, pacing induced a significant increase in LV end-diastolic pressure (from 8±1 to 20±3 mm Hg, P <.05), which was accompanied by a significant decrease of subendocardial/subepicardial (Endo/Epi) blood flow ratio (from 1.01±0.10 to 0.63±0.11, P <.05) and a significant decrease in subendocardial CP/ATP ratio (from 1.78±0.07 to 1.61±0.10, P <.05) and increase of ΔP i /ATP ratio (from 0 to 0.24±0.05, P <.01). The decrease in subendocardial CP/ATP ratio was correlated with the decrease in Endo/Epi blood flow ratio ( r =.79, P <.05). Conclusions These results demonstrate that alterations in myocardial high-energy phosphate levels are correlated with the extent of LV remodeling. In remodeled hearts, pacing-induced tachycardia produces further changes of myocardial high-energy phosphate levels in the subendocardium that appear to be related to ventricular dysfunction and redistribution of blood flow away from the subendocardium.Keywords
This publication has 28 references indexed in Scilit:
- Transmural high energy phosphate distribution and response to alterations in workload in the normal canine myocardium as studied with spatially localized 31P NMR spectroscopyMagnetic Resonance in Medicine, 1990
- Cardiomyopathy of OverloadNew England Journal of Medicine, 1990
- Spectroscopic imaging and spatial localization using adiabatic pulses and applications to detect transmural metabolite distribution in the canine heartMagnetic Resonance in Medicine, 1989
- Transmural distribution of left ventricular glucose uptake in spontaneously hypertensive rats during rest and exerciseActa Physiologica Scandinavica, 1989
- Velocity of the creatine kinase reaction in the neonatal rabbit heart: role of mitochondrial creatine kinaseBiochemistry, 1988
- High performance liquid chromatography: a rapid isocratic method for determination of creatine compounds and adenine nucleotides in myocardial tissueJournal of Molecular and Cellular Cardiology, 1986
- Regional Myocardial Substrate Uptake in Hypertensive Rats: a Quantitative Autoradiographic MeasurementScience, 1985
- Physiologic cardiac hypertrophy corrects contractile protein abnormalities associated with pathologic hypertrophy in rats.Journal of Clinical Investigation, 1982
- Variables predictive of survival in patients with coronary disease. Selection by univariate and multivariate analyses from the clinical, electrocardiographic, exercise, arteriographic, and quantitative angiographic evaluations.Circulation, 1979
- Defective lipid metabolism in the failing heartJournal of Clinical Investigation, 1968