Circulation Research, Vol 73, 184-192, Copyright © 1993 by American Heart Association
ARTICLES |
AM Feldman, EO Weinberg, PE Ray and BH Lorell
Peter Belfer Laboratory for the Molecular Biology of Heart Failure, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Md 21205.
Left ventricular hypertrophy (LVH) is associated with reinduction of the fetal program of gene expression. It is unclear whether this pattern of cardiac gene expression changes with the development of left ventricular decompensation and failure. To answer these questions, we quantified steady-state levels of mRNA by the polymerase chain reaction in the left ventricular myocardium of rats 8 and 20 weeks after ascending aortic banding. Clinical and hemodynamic assessment identified two distinct groups of animals 20 weeks after aortic banding. The first group (20-week nonfailed LVH) demonstrated substantial LVH but no depression in systolic developed pressure per gram left ventricular weight compared with the age-matched control group. In contrast, a second group of rats exhibited clinical signs of congestive failure as well as a marked diminution in left ventricular developed pressure per gram. Assessment of the levels of mRNA encoding a panel of cardiac proteins demonstrated a greater than twofold increase in beta-myosin heavy chain mRNA and an approximately sixfold increase in atrial natriuretic factor mRNA in left ventricular myocardium of all three groups (8-week LVH, 20-week nonfailed LVH, 20- week failed LVH) when compared with appropriate age-matched control groups. In contrast, Ca(2+)-ATPase mRNA levels were decreased by 50% only in the left ventricular myocardium of animals with both clinical signs and hemodynamic indexes consistent with cardiac decompensation (20-week failed LVH). These results suggest that in rats with ascending aortic banding the hypertrophic phenotype is associated with a selective reinduction of the fetal gene program, which persists even after the development of left ventricular failure.(ABSTRACT TRUNCATED AT 250 WORDS)
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R. J. Wiesner, H. Ehmke, J. Faulhaber, R. Zak, and J. C. Ruegg Dissociation of Left Ventricular Hypertrophy, ß-Myosin Heavy Chain Gene Expression, and Myosin Isoform Switch in Rats After Ascending Aortic Stenosis Circulation, March 4, 1997; 95(5): 1253 - 1259. [Abstract] [Full Text] |
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R. J. Hajjar, J. X. Kang, J. K. Gwathmey, and A. Rosenzweig Physiological Effects of Adenoviral Gene Transfer of Sarcoplasmic Reticulum Calcium ATPase in Isolated Rat Myocytes Circulation, January 21, 1997; 95(2): 423 - 429. [Abstract] [Full Text] |
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P. Assayag, D. Charlemagne, J. de Leiris, F. Boucher, P.-E. Valere, S. Lortet, B. Swynghedauw, and S. Besse Senescent Heart Compared With Pressure Overload-Induced Hypertrophy Hypertension, January 1, 1997; 29(1): 15 - 21. [Abstract] [Full Text] |
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M. N. Sack, T. A. Rader, S. Park, J. Bastin, S. A. McCune, and D. P. Kelly Fatty Acid Oxidation Enzyme Gene Expression Is Downregulated in the Failing Heart Circulation, December 1, 1996; 94(11): 2837 - 2842. [Abstract] [Full Text] |
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Y. Kagaya, R. J. Hajjar, J. K. Gwathmey, W. H. Barry, and B. H. Lorell Long-term Angiotensin-Converting Enzyme Inhibition With Fosinopril Improves Depressed Responsiveness to Ca2+ in Myocytes From Aortic-Banded Rats Circulation, December 1, 1996; 94(11): 2915 - 2922. [Abstract] [Full Text] |
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H. Stromer, A. Cittadini, P. S. Douglas, and J. P. Morgan Exogenously Administered Growth Hormone and Insulin-like Growth Factor-I Alter Intracellular Ca2+ Handling and Enhance Cardiac Performance: In Vitro Evaluation in the Isolated Isovolumic Buffer-Perfused Rat Heart Circ. Res., August 1, 1996; 79(2): 227 - 236. [Abstract] [Full Text] |
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A. Cittadini, H. Stromer, S. E. Katz, R. Clark, A. C. Moses, J. P. Morgan, and P. S. Douglas Differential Cardiac Effects of Growth Hormone and Insulin-like Growth Factor1 in the Rat : A Combined In Vivo and In Vitro Evaluation Circulation, February 15, 1996; 93(4): 800 - 809. [Abstract] [Full Text] |
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A. Calderone, N. Takahashi, N. J. Izzo Jr, C. M. Thaik, and W. S. Colucci Pressure- and Volume-Induced Left Ventricular Hypertrophies Are Associated With Distinct Myocyte Phenotypes and Differential Induction of Peptide Growth Factor mRNAs Circulation, November 1, 1995; 92(9): 2385 - 2390. [Abstract] [Full Text] |
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E. Kiss, N. A. Ball, E. G. Kranias, and R. A. Walsh Differential Changes in Cardiac Phospholamban and Sarcoplasmic Reticular Ca2+-ATPase Protein Levels : Effects on Ca2+ Transport and Mechanics in Compensated Pressure-Overload Hypertrophy and Congestive Heart Failure Circ. Res., October 1, 1995; 77(4): 759 - 764. [Abstract] [Full Text] |
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S. E. Litwin, S. E. Katz, E. O. Weinberg, B. H. Lorell, G. P. Aurigemma, and P. S. Douglas Serial Echocardiographic-Doppler Assessment of Left Ventricular Geometry and Function in Rats With Pressure-Overload Hypertrophy : Chronic Angiotensin-Converting Enzyme Inhibition Attenuates the Transition to Heart Failure Circulation, May 15, 1995; 91(10): 2642 - 2654. [Abstract] [Full Text] |
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E. Loh, J. V. Barnett, A. M. Feldman, G. S. Couper, D. E. Vatner, W. S. Colucci, and J. B. Galper Decreased Adenylate Cyclase Activity and Expression of Gs{alpha} in Human Myocardium After Orthotopic Cardiac Transplantation Circ. Res., May 1, 1995; 76(5): 852 - 860. [Abstract] [Full Text] |
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G. Bruckschlegel, S. R. Holmer, K. Jandeleit, D. Grimm, F. Muders, E. P. Kromer, G. A. J. Riegger, and H. Schunkert Blockade of the Renin-Angiotensin System in Cardiac Pressure-Overload Hypertrophy in Rats Hypertension, February 1, 1995; 25(2): 250 - 259. [Abstract] [Full Text] |
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K. Haghighi, A. G. Schmidt, B. D. Hoit, A. G. Brittsan, A. Yatani, J. W. Lester, J. Zhai, Y. Kimura, G. W. Dorn II, D. H. MacLennan, et al. Superinhibition of Sarcoplasmic Reticulum Function by Phospholamban Induces Cardiac Contractile Failure J. Biol. Chem., June 22, 2001; 276(26): 24145 - 24152. [Abstract] [Full Text] [PDF] |
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