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Circulation Research. 1993;73:184-192

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*Heart Failure

Circulation Research, Vol 73, 184-192, Copyright © 1993 by American Heart Association


ARTICLES

Selective changes in cardiac gene expression during compensated hypertrophy and the transition to cardiac decompensation in rats with chronic aortic banding

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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A. D Wickenden, R. Kaprielian, Z. Kassiri, J. N Tsoporis, R. Tsushima, G. I Fishman, and P. H Backx
The role of action potential prolongation and altered intracellular calcium handling in the pathogenesis of heart failure
Cardiovasc Res, February 1, 1998; 37(2): 312 - 323.
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Cardiovasc ResHome page
R. M Phillips, P. Narayan, A. M Gomez, K. Dilly, L. R Jones, W.J. Lederer, and R. A Altschuld
Sarcoplasmic reticulum in heart failure: central player or bystander?
Cardiovasc Res, February 1, 1998; 37(2): 346 - 351.
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Cardiovasc ResHome page
K. Wong, K. R Boheler, J. Bishop, M. Petrou, and M. H Yacoub
Clenbuterol induces cardiac hypertrophy with normal functional, morphological and molecular features
Cardiovasc Res, January 1, 1998; 37(1): 115 - 122.
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Cardiovasc ResHome page
R. L Young, A. L Gundlach, and W. J Louis
Altered cardiac hormone and contractile protein messenger RNA levels following left ventricular myocardial infarction in the rat: an in situ hybridization histochemical study
Cardiovasc Res, January 1, 1998; 37(1): 187 - 201.
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Cardiovasc ResHome page
X. Sun and Y.-C. Ng
Effects of norepinephrine on expression of IGF-1/IGF-1R and SERCA2 in rat heart
Cardiovasc Res, January 1, 1998; 37(1): 202 - 209.
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Circ. Res.Home page
T. Shioi, A. Matsumori, Y. Kihara, M. Inoko, K. Ono, Y. Iwanaga, T. Yamada, A. Iwasaki, K. Matsushima, and S. Sasayama
Increased Expression of Interleukin-1ß and Monocyte Chemotactic and Activating Factor/Monocyte Chemoattractant Protein-1 in the Hypertrophied and Failing Heart With Pressure Overload
Circ. Res., November 19, 1997; 81(5): 664 - 671.
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CirculationHome page
K. Wong, K. R. Boheler, M. Petrou, and M. H. Yacoub
Pharmacological Modulation of Pressure-Overload Cardiac Hypertrophy : Changes in Ventricular Function, Extracellular Matrix, and Gene Expression
Circulation, October 7, 1997; 96(7): 2239 - 2246.
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Am. J. Physiol. Regul. Integr. Comp. Physiol.Home page
J. L. Segar, T. D. Scholz, K. A. Bedell, O. M. Smith, D. J. Huss, and E. N. Guillery
Angiotensin AT1 receptor blockade fails to attenuate pressure-overload cardiac hypertrophy in fetal sheep
Am J Physiol Regulatory Integrative Comp Physiol, October 1, 1997; 273(4): R1501 - R1508.
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CirculationHome page
F. J. Giordano, H. He, P. McDonough, M. Meyer, M. R. Sayen, and W. H. Dillmann
Adenovirus-Mediated Gene Transfer Reconstitutes Depressed Sarcoplasmic Reticulum Ca2+-ATPase Levels and Shortens Prolonged Cardiac Myocyte Ca2+ Transients
Circulation, July 15, 1997; 96(2): 400 - 403.
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CirculationHome page
N. Ito, J. Bartunek, K. W. Spitzer, and B. H. Lorell
Effects of the Nitric Oxide Donor Sodium Nitroprusside on Intracellular pH and Contraction in Hypertrophied Myocytes
Circulation, May 6, 1997; 95(9): 2303 - 2311.
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CirculationHome page
E. O. Weinberg, M. A. Lee, M. Weigner, K. Lindpaintner, S. P. Bishop, C. R. Benedict, K. K. L. Ho, P. S. Douglas, E. Chafizadeh, and B. H. Lorell
Angiotensin AT1 Receptor Inhibition : Effects on Hypertrophic Remodeling and ACE Expression in Rats With Pressure-Overload Hypertrophy due to Ascending Aortic Stenosis
Circulation, March 18, 1997; 95(6): 1592 - 1600.
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CirculationHome page
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.
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CirculationHome page
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.
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HypertensionHome page
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.
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CirculationHome page
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.
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CirculationHome page
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.
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Circ. Res.Home page
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.
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CirculationHome page
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.
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CirculationHome page
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.
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Circ. Res.Home page
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.
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CirculationHome page
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.
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Circ. Res.Home page
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.
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HypertensionHome page
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.
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J. Biol. Chem.Home page
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]