31P-NMR analysis of congestive heart failure in the SHHF/Mcc-facp rat heart

J Mol Cell Cardiol. 1998 Feb;30(2):235-41. doi: 10.1006/jmcc.1997.0587.

Abstract

31P-NMR was used to monitor myocardial bioenergetics in compensated and failing SHHF/MCC-fa(cp) (SHF) rat hearts. The SHHF/Mcc-fa(cp) (spontaneous hypertension and heart failure) rat is a relatively new genetic model in which all individuals spontaneously develop congestive heart failure, most during the second year of life. Failing SHF rat hearts displayed a pronounced decrease in resting PCr:ATP ratios (P<0.001), which was explained by a significant (P<0. 0001) drop in total creatine (47.2+/-3.1 nmol/mg protein) v age matched controls (106+/-3 nmol/mg protein). In end stage failure, NMR determined PCr was 2.9+/-0.1 micro mol/g wet weight under basal conditions. In contrast, 6- and 20-month-old controls and compensated SHFs had PCr values of 5.3+/-0.1, and 5.1+/-0.5 and 5. 1+/-0.2 micro mol/g wet weight. Both compensated and failing SHF hearts were metabolically compromised when the rate pressure product (RPP) was increased, as evidenced by an increase in Pi and a drop in PCr. Compensated SHF hearts, however, were able to increase rate pressure products (RRP, mmHg X beats/min) from 44.5+/-1.4 to 66.6+/-3. 4 K with dobutamine infusion, whereas hearts in end-stage failure were able to increase their RPP from baseline values of 27+/-4 K to only 37+/-7 K. The data indicate that a pronounced decline in PCr and total creatine signals the transition from compensatory hypertrophy to decompensation and failure in the SHF rat model of hypertensive cardiomyopathy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adenine Nucleotides / metabolism
  • Adenosine Triphosphate / metabolism
  • Animals
  • Creatine / metabolism
  • Disease Models, Animal
  • Energy Metabolism
  • Heart Failure / genetics
  • Heart Failure / metabolism*
  • Heart Failure / physiopathology
  • In Vitro Techniques
  • Magnetic Resonance Spectroscopy
  • Male
  • Myocardium / metabolism*
  • Perfusion
  • Phosphocreatine / metabolism
  • Phosphorus Isotopes
  • Rats
  • Rats, Inbred F344
  • Rats, Mutant Strains
  • Rats, Sprague-Dawley
  • Ventricular Dysfunction, Left / genetics
  • Ventricular Dysfunction, Left / metabolism
  • Ventricular Dysfunction, Left / physiopathology

Substances

  • Adenine Nucleotides
  • Phosphorus Isotopes
  • Phosphocreatine
  • Adenosine Triphosphate
  • Creatine