Decreased [3H]ouabain binding sites in skeletal muscle of rats with chronic heart failure

J Appl Physiol (1985). 1997 Jul;83(1):323-7. doi: 10.1152/jappl.1997.83.1.323.

Abstract

Abnormalities intrinsic to skeletal muscle are thought to contribute to decrements in exercise capacity found in individuals with chronic heart failure (CHF). Na+-K+-adenosinetriphosphatase (the Na+ pump) is essential for maintaining muscle excitability and contractility. Therefore, we investigated the possibility that the number and affinity of Na+ pumps in locomotor muscles of rats with CHF are decreased. Myocardial infarction (MI) was induced in 8 rats, and a sham operation was performed in 12 rats. The degree of CHF was assessed approximately 180 days after surgery. Soleus and plantaris muscles were harvested, and Na+ pumps were quantified by using a [3H]ouabain binding assay. At the time of muscle harvest, MI and sham-operated rats were similar in age (458 +/- 54 vs. 447 +/- 34 days old, respectively). Compared with their sham-operated counterparts, MI rats had a significant amount of heart failure, right ventricular-to-body weight ratio was greater (48%), and the presence of pulmonary congestion was suggested by an elevated lung-to-body weight ratio (29%). Left ventricular end-diastolic pressure was significantly increased in the MI rats (11 +/- 1 mmHg) compared with the sham-operated controls (1 +/- 1 mmHg). In addition, mean arterial blood pressure was lower in the MI rats compared with their control counterparts. [3H]ouabain binding sites were reduced 18% in soleus muscle (136 +/- 12 vs. 175 +/- 13 pmol/g wet wt, MI vs. sham, respectively) and 22% in plantaris muscle (119 +/- 12 vs. 147 +/- 8 pmol/g wet wt, MI vs. sham, respectively). The affinity of these [3H]ouabain binding sites was similar for the two groups. The relationship between the reduction in Na+ pump number and the reduced exercise capacity in individuals with CHF remains to be determined.

Publication types

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

MeSH terms

  • Animals
  • Binding Sites
  • Chronic Disease
  • Female
  • Heart Failure / metabolism*
  • Locomotion / physiology
  • Muscle Contraction / physiology
  • Muscle, Skeletal / chemistry
  • Muscle, Skeletal / metabolism*
  • Myocardial Infarction / physiopathology
  • Ouabain / metabolism*
  • Rats
  • Rats, Wistar
  • Sodium Channels / metabolism
  • Sodium-Potassium-Exchanging ATPase / metabolism
  • Ventricular Dysfunction, Left / physiopathology

Substances

  • Sodium Channels
  • Ouabain
  • Sodium-Potassium-Exchanging ATPase