ISOFORM-SPECIFIC REGULATION OF MYOCARDIAL NA,K-ATPASE ALPHA-SUBUNIT IN CONGESTIVE-HEART-FAILURE - ROLE OF NOREPINEPHRINE

Background Myocardial ouabain-binding sites and Na,K-ATPase activity a re reduced in congestive heart failure (CHF), but the mechanisms by wh ich CHF reduces the Na,K-ATPase remain unknown. We proposed to investi gate whether the changes are accompanied by isoform-specific reduction s of the Na,K-ATPase alpha-subunit proteins in CHF and whether similar changes could be produced by exogenous norepinephrine administration. Methods and Results CHF was induced in dogs by rapid ventricular paci ng at a rate of 225 beats per minute for 8 weeks (protocol 1). A secon d group of dogs were paced at 100 beats per minute and served as contr ols. In protocol 2, norepinephrine was infused in normal dogs using a subcutaneous osmotic minipump for 8 weeks. The control dogs received n ormal saline through the pump. Animals were studied after 8 weeks of p acing or norepinephrine infusion. After the baseline hemodynamics and interstitial norepinephrine concentration had been obtained, the heart s were removed for measuring [H-3]]ouabain-binding sites and Na,K-ATPa se alpha-subunit proteins using isoform-specific monoclonal antibodies . Results Myocardial [H-3]ouabain-binding sites were reduced in dogs w ith CHF and chronic norepinephrine infusion. The Western blot analysis showed that adult canine hearts possess both alpha(1) and alpha(3) is oforms of the Na,K-ATPase alpha-subunit but not the alpha(2) isoform p rotein. CHF and NE infusion had no effect on the Na,K-ATPase alpha(1)- subunit protein but did reduce the alpha(3) isoform protein significan tly. In addition, there was a significant inverse correlation between the amount of myocardial alpha(3) isoform protein and interstitial nor epinephrine content in the dogs. In contrast, the specific activity of the sarcolemmal marker 5'-nucleotidase did not differ among the group s of animals. Conclusions The reduction of myocardial Na,K-ATPase in C HF is limited to the alpha(3) isoform. Furthermore, because similar ch anges in myocardial ouabain-binding sites and Na,K-ATPase alpha(3) iso form were produced by chronic norepinephrine infusion, the decrease in the Na,K-ATPase in CHF is most likely mediated via excess sympathetic stimulation.