Digoxin and exercise effects on skeletal muscle Na+,K+‐ATPase isoform gene expression in healthy humans

Author:

McKenna Michael J.1ORCID,Gong Xiaofei1,Petersen Aaron C.1ORCID,Sostaric Simon1ORCID,Goodman Craig A.12ORCID,Garnham Andrew1ORCID,Aw Tai‐Juan3ORCID,Steward Collene H.1ORCID,Murphy Kate T.12ORCID,Carey Kate A.4ORCID,Krum Henry3ORCID,Snow Rodney J.5ORCID,Cameron‐Smith David6ORCID

Affiliation:

1. Institute for Health and Sport Victoria University Melbourne Australia

2. Centre for Muscle Research, Department of Anatomy and Physiology University of Melbourne Melbourne Australia

3. Department of Epidemiology and Preventive Medicine Monash University Alfred Hospital Melbourne Australia

4. Institute for Breathing and Sleep Melbourne Australia

5. Institute of Physical Activity and Nutrition, School of Exercise and Nutrition Sciences Deakin University Melbourne Australia

6. Department of Nutrition Singapore Institute of Food and Biotechnology Innovation (SIFBI) Singapore Singapore

Abstract

AbstractIn muscle, digoxin inhibits Na+,K+‐ATPase (NKA) whereas acute exercise can increase NKA gene expression, consistent with training‐induced increased NKA content. We investigated whether oral digoxin increased NKA isoform mRNA expression (qPCR) in muscle at rest, during and post‐exercise in 10 healthy adults, who received digoxin (DIG, 0.25 mg per day) or placebo (CON) for 14 days, in a randomised, double‐blind and cross‐over design. Muscle was biopsied at rest, after cycling 20 min (10 min each at 33%, then 67% ), then to fatigue at 90% and 3 h post‐exercise. No differences were found between DIG and CON for NKA α1–3 or β1–3 isoform mRNA. Both α1 (354%, P = 0.001) and β3 mRNA (P = 0.008) were increased 3 h post‐exercise, with α2 and β1–2 mRNA unchanged, whilst α3 mRNA declined at fatigue (−43%, P = 0.045). In resting muscle, total β mRNA (∑(β123)) increased in DIG (60%, P = 0.025) and also when transcripts for each isoform were normalised to CON then either summed (P = 0.030) or pooled (n = 30, P = 0.034). In contrast, total α mRNA (∑(α123), P = 0.348), normalised then summed (P = 0.332), or pooled transcripts (n = 30, P = 0.717) did not differ with DIG. At rest, NKA α1–2 and β1–2 protein abundances were unchanged by DIG. Post‐exercise, α1 and β1–2 proteins were unchanged, but α2 declined at 3 h (19%, P = 0.020). In conclusion, digoxin did not modify gene expression of individual NKA isoforms at rest or with exercise, indicating NKA gene expression was maintained consistent with protein abundances. However, elevated resting muscle total β mRNA with digoxin suggests a possible underlying β gene‐stimulatory effect.Highlights What is the central question of this study?Na+,K+‐ATPase (NKA) in muscle is important for Na+/K+ homeostasis. We investigated whether the NKA‐inhibitor digoxin stimulates increased NKA gene expression in muscle and exacerbates NKA gene responses to exercise in healthy adults. What is the main finding and its importance?Digoxin did not modify exercise effects on muscle NKA α1–3 and β1–3 gene transcripts, which comprised increased post‐exercise α1 and β3 mRNA and reduced α3 mRNA during exercise. However, in resting muscle, digoxin increased NKA total β isoform mRNA expression. Despite inhibitory‐digoxin or acute exercise stressors, NKA gene regulation in muscle is consistent with the maintenance of NKA protein contents.

Publisher

Wiley

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