Reduced aerobic capacity causes leaky ryanodine receptors that trigger arrhythmia in a rat strain artificially selected and bred for low aerobic running capacity

M. A. Høydal, T. O. Stølen, A. B. Johnsen, M. Alvez, D. Catalucci, G. Condorelli, L. G. Koch, S. L. Britton, G. L. Smith, U. Wisløff

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Aim: Rats selectively bred for inborn low capacity of running (LCR) display a series of poor health indices, whereas rats selected for high capacity of running (HCR) display a healthy profile. We hypothesized that selection of low aerobic capacity over generations leads to a phenotype with increased diastolic Ca2+ leak that trigger arrhythmia. Methods: We used rats selected for HCR (N = 10) or LCR (N = 10) to determine the effect of inborn aerobic capacity on Ca2+ leak and susceptibility of ventricular arrhythmia. We studied isolated Fura-2/AM-loaded cardiomyocytes to detect Ca2+ handling and function on an inverted epifluorescence microscope. To determine arrhythmogenicity, we did a final experiment with electrical burst pacing in Langendorff-perfused hearts. Results: Ca2+ handling was impaired by reduced Ca2+ amplitude, prolonged time to 50% Ca2+ decay and reduced sarcoplasmic reticulum (SR) Ca2+ content. Impaired Ca2+ removal was influenced by reduced SR Ca2+ATP-ase 2a (SERCA2a) function and increased sodium/Ca2+ exchanger (NCX) in LCR rats. Diastolic Ca2 leak was 87% higher in LCR rats. The leak was reduced by CaMKII inhibition. Expression levels of phosphorylated threonine 286 CaMKII levels and increased RyR2 phosphorylation at the serine 2814 site mechanistically support our findings of increased leak in LCR. LCR rats had significantly higher incidence of ventricular fibrillation. Conclusion: Selection of inborn low aerobic capacity over generations leads to a phenotype with increased risk of ventricular fibrillation. Increased phosphorylation of CaMKII at serine 2814 at the cardiac ryanodine receptor appears as an important mechanism of impaired Ca2+ handling and diastolic Ca2+ leak that results in increased susceptibility to ventricular fibrillation.

Original languageEnglish
Pages (from-to)854-864
Number of pages11
JournalActa Physiologica
Volume210
Issue number4
DOIs
Publication statusPublished - 2014

Fingerprint

Ryanodine Receptor Calcium Release Channel
Running
Cardiac Arrhythmias
Calcium-Calmodulin-Dependent Protein Kinase Type 2
Ventricular Fibrillation
Sarcoplasmic Reticulum
Serine
Phosphorylation
Phenotype
Fura-2
Threonine
Cardiac Myocytes
Adenosine Triphosphate
Sodium
Incidence
Health

Keywords

  • Aerobic capacity
  • Arrhytmia
  • Calcium

ASJC Scopus subject areas

  • Physiology

Cite this

Reduced aerobic capacity causes leaky ryanodine receptors that trigger arrhythmia in a rat strain artificially selected and bred for low aerobic running capacity. / Høydal, M. A.; Stølen, T. O.; Johnsen, A. B.; Alvez, M.; Catalucci, D.; Condorelli, G.; Koch, L. G.; Britton, S. L.; Smith, G. L.; Wisløff, U.

In: Acta Physiologica, Vol. 210, No. 4, 2014, p. 854-864.

Research output: Contribution to journalArticle

Høydal, M. A. ; Stølen, T. O. ; Johnsen, A. B. ; Alvez, M. ; Catalucci, D. ; Condorelli, G. ; Koch, L. G. ; Britton, S. L. ; Smith, G. L. ; Wisløff, U. / Reduced aerobic capacity causes leaky ryanodine receptors that trigger arrhythmia in a rat strain artificially selected and bred for low aerobic running capacity. In: Acta Physiologica. 2014 ; Vol. 210, No. 4. pp. 854-864.
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abstract = "Aim: Rats selectively bred for inborn low capacity of running (LCR) display a series of poor health indices, whereas rats selected for high capacity of running (HCR) display a healthy profile. We hypothesized that selection of low aerobic capacity over generations leads to a phenotype with increased diastolic Ca2+ leak that trigger arrhythmia. Methods: We used rats selected for HCR (N = 10) or LCR (N = 10) to determine the effect of inborn aerobic capacity on Ca2+ leak and susceptibility of ventricular arrhythmia. We studied isolated Fura-2/AM-loaded cardiomyocytes to detect Ca2+ handling and function on an inverted epifluorescence microscope. To determine arrhythmogenicity, we did a final experiment with electrical burst pacing in Langendorff-perfused hearts. Results: Ca2+ handling was impaired by reduced Ca2+ amplitude, prolonged time to 50{\%} Ca2+ decay and reduced sarcoplasmic reticulum (SR) Ca2+ content. Impaired Ca2+ removal was influenced by reduced SR Ca2+ATP-ase 2a (SERCA2a) function and increased sodium/Ca2+ exchanger (NCX) in LCR rats. Diastolic Ca2 leak was 87{\%} higher in LCR rats. The leak was reduced by CaMKII inhibition. Expression levels of phosphorylated threonine 286 CaMKII levels and increased RyR2 phosphorylation at the serine 2814 site mechanistically support our findings of increased leak in LCR. LCR rats had significantly higher incidence of ventricular fibrillation. Conclusion: Selection of inborn low aerobic capacity over generations leads to a phenotype with increased risk of ventricular fibrillation. Increased phosphorylation of CaMKII at serine 2814 at the cardiac ryanodine receptor appears as an important mechanism of impaired Ca2+ handling and diastolic Ca2+ leak that results in increased susceptibility to ventricular fibrillation.",
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T1 - Reduced aerobic capacity causes leaky ryanodine receptors that trigger arrhythmia in a rat strain artificially selected and bred for low aerobic running capacity

AU - Høydal, M. A.

AU - Stølen, T. O.

AU - Johnsen, A. B.

AU - Alvez, M.

AU - Catalucci, D.

AU - Condorelli, G.

AU - Koch, L. G.

AU - Britton, S. L.

AU - Smith, G. L.

AU - Wisløff, U.

PY - 2014

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N2 - Aim: Rats selectively bred for inborn low capacity of running (LCR) display a series of poor health indices, whereas rats selected for high capacity of running (HCR) display a healthy profile. We hypothesized that selection of low aerobic capacity over generations leads to a phenotype with increased diastolic Ca2+ leak that trigger arrhythmia. Methods: We used rats selected for HCR (N = 10) or LCR (N = 10) to determine the effect of inborn aerobic capacity on Ca2+ leak and susceptibility of ventricular arrhythmia. We studied isolated Fura-2/AM-loaded cardiomyocytes to detect Ca2+ handling and function on an inverted epifluorescence microscope. To determine arrhythmogenicity, we did a final experiment with electrical burst pacing in Langendorff-perfused hearts. Results: Ca2+ handling was impaired by reduced Ca2+ amplitude, prolonged time to 50% Ca2+ decay and reduced sarcoplasmic reticulum (SR) Ca2+ content. Impaired Ca2+ removal was influenced by reduced SR Ca2+ATP-ase 2a (SERCA2a) function and increased sodium/Ca2+ exchanger (NCX) in LCR rats. Diastolic Ca2 leak was 87% higher in LCR rats. The leak was reduced by CaMKII inhibition. Expression levels of phosphorylated threonine 286 CaMKII levels and increased RyR2 phosphorylation at the serine 2814 site mechanistically support our findings of increased leak in LCR. LCR rats had significantly higher incidence of ventricular fibrillation. Conclusion: Selection of inborn low aerobic capacity over generations leads to a phenotype with increased risk of ventricular fibrillation. Increased phosphorylation of CaMKII at serine 2814 at the cardiac ryanodine receptor appears as an important mechanism of impaired Ca2+ handling and diastolic Ca2+ leak that results in increased susceptibility to ventricular fibrillation.

AB - Aim: Rats selectively bred for inborn low capacity of running (LCR) display a series of poor health indices, whereas rats selected for high capacity of running (HCR) display a healthy profile. We hypothesized that selection of low aerobic capacity over generations leads to a phenotype with increased diastolic Ca2+ leak that trigger arrhythmia. Methods: We used rats selected for HCR (N = 10) or LCR (N = 10) to determine the effect of inborn aerobic capacity on Ca2+ leak and susceptibility of ventricular arrhythmia. We studied isolated Fura-2/AM-loaded cardiomyocytes to detect Ca2+ handling and function on an inverted epifluorescence microscope. To determine arrhythmogenicity, we did a final experiment with electrical burst pacing in Langendorff-perfused hearts. Results: Ca2+ handling was impaired by reduced Ca2+ amplitude, prolonged time to 50% Ca2+ decay and reduced sarcoplasmic reticulum (SR) Ca2+ content. Impaired Ca2+ removal was influenced by reduced SR Ca2+ATP-ase 2a (SERCA2a) function and increased sodium/Ca2+ exchanger (NCX) in LCR rats. Diastolic Ca2 leak was 87% higher in LCR rats. The leak was reduced by CaMKII inhibition. Expression levels of phosphorylated threonine 286 CaMKII levels and increased RyR2 phosphorylation at the serine 2814 site mechanistically support our findings of increased leak in LCR. LCR rats had significantly higher incidence of ventricular fibrillation. Conclusion: Selection of inborn low aerobic capacity over generations leads to a phenotype with increased risk of ventricular fibrillation. Increased phosphorylation of CaMKII at serine 2814 at the cardiac ryanodine receptor appears as an important mechanism of impaired Ca2+ handling and diastolic Ca2+ leak that results in increased susceptibility to ventricular fibrillation.

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KW - Arrhytmia

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