| First Author | Aschar-Sobbi R | Year | 2015 |
| Journal | Nat Commun | Volume | 6 |
| Pages | 6018 | PubMed ID | 25598495 |
| Mgi Jnum | J:219724 | Mgi Id | MGI:5629621 |
| Doi | 10.1038/ncomms7018 | Citation | Aschar-Sobbi R, et al. (2015) Increased atrial arrhythmia susceptibility induced by intense endurance exercise in mice requires TNFalpha. Nat Commun 6:6018 |
| abstractText | Atrial fibrillation (AF) is the most common supraventricular arrhythmia that, for unknown reasons, is linked to intense endurance exercise. Our studies reveal that 6 weeks of swimming or treadmill exercise improves heart pump function and reduces heart-rates. Exercise also increases vulnerability to AF in association with inflammation, fibrosis, increased vagal tone, slowed conduction velocity, prolonged cardiomyocyte action potentials and RyR2 phosphorylation (CamKII-dependent S2814) in the atria, without corresponding alterations in the ventricles. Microarray results suggest the involvement of the inflammatory cytokine, TNFalpha, in exercised-induced atrial remodelling. Accordingly, exercise induces TNFalpha-dependent activation of both NFkappaB and p38MAPK, while TNFalpha inhibition (with etanercept), TNFalpha gene ablation, or p38 inhibition, prevents atrial structural remodelling and AF vulnerability in response to exercise, without affecting the beneficial physiological changes. Our results identify TNFalpha as a key factor in the pathology of intense exercise-induced AF. |
