The research led by the University of Bristol and funded by the Medical Research Council (MRC) is published in the Proceedings of the National Academy of Sciences (PNAS).
Heart cardiogram. Image credit: Виталий Смолыгин via publicdomainpictures.net, CC0 Public Domain
Around 26 million people worldwide suffer from heart failure, with more than 50 per cent dying suddenly most likely due to the spontaneous onset of a heart rhythm problem, known as an arrhythmia. The link between the electrical signal that triggers the heart cell to contract (action potential) and consequent ability of the heart to pump blood has been known for nearly 40 years but understanding how and why the heart's electrical rhythm becomes disturbed has remained a major research problem.
At the cellular level, and identified initiator of cardiac arrhythmias are early after-depolarizations (EADs), but the cellular trigger for EADs in heart failure is unclear. EADs occur during the repolarization phase of the cardiac action potential (AP) where several ionic currents interact to control repolarization. EADs may be produced by reactivation of ionic currents during AP repolarization when the potassium currents forming the “repolarization reserve” are insufficient to maintain the repolarization trajectory of the AP, although why this should occur spontaneously within a steady train of APs is uncertain. Spontaneous calcium (Ca2+) waves inside the cell have also been implicated in EAD generation, but it is unclear how such waves might be initiated.
The study has shown that the reduction in synchronous Ca2+ release early in the AP of failing heart muscle cells promotes the appearance of “late Ca2+ sparks” (microscopic Ca2+ release events) which can propagate, forming Ca2+ ripples and waves. These, in turn, produce an inward sodium-calcium exchange current which opposes AP repolarization. Restoration of AP phase 1 repolarization improved Ca2+ release synchrony and reduced late Ca2+ spark rate, suggesting an entirely new approach to reducing the risk of sudden death in heart failure.
Professor Mark Cannell, Chair in Cardiac Cell Biology in the University of Bristol's School of Physiology, Pharmacology, and Neuroscience, who led the research, said: “Our findings suggest that new therapies should be developed with the aim of improving early Ca2+ release by restoring AP phase 1 repolarization and/or restoring t-tubule regularity. This will reduce the risk of potentially lethal heart rhythm problems as well as mitigating the defective excitation-contraction coupling seen in heart failure. Our research proposes an entirely new approach to reducing the risk of sudden death in heart failure and the next step will be to move towards a clinical trial of new drugs.”
Source: University of Bristol