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American Journal of Clinical Nutrition, Vol. 71, No. 1, 202S-207S, January 2000
© 2000 American Society for Clinical Nutrition


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Prevention of fatal cardiac arrhythmias by polyunsaturated fatty acids1,2,3

Jing X Kang and Alexander Leaf

1 From the Department of Medicine, Massachusetts General Hospital, Boston; the Brockton/West Roxbury Veterans Affairs Medical Center, West Roxbury, MA; and the Harvard Medical School, Boston.

In animal feeding studies, and probably in humans, n–3 polyunsaturated fatty acids (PUFAs) prevent fatal ischemia-induced cardiac arrhythmias. We showed that n–3 PUFAs also prevented such arrhythmias in surgically prepared, conscious, exercising dogs. The mechanism of the antiarrhythmic action of n–3 PUFAs has been studied in spontaneously contracting cultured cardiac myocytes of neonatal rats. Adding arrhythmogenic toxins (eg, ouabain, high Ca2+, lysophosphatidylcholine, ß-adrenergic agonist, acylcarnitine, and the Ca2+ ionophore) to the myocyte perfusate caused tachycardia, contracture, and fibrillation of the cultured myocytes. Adding eicosapentaenoic acid (EPA: 5–15 µmol/L) to the superfusate before adding the toxins prevented the expected tachyarrhythmias. If the arrhythmias were first induced, adding the EPA to the superfusate terminated the arrhythmias. This antiarrhythmic action occurred with dietary n–3 and n–6 PUFAs; saturated fatty acids and the monounsaturated oleic acid induced no such action. Arachidonic acid (AA; 20:4n–6) is anomalous because in one-third of the tests it provoked severe arrhythmias, which were found to result from cyclooxygenase metabolites of AA. When cyclooxygenase inhibitors were added with the AA, the antiarrhythmic effect was like those of EPA and DHA. The action of the n–3 and n–6 PUFAs is to stabilize electrically every myocyte in the heart by increasing the electrical stimulus required to elicit an action potential by {approx}50% and prolonging the relative refractory time by {approx}150%. These electrophysiologic effects result from an action of the free PUFAs to modulate sodium and calcium currents in the myocytes. The PUFAs also modulate sodium and calcium channels and have anticonvulsant activity in brain cells.

Key Words: n–3 Fatty acids • n–6 fatty acids • ventricular fibrillation • sudden cardiac death • cardiac arrhythmias




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