PDE4 in the human heart – major player or little helper?

• Published in: British journal of pharmacology Vol. 169; no. 3; pp. 524 - 527
• Main Author: Eschenhagen, Thomas
• Format: Journal Article
• Language: English
• Published: England Blackwell Publishing Ltd 01.06.2013
• Subjects: Adrenergic beta-1 Receptor Antagonists - adverse effects; arrhythmias; contractility; Cyclic Nucleotide Phosphodiesterases, Type 3 - metabolism; Heart Failure - drug therapy; Heart Ventricles - drug effects; human heart; Humans; Metoprolol - adverse effects; PDE inhibitors; PDE isoforms; Receptors, Adrenergic, beta-1 - metabolism; Receptors, Adrenergic, beta-2 - metabolism; Research Paper with; Rodents; roflumilast
• ISSN: 0007-1188; 1476-5381
• DOI: 10.1111/bph.12168

PDEs restrict the positive inotropic effects of β‐adrenoceptor stimulation by degrading cAMP. Hence, PDE inhibitors sensitize the heart to catecholamines and are therefore used as positive inotropes. On the downside, this is accompanied by exaggerated energy expenditure, cell death and arrhythmias. For many years, PDE3 was considered to be the major isoform responsible for the control of cardiac force and rhythm. However, recent work in gene‐targeted mice and rodent cells has indicated that PDE4 is also involved. Furthermore, selective PDE4 inhibitors augment catecholamine‐stimulated cAMP levels and induce arrhythmias in human atrial preparations, which suggests that PDE4 has a more prominent role in the human heart than anticipated, and that PDE4 inhibitors such as roflumilast may carry an arrhythmogenic risk. In this issue of the journal, a team of researchers from three laboratories report on the effect of PDE3 and PDE4 inhibitors on ventricular trabeculae from explanted human hearts. The key result is that the PDE4 inhibitor rolipram does not affect the positive inotropic effects of β1‐ or β2‐adrenoceptor stimulation. Given that the ventricle rather than the atria is the critical region in terms of arrhythmogenic consequences, this is an important and reassuring finding. Linked Article This article is a commentary on the research paper by Molenaar et al., pp. 528–538 of this issue. To view this paper visit http://dx.doi.org/10.1111/bph.12167