Back to Search Start Over

Chronic atrial fibrillation alters the functional properties of If in the human atrium.

Authors :
Stillitano F
Lonardo G
Giunti G
Del Lungo M
Coppini R
Spinelli V
Sartiani L
Poggesi C
Mugelli A
Cerbai E
Source :
Journal of cardiovascular electrophysiology [J Cardiovasc Electrophysiol] 2013 Dec; Vol. 24 (12), pp. 1391-400. Date of Electronic Publication: 2013 Jul 19.
Publication Year :
2013

Abstract

Introduction: Despite the evidence that the hyperpolarization-activated current (If) is highly modulated in human cardiomyopathies, no definite data exist in chronic atrial fibrillation (cAF). We investigated the expression, function, and modulation of If in human cAF.<br />Methods and Results: Right atrial samples were obtained from sinus rhythm (SR, n = 49) or cAF (duration >1 year, n = 31) patients undergoing corrective cardiac surgery. Among f-channel isoforms expressed in the human atrium (HCN1, 2 and 4), HCN4 mRNA levels measured by RT-PCR were significantly reduced. However, protein expression was preserved in cAF compared to SR (+85% for HCN4); concurrently, miR-1 expression was significantly reduced. In patch-clamped atrial myocytes, current-specific conductance (gf) was significantly increased in cAF at voltages around the threshold for If activation (-60 to -80 mV); accordingly, a 10-mV rightward shift of the activation curve occurred (P < 0.01). β-Adrenergic and 5-HT4 receptor stimulation exerted similar effects on If in cAF and SR cells, while the ANP-mediated effect was significantly reduced (P < 0.02), suggesting downregulation of natriuretic peptide signaling.<br />Conclusions: In human cAF modifications in transcriptional and posttranscriptional mechanisms of HCN channels occur, associated with a slight yet significant gain-of-function of If , which may contribute to enhanced atrial ectopy.<br /> (© 2013 Wiley Periodicals, Inc.)

Details

Language :
English
ISSN :
1540-8167
Volume :
24
Issue :
12
Database :
MEDLINE
Journal :
Journal of cardiovascular electrophysiology
Publication Type :
Academic Journal
Accession number :
23869794
Full Text :
https://doi.org/10.1111/jce.12212