Skip Navigation

Cardiovascular Research 2004 64(2):250-259; doi:10.1016/j.cardiores.2004.07.001
© 2004 by European Society of Cardiology
This Article
Right arrow Full Text Freely available
Right arrow FREE Full Text (PDF) Freely available
Right arrow E-letters: Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when E-letters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Right arrow Disclaimer
Google Scholar
Right arrow Articles by Zorn-Pauly, K.
Right arrow Articles by Koidl, B.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Zorn-Pauly, K.
Right arrow Articles by Koidl, B.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Copyright © 2004, European Society of Cardiology

If in left human atrium: a potential contributor to atrial ectopy

Klaus Zorn-Paulya, Peter Schaffera, Brigitte Pelzmanna, Petra Langa, Heinrich Mächlerb, Bruno Riglerb and Bernd Koidla,*

aInstitut für Medizinische Physik und Biophysik, Medizinische Universität Graz, Harrachgasse 21, A-8010 Graz, Austria
bUniversitätsklinik für Chirugie, Medizinische Universität Graz, Auenbruggerplatz 5, A-8036 Graz, Austria

* Corresponding author. Tel.: +43 316 380 4137; fax: +43 316 380 7746. Email address: bernd.koidl{at}meduni-graz.at

Objective: The left human atrium plays an important role in initiation of atrial fibrillation (AF) and the hyperpolarization activated cation current (If) is a candidate for contributing to abnormal automaticity. However, electrophysiological data concerning If are not available in this cardiac region and we therefore investigated If in human left atrial tissue.

Methods: Human atrial myocytes were isolated from the left atrial appendage (LAA) and the left atrial wall (LAW) obtained from patients undergoing open heart surgery. If was measured with the whole-cell patch-clamp technique.

Results: If densities between –70 and –110 mV were found to be significantly higher in LAA than in LAW cells. Furthermore, in the group of LAA cells the half maximal activation potential (V1/2) was found to be less negative (V1/2 of –84.3±1.9 mV, n=14/9) compared to LAW cells (V1/2 of –97.8±2.1 mV, n=28/9). Beta-adrenergic receptor stimulation with isoproterenol (1 µM) caused an acceleration of current activation and a V1/2 shift to more positive potentials in cells of both regions (LAA: 8.8±2.3 mV, n=6/4 and LAW: 8.9±2.6 mV, n=6/4). Simulations using a mathematical model of the human atrial myocyte demonstrated that If was able to induce spontaneous activity in the model at a regular rhythm due to the interplay of If, Na+/Ca2+ exchange current and Ca2+ release of the sarcoplasmic reticulum (SR).

Conclusions: Our study revealed the presence of If in left atrial myocytes and showed that If parameters depend on atrial region. If current densities were sufficient to convert the mathematical model of a quiescent human atrial cell into a "pacemaker cell". These data support the hypothesis of If as a contributor to abnormal automaticity in human atrial tissue.

KEYWORDS Human left atrial myocytes; Patch clamp; Pacemaker current; Computer modeling; Atrial ectopy


Time for primary review 26 days


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Physiol. Rev.Home page
M. Biel, C. Wahl-Schott, S. Michalakis, and X. Zong
Hyperpolarization-Activated Cation Channels: From Genes to Function
Physiol Rev, July 1, 2009; 89(3): 847 - 885.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
E. A. Woodcock, P. M. Kistler, and Y.-K. Ju
Phosphoinositide signalling and cardiac arrhythmias
Cardiovasc Res, May 1, 2009; 82(2): 286 - 295.
[Abstract] [Full Text] [PDF]


Home page
Cardiovasc ResHome page
P. Kohl
Cardiac cellular heterogeneity and remodelling
Cardiovasc Res, November 1, 2004; 64(2): 195 - 197.
[Full Text] [PDF]



Disclaimer: Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.