AJP - Heart Track the topics, authors and articles important to you
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


Am J Physiol Heart Circ Physiol 292: H1487-H1497, 2007. First published November 10, 2006; doi:10.1152/ajpheart.00909.2006
0363-6135/07 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
292/3/H1487    most recent
00909.2006v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Iribe, G.
Right arrow Articles by Kohl, P.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Iribe, G.
Right arrow Articles by Kohl, P.

Force-length relations in isolated intact cardiomyocytes subjected to dynamic changes in mechanical load

Gentaro Iribe,1 Michiel Helmes,1,2 and Peter Kohl1

1Oxford University, Oxford, United Kingdom; and 2IonOptix Europe, Wageningen, The Netherlands

Submitted 23 August 2006 ; accepted in final form 9 November 2006

We developed a dynamic force-length (FL) control system for single intact cardiomyocytes that uses a pair of compliant, computer-controlled, and piezo translator (PZT)-positioned carbon fibers (CF). CF are attached to opposite cell ends to afford dynamic and bidirectional control of the cell's mechanical environment. PZT and CF tip positions, as well as sarcomere length (SL), are simultaneously monitored in real time, and passive/active forces are calculated from CF bending. Cell force and length were dynamically adjusted by corresponding changes in PZT position, to achieve isometric, isotonic, or work-loop style contractions. Functionality of the technique was assessed by studying FL behavior of guinea pig intact cardiomyocytes. End-diastolic and end-systolic FL relations, obtained with varying preload and/or afterloads, were near linear, independent of the mode of contraction, and overlapping for the range of end-diastolic SLs tested (1.85–2.05 µm). Instantaneous elastance curves, obtained from FL relation curves, showed an afterload-dependent decrease in time to peak elastance and slowed relaxation with both increased preload and afterload. The ability of the present system to independently and dynamically control preload, afterload, and transition between end-diastolic and end-systolic FL coordinates provides a valuable extension to the range of tools available for the study of single cardiomyocyte mechanics, to foster its interrelation with whole heart pathophysiology.

single cell mechanics; preload; afterload; time-varying elastance



Address for reprint requests and other correspondence: G. Iribe, Cardiac Mechano-Electric Feedback Group, Dept. of Physiology, Anatomy and Genetics, Univ. of Oxford, Sherrington Bldg., Parks Road, Oxford, UK OX1 3PT (e-mail: gentaro.iribe{at}dpag.ox.ac.uk)




This article has been cited by other articles:


Home page
Exp Biol MedHome page
K. A. Addae-Mensah and J. P. Wikswo
Measurement Techniques for Cellular Biomechanics In Vitro
Exp Biol Med, July 1, 2008; 233(7): 792 - 809.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2007 by the American Physiological Society.