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1Department of Cardiovascular Medicine, Graduate School of Medicine, and 2Biomechanics Division, Institute of Environmental Studies, Graduate School of Frontier Sciences, University of Tokyo, Tokyo 113-0033; 3Department of Physiology, School of Dental Medicine, Tsurumi University, Kanagawa 230-5801; and 4Department of Cardiovascular Dynamics, National Cardiovascular Center Research Institute, Osaka 565-8565, Japan
Submitted 10 October 2003 ; accepted in final form 2 March 2004
One of the most salient characteristics of the heart is its ability to adjust work output to external load. To examine whether a single cardiomyocyte preparation retains this property, we measured the contractile function of a single rat cardiomyocyte under a wide range of loading conditions using a force-length measurement system implemented with adaptive control. A pair of carbon fibers was used to clamp the cardiomyocyte, attached to each end under a microscope. One fiber was stiff, serving as a mechanical anchor, while the bending motion of the compliant fiber was monitored for force-length measurement. Furthermore, by controlling the position of the compliant fiber using a piezoelectric translator based on adaptive control, we could change load dynamically during contractions. Under unloaded conditions, maximal shortening velocity was 106 ± 8.9 µm/s (n = 13 cells), and, under isometric conditions, peak developed force reached 5,720 nN (41.6 ± 5.6 mN/mm2; n = 17 cells). When we simulated physiological working conditions consisting of an isometric contraction, followed by shortening and relaxation, the average work output was 828 ± 123 J/m3 (n = 20 cells). The top left corners of tension-length loops obtained under all of these conditions approximate a line, analogous to the end-systolic pressure-volume relation of the ventricle. All of the functional characteristics described were analogous to those established by studies using papillary muscle or trabeculae preparations. In conclusion, the present results confirmed the fact that each myocyte forms the functional basis for ventricular function and that single cell mechanics can be a link between subcellular events and ventricular mechanics.
cardiomyocyte; mechanics; carbon fiber
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