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Am J Physiol Heart Circ Physiol 279: H2568-H2573, 2000;
0363-6135/00 $5.00
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Vol. 279, Issue 5, H2568-H2573, November 2000

SPECIAL COMMUNICATION
Myofilament lattice spacing as a function of sarcomere length in isolated rat myocardium

Thomas C. Irving1, John Konhilas2, Darold Perry1, Robert Fischetti1, and Pieter P. de Tombe2

1 Center for Synchrotron Radiation Research and Instrumentation and Department of Biological, Chemical, and Physical Sciences, Illinois Institute of Technology, Chicago 60616 and 2 Department of Physiology and Biophysics, University of Illinois at Chicago, Chicago, Illinois 60607-7171

The Frank-Starling relationship of the heart has, as its molecular basis, an increase in the activation of myofibrils by calcium as the sarcomere length increases. It has been suggested that this phenomenon may be due to myofilaments moving closer together at longer lengths, thereby enhancing the probability of favorable acto-myosin interaction, resulting in increased calcium sensitivity. Accordingly, we have developed an apparatus so as to obtain accurate measurements of myocardial interfilament spacing (by synchrotron X-ray diffraction) as a function of sarcomere length (by video microscopy) over the working range of the heart, using skinned as well as intact rat trabeculas as model systems. In both these systems, lattice spacing decreased significantly as sarcomere length was increased. Furthermore, lattice spacing in the intact muscle was significantly smaller than that in the skinned muscle at all sarcomere lengths studied. These observations are consistent with the hypothesis that lattice spacing underlies length-dependent activation in the myocardium.

trabeculas; length-dependent activation; X-ray diffraction


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