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Am J Physiol Heart Circ Physiol 288: H1662-H1667, 2005. First published December 2, 2004; doi:10.1152/ajpheart.00906.2004
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Effects of BDM, [Ca2+]o, and temperature on the dynamic stiffness of quiescent cardiac trabeculae from rat

R. S. Kirton,1,3 A. J. Taberner,1,5 P. M. F. Nielsen,1,3 A. A. Young,1,2,4 and D. S. Loiselle1,4

1Bioengineering Institute and Departments of 2Anatomy, 3Engineering Science, and 4Physiology, University of Auckland, Auckland, New Zealand; and 5Department of Mechanical Engineering, Massachusetts Institute of Technology, Cambridge, Massachusetts

Submitted 2 September 2004 ; accepted in final form 22 November 2004

Studies of the passive mechanical properties of cardiac tissue have traditionally been conducted at subphysiological temperatures and various concentrations of extracellular Ca2+ ([Ca2+]o). More recently, the negative inotropic agent 2,3-butanedione monoxime (BDM) has been used. However, there remains a lack of data regarding the influence of temperature, Ca2+, and BDM on the passive mechanical properties of cardiac tissue. We have used the dynamic stiffness technique, a sensitive measurement of cross-bridge activity, in which minute (~0.2% of muscle length) sinusoidal perturbations are applied at various frequencies (0.2–100 Hz) to quiescent, viable right ventricular rat trabeculae at two temperatures (20°C and 26°C) and at two [Ca2+]o (0.5 and 1.25 mM) in the presence and absence of BDM (20 mM). The stiffness spectra (amplitude and phase) were sensitive to temperature and [Ca2+]o in the absence of BDM but insensitive in the presence of BDM. From the index of cross-bridge cycling (the ratio of high- to low-frequency stiffness amplitude), we infer that BDM inhibits a small degree of spontaneous sarcomere activity, thereby allowing the true passive properties of trabeculae to be determined. In the absence of BDM, the extent of spontaneous sarcomere activity decreases with increasing temperature. We caution that the measured mechanical properties of passive cardiac tissue are critically dependent on the experimental conditions under which they are measured. Experiments must be performed at sufficiently high temperatures (>25°C) to ensure a low resting concentration of intracellular Ca2+ or in the presence of an inhibitor of cross-bridge cycling.

cardiac muscle; sinusoidal length perturbation; passive mechanics; 2,3-butanedione monoxime; extracellular calcium concentration



Address for reprint requests and other correspondence: R. S. Kirton, Bioengineering Institute, Univ. of Auckland, 70 Symonds St., Auckland, New Zealand (E-mail: r.kirton{at}auckland.ac.nz)




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