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Force‐velocity and power‐load curves in rat skinned cardiac myocytes
Author(s) -
McDonald Kerry S.,
Wolff Matthew R.,
Moss Richard L.
Publication year - 1998
Publication title -
the journal of physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.802
H-Index - 240
eISSN - 1469-7793
pISSN - 0022-3751
DOI - 10.1111/j.1469-7793.1998.519bh.x
Subject(s) - sarcomere , myocyte , chemistry , isometric exercise , biophysics , contraction (grammar) , mechanics , materials science , anatomy , medicine , physics , biology
1 This study utilized a skinned myocyte preparation with low end compliance to examine force‐velocity and power‐load curves at 12 °C in myocytes from rat hearts. 2 In maximally activated myocyte preparations, shortening velocities appeared to remain constant during load clamps in which shortening took place over a sarcomere length range of ≈2.30‐2.00 μm. These results suggest that previously reported curvilinear length traces during load clamps of multicellular preparations were due in part to extracellular viscoelastic structures that give rise to restoring forces during myocardial shortening. 3 During submaximal Ca 2+ activations, the velocity of shortening at low loads slowed and the time course of shortening became curvilinear, i.e. velocity progressively slowed as shortening continued. This result implies that cross‐bridge cycling kinetics are slower at low levels of activation and that an internal load arises during shortening of submaximally activated myocytes, perhaps due to slowly detaching cross‐bridges. 4 Reduced levels of activator Ca 2+ also reduced maximal power output and increased the relative load at which power output was optimal. For a given absolute load, the shift has the effect of maintaining power output near the optimum level despite reductions in cross‐bridge number and force generating capability at lower levels of Ca 2+ .