Key result
Eccentric lengthenings in cat soleus muscles showed that total steady-state force enhancement increased with stretching amplitude, but had no correlation with the rate of force decay.
Force enhancement in lengthening muscle contractions involves a combination of mechanisms including cross-bridge kinetics and passive elastic elements, rather than being solely the opposite of force depression.
Transient force analysis suggests combined mechanisms underlie force enhancement; leaves open the precise role of cross-bridge kinetics.
Force enhancement (FE) associated with lengthening is a well-accepted phenomenon of active skeletal muscle, but the underlying mechanism(s) remain unknown. Similar to force depression (FD) following active shortening, the mechanism of FE may be attributed, at least in part, to cross-bridge kinetics. To examine this relationship, a post hoc analysis was performed on the transient force relaxation phase of previous in-situ FE experiments in soleus muscle-tendon units of anesthetized cats. For each muscle (n = 8), nine eccentric lengthenings (3 amplitudes, 3 velocities) were performed while tetanically stimulated (3T at 30 Hz, 3× α motorneuron, 35 ± 1°C). To determine transient aspects of FE, the period immediately following stretching was fit with an exponential decay function (R (2) > 0.95). Statistical analyses revealed that total steady-state FE (FESS) increased with stretching amplitude and applied mechanical work. A positive relationship was observed between the active FESS and rate of force decay (k), indicating that a kinetic mechanism may explain active FE. However, for all muscles and stretch conditions, there was no correlation between the total amount of FESS and rate of decay. Therefore, FE cannot be explained solely by an active FE mechanism involving the interaction of actin and myosin. Rather, these findings suggest a combination of underlying mechanisms, including a kinetic mechanism for active FE, contributions of a passive elastic element, and possibly an activatable passive component operating outside of actin-myosin cross-bridging. Moreover, this transient analysis identifies that FE is not simply the opposite of FD, and its underlying mechanism(s) cannot simply be the opposite in nature.
No takes yet. Share an insight, caveat, or question.
Koppes et al. (2013) studied Anesthetized cats (soleus muscle-tendon units) (n=8). Eccentric lengthenings was evaluated on Relationship between total steady-state force enhancement (FESS) and rate of force decay (k). Eccentric lengthenings in cat soleus muscles showed that total steady-state force enhancement increased with stretching amplitude, but had no correlation with the rate of force decay.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: