scholarly journals Influence of residual force enhancement and elongation of attached cross-bridges on stretch-shortening cycle in skinned muscle fibers

2017 ◽  
Vol 5 (22) ◽  
pp. e13477 ◽  
Author(s):  
Atsuki Fukutani ◽  
Venus Joumaa ◽  
Walter Herzog
Keyword(s):  
Muscle Fibers ◽  
Force Enhancement ◽  
Skinned Muscle ◽  
Skinned Muscle Fibers ◽  
Residual Force ◽  
Stretch Shortening Cycle ◽  
Residual Force Enhancement ◽  
Cross Bridges

scholarly journals Effect of Active Lengthening and Shortening on Small-Angle X-ray Reflections in Skinned Skeletal Muscle Fibres

2021 ◽  
Vol 22 (16) ◽  
pp. 8526
Author(s):  
Venus Joumaa ◽  
Ian C. Smith ◽  
Atsuki Fukutani ◽  
Timothy R. Leonard ◽  
Weikang Ma ◽  
...  
Keyword(s):  
Steady State ◽  
Small Angle ◽  
Isometric Contraction ◽  
Sarcomere Length ◽  
Force Enhancement ◽  
X Ray ◽  
Cross Bridge ◽  
Residual Force ◽  
Residual Force Enhancement ◽  
Cross Bridges

Our purpose was to use small-angle X-ray diffraction to investigate the structural changes within sarcomeres at steady-state isometric contraction following active lengthening and shortening, compared to purely isometric contractions performed at the same final lengths. We examined force, stiffness, and the 1,0 and 1,1 equatorial and M3 and M6 meridional reflections in skinned rabbit psoas bundles, at steady-state isometric contraction following active lengthening to a sarcomere length of 3.0 µm (15.4% initial bundle length at 7.7% bundle length/s), and active shortening to a sarcomere length of 2.6 µm (15.4% bundle length at 7.7% bundle length/s), and during purely isometric reference contractions at the corresponding sarcomere lengths. Compared to the reference contraction, the isometric contraction after active lengthening was associated with an increase in force (i.e., residual force enhancement) and M3 spacing, no change in stiffness and the intensity ratio I1,1/I1,0, and decreased lattice spacing and M3 intensity. Compared to the reference contraction, the isometric contraction after active shortening resulted in decreased force, stiffness, I1,1/I1,0, M3 and M6 spacings, and M3 intensity. This suggests that residual force enhancement is achieved without an increase in the proportion of attached cross-bridges, and that force depression is accompanied by a decrease in the proportion of attached cross-bridges. Furthermore, the steady-state isometric contraction following active lengthening and shortening is accompanied by an increase in cross-bridge dispersion and/or a change in the cross-bridge conformation compared to the reference contractions.

scholarly journals Passive force enhancement in striated muscle

2019 ◽  
Vol 126 (6) ◽  
pp. 1782-1789 ◽  
Author(s):  
Walter Herzog
Keyword(s):  
Molecular Mechanisms ◽  
Striated Muscle ◽  
Isometric Force ◽  
Muscle Length ◽  
Passive Force ◽  
Force Enhancement ◽  
Sarcomeric Protein ◽  
Residual Force ◽  
Residual Force Enhancement ◽  
Cross Bridges

Passive force enhancement is defined as the increase in passive, steady-state, isometric force of an actively stretched muscle compared with the same muscle stretched passively to that same length. Passive force enhancement is long lasting, increases with increasing muscle length and increasing stretch magnitudes, contributes to the residual force enhancement in skeletal and cardiac muscle, and is typically only observed at muscle lengths at which passive forces occur naturally. Passive force enhancement is typically equal to or smaller than the total residual force enhancement, it persists when a muscle is deactivated and reactivated, but can be abolished instantaneously when a muscle is shortened quickly from its stretched length. There is strong evidence that the passive force enhancement is caused by the filamentous sarcomeric protein titin, although the detailed molecular mechanisms underlying passive force enhancement remain unknown. Here I propose a tentative mechanism based on experimental evidence that associates passive force enhancement with the shortening of titin’s free spring length in the I-band region of sarcomeres. I suggest that this shortening is accomplished by titin binding to actin and that the trigger for titin-actin interactions is associated with the formation of strongly bound cross bridges between actin and myosin that exposes actin attachment sites for titin through movement of the regulatory proteins troponin and tropomyosin.

scholarly journals Both the elongation of attached crossbridges and residual force enhancement contribute to joint torque enhancement by the stretch-shortening cycle

2017 ◽  
Vol 4 (2) ◽  
pp. 161036 ◽  
Author(s):  
Atsuki Fukutani ◽  
Jun Misaki ◽  
Tadao Isaka
Keyword(s):  
Elastic Energy ◽  
Time Frame ◽  
Joint Torque ◽  
Force Enhancement ◽  
Fascicle Length ◽  
Joint Torques ◽  
Concentric Contraction ◽  
Residual Force ◽  
Stretch Shortening Cycle ◽  
Residual Force Enhancement

This study examined the influence of the elongation of attached crossbridges and residual force enhancement on joint torque enhancement by the stretch-shortening cycle (SSC). Electrically evoked submaximal tetanic plantar flexions were adopted. Concentric contractions were evoked in the following three conditions: after 2 s isometric preactivation (ISO condition), after 1 s isometric then 1 s eccentric preactivation (ECC condition), and after 1 s eccentric then 1 s isometric preactivation (TRAN condition). Joint torque and fascicle length were measured during the concentric contraction phase. While no differences in fascicle length were observed among conditions at any time points, joint torque was significantly higher in the ECC than TRAN condition at the onset of concentric contraction. This difference would be caused by the dissipation of the elastic energy stored in the attached crossbridges induced by eccentric preactivation in TRAN condition due to 1 s transition phase. Furthermore, joint torques observed 0.3 and 0.6 s after concentric contraction were significantly larger in the ECC and TRAN conditions than in the ISO condition while no difference was observed between the ECC and TRAN conditions. Since the elastic energy stored in the attached crossbridges would have dissipated over this time frame, this result suggests that residual force enhancement induced by eccentric preactivation also contributes to joint torque enhancement by the SSC.

scholarly journals Energy Cost of Force Production After a Stretch-Shortening Cycle in Skinned Muscle Fibers: Does Muscle Efficiency Increase?

2021 ◽  
Vol 11 ◽  
Author(s):  
Venus Joumaa ◽  
Atsuki Fukutani ◽  
Walter Herzog
Keyword(s):  
Steady State ◽  
Energy Cost ◽  
Muscle Force ◽  
Metabolic Energy ◽  
Total Force ◽  
Force Enhancement ◽  
Residual Force ◽  
Stretch Shortening Cycle ◽  
Residual Force Enhancement ◽  
Shortening Contractions

Muscle force is enhanced during shortening when shortening is preceded by an active stretch. This phenomenon is known as the stretch-shortening cycle (SSC) effect. For some stretch-shortening conditions this increase in force during shortening is maintained following SSCs when compared to the force following a pure shortening contraction. It has been suggested that the residual force enhancement property of muscles, which comes into play during the stretch phase of SSCs may contribute to the force increase after SSCs. Knowing that residual force enhancement is associated with a substantial reduction in metabolic energy per unit of force, it seems reasonable to assume that the metabolic energy cost per unit of force is also reduced following a SSC. The purpose of this study was to determine the energy cost per unit of force at steady-state following SSCs and compare it to the corresponding energy cost following pure shortening contractions of identical speed and magnitude. We hypothesized that the energy cost per unit of muscle force is reduced following SSCs compared to the pure shortening contractions. For the SSC tests, rabbit psoas fibers (n = 12) were set at an average sarcomere length (SL) of 2.4 μm, activated, actively stretched to a SL of 3.2 μm, and shortened to a SL of 2.6 or 3.0 μm. For the pure shortening contractions, the same fibers were activated at a SL of 3.2 μm and actively shortened to a SL of 2.6 or 3.0 μm. The amount of ATP consumed was measured over a 40 s steady-state total isometric force following either the SSCs or the pure active shortening contractions. Fiber stiffness was determined in an additional set of 12 fibers, at steady-state for both experimental conditions. Total force, ATP consumption, and stiffness were greater following SSCs compared to the pure shortening contractions, but ATP consumption per unit of force was the same between conditions. These results suggest that the increase in total force observed following SSCs was achieved with an increase in the proportion of attached cross-bridges and titin stiffness. We conclude that muscle efficiency is not enhanced at steady-state following SSCs.

scholarly journals Influence of muscle length on the stretch-shortening cycle in skinned rabbit soleus

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Atsuki Fukutani ◽  
Tadao Isaka
Keyword(s):  
Muscle Force ◽  
Muscle Length ◽  
Relative Increase ◽  
Mechanical Work ◽  
Skinned Fibers ◽  
Force Enhancement ◽  
Residual Force ◽  
Stretch Shortening Cycle ◽  
Residual Force Enhancement

AbstractMuscle force generated during shortening is instantaneously increased after active stretch. This phenomenon is called as stretch-shortening cycle (SSC) effect. It has been suggested that residual force enhancement contributes to the SSC effect. If so, the magnitude of SSC effect should be larger in the longer muscle length condition, because the residual force enhancement is prominent in the long muscle length condition. This hypothesis was examined by performing the SSC in the short and long muscle length conditions. Skinned fibers obtained from rabbit soleus (N = 20) were used in this study. To calculate the magnitude of SSC effect, the SSC trial (isometric-eccentric-concentric-isometric) and the control trial (isometric-concentric-isometric) were conducted in the short (within the range of 2.4 to 2.7 μm) and long muscle (within the range of 3.0 to 3.3 μm). The magnitude of SSC effect was calculated as the relative increase in the mechanical work attained during the shortening phase between control and SSC trials. As a result, the magnitude of SSC effect was significantly larger in the long (176.8 ± 18.1%) than in the short muscle length condition (157.4 ± 8.5%) (p < 0.001). This result supports our hypothesis that the magnitude of SSC effect is larger in the longer muscle length condition, possibly due to the larger magnitude of residual force enhancement.

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