Activation heat and latency relaxation in relation to calcium movement in skeletal and cardiac muscle

1982 ◽  
Vol 60 (4) ◽  
pp. 529-541 ◽  
Author(s):  
Louis A. Mulieri ◽  
Norman R. Alpert
Keyword(s):  
Skeletal Muscle ◽  
Refractory Period ◽  
Muscle Activation ◽  
Slow Component ◽  
Isometric Force ◽  
Fast Component ◽  
Bathing Solution ◽  
Latency Relaxation ◽  
In Series ◽  
Activation Heat

Measurements of activation heat, initial heat, twitch tension, and latency relaxation were made using thin-layer, vacuum-deposited thermopiles and isometric force transducers, respectively. Experiments were performed on frog skeletal muscle fiber bundles and on rabbit right ventricular papillary muscles at 0, 15, and 21 °C in normal and 1.75× to 2.5× mannitol hyperosmotic bathing solutions. In skeletal muscle, activation heat, obtained by stretching to zero overlap, was only slightly affected by 1.75× hyperosmotic solution and consisted of a fast and a slow component. Both components have a refractory period and a relatively refractory period which can be demonstrated by double pulse stimulation. The twitch potentiators Zn2+ and caffeine increase the total activation heat and the magnitude and rate of the fast component. The temporal relation between the latency relaxation and activation heat is demonstrated. The latency relaxation is independent of the number of sarcomeres in series in a muscle. Activation heat and latency relaxation records from heart muscle are obtained in 2.5× hyperosmotic bathing solution. A model of excitation–contraction coupling is presented which indicates that (1) the downstroke of the latency relaxation monitors the functioning of the Ca2+ -permeability or debinding mechanism in the terminal cisternae, (2) the fast component of activation heat monitors the amount of Ca2+ bound to troponin C, and (3) the total amplitude of activation heat is a measure of the total quantity of Ca2+ cycled in a twitch.

scholarly journals Tracking Voltage-dependent Conformational Changes in Skeletal Muscle Sodium Channel during Activation

2002 ◽  
Vol 120 (5) ◽  
pp. 629-645 ◽  
Author(s):  
Baron Chanda ◽  
Francisco Bezanilla
Keyword(s):  
Skeletal Muscle ◽  
Sodium Channel ◽  
Slow Component ◽  
Fast Component ◽  
Lag Phase ◽  
Kinetic Properties ◽  
Charge Movement ◽  
Voltage Dependent ◽  
Domain Iii ◽  
Domain I

The primary voltage sensor of the sodium channel is comprised of four positively charged S4 segments that mainly differ in the number of charged residues and are expected to contribute differentially to the gating process. To understand their kinetic and steady-state behavior, the fluorescence signals from the sites proximal to each of the four S4 segments of a rat skeletal muscle sodium channel were monitored simultaneously with either gating or ionic currents. At least one of the kinetic components of fluorescence from every S4 segment correlates with movement of gating charge. The fast kinetic component of fluorescence from sites S216C (S4 domain I), S660C (S4 domain II), and L1115C (S4 domain III) is comparable to the fast component of gating currents. In contrast, the fast component of fluorescence from the site S1436C (S4 domain IV) correlates with the slow component of gating. In all the cases, the slow component of fluorescence does not have any apparent correlation with charge movement. The fluorescence signals from sites reflecting the movement of S4s in the first three domains initiate simultaneously, whereas the fluorescence signals from the site S1436C exhibit a lag phase. These results suggest that the voltage-dependent movement of S4 domain IV is a later step in the activation sequence. Analysis of equilibrium and kinetic properties of fluorescence over activation voltage range indicate that S4 domain III is likely to move at most hyperpolarized potentials, whereas the S4s in domain I and domain II move at more depolarized potentials. The kinetics of fluorescence changes from sites near S4-DIV are slower than the activation time constants, suggesting that the voltage-dependent movement of S4-DIV may not be a prerequisite for channel opening. These experiments allow us to map structural features onto the kinetic landscape of a sodium channel during activation.

scholarly journals Dynamics of Primate Oculomotor Plant Revealed by Effects of Abducens Microstimulation

2009 ◽  
Vol 101 (6) ◽  
pp. 2907-2923 ◽  
Author(s):  
Sean R. Anderson ◽  
John Porrill ◽  
Sokratis Sklavos ◽  
Neeraj J. Gandhi ◽  
David L. Sparks ◽  
...  
Keyword(s):  
Steady State ◽  
Muscle Activation ◽  
Isometric Force ◽  
Force Production ◽  
Rectus Muscle ◽  
Linear Component ◽  
Abducens Nucleus ◽  
In Series ◽  
Tension Increase ◽  
Movement Parameters

Despite their importance for deciphering oculomotor commands, the mechanics of the extraocular muscles and orbital tissues (oculomotor plant) are poorly understood. In particular, the significance of plant nonlinearities is uncertain. Here primate plant dynamics were investigated by measuring the eye movements produced by stimulating the abducens nucleus with brief pulse trains of varying frequency. Statistical analysis of these movements indicated that the effects of stimulation lasted about 40 ms after the final pulse, after which the eye returned passively toward its position before stimulation. Behavior during the passive phase could be approximated by a linear plant model, corresponding to Voigt elements in series, with properties independent of initial eye position. In contrast, behavior during the stimulation phase revealed a sigmoidal relation between stimulation frequency and estimated steady-state tetanic tension, together with a frequency-dependent rate of tension increase, that appeared very similar to the nonlinearities previously found for isometric-force production in primate lateral rectus muscle. These results suggest that the dynamics of the oculomotor plant have an approximately linear component related to steady-state viscoelasticity and a nonlinear component related to changes in muscle activation. The latter may in part account for the nonlinear relations observed between eye-movement parameters and single-unit firing patterns in the abducens nucleus. These findings point to the importance of recruitment as a simplifying factor for motor control with nonlinear plants.

Injury to skeletal muscle fibers of mice following lengthening contractions

1985 ◽  
Vol 59 (1) ◽  
pp. 119-126 ◽  
Author(s):  
K. K. McCully ◽  
J. A. Faulkner
Keyword(s):  
Skeletal Muscle ◽  
Isometric Force ◽  
Muscle Fibers ◽  
Lengthening Contractions ◽  
Control Value ◽  
Skeletal Muscle Fibers ◽  
Maximum Isometric Force ◽  
Distal Tendon ◽  
Shortening Contractions

We tested the hypothesis that lengthening contractions result in greater injury to skeletal muscle fibers than isometric or shortening contractions. Mice were anesthetized with pentobarbital sodium and secured to a platform maintained at 37 degrees C. The distal tendon of the extensor digitorum longus muscle was attached to a servomotor. A protocol consisting of isometric, shortening, or lengthening contractions was performed. After the contraction protocol the distal tendon was reattached, incisions were closed, and the mice were allowed to recover. The muscles were removed after 1–30 days, and maximum isometric force (Po) was measured in vitro at 37 degrees C. Three days after isometric and shortening contractions and sham operations, histological appearance was not different from control and Po was 80% of the control value. Three days after lengthening contractions, histological sections showed that 37 +/- 4% of muscle fibers degenerated and Po was 22 +/- 3% of the control value. Muscle regeneration, first seen at 4 days, was nearly complete by 30 days, when Po was 84 +/- 3% of the control value. We conclude that, with the protocol used, lengthening, but not isometric or shortening contractions, caused significant injury to muscle fibers.

scholarly journals Caffeine-Induced Effects on Human Skeletal Muscle Contraction Time and Maximal Displacement Measured by Tensiomyography

Nutrients ◽  
2021 ◽  
Vol 13 (3) ◽  
pp. 815
Author(s):  
Przemysław Domaszewski ◽  
Paweł Pakosz ◽  
Mariusz Konieczny ◽  
Dawid Bączkowicz ◽  
Ewa Sadowska-Krępa
Keyword(s):  
Skeletal Muscle ◽  
Muscle Activation ◽  
Electric Pulse ◽  
Professional Athletes ◽  
Mechanical Activity ◽  
The Novel ◽  
Contraction Time ◽  
Novel Approach ◽  
Skeletal Muscle Contraction ◽  
Maximal Displacement

Studies on muscle activation time in sport after caffeine supplementation confirmed the effectiveness of caffeine. The novel approach was to determine whether a dose of 9 mg/kg/ body mass (b.m.) of caffeine affects the changes of contraction time and the displacement of electrically stimulated muscle (gastrocnemius medialis) in professional athletes who regularly consume products rich in caffeine and do not comply with the caffeine discontinuation period requirements. The study included 40 professional male handball players (age = 23.13 ± 3.51, b.m. = 93.51 ± 15.70 kg, height 191 ± 7.72, BMI = 25.89 ± 3.10). The analysis showed that in the experimental group the values of examined parameters were significantly reduced (p ≤ 0.001) (contraction time: before = 20.60 ± 2.58 ms/ after = 18.43 ± 3.05 ms; maximal displacement: before = 2.32 ± 0.80 mm/after = 1.69 ± 0.51 mm). No significant changes were found in the placebo group. The main achievement of this research was to demonstrate that caffeine at a dose of 9 mg/kg in professional athletes who regularly consume products rich in caffeine has a direct positive effect on the mechanical activity of skeletal muscle stimulated by an electric pulse.

V˙o 2 and heart rate kinetics in cycling: transitions from an elevated baseline

2001 ◽  
Vol 90 (6) ◽  
pp. 2081-2087 ◽  
Author(s):  
S. E. Bearden ◽  
R. J. Moffatt
Keyword(s):  
Heart Rate ◽  
Base Excess ◽  
Slow Component ◽  
Lactate Concentration ◽  
Fast Component ◽  
Square Wave ◽  
Mean Response Time ◽  
Rate Kinetics ◽  
Component Amplitude ◽  
Heart Rate Kinetics

The purpose of this study was to examine oxygen consumption (V˙o 2) and heart rate kinetics during moderate and repeated bouts of heavy square-wave cycling from an exercising baseline. Eight healthy, male volunteers performed square-wave bouts of leg ergometry above and below the gas exchange threshold separated by recovery cycling at 35%V˙o 2 peak.V˙o 2 and heart rate kinetics were modeled, after removal of phase I data by use of a biphasic on-kinetics and monoexponential off-kinetics model. Fingertip capillary blood was sampled 45 s before each transition for base excess, HCO[Formula: see text] and lactate concentration, and pH. Base excess and HCO[Formula: see text] concentration were significantly lower, whereas lactate concentration and pH were not different before the second bout. The results confirm earlier reports of a smaller mean response time in the second heavy bout. This was the result of a significantly greater fast-component amplitude and smaller slow-component amplitude with invariant fast-component time constant. A role for local oxygen delivery limitation in heavy exercise transitions with unloaded but not moderate baselines is presented.

Hypertrophy, Resistance Training, and the Nature of Skeletal Muscle Activation

1995 ◽  
Vol 9 (3) ◽  
pp. 155-159 ◽  
Author(s):  
Christine L. Ruther ◽  
Catherine L. Golden ◽  
Robert T. Harris ◽  
Gary A. Dudley
Keyword(s):  
Skeletal Muscle ◽  
Resistance Training ◽  
Muscle Activation

scholarly journals Mechanism of retraction of the trailing edge during fibroblast movement.

1981 ◽  
Vol 90 (1) ◽  
pp. 187-200 ◽  
Author(s):  
W T Chen
Keyword(s):  
Slow Component ◽  
Fast Component ◽  
Slow Phase ◽  
Main Body ◽  
Elastic Recoil ◽  
Forward Movement ◽  
Trailing Edge ◽  
Fast Phase ◽  
Focal Contacts

Retraction of the taut, trailing portion of a moving chick heart fibroblast in vitro is an abrupt dynamic process. Upon retraction, the fibroblast tail always ruptures, leaving a small amount of itself attached to the substratum by focal contacts. Time-lapse cinemicrography shows that retraction produces a sudden, massive movement of both surface and cytoplasmic material toward a cluster of focal contacts near the main body of the cell. The appearance of folds on the upper cell surface at this time and the absence of endocytotic vesicles are consistent with this forward movement. Retraction of the trailing edge, either occurring naturally or produced artificially with a microneedle, consists of an initial fast component followed and overlapped by a slow component. Upon artificial detachment in the presence of iodoacetate, dinitrophenol, and sodium fluoride, and at 4 degrees C, the slow component is strongly inhibited and the fast one only slightly inhibited. Moreover of the bundles of microfilaments oriented parallel to the long axis of the tail seen in TEM. Most of the birefringence is lost during the fast phase and the rest during the slow phase of retraction. Concurrently, the bundles of microfilaments disappear during the fast phase of retraction and are replaced by a microfilament meshwork. All of these results are consistent with the hypothesis that the initial fast component of retraction is a passive elastic recoil, associated with the oriented bundles of microfilaments, and that the slow component of retraction is an active contraction, associated with a meshwork of microfilaments.

Internal defibrillation with minimal skeletal muscle activation: A new paradigm toward painless defibrillation

Heart Rhythm ◽  
2005 ◽  
Vol 2 (10) ◽  
pp. 1108-1113 ◽  
Author(s):  
Vinod Jayam ◽  
Menekhem Zviman ◽  
Venku Jayanti ◽  
Ariel Roguin ◽  
Henry Halperin ◽  
...  
Keyword(s):  
Skeletal Muscle ◽  
Muscle Activation ◽  
New Paradigm ◽  
Internal Defibrillation
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