scholarly journals Release of fascial compartment boundaries reduces muscle force output

2019 ◽  
Vol 126 (3) ◽  
pp. 593-598 ◽  
Author(s):  
Roy J. Ruttiman ◽  
David A. Sleboda ◽  
Thomas J. Roberts
Keyword(s):  
Muscle Force ◽  
Muscle Length ◽  
Close Packing ◽  
Muscle Performance ◽  
Maximum Force ◽  
Force Output ◽  
Reduction In Force ◽  
Limb Muscles ◽  
Wild Turkeys

Most limb muscles operate within a compartment defined by fascial layers that enclose a muscle or groups of muscles within a defined space. These compartments are important clinically, because fluid accumulation can cause ischemia and tissue necrosis if untreated. Little is known, however, about how fascial enclosures influence healthy muscle function. One previous study showed that removing a fascial covering reduced the force output of a muscle under maximal stimulation. We hypothesized that such reduction in force output was due to a change in the muscle length following fasciotomy and that a reduced force output could be explained by the length-tension relationship of muscle. Thus we predicted that the maximum force across a range of lengths would be unchanged following fasciotomy. We measured maximal tetanic force output in a wing muscle in wild turkeys both before and after removal of fascia that enclosed the muscle in a compartment. Our hypothesis was not supported. The length-tension curve of this muscle showed that removal of fascia reduced maximum force output to 72 ± 10% of the prefascial release condition. Thus a reduction in muscle force following fasciotomy was not explained by a change in muscle length. The mechanism underlying reduction in force is unclear, but it suggests that the assumption underlying most isolated muscle experiments, i.e., removal of a muscle from its situation in vivo does not influence its maximal mechanical output, may need reexamining. NEW & NOTEWORTHY Most limb muscles are enclosed within compartments bound by robust fascial sheets. The mechanical significance of the close packing of muscle and fascia is largely unexplored. We used an animal model to show that removal of a fascial covering reduces the maximal force developed during contraction. These results raise questions about the use of isolated muscles to estimate muscle performance and suggest that a muscle's mechanical surrounding influences performance by mechanisms that are not understood.

MUSCLE BULGING REDUCES MUSCLE FORCE AND LIMITS THE MAXIMAL EFFECTIVE MUSCLE SIZE

2006 ◽  
Vol 06 (03) ◽  
pp. 229-239 ◽  
Author(s):  
KARL DAGGFELDT
Keyword(s):  
Muscle Force ◽  
Muscle Length ◽  
Biomechanical Model ◽  
Muscle Performance ◽  
Muscle Size ◽  
Intramuscular Pressure ◽  
Shortening Velocity ◽  
Muscle Shortening ◽  
Force Reduction ◽  
Total Muscle

A biomechanical model was generated in order to investigate the possible mechanisms behind reductions in muscle performance due to muscle bulging. It was shown that the proportion of fiber force contributing to the total muscle force is reduced with fiber bulging and that the cause of this reduction is due to the intramuscular pressure (IMP) created by the bulging fibers. Moreover, it was established that the amount of IMP generated muscle force reduction is determined by the extent to which muscle thickening restricts muscle fibers from shortening, thereby limiting their power contribution. It was shown that bulging can set a limit to the maximal size a muscle can take without losing force and power producing capability. Possible effects, due to bulging, on maximal muscle force in relation to both muscle length and muscle shortening velocity were also demonstrated by the model.

scholarly journals How muscles deal with real-world loads: the influence of length trajectory on muscle performance

1999 ◽  
Vol 202 (23) ◽  
pp. 3377-3385 ◽  
Author(s):  
R.L. Marsh
Keyword(s):  
Velocity Profile ◽  
Real World ◽  
Skeletal Muscles ◽  
External Environment ◽  
The Body ◽  
Muscle Performance ◽  
Force Output ◽  
Optimal Velocity ◽  
Level Running

The performance of skeletal muscles in vivo is determined by the feedback received when the muscle interacts with the external environment via various morphological structures. This interaction between the muscle and the ‘real-world load’ forces us to reconsider how muscles are adapted to suit their in vivo function. We must consider the co-evolution of the muscles and the morphological structures that ‘create’ the load in concert with the properties of the external environment. This complex set of interactions may limit muscle performance acutely and may also constrain the evolution of morphology and physiology. The performance of skeletal muscle is determined by the length trajectory during movement and the pattern of stimulation. Important features of the length trajectory include its amplitude, frequency, starting length and shape (velocity profile). Many of these parameters interact. For example, changing the velocity profile during shortening may change the optimum values of the other parameters. The length trajectory that maximizes performance depends on the task to be performed. During cyclical work, muscles benefit from using asymmetric cycles with longer shortening than lengthening phases. Modifying this ‘sawtooth’ cycle by increasing the velocity during shortening may further increase power by augmenting force output and speeding deactivation. In contrast, when accelerating an inertial load, as in jumping, the predicted ‘optimal’ velocity profile has two peak values, one early and one late in shortening. During level running at constant speed, muscles perform tasks other than producing work and power. Producing force to support the body weight is performed with nearly isometric contractions in some of the limb muscles of vertebrates. Muscles also play a key role in producing stability during running, and the intrinsic properties of the musculoskeletal system may be particularly important in stabilizing rapid running. Recently, muscles in running invertebrates and vertebrates have been described that routinely absorb large amounts of work during running. These muscles are hypothesized to play a key role in stability.

scholarly journals Characteristics of Tetanic Force Produced by the Sternomastoid Muscle of the Rat

2010 ◽  
Vol 2010 ◽  
pp. 1-11 ◽  
Author(s):  
Stanislaw Sobotka ◽  
Liancai Mu
Keyword(s):  
Electrical Stimulation ◽  
Muscle Contraction ◽  
Muscle Force ◽  
Muscle Length ◽  
Threshold Current ◽  
Contractile Properties ◽  
Normative Values ◽  
Muscle Reinnervation ◽  
Stimulation Current

The sternomastoid (SM) muscle plays an important role in supporting breathing. It also has unique anatomical advantages that allow its wide use in head and neck tissue reconstruction and muscle reinnervation. However, little is known about its contractile properties. The experiments were run on rats and designed to determine in vivo the relationship between muscle force (active muscle contraction to electrical stimulation) with passive tension (passive force changing muscle length) and two parameters (intensity and frequency) of electrical stimulation. The threshold current for initiating noticeable muscle contraction was 0.03 mA. Maximal muscle force (0.94 N) was produced by using moderate muscle length/tension (28 mm/0.08 N), 0.2 mA stimulation current, and 150 Hz stimulation frequency. These data are important not only to better understand the contractile properties of the rat SM muscle, but also to provide normative values which are critical to reliably assess the extent of functional recovery following muscle reinnervation.

Mechanical actions of heterogenic reflexes linking long toe flexors with ankle and knee extensors of the cat hindlimb

1994 ◽  
Vol 71 (3) ◽  
pp. 1096-1110 ◽  
Author(s):  
S. J. Bonasera ◽  
T. R. Nichols
Keyword(s):  
Muscle Activation ◽  
Muscle Force ◽  
Muscle Length ◽  
Knee Extensors ◽  
Flexor Hallucis Longus ◽  
Force Output ◽  
Small Magnitude ◽  
Dramatic Decline ◽  
Muscle Pair ◽  
Length Changes

1. To study the means whereby ankle biomechanics are represented in the interneuronal circuitry of the spinal cord we examined stretch-evoked reflex interactions between the physiological extensors flexor hallucis longus (FHL) and flexor digitorum longus (FDL) as well as their interactions with gastrocnemius (G), soleus (S), and the quadriceps group (Q) in 34 unanesthetized decerebrate cats. To evoke stretch, DC motors provided ramp-hold-release length changes to tendons detached from their bony insertions. Semiconductor myographs measured resultant muscle force response. Reflexes were examined under both quiescent (no active force generation) and activated conditions; muscle activation was achieved through either crossed-extension or flexion reflexes. 2. FHL and FDL share mutual excitatory stretch-evoked interactions under most conditions examined. These interactions depended on muscle length, were asymmetric (with FHL contributing a larger magnitude of reflex excitation onto FDL), and occurred at a latency of 16 ms. Mutual Ia synergism previously described for these two muscles provides a basis for all of the above findings. Our data demonstrate that for this muscle pair, reflex connectivities revealed at the intracellular level can be extrapolated to cover the entire motoneuron pool; further, our data directly demonstrate the net mechanical result of ensemble synaptic events. 3. FHL was found to share strong, mutually inhibitory stretch-evoked interactions with G, S, and Q. Stepwise regression statistical analyses determined that these interactions depended on recipient muscle force and donor muscle force. These reflex interactions all occurred at a latency of 28 +/- 4 (SE) ms. Further, the heterogenic inhibition between FHL/G and FHL/S was attenuated by strychnine infusion (intravenous) but unaffected by either mecamylamine, picrotoxin, or baclofen infusion (intravenous, intrathecal). Disynaptic Ib inhibition previously described among hindlimb extensors provides a basis for the above findings; our data demonstrate that under certain conditions the ensemble activity of this system can cause a dramatic decline in whole muscle force output. 4. By contrast, FDL was found to share mutually inhibitory, stretch-evoked reflex interactions with G, S, and Q that were much weaker than those observed between FHL and these same muscles. The small magnitude of inhibition observed in these interactions made it difficult to assess reflex latency or to determine the factor(s) that best predicted the heterogenic inhibition. 5. This study provides further evidence of intrinsic differences in interneuronal organization between muscles whose activity occurs in a periodic manner during locomotion ("stereotypical") and a muscle whose locomotor activity is characterized by both periodic and nonperiodic components ("facultative").(ABSTRACT TRUNCATED AT 400 WORDS)

scholarly journals Muscle-tendon length and force affect human tibialis anterior central aponeurosis stiffness in vivo

2018 ◽  
Vol 115 (14) ◽  
pp. E3097-E3105 ◽  
Author(s):  
Brent James Raiteri ◽  
Andrew Graham Cresswell ◽  
Glen Anthony Lichtwark
Keyword(s):  
Tibialis Anterior ◽  
Muscle Force ◽  
Fundamental Property ◽  
Muscle Performance ◽  
Tendon Length ◽  
Muscle Fascicle ◽  
Length Relationship ◽  
Longitudinal Stiffness ◽  
Passive Muscle

The factors that drive variable aponeurosis behaviors in active versus passive muscle may alter the longitudinal stiffness of the aponeurosis during contraction, which may change the fascicle strains for a given muscle force. However, it remains unknown whether these factors can drive variable aponeurosis behaviors across different muscle-tendon unit (MTU) lengths and influence the subsequent fascicle strains during contraction. Here, we used ultrasound and elastography techniques to examine in vivo muscle fascicle behavior and central aponeurosis deformations of human tibialis anterior (TA) during force-matched voluntary isometric dorsiflexion contractions at three MTU lengths. We found that increases in TA MTU length increased both the length and apparent longitudinal stiffness of the central aponeurosis at low and moderate muscle forces (P < 0.01). We also found that increased aponeurosis stiffness was directly related to reduced magnitudes of TA muscle fascicle shortening for the same change in force (P < 0.01). The increase in slope and shift to longer overall lengths of the active aponeurosis force–length relationship as MTU length increased was likely due to a combination of parallel lengthening of aponeurosis and greater transverse aponeurosis strains. This study provides in vivo evidence that human aponeurosis stiffness is increased from low to moderate forces and that the fascicle strains for a given muscle force are MTU length dependent. Further testing is warranted to determine whether MTU length-dependent stiffness is a fundamental property of the aponeurosis in pennate muscles and evaluate whether this property can enhance muscle performance.

scholarly journals Muscle size explains low passive skeletal muscle force in heart failure patients

PeerJ ◽  
2016 ◽  
Vol 4 ◽  
pp. e2447 ◽  
Author(s):  
Fausto Antonio Panizzolo ◽  
Andrew J. Maiorana ◽  
Louise H. Naylor ◽  
Lawrence G. Dembo ◽  
David G. Lloyd ◽  
...  
Keyword(s):  
Heart Failure ◽  
Skeletal Muscle ◽  
Muscle Force ◽  
Muscle Length ◽  
Muscle Size ◽  
Clear Understanding ◽  
Passive Force ◽  
Force Output ◽  
Skeletal Muscle Function ◽  
Cross Sectional

BackgroundAlterations in skeletal muscle function and architecture have been linked to the compromised exercise capacity characterizing chronic heart failure (CHF). However, how passive skeletal muscle force is affected in CHF is not clear. Understanding passive force characteristics in CHF can help further elucidate the extent to which altered contractile properties and/or architecture might affect muscle and locomotor function. Therefore, the aim of this study was to investigate passive force in a single muscle for which non-invasive measures of muscle size and estimates of fiber force are possible, the soleus (SOL), both in CHF patients and age- and physical activity-matched control participants.MethodsPassive SOL muscle force and size were obtained by means of a novel approach combining experimental data (dynamometry, electromyography, ultrasound imaging) with a musculoskeletal model.ResultsWe found reduced passive SOL forces (∼30%) (at the same relative levels of muscle stretch) in CHF vs. healthy individuals. This difference was eliminated when force was normalized by physiological cross sectional area, indicating that reduced force output may be most strongly associated with muscle size. Nevertheless, passive force was significantly higher in CHF at a given absolute muscle length (non length-normalized) and likely explained by the shorter muscle slack lengths and optimal muscle lengths measured in CHF compared to the control participants. This later factor may lead to altered performance of the SOL in functional tasks such gait.DiscussionThese findings suggest introducing exercise rehabilitation targeting muscle hypertrophy and, specifically for the calf muscles, exercise that promotes muscle lengthening.

In vivo length-force relationship of canine diaphragm

1986 ◽  
Vol 60 (1) ◽  
pp. 63-70 ◽  
Author(s):  
J. Road ◽  
S. Newman ◽  
J. P. Derenne ◽  
A. Grassino
Keyword(s):  
Muscle Length ◽  
Elastic Recoil ◽  
Force Output ◽  
Transdiaphragmatic Pressure ◽  
Residual Capacity ◽  
Equilibrium Length ◽  
Crural Diaphragm ◽  
Tension Curves

Diaphragmatic length was measured by sonomicrometry and transdiaphragmatic pressure (Pdi) by conventional latex balloons in eight dogs anesthetized with pentobarbital sodium under passive conditions and during supramaximal phrenic stimulation. The passive length-pressure relationship indicates that the crural part of the diaphragm is more compliant than the costal part. With supramaximal stimulation the costal diaphragm showed a length-pressure relationship similar in shape to in vitro length-tension curves previously described for the canine diaphragm. The crural part has a smaller pressure-length slope than the costal part in the length range from 80% of optimum muscle length (Lo) to Lo. At supine functional residual capacity (FRC) the resting length (LFRC) of the costal and crural diaphragms are not at Lo. The costal part is distended to 105% of Lo, and crural is shortened to 92% of Lo. Tidal shortening will increase the force output of costal while decreasing that of the crural diaphragm. The major forces setting the passive supine LFRC are the abdominal weight (pressure) and the elastic recoil of the lungs. The equilibrium length (resting length of excised diaphragmatic strips) was 79 +/- 3.6% LFRC for the costal diaphragm and 87 +/- 3.9% LFRC for the crural diaphragm. Similar shortening was obtained in the upright position, indicating passive diaphragmatic stretch at supine LFRC.

Impact of muscle length during stretch-shortening contractions on real-time and temporal muscle performance measures in rats in vivo

2004 ◽  
Vol 96 (2) ◽  
pp. 507-516 ◽  
Author(s):  
R. G. Cutlip ◽  
K. B. Geronilla ◽  
B. A. Baker ◽  
M. L. Kashon ◽  
G. R. Miller ◽  
...  
Keyword(s):  
Real Time ◽  
Isometric Force ◽  
Muscle Length ◽  
Muscle Performance ◽  
Temporal Muscle ◽  
Time Changes ◽  
The Impact ◽  
Force Difference ◽  
Shortening Contractions

The objective of the present study was to investigate the impact of muscle length during stretch-shortening cycles on static and dynamic muscle performance. Animals were randomly assigned to an isometric (control, Con, n = 12), a short-muscle-length (S-Inj, 1.22-2.09 rad, n = 12), or a long-muscle-length (L-Inj, 1.57-2.44 rad, n = 12) group. The dorsiflexor muscles were exposed in vivo to 7 sets of 10 stretch-shortening contractions (conducted at 8.72 rad/s) or 7 sets of isometric contractions of the same stimulation duration by using a custom-designed dynamometer. Performance was characterized by multipositional isometric exertions and positive, negative, and net work before exposure, 6 h after exposure, and 48 h after exposure to contractions. Real-time muscle performance during the stretch-shortening cycles was characterized by stretch-shortening parameters and negative, positive, and net work. The S-Inj group recovery (force difference) was similar to the Con group force difference at 48 h, whereas the L-Inj group force difference was statistically greater at 1.39, 1.57, and 1.74 rad than the Con group force difference ( P < 0.05). Negative work ( P < 0.05) and net work ( P < 0.05) were statistically lower in the S-Inj and L-Inj groups than in the Con group 48 h after exposure to contractions. Of the real-time parameters, there was a difference in cyclic force with treatment during the stretch-shortening cycles ( P < 0.0001), with the L-Inj group being the most affected. Thus longer ranges of motion result in a more profound isometric force decrement 48 h after exposure to contractions and in real-time changes in eccentric forces.

Effects of hypoxia and hypercapnia on geniohyoid contractility and endurance

1991 ◽  
Vol 71 (2) ◽  
pp. 709-715 ◽  
Author(s):  
R. J. Salmone ◽  
E. Van Lunteren
Keyword(s):  
Force Production ◽  
Upper Airway ◽  
Muscle Performance ◽  
Severe Hypoxia ◽  
Force Frequency ◽  
Force Output ◽  
Frequency Curve ◽  
Dilator Muscle ◽  
Index Ratio ◽  
Mild Hypoxia

Sleep apnea and other respiratory diseases produce hypoxemia and hypercapnia, factors that adversely affect skeletal muscle performance. To examine the effects of these chemical alterations on force production by an upper airway dilator muscle, the contractile and endurance characteristics of the geniohyoid muscle were examined in situ during severe hypoxia (arterial PO2 less than 40 Torr), mild hypoxia (PO2 45–65 Torr), and hypercapnia (PCO2 55–80 Torr) and compared with hyperoxic-normocapnic conditions in anesthetized cats. Muscles were studied at optimal length, and contractile force was assessed in response to supramaximal electrical stimulation of the hypoglossal nerve (n = 7 cats) or geniohyoid muscle (n = 2 cats). There were no significant changes in the twitch kinetics or force-frequency curve of the geniohyoid muscle during hypoxia or hypercapnia. However, the endurance of the geniohyoid, as reflected in the fatigue index (ratio of force at 2 min to initial force in response to 40-Hz stimulation at a duty cycle 0.33), was significantly reduced by severe hypoxia but not by hypercapnia or mild hypoxia. In addition, the downward shift in the force-frequency curve after the repetitive stimulation protocol was greater during hypoxia than hyperoxia, especially at higher frequencies. In conclusion, the ability of the geniohyoid muscle to maintain force output during high levels of activation is adversely affected by severe hypoxia but not mild hypoxia or hypercapnia. However, none of these chemical perturbations affected muscle contractility acutely.

scholarly journals ANALYSIS OF BIOMECHANICAL PARAMETERS IN COLONIC ANASTOMOSIS

2016 ◽  
Vol 29 (2) ◽  
pp. 90-92 ◽  
Author(s):  
Tiago Cavalcanti IWANAGA ◽  
José Lamartine de Andrade AGUIAR ◽  
Euclides Dias MARTINS-FILHO ◽  
Flávio KREIMER ◽  
Fernando Luiz SILVA-FILHO ◽  
...  
Keyword(s):  
Modulus Of Elasticity ◽  
Treatment Time ◽  
Intestinal Wall ◽  
Maximum Force ◽  
Sugarcane Molasses ◽  
Rupture Force ◽  
Treatment Groups ◽  
Biomechanical Parameters ◽  
Medical Interest

ABSTRACT Background: The use of measures in colonic anastomoses to prevent dehiscences is of great medical interest. Sugarcane molasses, which has adequate tolerability and compatibility in vivo, has not yet been tested for this purpose. Aim: To analyze the biomechanical parameters of colonic suture in rats undergoing colectomy, using sugarcane molasses polysaccharide as tape or gel. Methods: 45 Wistar rats (Rattus norvegicus albinus) were randomized into three groups of 15 animals: irrigation of enteric sutures with 0.9% saline solution; application of sugarcane molasses polysaccharide as tape; and sugarcane molasses polysaccharide as gel. The rats underwent colon ressection, with subsequent reanastomosis using polypropylene suture; they were treated according to their respective groups. Five rats from each group were evaluated at different times after the procedure: 30, 90 and 180 days postoperatively. The following variables were evaluated: maximum rupture force, modulus of elasticity and specific deformation of maximum force. Results: The biomechanical variables among the scheduled times and treatment groups were statistically calculated. The characteristics of maximum rupture force and modulus of elasticity of the specimens remained identical, regardless of treatment with saline, polysaccharide gel or tape, and treatment time. However, it was found that the specific deformation of maximum force of the intestinal wall was higher after 180 days in the group treated with sugarcane polysaccharide gel (p=0.09). Conclusion: Compared to control, it was detected greater elasticity of the intestinal wall in mice treated with sugarcane polysaccharide gel, without changing other biomechanical characteristics, regardless of type or time of treatment.

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