Abstract:There is increasing evidence that the architectural design and arrangement of the fibers within a motor unit have important physiological and developmental ramifications. Limited data, however, are available to directly address this issue. In the present study the physiological properties of one motor unit in each of seven cat tibialis anterior (TA) muscles were determined. Each of these units then was repetitively stimulated to deplete the glycogen in all muscle fibers within the unit. Subsequently, the lengt… Show more
“…Although there are specialized structures where they insert to the tendon plate, because the fibers always taper, the connective tissue matrix is likely to transmit some of the force. Furthermore, recent evidence shows that many muscles have fibers that do not run the length of the muscle (18,20,24). These fibers by necessity transmit their force to this endomysial connective tissue matrix.…”
Section: Discussionmentioning
confidence: 99%
“…The links between neighboring fibers may prevent sarcomere length heterogeneity observed in isolated fibers, thus preventing damage and altering muscle force (8,21). In some muscles, fibers do not run the length of the muscle but rather rely on this extracellular matrix and other muscle fibers to transmit force (18,24). Thus neighboring fibers are not mechanically independent.…”
The complex connective tissue structure of muscle and tendon suggests that forces from two parts of a muscle may not summate linearly. This study measured the nonlinear summation of force (Fnl) in whole cat soleus during isometric and ramp movements. In six anesthetized cats, the soleus was attached to a servomechanism to control muscle length and record force. The ventral roots were divided into two bundles, each innervating about half the soleus; thus the two parts could be stimulated alone or together. In all experiments, Fnl was small (<6% of maximum tetanic tension). Peak Fnl occurred during changes in muscle force, either as a result of imposed muscle movement or the onset or offset of a stimulus train. The data were fit to a model in which both parts of the muscle were assumed to stretch to a common elasticity. The servomechanism was programmed to compensate for reduced stretch of the common elasticity during partial compared with whole muscle activation. These compensatory movements showed how the model could account for most, but not all, of Fnl.
“…Although there are specialized structures where they insert to the tendon plate, because the fibers always taper, the connective tissue matrix is likely to transmit some of the force. Furthermore, recent evidence shows that many muscles have fibers that do not run the length of the muscle (18,20,24). These fibers by necessity transmit their force to this endomysial connective tissue matrix.…”
Section: Discussionmentioning
confidence: 99%
“…The links between neighboring fibers may prevent sarcomere length heterogeneity observed in isolated fibers, thus preventing damage and altering muscle force (8,21). In some muscles, fibers do not run the length of the muscle but rather rely on this extracellular matrix and other muscle fibers to transmit force (18,24). Thus neighboring fibers are not mechanically independent.…”
The complex connective tissue structure of muscle and tendon suggests that forces from two parts of a muscle may not summate linearly. This study measured the nonlinear summation of force (Fnl) in whole cat soleus during isometric and ramp movements. In six anesthetized cats, the soleus was attached to a servomechanism to control muscle length and record force. The ventral roots were divided into two bundles, each innervating about half the soleus; thus the two parts could be stimulated alone or together. In all experiments, Fnl was small (<6% of maximum tetanic tension). Peak Fnl occurred during changes in muscle force, either as a result of imposed muscle movement or the onset or offset of a stimulus train. The data were fit to a model in which both parts of the muscle were assumed to stretch to a common elasticity. The servomechanism was programmed to compensate for reduced stretch of the common elasticity during partial compared with whole muscle activation. These compensatory movements showed how the model could account for most, but not all, of Fnl.
“…The fascicle length is defined as the distance between the insertions of the fascicle into superficial and deep aponeurosis (Kubo et al 2000; figure 19), and it is sometimes regarded as equivalent to muscle fiber length, based on observations of tendon-to-tendon fiber arrangement within a fascicle . Although the orientation of fascicles is the same as muscle fibers, the fascicle length may not correspond to the muscle fiber length, because muscle fibers may terminate mid-fascicularly (Ounjian et al 1991). In spite of the fact that fascicle length measurements do not give accurate representation of fiber or sarcomere function due to inhomogeneities in sarcomere lengths in series and compliance of connective tissue, the ultrasonographic method can give more detailed information about muscular function in vivo as compared to the muscle-tendon unit length estimations alone (Finni et al 2001).…”
Section: Assessment Of Muscle Tendon Complex Mechanical Behaviourmentioning
Valadão, Pedro Frederico, 2012. Effects of muscle action type on corticospinal excitability and triceps surae muscle-tendon mechanics. Department of Biology of Physical Activity, University of Jyväskylä. Master's Thesis in Biomechanics. 105 pp.The present study was designed to investigate corticospinal excitability modulation during maximum isometric and eccentric muscle actions with two different velocities. Moreover, the study aimed to clarify the effect of muscle action type on muscle-tendon mechanical behavior in order to shed light into the possible role of sensory information in modulating corticospinal excitability during different muscle actions. We compared motor evoked potentials (MEPs) to transcranial magnetic stimulation and Hoffman reflexes (H-reflex) in soleus muscle during isometric, slow eccentric (25 deg/s) and fast eccentric (100 deg/s) muscle actions. Concomitantly, ultrasonography was utilized to access soleus and medial gastrocnemius fascicle behavior, characterized by fascicle length, velocity and pennation angle.The main finding was that soleus H-reflex was depressed (P < 0.001) during both fast and slow eccentric protocols as compared to isometric, while no differences in fascicle length (P = 0.569) and pennation angle (P = 0.293) were found among the three protocols.Furthermore, although the fast eccentric protocol had a greater fascicle velocity than slow eccentric (P < 0.05), there were no differences in H-reflex (P > 0.05). No differences in MEP sizes were found among the three protocols (P = 0.750), while absolute silent period was significantly shorter (P = 0.009) for both eccentric protocols as compared to isometric.Taken together, the present results corroborates with the idea that the central nervous system has an unique activation strategy during eccentric muscle actions , Enoka 1996, and further refutes the hypothesis that sensory information plays an important role in modulating these actions.
“…Other investigators have speculated that such an arrangement could lead to a loss of expected force when the muscle contracts (Katz, 1939;Demieville and Partridge, 1980;Goldberg et al, 1997b). Other skeletal muscles have been shown to have serially arranged and interdigitated fibers as well, and such arrangements could significantly alter the contractile properties of a motor unit as it acts in concert with other units (Loeb et al, 1987;Ounjian et al, 1991;Roy et al, 1995;Trotter et al, 1995).…”
Section: Motor Units and The Whole Musclementioning
Because primate studies provide data for the current experimental models of the human oculomotor system, we investigated the relationship of lateral rectus muscle motoneuron firing to muscle unit contractile characteristics in the squirrel monkey. Also examined was the correlation of whole-muscle contractile force with the degree of evoked eye displacement. A force transducer was used to record lateral rectus whole-muscle or muscle unit contraction in response to abducens whole-nerve stimulation or stimulation of single abducens motoneurons or axons. Horizontal eye displacement was recorded using a magnetic search coil.(1) Motor units could be categorized based on contraction speed (fusion frequency) and fatigue. (2) The kt value (change in motoneuronal firing necessary to increase motor unit force by 1.0 mg) of the units correlated with maximum tetanic tension. (3) There was some tendency for maximum tetanic tension of this unit population to separate into three groups. (4) At a constant frequency of 100 Hz, 95% of the motor units demonstrated significantly different force levels dependent on immediately previous stimulation history (hysteresis). (5) A mean force change of 0.32 gm/° and a mean frequency change of 4.7 Hz/° of eye displacement were observed in response to whole-nerve stimulation.These quantitative data provide the first contractile measures of primate extraocular motor units. Models of eye movement dynamics may need to consider the nonlinear transformations observed between stimulation rate and muscle tension as well as the probability that as few as two to three motor units can deviate the eye 1°.
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