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Muscle fiber conduction velocity (MFCV) can be affected by muscle fiber geometry at different joint angles and during joint movements. This study aimed to investigate MFCV during electrically evoked contraction at different joint angles, during joint movements, and during voluntary contractions. Sixteen healthy young men participated. A stimulation electrode was attached on the innervation zone of the vastus lateralis, and a linear electrode array was attached on the vastus lateralis. Under a static condition, electrically evoked electromyography signals were recorded at knee joint angles set every 15° between 0° and 105°. Under a passive movement condition, signals were recorded during knee extension and flexion passively. Under a voluntary contraction condition, signals were recorded while performing 30% or 60% of maximum voluntary contraction. MFCV was calculated using cross-correlation coefficients. Under the static condition, there were no differences in MFCV among various joint angles. Under the passive movement condition, MFCV was significantly greater during high velocity or shortening. Under the voluntary contraction condition, MFCV was significantly greater during high-intensity voluntary contraction and with a shortened muscle length. Joint angles do not influence MFCV markedly during relaxation, but it is possible to overestimate MFCV during movement or voluntary contraction. [ABSTRACT FROM AUTHOR]

The uncoupling behaviour between muscle belly and fascicle shortening velocity (i.e. belly gearing), affects mechanical output by allowing the muscle to circumvent the limits imposed by the fascicles' force-velocity relationship. However, little is known about the 'metabolic effect' of a decrease/increase in belly gearing. In this study, we manipulated the plantar flexor muscles' capacity to change in shape (and hence belly gearing) by using compressive multidirectional loads. Metabolic, kinetic, electromyography activity and ultrasound data (in soleus and gastrocnemius medialis) were recorded during cyclic fixed-end contractions of the plantar flexor muscles in three different conditions: no load, +5 kg and +10 kg of compression. No differences were observed in mechanical power and electrophysiological variables as a function of compression intensity, whereas metabolic power increased as a function of it. At each compression intensity, differences in efficiency were observed when calculated based on fascicle or muscle behaviour and significant positive correlations (R2 range: 0.7–0.8 and p > 0.001) were observed between delta efficiency (ΔEff: Effmus−Efffas) and belly gearing (Vmus/Vfas) or ΔV (Vmus−Vfas). Thus, changes in the muscles' capacity to change in shape (e.g. in muscle stiffness or owing to compressive garments) affect the metabolic demands and the efficiency of muscle contraction. [ABSTRACT FROM AUTHOR]

In their physiological condition, muscles are surrounded by connective tissue, other muscles and bone. These tissues exert transverse forces that change the three-dimensional shape of the muscle compared to its isolated condition, in which all surrounding tissues are removed. A change in shape affects the architecture of a muscle and therefore its mechanical properties. The rabbit M. plantaris is a multi-pennate calf muscle consisting of two compartments. A smaller, bi-pennate inner muscle compartment is embedded in a larger, uni-pennate outer compartment (Böl et al., 2015). As part of the calf, the plantaris is tightly packed between other muscles. It is unclear how packing affects the shape and architecture of the plantaris. Therefore, we examined the isolated and packed plantaris of the contralateral legs of three rabbits to determine the influence of the surrounding muscles on its shape and architectural properties using photogrammetric reconstruction and manual digitization, respectively. In the packed condition, the plantaris showed a 27% increase in fascicle pennation and a 54% increase in fascicle curvature compared to the isolated condition. Fascicle length was not affected by muscle packing. The change in muscle architecture occurred mainly in the outer compartment of the plantaris. Furthermore, the isolated plantaris showed a more circular shape and a reduced width of its muscle belly. It can be concluded that the packed plantaris is flattened by the forces exerted by the surrounding muscles, causing a complex architectural change. The data provided improve our understanding of muscle packages in general and can be used to develop and validate realistic three-dimensional muscle models., Competing Interests: Declaration of competing interest The authors declare that they have no known competing financial interests or personal relationships that could have appeared to influence the work reported in this paper., (Copyright © 2024 The Authors. Published by Elsevier Ltd.. All rights reserved.)

Changes in muscle shape could play an important role during contraction allowing to circumvent some limits imposed by the fascicle force–velocity (F–V) and power–velocity (P–V) relationships. Indeed, during low-force high-velocity contractions, muscle belly shortening velocity could exceed muscle fascicles shortening velocity, allowing the muscles to operate at higher F–V and P–V potentials (i.e., at a higher fraction of maximal force/power in accordance to the F–V and P–V relationships). By using an ultrafast ultrasound, we investigated the role of muscle shape changes (vastus lateralis) in determining belly gearing (muscle belly velocity/fascicle velocity) and the explosive torque during explosive dynamic contractions (EDC) at angular accelerations ranging from 1000 to 4000°.s–2. By means of ultrasound and dynamometric data, the F–V and P–V relationships both for fascicles and for the muscle belly were assessed. During EDC, fascicle velocity, belly velocity, belly gearing, and knee extensors torque data were analysed from 0 to 150 ms after torque onset; the fascicles and belly F–V and P–V potentials were thus calculated for each EDC. Absolute torque decreased as a function of angular acceleration (from 80 to 71 Nm, for EDC at 1000 and 4000°.s–1, respectively), whereas fascicle velocity and belly velocity increased with angular acceleration (P < 0.001). Belly gearing increased from 1.11 to 1.23 (or EDC at 1000 and 4000°.s–1, respectively) and was positively corelated with the changes in muscle thickness and pennation angle (the changes in latter two equally contributing to belly gearing changes). For the same amount of muscle’s mechanical output (force or power), the fascicles operated at higher F–V and P–V potential than the muscle belly (e.g., P–V potential from 0.70 to 0.56 for fascicles and from 0.65 to 0.41 for the muscle belly, respectively). The present results experimentally demonstrate that belly gearing could play an important role during explosive contractions, accommodating the largest part of changes in contraction velocity and allowing the fascicle to operate at higher F–V and P–V potentials.

Changes in muscle shape could play an important role during contraction allowing to circumvent some limits imposed by the fascicle force–velocity (F–V) and power–velocity (P–V) relationships. Indeed, during low-force high-velocity contractions, muscle belly shortening velocity could exceed muscle fascicles shortening velocity, allowing the muscles to operate at higher F–V and P–V potentials (i.e., at a higher fraction of maximal force/power in accordance to the F–V and P–V relationships). By using an ultrafast ultrasound, we investigated the role of muscle shape changes (vastus lateralis) in determining belly gearing (muscle belly velocity/fascicle velocity) and the explosive torque during explosive dynamic contractions (EDC) at angular accelerations ranging from 1000 to 4000°.s–2. By means of ultrasound and dynamometric data, the F–V and P–V relationships both for fascicles and for the muscle belly were assessed. During EDC, fascicle velocity, belly velocity, belly gearing, and knee extensors torque data were analysed from 0 to 150 ms after torque onset; the fascicles and belly F–V and P–V potentials were thus calculated for each EDC. Absolute torque decreased as a function of angular acceleration (from 80 to 71 Nm, for EDC at 1000 and 4000°.s–1, respectively), whereas fascicle velocity and belly velocity increased with angular acceleration (P < 0.001). Belly gearing increased from 1.11 to 1.23 (or EDC at 1000 and 4000°.s–1, respectively) and was positively corelated with the changes in muscle thickness and pennation angle (the changes in latter two equally contributing to belly gearing changes). For the same amount of muscle's mechanical output (force or power), the fascicles operated at higher F–V and P–V potential than the muscle belly (e.g., P–V potential from 0.70 to 0.56 for fascicles and from 0.65 to 0.41 for the muscle belly, respectively). The present results experimentally demonstrate that belly gearing could play an important role during explosive contractions, accommodating the largest part of changes in contraction velocity and allowing the fascicle to operate at higher F–V and P–V potentials. [ABSTRACT FROM AUTHOR]

The function of a muscle is highly dependent on its architecture, which is characterized by the length, pennation, and curvature of the fascicles, and the geometry of the aponeuroses. During in vivo function, muscles regularly undergo changes in length, thereby altering their architecture. During passive muscle lengthening, fascicle length (FL) generally increases and the angle of fascicle pennation (FP) and the fascicle curvature (FC) decrease, while the aponeuroses increase in length but decrease in width. Muscles are differently structured, making their change during muscle lengthening complex and multifaceted. To obtain comprehensive data on architectural changes in muscles during passive length, the present study determined the three-dimensional fascicle geometry of rabbit M. gastrocnemius medialis (GM), M. gastrocnemius lateralis (GL), and M. plantaris (PLA). For this purpose, the left and right legs of three rabbits were histologically fixed at targeted ankle joint angles of 95° (short muscle length [SML]) and 60° (long muscle length [LML]), respectively, and the fascicles were tracked by manual three-dimensional digitization. In a second set of experiments, the GM aponeurosis dimensions of ten legs from five rabbits were determined at varying muscle lengths via optical marker tracking. The GM consisted of a uni-pennated compartment, whereas the GL and PLA contained multiple compartments of differently pennated fascicles. In the LML compared to the SML, the GM, GL, and PLA had on average a 41%, 29%, and 41% increased fascicle length, and a 30%, 25%, and 33% decrease in fascicle pennation and a 32%, 11%, and 35% decrease in fascicle curvature, respectively. Architectural properties were also differentiated among the different compartments of the PLA and GL, allowing for a more detailed description of their fascicle structure and changes. It was shown that the compartments change differently with muscle length. It was also shown that for each degree of ankle joint angle reduction, the proximal GM aponeurosis length increased by 0.11%, the aponeurosis width decreased by 0.22%, and the area was decreased by 0.20%. The data provided improve our understanding of muscles and can be used to develop and validate muscle models. [ABSTRACT FROM AUTHOR]

Summary: Rate of force development (RFD) refers to the ability of the neuromuscular system to increase contractile force from a low or resting level when muscle activation is performed as quickly as possible, and it is considered an important muscle strength parameter, especially for athletes in sports requiring high‐speed actions. The assessment of RFD has been used for strength diagnosis, to monitor the effects of training interventions in both healthy populations and patients, discriminate high‐level athletes from those of lower levels, evaluate the impairment in mechanical muscle function after acute bouts of eccentric muscle actions and estimate the degree of fatigue and recovery after acute exhausting exercise. Notably, the evaluation of RFD in human skeletal muscle is a complex task as influenced by numerous distinct methodological factors including mode of contraction, type of instruction, method used to quantify RFD, devices used for force/torque recording and ambient temperature. Another important aspect is our limited understanding of the mechanisms underpinning rapid muscle force production. Therefore, this review is primarily focused on (i) describing the main mechanical characteristics of RFD; (ii) analysing various physiological factors that influence RFD; and (iii) presenting and discussing central biomechanical and methodological factors affecting the measurement of RFD. The intention of this review is to provide more methodological and analytical coherency on the RFD concept, which may aid to clarify the thinking of coaches and sports scientists in this area. [ABSTRACT FROM AUTHOR]

Isolated and packed muscles (e.g. in the calf) exhibit different three-dimensional muscle shapes. In packed muscles, cross-sections are more angular compared to the more elliptical ones in isolated muscles. As far as we know, it has not been examined yet, whether the shape of the muscle in its packed condition influences its internal arrangement of muscle fascicles and accordingly the contraction behavior in comparison to the isolated condition. To evaluate the impact of muscle packing, we examined the three-dimensional muscle architecture of isolated and packed rabbit M. soleus for different ankle angles (65°, 75°, 85°, 90°, and 95°) using manual digitization (MicroScribe ® MLX). In general, significantly increased values of pennation angle and fascicle curvature were found in packed compared to isolated M. soleus (except for fascicle curvature at 90° ankle angle). On average, fascicle length of isolated muscles exceeded fascicle lengths of packed muscles by 2.6%. Reduction of pennation angle in the packed condition had only marginal influence on force generation (about 1% of maximum isometric force) in longitudinal direction (along the line of action) although an increase of transversal force component (perpendicular to the line of action) of about 26% is expected. Results of this study provide initial evidence that muscle packing limits maximum muscle performance observed in isolated M. soleus . Besides an enhanced understanding of the impact of muscle packing on architectural parameters, the outcomes of this study are essential for realistic three-dimensional muscle modeling and model validation. [ABSTRACT FROM AUTHOR]

Accurate muscle geometry (muscle length and moment arm) is required to estimate muscle function when using musculoskeletal modelling. In shoulder, muscles are often modelled as a collection of independent line segments, leading to non-physiological muscles trajectory, especially for the rotator cuff muscles. To prevent this, a surface mesh model was developed and validated against 7 MRI positions in one participant. Mean moment arm errors was 11.4% for the line vs. 8.8% for the mesh model. While the model with independent lines led to some non-physiological trajectories, the mesh model gave lower misestimations of muscle lengths and moment arms. [ABSTRACT FROM AUTHOR]

Background Accurate geometry of the trunk musculature is essential for reliably estimating spinal loads in biomechanical models. Currently, many models employ straight muscle path assumptions that yield far less accurate tissue loads, particularly in extreme postures. Precise muscle moment-arms and physiological cross-sectional areas are important when incorporating curved muscle geometry in biomechanical models. The objective of this study was to develop a predictive model of moment arms and physiological cross-sectional areas of trunk musculature at multiple levels in the thoracic/lumbar spine as a function of anthropometric measures. Methods Based on magnetic resonance imaging data from thirty subjects (10 male and 20 female) reported in a previous study, a polynomial regression analysis was conducted to estimate the muscle moment-arms and physiological cross-sectional areas of trunk muscles through thoracic/lumbar spine as a function of vertebral level, gender, age, height, and body mass. Findings Gender, body mass, and height were the best predictors of muscle moment-arms and physiological cross-sectional areas. The predictability of muscle parameters tended to be higher for erector spinae than other muscles. Most muscles showed a curved muscle path along the thoracic/lumbar spine. Interpretation The polynomial regression model of the muscle geometry in this study generally showed good predictability compared to previous reports. The predictive model in this study will be useful to develop personalized biomechanical models that incorporate curved trunk muscle geometries. [ABSTRACT FROM AUTHOR]

Using a cross-sectional design, the purpose of this study was to determine how pennate gastrocnemius medialis (GM) muscle geometry changes as a function of adolescent age. Sixteen healthy adolescent males (aged 10-19 years) participated in this study. GM muscle geometry was measured within the mid-longitudinal plane obtained from a 3D voxel-array composed of transverse ultrasound images. Images were taken at footplate angles corresponding to standardised externally applied footplate moments (between 4 Nm plantar flexion and 6 Nm dorsal flexion). Muscle activity was recorded using surface electromyography ( EMG), expressed as a percentage of maximal voluntary contraction (% MVC). To minimise the effects of muscle excitation, EMG inclusion criteria were set at < 10% of MVC. In practice, however, normalised EMG levels were much lower. For adolescent subjects with increasing ages, GM muscle (belly) length increased due to an increase in the length component of the physiological cross-sectional area measured within the mid-longitudinal plane. No difference was found between fascicles at different ages, but the aponeurosis length and pennation angle increased by 0.5 cm year−1 and 0.5 ° per year, respectively. Footplate angles corresponding to externally applied 0 and 4 Nm plantarflexion moments were not associated with different adolescent ages. In contrast, footplate angles corresponding to externally applied 4 and 6 Nm dorsal flexion moments decreased by 10 ° between 10 and 19 years. In conclusion, we found that in adolescents' pennate GM muscles, longitudinal muscle growth is mediated predominantly by increased muscle fascicle diameter. [ABSTRACT FROM AUTHOR]

Musculoskeletal models allow estimation of muscle function during complex tasks. We used objective methods to determine possible attachment locations for index finger muscles in an OpenSim upper-extremity model. Data-driven optimization algorithms, Simulated Annealing and Hook-Jeeves, estimated tendon locations crossing the metacarpophalangeal (MCP), proximal interphalangeal (PIP) and distal interphalangeal (DIP) joints by minimizing the difference between model-estimated and experimentally-measured moment arms. Sensitivity analysis revealed that multiple sets of muscle attachments with similar optimized moment arms are possible, requiring additional assumptions or data to select a single set of values. The most smooth muscle paths were assumed to be biologically reasonable. Estimated tendon attachments resulted in variance accounted for (VAF) between calculated moment arms and measured values of 78% for flex/extension and 81% for ab/adduction at the MCP joint. VAF averaged 67% at the PIP joint and 54% at the DIP joint. VAF values at PIP and DIP joints partially reflected the constant moment arms reported for muscles about these joints. However, all moment arm values found through optimization were non-linear and non-constant. Relationships between moment arms and joint angles were best described with quadratic equations for tendons at the PIP and DIP joints. [ABSTRACT FROM AUTHOR]

There exists several numerical approaches to describe the active contractile behaviour of skeletal muscles. These models range from simple one-dimensional to more advanced three-dimensional ones; especially, three-dimensional models take up the cause of describing complex contraction modes in a realistic way. However, the validation of such concepts is challenging, as the combination of geometry, material and force characteristics is so far not available from the same muscle. To this end, we present in this study a comprehensive data set of the rabbit soleus muscle consisting of the muscles’ characteristic force responses (active and passive), its three-dimensional shape during isometric, isotonic and isokinetic contraction experiments including the spatial arrangement of muscle tissue and aponeurosis–tendon complex, and the fascicle orientation throughout the whole muscle at its optimal length. In this way, an extensive data set is available giving insight into the three-dimensional geometry of the rabbit soleus muscle and, further, allowing to validate three-dimensional numerical models. [ABSTRACT FROM AUTHOR]

In the last decade, diffusion tensor imaging ( DTI) has been used increasingly to investigate three-dimensional (3 D) muscle architectures. So far there is no study that has proved the validity of this method to determine fascicle lengths and pennation angles within a whole muscle. To verify the DTI method, fascicle lengths of m. soleus as well as their pennation angles have been measured using two different methods. First, the 3 D muscle architecture was analyzed in vivo applying the DTI method with subsequent deterministic fiber tractography. In a second step, the muscle architecture of the same muscle was analyzed using a standard manual digitization system ( MicroScribe MLX). Comparing both methods, we found differences for the median pennation angles ( P < 0.001) but not for the median fascicle lengths ( P = 0.216). Despite the statistical results, we conclude that the DTI method is appropriate to determine the global fiber orientation. The difference in median pennation angles determined with both methods is only about 1.2° (median pennation angle of Micro Scribe: 9.7°; DTI: 8.5°) and probably has no practical relevance for muscle simulation studies. Determining fascicle lengths requires additional restriction and further development of the DTI method. [ABSTRACT FROM AUTHOR]

Abstract: Generating muscle-driven forward dynamics simulations of human movement using detailed musculoskeletal models can be computationally expensive. This is due in part to the time required to calculate musculotendon geometry (e.g., musculotendon lengths and moment arms), which is necessary to determine and apply individual musculotendon forces during the simulation. Modeling upper-extremity musculotendon geometry can be especially challenging due to the large number of multi-articular muscles and complex muscle paths. To accurately represent this geometry, wrapping surface algorithms and/or other computationally expensive techniques (e.g., phantom segments) are used. This paper provides a set of computationally efficient polynomial regression equations that estimate musculotendon length and moment arms for thirty-two (32) upper-extremity musculotendon actuators representing the major muscles crossing the shoulder, elbow and wrist joints. Equations were developed using a least squares fitting technique based on geometry values obtained from a validated public-domain upper-extremity musculoskeletal model that used wrapping surface elements (). In general, the regression equations fit well the original model values, with an average root mean square difference for all musculotendon actuators over the represented joint space of 0.39mm (1.1% of peak value). In addition, the equations reduced the computational time required to simulate a representative upper-extremity movement (i.e., wheelchair propulsion) by more than two orders of magnitude (315 versus 2.3s). Thus, these equations can assist in generating computationally efficient forward dynamics simulations of a wide range of upper-extremity movements. [Copyright &y& Elsevier]

During development, muscle growth is usually finely adapted to meet functional demands in daily activities. However, how muscle geometry changes in typically developing children and how these changes are related to functional and mechanical properties is largely unknown. In rodents, longitudinal growth of the pennate m. gastrocnemius medialis (GM) has been shown to occur mainly by an increase in physiological cross-sectional area and less by an increase in fibre length. Therefore, we aimed to: (i) determine how geometry of GM changes in healthy children between the ages of 5 and 12 years, (ii) test whether GM geometry in these children is affected by gender, (iii) compare normalized growth of GM geometry in children with that in rats at similar normalized ages, and (iv) investigate how GM geometry in children relates to range of motion of angular foot movement at a given moment. Thirty children (16 females, 14 males) participated in the study. Moment-angle data were collected over a range of angles by rotating the foot from plantar flexion to dorsal flexion at standardized moments. GM geometry in the mid-longitudinal plane was measured using three-dimensional ultrasound imaging. This geometry was compared with that of GM geometry in rats. During growth from 5 to 12 years of age, the mean neutral footplate angle (0 Nm) occurred at −5° (SD 7°) and was not a function of age. Measured at standardized moments (4 Nm), footplate angles towards plantar flexion and dorsal flexion decreased by 25 and 40%, respectively. In both rats and children, GM muscle length increased proportionally with tibia length. In children, the length component of the physiological cross-sectional area and fascicle length increased by 7 and 5% per year, respectively. Fascicle angle did not change over the age range measured. In children, the Achilles tendon length increased by 6% per year. GM geometry was not affected by gender. We conclude that, whereas the length of GM in rat develops mainly by an increase in physiological cross-sectional area of the muscle, GM in children develops by uniform scaling of the muscle. This effect is probably related to the smaller fascicle angle in human GM, which entails a smaller contribution of radial muscle growth to increased GM muscle length. The net effect of uniform scaling of GM muscle belly causes it to be stiffer, explaining the decrease in range of motion of angular foot movement at 4 Nm towards dorsal flexion during growth. [ABSTRACT FROM AUTHOR]

The article presents a study that examined the impact of a 12-week strength-training regimen on the muscle thickness (MT) and pennation angle (PA) in three different sites of the triceps brachii and biceps brachii muscles. MT and PT increased by significant amounts at all 3 sites for the triceps brachii, as did MT in one of the sites for biceps brachii.

Reconstruction of a cleft lip leads inevitably to scar tissue formation. Scar tissue within the restored oral orbicular muscle might be assessed by quantification of the local contractility of this muscle. Furthermore, information about the contraction capability of the oral orbicular muscle is crucial for planning the revision surgery of an individual patient. We used ultrasound elastography to determine the local deformation (strain) of the upper lip and to differentiate contracting muscle from passive scar tissue. Raw ultrasound data (radio-frequency format; rf-) were acquired, while the lips were brought from normal state into a pout condition and back in normal state, in three patients and three normal individuals. During this movement, the oral orbicular muscle contracts and, consequently, thickens in contrast to scar tissue that will not contract, or even expand. An iterative coarse-to-fine strain estimation method was used to calculate the local tissue strain. Analysis of the raw ultrasound data allows estimation of tissue strain with a high precision. The minimum strain that can be assessed reproducibly is 0.1%. In normal individuals, strain of the orbicular oral muscle was in the order of 20%. Also, a uniform strain distribution in the oral orbicular muscle was found. However, in patients deviating values were found in the region of the reconstruction and the muscle tissue surrounding that. In two patients with a successful reconstruction, strain was reduced by 6% in the reconstructed region with respect to the normal parts of the muscle (from 22% to 16% and from 25% to 19%). In a patient with severe esthetical and functional disability, strain decreased from 30% in the normal region to 5% in the reconstructed region. With ultrasound elastography, the strain of the oral orbicular muscle can be quantified. In healthy subjects, the strain profiles and maximum strain values in all parts of the muscle were similar. The maximum strain of the muscle during pout was 20% ± 1%. In surgically repaired cleft lips, decreased deformation was observed. [ABSTRACT FROM AUTHOR]

Abstract: Functions of the extrinsic tongue muscles in vowel production were examined by measurements of muscle length and tongue tissue deformation using MRI (magnetic resonance imaging). Results from the analysis of Japanese vowel data suggested: (1) Contraction and relaxation of the three subdivisions of the genioglossus (GG) play a dominant role in forming tongue shapes for vowels. (2) The extra-lingual part of the styloglossus (SG), which was previously thought to cause a high-back tongue position by pulling its insertion point in the tongue, was found to be nearly constant across all vowels both in length and orientation. (3) The tongue shape for back vowels is mainly achieved by internal deformation of the tongue tissue, and the medial tissue of the tongue showed lateral expansion in front vowels, and medial compression in back vowels. [Copyright &y& Elsevier]

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. [ABSTRACT FROM AUTHOR]

The purpose of this study was to examine whether the human gastrocnemius medialis (GM) fascicle length and pennation angle alter during a sustained submaximal isometric plantar flexion. Fourteen male subjects performed maximal voluntary plantar flexions (MVC) on a dynamometer before and after a fatiguing task. This task consisted of a sustained submaximal isometric fatiguing contraction (40% MVC) until failure to hold the defined moment. Ultrasonography was used to visualise the muscle belly of the GM. Leg kinematics were recorded (120 Hz) to calculate the joint moment using inverse dynamics. The exerted moments and the EMG signals from GM and lateralis, soleus and tibialis anterior were measured at 1,080 Hz. The root mean square (RMS) of the EMG signal of the three triceps surae muscles increased significantly ( P≤0.05) between 17% and 28% with fatigue. Further, the fascicle length of the GM significantly decreased from 47.1±8.0 mm at the beginning to 41.8±6.7 mm at the end of fatigue and the pennation angle increased from 23.5±4.1° to 26.3±2.2° ( P≤0.05). The changes in fascicle length and pennation angle of the GM during the contraction can influence the force potential of the muscle due to the force–length relationship and the force transmission to the tendon. This provides evidence on that an additional mechanical mechanism, namely tendon creep, can contribute to the increase in the EMG activity of the GM during submaximal isometric sustained contractions. [ABSTRACT FROM AUTHOR]

This paper presents a set of polynomial expressions that can be used as regression equations to estimate length and three-dimensional moment arms of 43 lower-limb musculotendon actuators. These equations allow one to find, at a low computational cost, the musculotendon geometric parameters required for numerical simulation of large musculoskeletal models. Nominal values for these biomechanical parameters were established using a public-domain musculoskeletal model of the lower limb (IEEE Trans. Biomed. Eng. 37 (1990) 757). To fit these nominal values, regression equations with different levels of complexity were generated, based on the number of generalized coordinates of the joints spanned by each musculotendon actuator. Least squares fitting was used to identify regression equation coefficients. The goodness of the fit and confidence intervals were assessed, and the best fitting equations selected. [Copyright &y& Elsevier]

Muscle architecture has a significant influence on the mechanical properties of skeletal muscles. Important parameters include the fascicle length, the angle of pennation, the physiological cross-sectional area (PCSA) as well as aponeurosis and tendon dimensions. During growth, skeletal muscles have to react to an increasing body mass and size demanding adaptations in muscle dimensions. Investigations of muscle architectural changes during growth are sparse, and existing studies often confine their scope to specific parameters or regions of the muscle. For this cross-sectional study, we determined the entire three-dimensional fascicle architecture of rabbit M. soleus via manual digitization. To this end, the investigations covered nine rabbits in the age-range between 29 days and 109 days. Fascicle length, muscle belly length, and aponeurosis length increased by 40%, 107%, and 111%, respectively. As the pennation angle remained almost constant and the contribution of fascicle length growth to muscle belly growth was minor, the increase in muscle mass primarily led to an increase in PCSA (462%), which required a similar increase in aponeurosis area (434%). Results gain new insight into the build-up of rabbit M. soleus and reveal that increases in muscle belly length are primarily connected to increases in aponeurosis length (83%). Contributions from fascicle length increase (17%) only play a minor role. [ABSTRACT FROM AUTHOR]