Architecture of Contracting Human Muscles and Its Functional Significance
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This paper reviews three of our recent studies on human muscle architecture in vivo. 1. Hypertrophic changes: From B-mode ultrasonograms, pennation angles and thickness of triceps brachii were determined for normal subjects and highly-trained bodybuilders. There was a significant correlation between muscle thickness and pennation angles. It was confirmed that hypertrophy was accompanied by an increase in pennation angles. 2. Variation of fascicle architecture: Fascicle lengths and pennation angles were obtained from different positions in the gastrocnemius muscle while the subjects relaxed and performed isometric plantar flexion. The fascicle length was uniform throughout the muscle and shortened by contraction (30-34% at 50% of the maximal force). On the other hand, pennation angles differed among positions and increased by contraction. The muscle thickness did not change by contraction. Pen-nation angles were significantly correlated with muscle thickness within muscle. 3. Joint position-fascicle length relationships: Ultrasonic images of the gastrocnemius and soleus muscles were obtained while the subject performed maximal isometric plantarflexion at various joint positions, from which fascicle lengths and angles were determined. The length-force relationship of each muscle was estimated. It was suggested that human muscle architecture has an ability to make substantial changes to adapt to environmental conditions.Keywords:
Fascicle
Muscle architecture
Muscle belly
We evaluated the effects of differential muscle architectural adaptations on neuromuscular fatigue resistance. Seven young males and six females participated in this study. Using a longitudinal within-subject design, legs were randomly assigned to perform isometric training of the tibialis anterior (TA) three times per week for 8 wk at a short (S-group) or long muscle-tendon unit length (L-group). Before and following training, fascicle length (FL) and pennation angle (PA) of the TA were assessed. As well, fatigue-related time course changes in isometric maximal voluntary contraction (MVC) torque and isotonic peak power (20% MVC resistance) were determined before, immediately after, and 1, 2, 5, and 10 min following task failure. The fatiguing task consisted of repeated maximal effort isotonic (20% MVC resistance) contractions over a 40° range of motion until the participant reached a 40% reduction in peak power. Although there was no clear improvement in neuromuscular fatigue resistance following training in either group (P = 0.081; S-group: ∼20%; L-group: ∼51%), the change in neuromuscular fatigue resistance was related positively to the training-induced increase in PA (∼6%, P < 0.001) in the S-group (r = 0.739, P = 0.004) and negatively to the training-induced increase in FL (∼4%, P = 0.001) in the L-group (r = -0.568, P = 0.043). Both groups recovered similarly for MVC torque and peak power after the fatiguing task as compared with before training. We suggest that the relationships between the changes in muscle architecture and neuromuscular fatigue resistance depend on the muscle-tendon unit lengths at which the training is performed.NEW & NOTEWORTHY Eight weeks of isometric training at a long or short muscle-tendon unit length increased and did not change fascicle length, respectively. The "width" of the torque-angle relationship plateau became broader following isometric training at the long length. Despite marked differences in muscle architecture and functional adaptations between the groups, there was only a small-magnitude improvement in neuromuscular fatigue resistance, which was surprisingly negatively related to increased fascicle length in the long length-training group.
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Background Most data on the architecture of the human soleus muscle have been obtained from cadaveric dissection or two-dimensional ultrasound imaging. We present the first comprehensive, quantitative study on the three-dimensional anatomy of the human soleus muscle in vivo using diffusion tensor imaging (DTI) techniques. Methods We report three-dimensional fascicle lengths, pennation angles, fascicle curvatures, physiological cross-sectional areas and volumes in four compartments of the soleus at ankle joint angles of 69 ± 12° (plantarflexion, short muscle length; average ± SD across subjects) and 108 ± 7° (dorsiflexion, long muscle length) of six healthy young adults. Microdissection and three-dimensional digitisation on two cadaveric muscles corroborated the compartmentalised structure of the soleus, and confirmed the validity of DTI-based muscle fascicle reconstructions. Results The posterior compartments of the soleus comprised 80 ± 5% of the total muscle volume (356 ± 58 cm 3 ). At the short muscle length, the average fascicle length, pennation angle and curvature was 37 ± 8 mm, 31 ± 3° and 17 ± 4 /m, respectively. We did not find differences in fascicle lengths between compartments. However, pennation angles were on average 12° larger ( p < 0.01) in the posterior compartments than in the anterior compartments. For every centimetre that the muscle-tendon unit lengthened, fascicle lengths increased by 3.7 ± 0.8 mm, pennation angles decreased by −3.2 ± 0.9° and curvatures decreased by −2.7 ± 0.8 /m. Fascicles in the posterior compartments rotated almost twice as much as in the anterior compartments during passive lengthening. Discussion The homogeneity in fascicle lengths and inhomogeneity in pennation angles of the soleus may indicate a functionally different role for the anterior and posterior compartments. The data and techniques presented here demonstrate how DTI can be used to obtain detailed, quantitative measurements of the anatomy of complex skeletal muscles in living humans.
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Fascicle
Aponeurosis
Muscle belly
Muscle architecture
Tibialis anterior muscle
Gastrocnemius muscle
Flexor Digitorum Longus
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This paper reviews three of our recent studies on human muscle architecture in vivo. 1. Hypertrophic changes: From B-mode ultrasonograms, pennation angles and thickness of triceps brachii were determined for normal subjects and highly-trained bodybuilders. There was a significant correlation between muscle thickness and pennation angles. It was confirmed that hypertrophy was accompanied by an increase in pennation angles. 2. Variation of fascicle architecture: Fascicle lengths and pennation angles were obtained from different positions in the gastrocnemius muscle while the subjects relaxed and performed isometric plantar flexion. The fascicle length was uniform throughout the muscle and shortened by contraction (30-34% at 50% of the maximal force). On the other hand, pennation angles differed among positions and increased by contraction. The muscle thickness did not change by contraction. Pen-nation angles were significantly correlated with muscle thickness within muscle. 3. Joint position-fascicle length relationships: Ultrasonic images of the gastrocnemius and soleus muscles were obtained while the subject performed maximal isometric plantarflexion at various joint positions, from which fascicle lengths and angles were determined. The length-force relationship of each muscle was estimated. It was suggested that human muscle architecture has an ability to make substantial changes to adapt to environmental conditions.
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There are few comprehensive investigations of the changes in muscle architecture that accompany muscle contraction or change in muscle length in vivo. For this study, we measured changes in the three-dimensional architecture of the human medial gastrocnemius at the whole muscle level, the fascicle level and the fiber level using anatomical MRI and diffusion tensor imaging (DTI). Data were obtained from eight subjects under relaxed conditions at three muscle lengths. At the whole muscle level, a 5.1% increase in muscle belly length resulted in a reduction in both muscle width (mean change -2.5%) and depth (-4.8%). At the fascicle level, muscle architecture measurements obtained at 3,000 locations per muscle showed that for every millimeter increase in muscle-tendon length above the slack length, average fascicle length increased by 0.46 mm, pennation angle decreased by 0.27° (0.17° in the superficial part and 0.37° in the deep part), and fascicle curvature decreased by 0.18 m-1 There was no evidence of systematic variation in architecture along the muscle's long axis at any muscle length. At the fiber level, analysis of the diffusion signal showed that passive lengthening of the muscle increased diffusion along fibers and decreased diffusion across fibers. Using these measurements across scales, we show that the complex shape changes that muscle fibers, whole muscles, and aponeuroses of the medial gastrocnemius undergo in vivo cannot be captured by simple geometrical models. This justifies the need for more complex models that link microstructural changes in muscle fibers to macroscopic changes in architecture.NEW & NOTEWORTHY Novel MRI and DTI techniques revealed changes in three-dimensional architecture of the human medial gastrocnemius during passive lengthening. Whole muscle belly width and depth decreased when the muscle lengthened. Fascicle length, pennation, and curvature changed uniformly or near uniformly along the muscle during passive lengthening. Diffusion of water molecules in muscle changes in the same direction as fascicle strains.
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Fascicles in human vastus lateralis muscle (VL) were visualized as ultrasonic echoes and fascicle lengths were measured for healthy male volunteers (n=6). When the knee was fully extended from flexed position(110°) passively without muscle contraction (relaxed condition), the fascicle length decreased by 28%, from 133 to 97 mm. When VL was statically contracted with 10% of maximal voluntary contraction strength (tensed condition), shortening of fascicles (5.30%) were observed which was more pronounced when the knee was extended (30%) than when flexed (5%). Angle of pennation (fascicle angle), defined as the angle between fascicles and aponeurosis, was larger in tensed than in relaxed condition, especially when the knee was extended.Larger fascicle angles at the extended positions would cause more mechanical disadvantage in the force transmission.During relaxed condition, when the knee is fixed at above 90°, passive tension would be generated in fascicles. By contraction the force generated by muscle fibers lengthed the tendon slightly, which could result in a slim shortening of fascicles. Because a skeletal muscle consists of muscle fibers (contractile component) and tendinous tissues (elastic component), the differences in length and angle of fascicle between the relaxed and tensed conditions might be caused by the laxity of either or both of two components. The present results clearly show that the architecture of contracting muscle fibers is greatly different from that with no activation. The use of cadaver's data in the study of architecture and function of muscles would result in inaccurate, and in some cases even erroneous conclusions.
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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.
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Fascicle
Aponeurosis
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