Predictability of skeletal muscle tension from architectural determinations in guinea pig hindlimbs.

The maximum tetanic tension (Po) generated by a skeletal muscle is determined by its functional cross-sectional area (CSA) and its specific tension (tension/CSA). Measurements of average fiber length (normalized to a sarcomere length of 2.2 micron), muscle mass, and approximate angle of pinnation of muscle fibers within a muscle were taken from 26 different guinea pig hindlimb muscles and were used to calculate CSA. The specific tension was assumed to be 22.5 N X cm-2 and was used to determine the estimated Po of each muscle studied. In a second group of guinea pigs the in situ Po of 11 selected hindlimb muscles and muscle groups were determined. Estimated and measured Po values were found to have a strong linear relationship (r = 0.99) for muscle and muscle groups tested. The specific tension of the soleus, a homogeneously slow-twitch muscle, was shown to be approximately 15.4 N X cm-2 (P less than 0.01). Therefore, in our hands a specific tension value of 22.5 N X cm-2 appears to be a reasonable value for all mixed muscles studied in the guinea pig hindlimb and can be used to estimate their Po.

Architectural design and fiber-type distribution of the major elbow flexors and extensors of the monkey (cynomolgus).

Because the architectural and biochemical properties of skeletal muscle dictate its force, velocity, and displacement properties, the major extensors (triceps brachii) and flexors (biceps brachii, brachialis, and brachioradialis) of the elbow in a primate (cynomolgus, monkey) were studied. Functional cross-sectional areas (CSA) were calculated from muscle mass, mean fiber length (normalized to a 2.20 microns sarcomere length), and angle of fiber pinnation measurements from each muscle. Fiber-type distributions were determined and used as a gross index of the biochemical capacities of the muscle. The extensor group had a shorter mean fiber length (31 vs. 47 mm), a larger CSA (13 vs. 8 cm2), and a higher overall percentage of slow-twitch fibers (47 vs. 26%). Consequently, the elbow extensors had a relatively greater potential for force production and force maintenance than the flexors. In contrast, the flexors were designed to optimize their length-velocity potentials; i.e., they had relatively long fibers and a higher fast-twitch fiber composition than the extensors. These morphologic differences between antagonistic muscle groups should be considered when evaluating the motor control mechanisms regulating reciprocal movements about the elbow.

Architectural and histochemical analysis of the semitendinosus muscle in mice, rats, guinea pigs, and rabbits.

The architectural and histochemical properties of the anatomically distinct compartments of the semitendinosus muscle (ST) of mice, rats, guinea pigs, and rabbits show that the ST is composed of two separate compartments aligned in series--a distal compartment (STd) and a proximal one (STp). The STp is further subdivided into a ventral head (STpv) and a dorsal head (STpd). The muscle fibers were arranged in parallel to the line of muscle pull within each compartment. The STd has the longest and the STpv the shortest fibers in all species. The physiological cross-sectional area and the estimated tetanic tension was greatest in the STd. Based on the staining pattern for myosin ATPase (alkaline preincubation) and an oxidative indicator (NADH or SDH), the STpv has the highest percentage of slow-oxidative (SO) or SO plus fast-oxidative-glycolytic (FOG) fibers of any portion of the muscle. The differences in fiber-type distributions and architectural designs of the separate compartments suggest a specialization of function of the individual compartments.

Muscle architecture and force-velocity relationships in humans.

The in vivo torque-velocity relationships of the knee extensors (KE), knee flexors (KF), ankle plantarflexors (PF), and ankle dorsiflexors (DF) were determined in 12 untrained subjects using an isokinetic testing device (Cybex II). These data were then matched to the predicted maximum forces and shortening velocities derived from muscle architectural determinations made on three hemipelvectomies (36). The torque-velocity curves of all muscle groups resembled that predicted by Hill's (19, 20) equation except at the higher forces and lower velocities. The peak torques occurred at mean velocities ranging from 41-62 rad X s-1 for the KE, KF, and PF. Although the peak torque of the DF occurred at the isometric loading condition, it was also lower than that predicted by Hill's equation. The muscle fiber length and physiological cross-sectional area measurements indicate that the architecture of the human leg musculature has a major influence on the torque-velocity characteristics. These data corroborate previous findings (24) that some neural inhibitory mechanism exists in the control of the leg musculature, which limits the maximum forces that could be produced under optimal stimulating conditions.

Muscle architecture of the human lower limb.

The architectural features of the major knee extensors and flexors and ankle plantar flexors and dorsiflexors were determined in three human cadavers. There was marked uniformity of fiber length throughout a given muscle and a trend toward similar fiber lengths within muscles of a synergistic group. Muscle length/fiber length ratios were remarkably similar for all three limbs. Angles of fiber pinnation were relatively small (0 degree-15 degrees) and generally consistent throughout the muscle. From these architectural data, the performance of a muscle was studied with respect to its tension production and velocity of shortening potentials. The tension is a function of the number of sarcomeres in parallel, and the velocity of shortening is a function of the number of sarcomeres in series. Muscles were grouped according to whether they showed a predilection for tension or velocity of shortening.