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.

Hindlimb suspension (HS) results in whole muscle atrophic and metabolic changes that vary in magnitude in different hindlimb muscles. The present study was designed to investigate these effects in single fibers. Fiber type and size and the activities of two metabolic marker enzymes were determined in a deep (close to the bone) and a superficial (away from the bone) region of the medial gastrocnemius (MG) and the tibialis anterior (TA) of control (CON) and 28-day HS adult female rats. Fibers were classified as dark or light adenosinetriphosphatase (ATPase) based on their qualitative staining reaction for myosin ATPase following alkaline preincubation. Fiber area and succinate dehydrogenase (SDH) and alpha-glycerophosphate dehydrogenase (GPD) activities were determined in tissue sections by use of an image analysis system. After 28 days of HS, the mean body weights of the CON and HS were similar. MG atrophied 28%, whereas TA weight was maintained in the HS. Both dark and light ATPase fibers in the deep region of the MG had smaller cross-sectional areas following HS, with the atrophic response being approximately twice as great in the light ATPase fibers. No significant changes in fiber type composition in either muscle or in fiber sizes in the superficial region of the MG or in either region of the TA were observed. Mean SDH activities of both fiber types were significantly lower in the MG and TA following HS. In contrast, mean GPD activities were either increased or maintained in light and dark ATPase fibers of both muscles in HS. Changes in SDH and GPD activity could not be directly linked to changes in fiber cross-sectional area. In summary, these data suggest an independence of the mechanisms determining muscle fiber size and metabolic adaptations associated with HS.

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.

In view of the supposition that a dolphin can swim faster than would be predicted based on its physical features and presumed muscle power potential, studies were initiated to reevaluate the assumptions made in reaching these conclusions. Several previous studies have shown that the architectural and histochemical properties of a skeletal muscle dictate its force, velocity and displacement properties. This study examined the muscle fiber lengths and tendon arrangements of the dorsal and ventral axial muscles in dolphins (Tursiops truncatus). Fiber type and fiber size distributions were determined to reflect the general biochemical characteristics of the musculature. The dorsal muscles had a higher mean fiber length (167 Vs. 90 mm) and the range within and across different dorsal muscles was less (141–199 vs. 37–185 mm) than in the ventral muscles. Both the dorsal and ventral muscles consisted of an overall mean of 50 percent slow twitch and 50 percent fast twitch fiber types. The fast twitch fibers were 67 percent larger (2,200 vs. 1,317 μm2) than the slow twitch fibers in the ventral and 38 percent larger (1,213 Vs. 879 μm2) in the dorsal muscles. In addition, the mean cross sectional area of the fibers in the ventral muscles was approximately 65 percent greater (1,750 vs. 1,072 μm2) than those in the dorsal muscles. The shorter, larger‐diameter fibers of the ventral musculature give it a greater potential for force production for a given amount of muscle mass. In contrast, the dorsal muscles appear to be designed to optimize velocity and displacement, (i.e., longer fibers). These findings contribute to the information necessary for the determination of the power potential of the musculature of the dolphin.