The range of sarcomere lengths in the muscles of the human lower limb.

The lengths of the sarcomeres of some muscles of the human leg were determined for the anatomical position, using a method based on diffraction. Measurements were made of the muscle lengths and angles of pennation from cadavers, and these were used to predict sarcomere lengths at other limb positions. The measured and predicted sarcomere lengths were compared with the length-tension curve for human muscle, which showed the range of sarcomere length from both extremes of muscle length to cover the entire range of the length-tension curve.

Myofibrillar M-band structure and composition of physiologically defined rat motor units.

The isometric contraction time of 19 fast and slow rat motor units in the soleus and the anterior tibial muscles were recorded. The motor unit fibers, subsequently distinguished by glycogen depletion, were histochemically differentiated into fiber types and analyzed immunohistochemically for high molecular weight M-band proteins, as well as ultrastructurally for M-band fine structure, Z-disc width, and volume density of mitochondria. All fibers belonging to slow-twitch motor units in both the anterior tibialis and soleus muscles were histochemically classed as type 1. They lacked the Mr 165,000 M-protein, showed ultrastructurally a four-line M-band pattern, and had broad Z-discs, whereas the volume density of the mitochondria varied considerably. Muscle fibers belonging to the fast-twitch motor units were histochemically classed as types 2A and 2B in anterior tibialis and type 2A in soleus. They contained a three- or a five-line M-band pattern and medium-to-thin Z-discs in the anterior tibialis and a five-line M-band pattern and broad Z-discs in the soleus. Furthermore, the volume density of mitochondria showed considerable variation within and in between soleus and anterior tibialis type 2 fibers. As the differences in M-band composition and structure between fiber types overrode the intragroup variability in contraction times of slow and fast units within and between the two muscles, it is concluded that the M-band composition and structure is fundamentally related to whether the fiber is innervated by a slow or fast motor neuron, whereas other parameters such as contraction time, Z-disc width, and mitochondrial content of fibers of fast and slow units are relative and vary between muscles. Thus the M-band appearance can be used as a reliable marker to distinguish between fibers of slow- and fast-twitch motor units in rat leg muscles.

A laser diffraction method for measuring muscle sarcomere length in vivo for application to tendon transfers.

A technique that uses laser light diffraction to measure muscle sarcomere length allows direct determination of optimal muscle length during tendon transfers. Forearm muscle sarcomere length with the hand in the position of function is 2.4, and muscle length corresponds directly to sarcomere length. We have used these observations to restore optimal muscle length during tendon transfers. Standard high radial nerve tendon transfers in six fresh cadaver forearms demonstrated the efficacy of the laser diffraction method in accurately measuring sarcomere length. In two clinical trials with the laser, standard high radial nerve palsy tendon transfers were performed. In each case the clinical tendency was to overpull the muscle during the transfer. With the laser it was possible to identify excessive muscle stretch and restore optimal muscle length.

Recovery of reinnervating rat muscle after cast immobilization.

We evaluated the recovery of the reinnervating rat plantar flexor muscles after different periods of casting and then decasting the lower extremities. Four groups of 4-month-old, female Wistar rats underwent bilateral crush-denervation of the sciatic nerve at the sciatic notch. Two weeks after nerve crush, the hind legs of three groups of rats were immobilized with bilateral casts at the knee and ankle joints and the fourth group was a control group. Of the three casted groups, one was mobilized after 1 week and another group after 3 weeks of casting. The third experimental group remained casted until the end of 6 weeks. Six weeks after the nerve crush, all groups were evaluated for muscle weights of the soleus, plantaris, and gastrocnemius; absolute amounts of the myofibrillar, sarcoplasmic, and stromal proteins in the gastrocnemius; the fiber diameters and percent composition of type I and type II fibers in the soleus and plantaris; and the isometric contractile properties of the soleus muscle. Compared with the denervated control group, the experimental groups revealed the following: (i) Four weeks of casting caused a reduction in wet weight (range 30.6 to 40.4%, P less than 0.01) in the soleus, plantaris, and gastrocnemius muscles. Decasting led to an earlier recovery of the soleus than of the plantaris and gastrocnemius muscles. (ii) The myofibrillar protein returned to control values with 3 weeks of decasting but the stromal protein remained significantly elevated and the sarcoplasmic protein significantly depressed regardless of the period of mobilization. (iii) Except for the type I fibers in the plantaris, the remainder of the muscle fibers in the soleus and plantaris decreased in size due to casting. Only the type I muscle fibers of the soleus increased in size with longer periods of mobilization. (iv) Four weeks of casting significantly altered the maximum isometric twitch tension (-42.3%), contraction time (+17.1%), maximum tetanic tension (-38.1%), and half-fatigue time (+40.5%) in the soleus. The reinnervating soleus muscle appears to recover from the effects of casting sooner than the plantaris or gastrocnemius muscles.

Calcium- and length-dependent force production in rat ventricular muscle.

1. Trabeculae from the right ventricles of rat hearts were ;skinned' by immersion for 30 min in a solution containing the non-ionic detergent Brij-58 at a concentration of 1%.2. The average sarcomere length in the central region of the relaxed preparation was estimated by laser diffraction and set at pre-determined values within the range of 1.9-2.4 mum by adjustment of muscle length. Isometric contractions were then induced by raising the Ca(2+) concentration under carefully controlled chemical conditions.3. The dependence of Ca(2+)-activated force production on sarcomere length over the ascending limb of the length-force relation was examined at Ca(2+) concentrations giving partial and full activation of the contractile system of the muscle.4. The dependence of Ca(2+)-activated force on Ca(2+) concentration was compared at sarcomere lengths on the ascending limb and plateau of the length-force relation.5. The results obtained from both kinds of experiment showed that the sensitivity of the contractile system to Ca(2+) increases with sarcomere length over the ascending limb of the length-force relation.6. Possible explanations for this observation have been discussed.

Ultrastructure of muscle fibres in head and axial muscles of the perch (Perca fluviatilis L.). A quantitative study.

White, pink, red and deep red fibres, selected from a head muscle and from axial muscles of the perch, show significant differences in actin filament length, Z line thickness, Z line lattice space, myofibril girth, the percentages volume occupied by T system and terminal cisternae of the SR, and in the degree of T system/SR contact per sarcomere. In both muscles the degree of T system/SR contact decreases in the order: white, pink, red, deep red, which suggests a decrease of contraction velocity in the same order. The position of the T system (at the Z line or at the A/I junction) is related to the actin filament length. The actin filaments in the red fibres are appreciably longer than in the white, which suggests that the sarcomeres of the red fibres have a broader length-tension curve. The Z line thickness is positively correlated with the actin filament length and, in the white and the red fibres, negatively with the degree of sarcomere shortening. Thicker Z lines are suggested to allow greater sarcomere size (length or girth). The percentage volume occupied by mitochondria varies independently of the extent of membrane systems. The ultrastructural characteristics of the fibre types are in agreement with the functional roles as reported in literature.

The non-specific nature of the myocardial wavy fibre.

Wavy myocardial fibres were found in about half each of a series of 28 normal and 31 infarcted human hearts, as well as in the normal heart of an infant. Such fibres were also seen in rather more than half of a series of normal rat hearts. Thus, the wavy fibre is not a specific feature of acute ischaemic heart disease. Some experimental evidence was obtained that patchy loss or preservation of ATP promotes the formation of wavy fibres.

The ultrastructure of normal myogenesis in the limb of the mouse.

The ultrastructure of myogenesis in the mouse hind limb has been studied from day 12 to birth. Mononucleated cells with myofilaments are small and infrequent during myogenesis and never line myotubes. Only mononucleated cells without myofilaments cover the myotubes are involved in mass fusion. These mononucleated cells are pleomorphic and undifferentiated during early myogenesis. They have a heterochromatic nucleus and many accumulate mitochondria and lengthen during days 16-18. After day 18 they are normally elongate with a heterochromatic nucleus and packed with free ribosomes. The multinucleated cell development may be divided into four stages. 1. Immature myotube (days 14-15). Their fibrils are small, out of register and some poorly defined. Many myofilaments are not in rigid hexagonal alignment. The sarcoplasmic reticulum is simple and randomly oriented and triads are absent. Large clumps of glycogen occur between euchromatic nuclei which are in chain formation. 2. Mature myotube (days 16-18). Small groups of fibrils show alignment. Glycogen granules and sarcoplasmic reticulum become numerous between fibrils. Triads are sparse and mitochondria cluster in subsarcolemmal regions and between nuclei. 3. Young myofibers are present by day 19. More fibrils are aligned and compact. The filaments are in a rigid hexagonal array, the glycogen is dispersed and nuclei are peripherally located and moderately heterochromatic. Triads are frequent but often obliquely oriented and mitochondria are elongate and numerous between fibrils. 4. Mature myofibers occur postnatally (2 weeks).

The dependence of the latency relaxation on sarcomere length and other characteristics of isolated muscle fibres.

1. The latency relaxation has been examined in single fibres from frog striated muscle with particular attention given to its possible relation to Ca(2+) release during excitation-contraction coupling.2. Latency relaxations were recorded at 19-23 degrees C from massively stimulated (0.2 msec pulses) single fibres using two selected RCA 5734 transducer tubes in a bridge circuit.3. The depth of the latency relaxation has its full value when stimulus strength is between 40 and 400% above twitch threshold. Stronger stimuli reversibly diminish the latency relaxation.4. The variation in depth of latency relaxation with sarcomere length was found similar to that reported previously for multifibre preparations but in single fibres the peak of the curve consists of a plateau between sarcomere lengths of 2.8 mu and 3.2 mu.5. Sucrose hypertonicity increases the depth of the latency relaxation at sarcomere lengths below 2.8 mu but above this length it has either no effect or a depressant effect depending on the degree of hypertonicity.6. The maximal depth of the latency relaxation (measured at 3 mu) averaged 0.23% of the maximal tetanus tension (measured at 2.2 mu) and was strongly correlated (r = 0.87) with the latter in forty-five single fibres.7. The maximal depth of the latency relaxation is not correlated with the number of sarcomeres in series in a fibre.8. The results of this study are shown to fully support and extend Sandow's (1966) hypothesis that the latency relaxation is caused by release of activator Ca(2+) from the sarcoplasmic reticulum.