Skeletal muscle fiber splitting with weight-lifting exercise in rats.

Adult male albino rats were assigned randomly to control (CON) and weight-lifting (WL) groups. The WL rats were subjected to a progressive weight-lifting program against high resistance for 8 weeks. During the last 2 weeks, each WL rat lifted a load equal to 130% of its body weight. The mean weight of the adductor longus muscle was significantly increased in the WL group ( p < 0.05). This increased muscle weight was shown to be due to an increase in the number of fibers per unit cross-sectional area ( p < 0.05), and the mean sizes of both fast-twitch oxidative glycolytic and slow-twitch oxidative fibers were significantly smaller in the WL rats than in the CON rats (p < 0.05). Light and electron microscopic examination showed that five out of eight WL rats exhibited longitudinally split muscle fibers, while only one CON rat had a few centrally placed nuclei. The splitting process appeared as either a "pinching-off" of a small segment from the parent fiber or an invagination of the sarcolemma deep into the muscle fiber in a plane parallel to the sarcomeres. There were preliminary indications that this work-induced fiber-splitting process may be a physiological adaptation of muscle to the stress of exercise.

Effects of an anabolic steroid and sprint training on selected histochemical and morphological observations in rat skeletal muscle types.

The effects on selected histochemical and morphological parameters of anabolic steroid administration and of high-intensity sprint running, separately, and in combination, were studied in young adult male rats. Dianabol (methandrostenolone) 1 mg/day for 8 weeks had no significant effects on phosphorylase or glycogen staining intensities and on fiber area in skeletal muscles of either trained or sedentary animals. The program of sprint training resulted in significantly decreased intensities of phosphorylase in all ten regions of the gastrocnemius, plantaris, and soleus muscles that were studied. Glycogen localization was significantly increased with training in five regions of the gastrocnemius and plantaris muscles which contained predominantly fast-switch fibers. No changes in fiber area occurred with the training program. We conclude from these results that (a) normal androgen levels in young, healthy male animals are sufficiently high so that the intake of large doses of anabolic steroid does not result in the stimulation of glycogen metabolism or hypertrophy of skeletal muscle; (b) the changes induced by high-intensity, short-duration sprint training suggest that the existing glycolytic capacity of muscle is adequate to supply the muscles energy needs even during the stress of very strenous exercise, and that more fast-twitch fibers were recruited by the exercise regimen than slow-twitch fibers.

Skeletal muscle function and structure after depletion of creatine.

Experiments were conducted to determine if normal skeletal muscle function and structure are dependent upon their ability to store large quantities of metabolic energy in the form of N-phosphorylcreatine. Muscle levels of creatine and N-phosphorylcreatine were reduced by feeding young male rats diets containing 1 per cent beta-guanidinopropionic acid (beta-GPA). Muscle function was evaluated by monitoring performance during a 4-week, short duration, high intensity exercise program in a control running wheel. Structural effects were determined by histochemistry, morphometric analysis, and routine histologic procedures using light microscopy. Evidence of abnormal creatine metabolism of rats fed beta-GPA included: excessive creatinuria, reduction in urine creatinine, reduced levels of muscle and brain creatine, and a reduced activity of muscle creatine kinase. In separate experiments, beta-GPA inhibited the reaction of creatine with creatine kinase in vitro. When muscle function was evaluated by running, the percentage of expected revolutions for the group of rats fed beta-GPA was below the expected normal values. The white (type II) fibers from the gastrocnemius of exercised rats fed beta-GPA were smaller than fibers from the same muscle areas of rats fed normal diets. The histochemical characteristics of red (type I) and white fibers of all rats tested were within normal limits. It is concluded that feeding beta-GPA will result in structural and functional changes in skeletal muscles of exercised young male rats. These changes are believed to result from the ability of beta-GPA to block creatine entry into muscle and thereby prevent muscle from accumulating and maintaining its normal complement of creatine and N-phosphorylcreatine.