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Fatigue during dynamic muscle contractions in male sprinters and marathon runners: relationships between performance, electromyographic activity, muscle cross-sectional area and morphology.

Knee extensor fatigue and endurance during repeated maximum isokinetic manoeuvres were studied in five sprinters and five marathon runners, all males. Fatigue and endurance were expressed in terms of output (contractional work, CW) and input (integrated electromyograms, iEMG), and was related to muscle fibre composition of m. vastus lateralis and to cross-sectional area (CSA) of m. quadriceps. The initially performed contractional work was positively related to the calculated absolute type II fibre area of m. vastus lateralis, but not to the cross-sectional area of m. quadriceps. During the first 25 contractions, sprinters fatigued, with a slope of decline in contractional work that was correlated to the absolute type II fibre area, also after correction of performed work for CSA of m. quadriceps. As the electromyographic activity decreased less than the contractional work, a drastic fall in the CW/iEMG ratio was found in the sprinter group. Three out of five sprinters could perform less than 50 knee extensions, due to subjective discomfort in tested thighs. In contrast, all marathon runners could, after a minor similar decline in electromyographic activity and contractional work during the first part of the experiment, maintain a steady-state endurance level of CW and iEMG throughout the test (200 knee extensions). In conclusion, fatigue during isokinetic maximal knee extensions is closely related to the muscle structure of m. vastus lateralis.

Adult↗

The pharmacology of clodanolene sodium, a new skeletal muscle contraction antagonist.

The pharmacology of hydrated 1 less than ([5-(3,4-dichlorophenyl)-2-furanyl]methylene) amino greater than-2,4,-imidazolidinedione sodium salt (clodanolene sodium), as skeletal-muscle contraction antagonist, is presented. Clodanolene sodium is remarkable in that it has no measurable direct effect on the peripheral or central nervous systmes. Skeletal muscle relaxation can be achieved with this drug at doses that do not affect motor coordination. Rats receiving clodanolene sodium for up to 30 days evidenced a downward trend in gross observation score of skeletal muscle relaxation, but the extent of twitch inhibition was the same on day 30 as on day 1. In an animal model of muscle spasticity (Straub-tail mouse), clodanolene sodium has been shown to be more efficacious for induction of skeletal muscle relaxation than neuromuscular blocking agents, local anesthetics, or centrally-acting muscle relaxants. Clodanolene sodium's mode of action has been identified as specific for skeletal muscle. It has no measurable effect on neuromuscular transmission or on the electrically excitable surface membrane. Indirect evidence indicates that the site of action of clodanolene sodium, like that of dantrolene sodium, is within the muscle cell and is related to caffeine-sensitive calcium stores. Its skeletal-muscle relaxant activity, we suggest results from a decrease in the release of calcium from the sarcoplasmic reticulum.

Administration, Oral↗

Temperature effects on mammalian muscle contraction.

Effects of temperature (range 37 degrees C to 8 degrees C) on isometric twitch and tetanic tensions of mammalian (rat) fast and slow muscles are re-examined. The twitch tension of a fast muscle increased in cooling it 20 degrees C but decreased on further cooling, whereas that of a slow muscle decreased monotonically with cooling. The cooling-potentiation in the fast muscle was evident within a week after birth but the cooling-depression in the slow muscle was not established until about the fourth week. The maximal tetanic tension in either muscle, and at all ages, decreased 10-20% in cooling to 25 degrees C but decreased more markedly in cooling below 20 degrees C; the tension at 10 degrees C was 40-50% of that at 35 degrees C. Preliminary observations made on fast muscle showed that the apparent stiffness/tension ratio was higher at low temperatures. It is postulated that the cooling depression of tetanic tension in mammalian muscle may be due to a direct effect on cross-bridges, whereas twitch tension variation may represent a net outcome of the same effect and the cooling-increase in the calcium sensitivity of myofibrillar activation.

Animals↗