Abstract
The skeletal musculature comprises the largest single tissue of the body, contributing up to 40%–45% of the adult body weight and 75% of its protein mass (Goldspink et al. 1985). Clearly this means that muscle is extremely important to the organism in metabolic terms, in addition to its well recognized mechanical functions of locomotion and maintenance of posture. Like many other tissues of the body, skeletal muscle undergoes atrophy in response to the loss of functional demands. In contrast, rapid adaptive growth can be induced either by the subsequent return of these functions or by the imposition of new, greater work demands. This plasticity (Pette 1980) represents part of the overall biological economy of the body in maintaining, or withdrawing, structures according to the changing requirements of the organism. Such features are regularly observed clinically; situations of disuse producing muscle wasting and weakness, while compensatory growth of the relevant musculature is often linked to patient recovery and rehabilitation.
This work was supported by a grant from NASA-Ames No. NAG 2–272 and the Wellcome Trust to G. Goldspink, D.F. Goldspink was the recipient of a Wellcome Trust travel award
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References
Booth FW, Seider MJ (1979) Early changes in skeletal muscle protein synthesis after immobilization of rats. J Appl Physiol 47: 974–977
Buller AJ, Eccles JC, Eccles RM (1960a) Differentiation of fast and slow muscles in the cat hind limb. J Physiol (Lond) 150: 399–416
Buller AJ, Eccles JC, Eccles RM (1960b) Interactions between motor neurones and muscles in respect of the characteristic speeds of their responses. J Physiol (Lond) 150: 417–439
Costili DL, Daniels J, Evans W, Fink W, Krahenbuhl G, Saltin B (1976) Skeletal muscle enzymes and fiber composition in male and female track athletes. J Appl Physiol 40: 149–154
Cotter M, Phillips P (1985) Chronic low-frequency activation prevents immobilization atrophy in rabbit soleus muscles. J Physiol (Lond) 361: 35P
Etlinger JD, Kameyama T, Van der Westhuysen D, Erlij D, Matsumoto K (1981) spivn In: Guba F, Marechal G, Takacs O (eds) Mechanisms of muscle adaptation to functional requirements. Pergamon, New York, pp 241–253
Feller DD, Ginoza HS, Morey ER (1981) Atrophy of rat skeletal muscles in stimulated weightlessness. Physiologist 24: S9–10
Fischback GD, Robbins N (1969) Changes in contractile properties of disused soleus muscles. J Physiol 201: 305–320
Garlick PJ, McNurlan MA, Preedy VR (1980) A rapid and convenient technique for measuring the rate of protein synthesis in tissues by injection of [3H] phenylalanine. Biochem J 192: 719–723
Goldberg AL, Etlinger JD, Goldspink DF, Jablecki C (1975) Mechanism of work-induced hypertrophy of skeletal muscle. Med Sci Sports 7: 248–261
Goldspink DF (1977) The influence of immobilization and stretch on protein turnover of rat skeletal muscle. J Physiol 264: 267–282
Goldspink DF (1978) The influence of passive stretch on the growth and protein turnover of the denervated EDL muscle. Biochem J 174: 595–602
Goldspink DF (1980) The influence of contractile activity and the nerve supply on muscle size and protein turnover. In: Pette D (ed) Plasticity of muscle. Walter de Gruyter, Berlin, pp 525–539
Goldspink G, Ward PS (1979) Changes in rodent muscle fibre types during post-natal growth, undernutrition and exercise. J Physiol 296–453–469
Goldspink DF, Garlick PJ, McNurlan MA (1983) Protein turnover measured in vivo and in vitro in muscles undergoing compensatory growth and subsequent denervation atrophy. Biochem J 210: 89–98
Goldspink DF, Lewis SEM, Kelly FJ (1985) Protein turnover and cathepsin B activity in several individual tissues of foetal and senescent rats. Comp Biochem Physiol 82: 849–853
Gutmann E (ed) (1962) The denervated muscle. Czechoslovakian Academy of Science, Prague
Hnik P, Vejsada R, Goldspink, DF, Kasicki S, Krekule I (1985) Quantitative evaluation of EMG activity in rat extensor and flexor muscles immobilized at different lengths. Exp Neurol 88: 515–528
Holly RG, Barnett JG, Ashmore CR, Taylor RG, Mole PA (1980) Stretch-induced growth in chicken wing muscles: a new model of stretch hypertrophy. Am J Physiol 238: C62–C71
Ianuzzo D, Patel P, Chen V, O’Brien P, Williams C (1977) Thyroidal trophic influence on skeletal muscle myosin. Nature 270: 74–76
Lewis SEM, Kelly FJ, Goldspink DF (1984) Pre- and post-natal growth and protein turnover in smooth muscle. heart and slow- and fast-twitch skeletal muscles of the rat. Biochem J 217: 517–526
Morey ER, Baylink DJ (1978) Inhibition of bone formation during space flight. Science 201: 1138–1141
Musacchia XJ, Deavers DR, Meininger GA, Davis TP (1980) A model for hypokinesia: effects on muscle atrophy in the rat. J Appl Physiol 48: 479–486
Palmer RM, Reeds PJ, Atkinson T, Smith RH (1983) The influence of changes in tension on protein synthesis and prostaglandin release in isolated rabbit muscles. Biochem J 214: 1011–1014
Pette D (ed) (1980) Plasticity of muscle. Walter de Gruyter, Berlin
Pette D (1984) Activity-induced fast to slow transitions in mammalian muscle. Med Sci Sports Exerc 16: 517–528
Rodemann HP, Goldberg AL (1982) Arachidonic acid, prostaglandin E2 and F2α influence rates of protein turnover in skeletal and cardiac muscle. J Biol Chem 257: 1632–1638
Salmons S, Henriksson J (1981) The adaptive response of skeletal muscle to increased use. Muscle Nerve 4: 94–105
Salmons S, Vrbová G (1969) The influence of activity on some contractile characteristics of mammalian fast and slow muscles. J Physiol (Lond) 210: 535–549
Waterlow JC, Garlick PJ, Millward DJ (eds) (1978) The effects of nutrition and hormones on protein turnover in muscle. In: Protein turnover in mammalian tissues and in the whole body. North-Holland, Amsterdam, pp 625–696
Watson PA, Stein JP, Booth FW (1984) Changes in actin synthesis and actin-mRNA content in rat muscle during immobilization. Am J Physiol 247: C39–C44
Watt PW, Kelly FJ, Goldspink DF, Goldspink G (1982) Exercise-induced morphological and biochemical changes in skeletal muscles of the rat. J Appl Physiol 53: 1144–1151
Williams PE, Goldspink G (1973) The effect of immobilization on the longitudinal growth of striated muscle. J Anat 116: 45–55
Young A, Hughes I, Round JM, Edwards RHT (1982) The effect of knee injury on the number of muscle fibres in the human quadriceps femoris. Clin Sci 62: 227–234
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© 1986 Springer-Verlag Berlin Heidelberg
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Goldspink, D.F., Goldspink, G. (1986). The Role of Passive Stretch in Retarding Muscle Atrophy. In: Nix, W.A., Vrbová, G. (eds) Electrical Stimulation and Neuromuscular Disorders. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-71337-8_10
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