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70 - Disorders of striated muscle

from PART VIII - NEUROMUSCULAR DISORDERS

Published online by Cambridge University Press:  05 August 2016

Richard W. Orrell
Affiliation:
Department of Clinical Neurosciences, Royal Free and University College Medical School, University College London, London, UK
Robert C. Griggs
Affiliation:
Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA
Arthur K. Asbury
Affiliation:
University of Pennsylvania School of Medicine
Guy M. McKhann
Affiliation:
The Johns Hopkins University School of Medicine
W. Ian McDonald
Affiliation:
University College London
Peter J. Goadsby
Affiliation:
University College London
Justin C. McArthur
Affiliation:
The Johns Hopkins University School of Medicine
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Summary

Muscle cells develop from mesenchymal cells in the embryo. They differentiate into two distinct morphologies, striated and non-striated. Striated muscle has an organized structure, and is able to contract rapidly. This is most commonly found as skeletal muscle, but also as cardiac muscle. Non-striated muscle, or smooth muscle, is generally not under voluntary control, maintains slow contraction, and is found in organs such as blood vessel walls, gastrointestinal tract, and urinary tract. In this chapter we deal with the skeletal form of striated muscle.

The basic unit of skeletal muscle is the muscle fibre. This is a single cell, with many nuclei. The muscle fibres are arranged in fascicles. Connective tissue within the fascicle is termed endomysium, the fascicle is surrounded by perimysium, and the whole muscle is surrounded by epimysium. Individual muscle fibres are 10–60 μ diameter, but are elongated, and may extend the full length of the muscle, up to 30 cm. The cytoplasm of the muscle fibre, or sarcoplasm, is composed of longitudinal threads of myofibrils, 1 μ diameter. In longitudinal section the myofibrils are transected by striations, or Z bands, which divide the myofibril into sarcomeres, 2.5 μ long at rest, and lead to the classification as striated muscle (Williams et al., 1989).

Within the sarcomere, two types of myofilament are present. Actin (5 nm diameter) attached to the Z band, and interdigitating myosin (12 nm diameter). In contracting muscle the actin filaments slide in relation to myosin. It is the making and breaking of connections between lateral projections on the myosin, and the actin, filaments, which causes the mechanical muscle contraction.

Within the muscle fibre are organelles and enzymes to provide the high level of energy necessary for muscle contraction. These include mitochondria, lipid vacuoles, and glycogen granules. Two main physiological groups of muscle fibres are recognized: slow (Type I) and fast (Type II). Slow muscles are more red than fast, and are rich in mitochondria and oxidative enzymes, but poor in phosphorylation. Slow fibres perform aerobic metabolism, in addition to the glycolytic metabolism which predominates in fast fibres. Slow muscles are particularly suited to sustained contraction, as in postural muscles, and fast muscle to more rapid movements. Most muscles contain a mixture of the two types of fibre.

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Diseases of the Nervous System
Clinical Neuroscience and Therapeutic Principles
, pp. 1163 - 1182
Publisher: Cambridge University Press
Print publication year: 2002

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  • Disorders of striated muscle
    • By Richard W. Orrell, Department of Clinical Neurosciences, Royal Free and University College Medical School, University College London, London, UK, Robert C. Griggs, Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.071
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  • Disorders of striated muscle
    • By Richard W. Orrell, Department of Clinical Neurosciences, Royal Free and University College Medical School, University College London, London, UK, Robert C. Griggs, Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.071
Available formats
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Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

  • Disorders of striated muscle
    • By Richard W. Orrell, Department of Clinical Neurosciences, Royal Free and University College Medical School, University College London, London, UK, Robert C. Griggs, Department of Neurology, University of Rochester School of Medicine and Dentistry, Rochester, NY, USA
  • Edited by Arthur K. Asbury, University of Pennsylvania School of Medicine, Guy M. McKhann, The Johns Hopkins University School of Medicine, W. Ian McDonald, University College London, Peter J. Goadsby, University College London, Justin C. McArthur, The Johns Hopkins University School of Medicine
  • Book: Diseases of the Nervous System
  • Online publication: 05 August 2016
  • Chapter DOI: https://doi.org/10.1017/CBO9781316134993.071
Available formats
×