Skip to main content

Abstract

The differentiation of muscle into red and white types is a feature of all vertebrates and, indeed, of chordates. Red muscles are slow-contracting and specialized for postural activity. They contain plentiful lipid droplets and glycogen granules and sparse mitochondria. White muscles, on the other hand, are faster contracting, suitable for short bursts of intense activity, but fatigue rapidly. They contain few lipid droplets, but plentiful mitochondria. In man these fibre types are not found exclusively in individual muscles but occur in a random distribution in all muscles. Although these two types of muscle fibre can be recognized in haematoxylin and eosin preparations of transverse sections of paraffin-embedded muscle, they can be more easily identified by the reciprocal relationship of their content of oxidative and non-oxidative enzymes (see Table 2.3). The red fibres react strongly for oxidative enzymes, e.g. succinic dehydrogenase, and are designated Type 1 fibres, and the white fibres react strongly for non-oxidative enzymes, e.g. myophosphorylase, and are designated Type 2 fibres (Dubowitz and Pearse, 1960). In cross section these two fibre types are arranged in a random mosaic pattern within muscle fascicles.

This is a preview of subscription content, log in via an institution to check access.

Access this chapter

Chapter
USD 29.95
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
eBook
USD 129.00
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 109.99
Price excludes VAT (USA)
  • Compact, lightweight edition
  • Dispatched in 3 to 5 business days
  • Free shipping worldwide - see info

Tax calculation will be finalised at checkout

Purchases are for personal use only

Institutional subscriptions

Preview

Unable to display preview. Download preview PDF.

Unable to display preview. Download preview PDF.

References

  • Brandstater, M. E. and Lambert, E. H. (1973), Motor unit anatomy. In New Developments in Electromyography and Clinical Neurophysiology, Vol. 1 (ed. J. E. Desmedt ), Karger, Basel, pp. 14–22.

    Google Scholar 

  • Dubowitz, V. and Pearse, A. G. E. (1960), Reciprocal relationship of phosphorylase and oxidative enzymes in skeletal muscle. Nature, 185, 701.

    Article  CAS  PubMed  Google Scholar 

  • Edstrom, L. and Kugelberg, E. (1968), Histochemical composition, distribution of fibres and fatiguability of single motor units. J. Neurol. Neurosurg. Psychiatry, 31, 424–33.

    Article  CAS  PubMed  Google Scholar 

  • Engel, W. K. (1967), Focal myopathic changes produced by electromyographic and hypodermic needles. Arch. Neurol., 16, 509–13.

    Article  CAS  PubMed  Google Scholar 

  • Swash, M. and Schwartz, M. S. (1981), Neuromuscular Diseases: A Practical Approach to Diagnosis, Springer-Verlag, Berlin, Heidelberg and New York.

    Google Scholar 

  • Walton, J. N. and Gardner-Medwin, D. (1981), Classification of neuromuscular disease In Disorders of Voluntary Muscle, 4th edn (ed. J. N. Walton), Churchill-Livingstone, Edinburgh.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

Copyright information

© 1984 M. Swash and M. S. Schwartz

About this chapter

Cite this chapter

Swash, M., Schwartz, M.S. (1984). Introduction. In: Biopsy Pathology of Muscle. Biopsy Pathology Series. Springer, Boston, MA. https://doi.org/10.1007/978-1-4899-3402-4_1

Download citation

  • DOI: https://doi.org/10.1007/978-1-4899-3402-4_1

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-0-412-24420-9

  • Online ISBN: 978-1-4899-3402-4

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics