Skip to main content

Part of the book series: Advances in Experimental Medicine and Biology ((AEMB,volume 72))

Abstract

A number of hypotheses have been proposed for the etiology of muscular dystrophy(1). Of these, in recent years, the neurogenic hypothesis has been widely used to describe the biochemical lesion of genetically linked muscular dystrophy of some human and animal diseases.

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 39.99
Price excludes VAT (USA)
  • Available as PDF
  • Read on any device
  • Instant download
  • Own it forever
Softcover Book
USD 54.99
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

  1. O. Appenzeller, and G. Ogin, Pathogenesis of muscular dystrophies. Sympathetic neurovascular components. Arch. Neurol. 32: 2–4 (1975).

    Article  Google Scholar 

  2. J. Folch, M. Lees, and G.H.S. Stanley, A simple method for the isolation and purification of total lipids from animal tissues, J. Biol. Chem. 226: 497–509 (1957).

    Google Scholar 

  3. J.J. Kabara, Brain cholesterol: V. Effect of hereditary dystrophia muscularis on acetate incorporation, Texas Rept. Biol. Med. 22: 126–133 (1964).

    Google Scholar 

  4. Y. Komiya, and L. Austin, Axoplasmic flow of protein in the sciatic nerve of normal and dystrophic mice, Exp. Neurol. 43: 1–12 (1974).

    Article  Google Scholar 

  5. J.L. Rabinowitz, Enzymic studies on dystrophic mice and their littermates (lipogenesis and cholesterolgenesis), Biochim. Biophys. Acta. 43: 337–338 (1960).

    Article  Google Scholar 

  6. R.K. Raheja, C. Kaur, A. Singh, and I.S. Bhatia, New colorimetric method for the quantitative estimation of phospholipids without acid digestion, J. Lipid Res. 14 695–697 (1973).

    Google Scholar 

  7. S.B. Rodan, R.L. Hintz, R.I. Shaafi, and G.A. Rodan, The activity of membrane bound enzymes in muscular dystrophic chicks. Nature 252: 589–591 (1974).

    Article  Google Scholar 

  8. R. Tanaka, A.J. Hudson, J. Jato-Rodriguez, C.H. Lin, and K.P. Strickland, The in vivo incorporation of labelled acetate into the cholesterol and fatty acids of tissues of dystrophic mice, Exp. Mol. Pathol. 11: 8–16 (1969).

    Article  Google Scholar 

  9. B.Y. Tang, Y. Komiya, and L. Austin, Axoplasmie flow of phospholipids and cholesterol in the sciatic nerve of normal and dystrophic mice, Exp. Neurol. 43: 13–20 (1974).

    Article  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Editor information

Editors and Affiliations

Rights and permissions

Reprints and permissions

Copyright information

© 1976 Plenum Press, New York

About this chapter

Cite this chapter

Austin, L., Kwok, C.T., Kuffer, A.D., Tang, B.Y. (1976). Phospholipid Metabolism in Murine Muscular Dystrophy. In: Porcellati, G., Amaducci, L., Galli, C. (eds) Function and Metabolism of Phospholipids in the Central and Peripheral Nervous Systems. Advances in Experimental Medicine and Biology, vol 72. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-0955-0_30

Download citation

  • DOI: https://doi.org/10.1007/978-1-4684-0955-0_30

  • Publisher Name: Springer, Boston, MA

  • Print ISBN: 978-1-4684-0957-4

  • Online ISBN: 978-1-4684-0955-0

  • eBook Packages: Springer Book Archive

Publish with us

Policies and ethics