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. 1958 Mar 31;107(4):475–496. doi: 10.1084/jem.107.4.475

A BIOCHEMICAL AND MORPHOLOGIC STUDY OF MYELINATION AND DEMYELINATION

I. LIPIDE BIOSYNTHESIS IN VITRO BY NORMAL NERVOUS TISSUE

Guido Majno 1, Manfred L Karnovsky 1
PMCID: PMC2136842  PMID: 13513913

Abstract

Samples of normal grey matter, white matter, and peripheral nerves obtained from rats were incubated in Warburg vessels with glucose and a labelled lipide precursor (acetate, phosphate, choline, glycerol, glucose). The total lipides were then extracted and their radioactivity measured. The preparations were compared with respect to dry weight, lipide content, O2 uptake, and ability to incorporate the various substrates into the lipides. Grey matter was found to be the least damaged by incubation, white matter the most. Damage to the tissue depressed lipogenesis to a greater extent than respiration. Five substrates were compared with respect to their degree of incorporation into the lipides of the various preparations. White matter, which had a greater oxygen uptake than peripheral nerves, showed the lowest degree of incorporation for most of the substrates studied. The results suggest that there are considerable quantitative differences in the metabolism of central and peripheral myelin. In the sciatic preparations, oxygen uptake and lipogenesis from acetate were found to decrease from the proximal to the distal end of the nerve. This finding may be relevant to the pathogenesis of peripheral neuropathies. The growth and metabolic activity of peripheral nerves were studied in rats aged 1 to 500 days, and the biochemical and histological findings were correlated. The results indicated that the lipogenetic activity of the Schwann cell was lowest in the newborn animal, and reached its peak at about 20 days. Comparative data were also obtained from the cerebral cortex. The growth pattern of peripheral nerves was distinctly different from that of the brain. With respect to changes in tissue weight, respiration, and lipogenesis, growing peripheral nerve correlated with body weight, while the brain matured much more rapidly.

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Selected References

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  1. BARROWS C. H., Jr Cellular metabolism and aging. Fed Proc. 1956 Sep;15(3):954–959. [PubMed] [Google Scholar]
  2. BEN GEREN B. The formation from the Schwann cell surface of myelin in the peripheral nerves of chick embryos. Exp Cell Res. 1954 Nov;7(2):558–562. doi: 10.1016/s0014-4827(54)80098-x. [DOI] [PubMed] [Google Scholar]
  3. DAWSON R. M. Studies on the labelling of brain phospholipids with radioactive phosphorus. Biochem J. 1954 Jun;57(2):237–245. doi: 10.1042/bj0570237. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. DAWSON R. M. The incorporation of labelled phosphate into the lipids of a brain dispersion. Biochem J. 1953 Oct;55(3):507–517. doi: 10.1042/bj0550507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. FINEAN J. B., HAWTHORNE J. N., PATTERSON J. D. Structural and chemical differences between optic and sciatic nerve myelins. J Neurochem. 1957;1(3):256–259. doi: 10.1111/j.1471-4159.1957.tb12080.x. [DOI] [PubMed] [Google Scholar]
  6. FOLCH J., ASCOLI I., LEES M., MEATH J. A., LeBARON N. Preparation of lipide extracts from brain tissue. J Biol Chem. 1951 Aug;191(2):833–841. [PubMed] [Google Scholar]
  7. FOLCH J., LEES M., SLOANE STANLEY G. H. A simple method for the isolation and purification of total lipides from animal tissues. J Biol Chem. 1957 May;226(1):497–509. [PubMed] [Google Scholar]
  8. GIDEZ L. I., KARNOVSKY M. L. The metabolism of C14-glycerol in the intact rat. J Biol Chem. 1954 Jan;206(1):229–242. [PubMed] [Google Scholar]
  9. HOKIN L. E., HOKIN M. R. Effects of acetylcholine on the turnover of phosphoryl units in individual phospholipids of pancreas slices and brain cortex slices. Biochim Biophys Acta. 1955 Sep;18(1):102–110. doi: 10.1016/0006-3002(55)90013-5. [DOI] [PubMed] [Google Scholar]
  10. Holmes E. G. Oxidations in central and peripheral nervous tissue. Biochem J. 1930;24(4):914–925. doi: 10.1042/bj0240914. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. KREBS H. A. Body size and tissue respiration. Biochim Biophys Acta. 1950 Jan;4(1-3):249–269. doi: 10.1016/0006-3002(50)90032-1. [DOI] [PubMed] [Google Scholar]
  12. KREBS H. A., JOHNSON W. A. Cell metabolism. Tabulae Biol. 1948;19(3):100–235. [PubMed] [Google Scholar]
  13. MAJNO G., BUNKER W. E. Preparation of tissue slices for metabolic studies: a hand-microtome especially suitable for brain. J Neurochem. 1957;2(1):11–14. doi: 10.1111/j.1471-4159.1957.tb12347.x. [DOI] [PubMed] [Google Scholar]
  14. NOBACK C. R. Metachromasia in the nervous system. J Neuropathol Exp Neurol. 1954 Jan;13(1):161–167. doi: 10.1097/00005072-195401000-00012. [DOI] [PubMed] [Google Scholar]
  15. RUDIN D. O., EISENMAN G. A method for dissection and electrical study in vitro of mammalian central nervous tissue. Science. 1951 Sep 21;114(2960):300–302. doi: 10.1126/science.114.2960.300-a. [DOI] [PubMed] [Google Scholar]
  16. Robinson C. V. Windowless, Flow Type, Proportional Counter for Counting C14. Science. 1950 Aug 18;112(2903):198–199. doi: 10.1126/science.112.2903.198. [DOI] [PubMed] [Google Scholar]
  17. SPERRY W. M., WAELSCH H. The chemistry of myelination and demyelination. Res Publ Assoc Res Nerv Ment Dis. 1950;28:255–267. [PubMed] [Google Scholar]
  18. STRICKLAND K. P. Factors affecting the incorporation of radioactive phosphate into the phospholipids of the slices of cat brain. Can J Biochem Physiol. 1954 Jan;32(1):50–59. [PubMed] [Google Scholar]
  19. VON BERTALANFFY L., PIROZYNSKI W. J. Tissue respiration and body size. Science. 1951 May 25;113(2943):599–600. doi: 10.1126/science.113.2943.599. [DOI] [PubMed] [Google Scholar]
  20. Vizoso A. D., Young J. Z. Internode length and fibre diameter in developing and regenerating nerves. J Anat. 1948 Apr;82(Pt 1-2):110–134.1. [PMC free article] [PubMed] [Google Scholar]
  21. WAGMAN I. H., LESSE H. Maximum conduction velocities of motor fibers of ulnar nerve in human subjects of various ages and sizes. J Neurophysiol. 1952 May;15(3):235–244. doi: 10.1152/jn.1952.15.3.235. [DOI] [PubMed] [Google Scholar]

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