Skip to main content
The Journal of General Physiology logoLink to The Journal of General Physiology
. 1961 Jan 1;44(3):487–498. doi: 10.1085/jgp.44.3.487

Quantitative Studies of White Matter

I. Enzymes involved in glucose-6-phosphate metabolism

D B McDougal Jr 1, DW Schulz 1, JV Passonneau 1, J R Clark 1, M A Reynolds 1, O H Lowry 1
PMCID: PMC2195104  PMID: 19873533

Abstract

Total lipid and six enzymes closely related to the metabolism of glucose-6-phosphate have been measured in ten tracts of the rabbit. Lipid content appears to be a valid indicator of the degree of myelination. Heavily myelinated tracts have much larger amounts of glucose-6-phosphate dehydrogenase than lightly myelinated ones but there is no corresponding difference in 6-phosphogluconate dehydrogenase. In fact the ratios between the two enzymes were found to vary over a ninefold range. Hexokinase is found in largest amounts in tracts with relatively little lipid, and this tends to be true for phosphofructokinase as well. The fibrillar layer of olfactory bulb is exceptional with regard to both enzymes, and to glucose-6-phosphate dehydrogenase. The enzymes are present in amounts which are more than adequate to support glucose metabolism at a rate commensurate with the known rates of O2 uptake by various tracts. The distribution of some of the enzymes is compatible with the notion that the nodes of Ranvier are regions of high metabolic activity. A simple algebraic relationship is found to hold fairly well for the distribution of four of the enzymes among the tracts.

Full Text

The Full Text of this article is available as a PDF (748.0 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ARDUINI A., WHITLOCK D. G. Spike discharges in pyramidal system during recruitment waves. J Neurophysiol. 1953 Jul;16(4):430–436. doi: 10.1152/jn.1953.16.4.430. [DOI] [PubMed] [Google Scholar]
  2. BISHOP G. H., CLARE M. H. Organization and distribution of fibers in the optic tract of the cat. J Comp Neurol. 1955 Oct;103(2):269–304. doi: 10.1002/cne.901030204. [DOI] [PubMed] [Google Scholar]
  3. BISHOP P. O., JEREMY D., LANCE J. W. Properties of pyramidal tract. J Neurophysiol. 1953 Sep;16(5):537–550. doi: 10.1152/jn.1953.16.5.537. [DOI] [PubMed] [Google Scholar]
  4. BISHOP P. O., JEREMY D., LANCE J. W. The optic nerve; properties of a central tract. J Physiol. 1953 Aug;121(2):415–432. doi: 10.1113/jphysiol.1953.sp004955. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. BOLLARD B. M., McILWAIN H. Metabolism and metabolic response to electrical pulses in white matter from the central nervous system. Biochem J. 1957 Aug;66(4):651–655. doi: 10.1042/bj0660651. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. BUELL M. V., LOWRY O. H., ROBERTS N. R., CHANG M. L., KAPPHAHN J. I. The quantitative histochemistry of the brain. V. Enzymes of glucose metabolism. J Biol Chem. 1958 Jun;232(2):979–993. [PubMed] [Google Scholar]
  7. CARPENTER F. G. Resting metabolism of immature nerve fibers in the developing chick. Am J Physiol. 1958 Oct;195(1):33–37. doi: 10.1152/ajplegacy.1958.195.1.33. [DOI] [PubMed] [Google Scholar]
  8. EISENMAN G., RUDIN D. O. Further studies on the functional properties of spinal axons in vivo. J Gen Physiol. 1954 Mar;37(4):495–503. doi: 10.1085/jgp.37.4.495. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. GASSER H. S. Olfactory nerve fibers. J Gen Physiol. 1956 Mar 20;39(4):473–496. doi: 10.1085/jgp.39.4.473. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. HESS A., YOUNG J. Z. Correlation of internodal length and fibre diameter in the central nervous system. Nature. 1949 Sep 17;164(4168):490–490. doi: 10.1038/164490a0. [DOI] [PubMed] [Google Scholar]
  11. LAPORTE Y., LUNDBERG A., OSCARSSON O. Functional organization of the dorsal spino-cerebellar tract in the cat. I. Recording of mass discharge in dissected Flechsig's fasciculus. Acta Physiol Scand. 1956 Mar 24;36(1-2):175–187. doi: 10.1111/j.1748-1716.1956.tb01316.x. [DOI] [PubMed] [Google Scholar]
  12. LLOYD D. P. C., McINTYRE A. K. Dorsal column conduction of group I muscle afferent impulses and their relay through Clarke's column. J Neurophysiol. 1950 Jan;13(1):39–54. doi: 10.1152/jn.1950.13.1.39. [DOI] [PubMed] [Google Scholar]
  13. LOWRY O. H., ROBERTS N. R., KAPPHAHN J. I. The fluorometric measurement of pyridine nucleotides. J Biol Chem. 1957 Feb;224(2):1047–1064. [PubMed] [Google Scholar]
  14. LOWRY O. H., ROBERTS N. R., LEWIS C. The quantitative histochemistry of the retina. J Biol Chem. 1956 Jun;220(2):879–892. [PubMed] [Google Scholar]
  15. LOWRY O. H. The quantitative histochemistry of the brain; histological sampling. J Histochem Cytochem. 1953 Nov;1(6):420–428. doi: 10.1177/1.6.420. [DOI] [PubMed] [Google Scholar]
  16. ROBINS E., ROBERTS N. R., EYDT K. M., LOWRY O. H., SMITH D. E. Microdetermination of alpha-keto acids with special reference to malic, lactic, and glutamic dehydrogenases in brain. J Biol Chem. 1956 Feb;218(2):897–909. [PubMed] [Google Scholar]
  17. RUDIN D. O., EISENMAN G. The action potential of spinal axons in vitro. J Gen Physiol. 1954 Mar;37(4):505–538. doi: 10.1085/jgp.37.4.505. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. STROMINGER J. L., LOWRY O. H. The quantitative histochemistry of brain. IV. Lactic, malic, and glutamic dehydrogenases. J Biol Chem. 1955 Apr;213(2):635–646. [PubMed] [Google Scholar]
  19. UMAR K., WANG G. H. Autonomic function of some small fibers in corticospinal tract of cat. J Neurophysiol. 1960 May;23:315–320. doi: 10.1152/jn.1960.23.3.315. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of General Physiology are provided here courtesy of The Rockefeller University Press

RESOURCES