Abstract
Bilateral transection was performed on rat sciatics. At varying intervals after the operation, samples of nerve were taken both distal and proximal to the level of transection, as well as from the tissue which bridged the gap between the stumps. These samples were incubated in Warburg flasks, with glucose and a labelled lipide precursor (acetate or phosphate). The total lipides were then extracted and their radioactivity was measured. Normal rat sciatics served as controls, and the biochemical and histological findings were correlated. In the distal portion undergoing Wallerian degeneration, the lipide content began to fall before any removal of myelin could be detected histologically. It is suggested that there is a period of "non-cellular removal" prior to the physical breakdown of the myelin. Changes in respiration and in lipogenesis from acetate followed a triphasic course, and agreed with the histological findings in that after a period of predominantly passive changes (approximately 1 to 3 days) there follows a period of cellular reaction (4 to 50 days) and a period of atrophy (from 50 days onward). The incorporation of phosphate into the lipides was increased at all stages examined, even as early as 22 hours after section. This increased P(32) incorporation could not be reproduced in nerves allowed to degenerate in vitro. It is suggested that the hypertrophying Schwann cells synthesize some lipide moieties at a considerably faster rate than others. Proximal to the level of transection, lipogenesis from acetate was depressed, for as long as 32 days postoperatively. It appears, therefore, that the maintenance of the myelin sheath is impaired also above the level of transection. In the "union tissue" which developed between the stumps, prior to the appearance of histologically visible myelin, lipogenesis was low; later it rose above levels for normal nerve. This pattern of lipogenesis in regenerating nerve is similar to that found in growing nerves.
Keywords
LIPIDS/metabolism
NERVES/metabolism
MeSH Terms
Adipogenesis
Animals
Demyelinating Diseases
Homeostasis
In Vitro Techniques
Lipid Metabolism
Lipids
Lipogenesis
Myelin Sheath
Nerve Regeneration
Rats
Schwann Cells
Sciatic Nerve
Synaptic Transmission
Authors & Affiliations
2 authors, click to expand affiliations / ORCID
MAJNO G
KARNOVSKY M L
References (25)
25 references, click to expand
-
[Increased capacity of phospholipid synthesis in the stump of amputated peripheral nerve; in vitro study with P32].
Boll Soc Ital Biol Sper. 1955 Jan-Feb;31(1-2):29-31
PMID: 13239792
-
Axon sprouting partially deneurotized nerves.
Brain. 1955;78(4):661-8
PMID: 13293274
-
The nucleic acid content of peripheral nerve in degeneration and activity.
Proc R Soc Lond B Biol Sci. 1956 Mar 13;144(917):520-7
PMID: 13310577
-
Myelin sheath during degeneration and regeneration. II. Histochemistry.
J Comp Neurol. 1956 Sep;105(2):333-53
PMID: 13385378
-
Changes in phosphatase activity following transection of the sciatic nerve.
J Histochem Cytochem. 1957 Jan;5(1):15-27
PMID: 13416564
-
A biochemical and morphologic study of myelination and demyelination. I. Lipide biosynthesis in vitro by normal nervous tissue.
J Exp Med. 1958 Apr 1;107(4):475-96
PMID: 13513913
-
On the changes in ali-esterase and pseudocholinesterase activity of chicken sciatic nerve during Wallerian degeneration and their correlation with cellular proliferation.
Q J Exp Physiol Cogn Med Sci. 1955 Jan;40(1):12-23
PMID: 14371986
-
Chemical studies of peripheral nerve during Wallerian degeneration; lipids after nerve crush (axonotmesis).
Biochem J. 1950 Sep;47(3):318-23
PMID: 14800886
-
Distribution exchange and migration of phosphate compounds in the nervous system.
Am J Physiol. 1951 Jan;164(1):1-15
PMID: 14810893
-
[Micro chemical studies of the amino acids of healthy and degenerate nerves].
Bull Soc Chim Biol (Paris). 1951;33(3-4):253-7
PMID: 14935591
-
Wallerian degeneration in the rat; a chemical study.
Can J Med Sci. 1952 Jun;30(3):173-9
PMID: 14945008
-
Chemistry of wallerian degeneration; a review of recent studies.
Arch Neurol Psychiatry. 1950 Jul;64(1):105-21
PMID: 15426456
-
The disposition of radioactive phosphorus in normal, as compared with regenerating and degenerating nervous tissue.
J Cell Physiol. 1950 Apr;35(2):155-77
PMID: 15428509
-
Recovery of fibre numbers and diameters in the regeneration of peripheral nerves.
J Physiol. 1943 Mar 25;101(4):489-518
PMID: 16991581
-
Conduction velocity and myelin thickness in regenerating nerve fibres.
J Physiol. 1946 Sep 18;105(2):152-74
PMID: 16991715
-
Quantitative histology of Wallerian degeneration: I. Nuclear population in rabbit sciatic nerve.
J Anat. 1946 Jan;80(Pt 1):37-50
PMID: 17104988
-
Internode length and fibre diameter in developing and regenerating nerves.
J Anat. 1948 Apr;82(Pt 1-2):110-134.1
PMID: 17105043
-
Quantitative histology of Wallerian degeneration: II. Nuclear population in two nerves of different fibre spectrum.
J Anat. 1948 Jul;82(Pt 3):135-45
PMID: 17105053
-
Experimental and Spontaneous Schwannomas (Peripheral Gliomas): I. Experimental Schwannomas.
Am J Pathol. 1932 Jul;8(4):367-388.1
PMID: 19970026
-
Histochemical studies of the myelin sheath and its fragmentation products during Wallerian (secondary) degeneration. I. Lipids.
J Comp Neurol. 1952 Oct;97(2):211-39
PMID: 12999990
-
Chemical studies of peripheral nerve during wallerian degeneration. V. B-Glucuronidase.
Biochem J. 1952 Dec;52(4):659-63
PMID: 13018297
-
Protein-bound phosphorus compounds in the proximal stump of peripheral nerve after nerve section or after nerve crush.
Can J Med Sci. 1952 Dec;30(6):457-62
PMID: 13019641
-
Cellular proliferation in the proximal segment of a sectioned or crushed peripheral nerve.
J Anat. 1953 Oct;87(4):419-22
PMID: 13117759
-
Chemical studies of peripheral nerve during wallerian degeneration. VI. Incorporation of radioactive phosphate into pentosenucleic acid and phospholipin in vitro.
Biochem J. 1954 Oct;58(2):243-9
PMID: 13208580
-
Some relationships between action potential, oxygen consumption and coenzyme content in degenerating peripheral axons.
J Cell Physiol. 1954 Dec;44(3):395-420
PMID: 13233292