Ultrastructural studies of the dying-back process

III. The evolution of experimental peripheral giant axonal Degeneration

Peter S. Spencer, Herbert H. Schaumburg

Research output: Contribution to journalArticle

237 Citations (Scopus)

Abstract

The spatio-temporal evolution of peripheral giant axonal degeneration has been studied in rats during the development of concurrent peripheral (PNS) and central (CNS) nervous system dying-back disease after chronic intoxication with the neurotoxic hexacarbons re-hexane (CH<inf>3</inf>COCH<inf>2</inf>CH<inf>2</inf>CH<inf>2</inf>CH<inf>3</inf>,), methyl n-butyl ketone (MBK) (CH<inf>3</inf>COCH<inf>2</inf>CH<inf>2</inf>CH<inf>2</inf>CH<inf>3</inf>), or 2,5-hexanedione (CH<inf>3</inf>COCH<inf>2</inf>CH<inf>2</inf>COCH<inf>3</inf>), a neurotoxic metabolite of MBK. Each compound caused animals insidiously to develop identical, symmetrical peripheral neuropathies characterized by eversion and drop of hindfeet, inability to extend hindlimbs and upper extremity weakness. Teased fiber studies demonstrated that giant axonal swellings first developed on the proximal sides of multiple paranodes sited in distal, non-terminal regions of large myelinated fibers. Later, swellings developed at internodal sites. Smaller myelinated and unmyelinated fibers also underwent multifocal, giant axonal swelling. In affected myelinated fibers, swollen nodal and paranodal axons were frequently associated with retracted paranodal myelin sheaths. Adjacent distal internodes were attenuated and corrugated. Demyelinated paranodes apparently underwent local shrinkage and remyelination before complete distal fiber breakdown commenced. The proximal limits of chains of homogeneous myelin ovoids were interfaced with proximal, preserved regions at sites of giant axonal swellings. Regeneration of myelinated axons also occurred during intoxication. Regenerating fibers were composed of multiple, short, branched internodes which sometimes appeared multifo- cally swollen. Interfaces between regenerating and preserved portions of fibers were unswollen. Thick section studies showed that pronounced endoneurial edema accompanied fiber degeneration in peripheral nerve trunks. Ultrastructural studies revealed multifocal, giant axonal swellings containing masses of 10 nm neurofilaments and, sometimes, clustered mitochondria, neurotubules and smooth endoplasmic reticulum. Enlarged granular mitochondria, interdigitated Schwann cell/axon networks and corrugated myelin sheaths were common findings. Dense granules, vesicles and hexagonal particles were also noted in the axoplasm. These findings provide new insights into the nature of the dying-back process: although there was a retrograde, temporal spread of axonal swelling up affected nerve trunks, axonal degeneration neither began in the nerve terminal nor spread seriatim centripetally along individual nerve fibers. The dying-back process was further examined in a companion study in this issue (32) which analyzed some of the factors determining the differential vulnerability of PNS and CNS fibers in animals intoxicated either with these neurotoxic hexacarbons or with acrylamide.

Original languageEnglish (US)
Pages (from-to)276-299
Number of pages24
JournalJournal of Neuropathology and Experimental Neurology
Volume36
Issue number2
StatePublished - 1977

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Methyl n-Butyl Ketone
Myelin Sheath
Axons
Mitochondria
Smooth Endoplasmic Reticulum
Intermediate Filaments
Acrylamide
Schwann Cells
Hexanes
Peripheral Nervous System Diseases
Hindlimb
Peripheral Nerves
Nerve Fibers
Upper Extremity
Regeneration
Edema
Chronic Disease
Central Nervous System

ASJC Scopus subject areas

  • Clinical Neurology
  • Pathology and Forensic Medicine
  • Cellular and Molecular Neuroscience
  • Neurology
  • Neuroscience(all)

Cite this

Ultrastructural studies of the dying-back process : III. The evolution of experimental peripheral giant axonal Degeneration. / Spencer, Peter S.; Schaumburg, Herbert H.

In: Journal of Neuropathology and Experimental Neurology, Vol. 36, No. 2, 1977, p. 276-299.

Research output: Contribution to journalArticle

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