Literature DB >> 720323

Distal axonopathy: one common type of neurotoxic lesion.

P S Spencer, H H Schaumburg.   

Abstract

Neurotoxic chemicals commonly produce retrograde degeneration of the axons of long and large nerve fibers in the central and peripheral nervous system. This produces a clinical picture of polyneuropathy in man and animals in which sensory and motor disturbances develop in the feet and hands then progress with time to the legs and arms. Distal axonopathy, as the underlying pathologic process is termed, is one of four principal types of neurotoxic diseases, the others including degeneration of neurons (neuronopathy), myelin sheaths (myelinopathy) and damage to the neurovasculature (neurovasculopathy). In the experimental animal, these four types of neurotoxic diseases can be distinguished by examining selected areas of brain and nerve tissues prepared by contemporary methods of tissue fixation. These procedures may form the basis of a new and sensitive assay for neurotoxicity.

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Year:  1978        PMID: 720323      PMCID: PMC1637239          DOI: 10.1289/ehp.782697

Source DB:  PubMed          Journal:  Environ Health Perspect        ISSN: 0091-6765            Impact factor:   9.031


  7 in total

1.  Degeneration in central and peripheral nervous systems produced by pure n-hexane: an experimental study.

Authors:  H H Schaumburg; P S Spencer
Journal:  Brain       Date:  1976-06       Impact factor: 13.501

2.  Ultrastructural studies of the dying-back process. I. Peripheral nerve terminal and axon degeneration in systemic acrylamide intoxication.

Authors:  H H Schaumburg; H M Wiśniewski; P S Spencer
Journal:  J Neuropathol Exp Neurol       Date:  1974-04       Impact factor: 3.685

Review 3.  Peripheral neuropathy caused by chemical agents.

Authors:  J B Cavanagh
Journal:  CRC Crit Rev Toxicol       Date:  1973-11

Review 4.  The significance of the "dying back" process in experimental and human neurological disease.

Authors:  J B Cavanagh
Journal:  Int Rev Exp Pathol       Date:  1964

5.  Side effects of organophosphorus compounds: delayed neurotoxicity.

Authors:  W N Aldridge; M K Johnson
Journal:  Bull World Health Organ       Date:  1971       Impact factor: 9.408

6.  Ultrastructural studies of the dying-back process. IV. Differential vulnerability of PNS and CNS fibers in experimental central-peripheral distal axonopathies.

Authors:  P S Spencer; H H Schaumburg
Journal:  J Neuropathol Exp Neurol       Date:  1977 Mar-Apr       Impact factor: 3.685

7.  Ultrastructural studies of the dying-back process. III. The evolution of experimental peripheral giant axonal degeneration.

Authors:  P S Spencer; H H Schaumburg
Journal:  J Neuropathol Exp Neurol       Date:  1977 Mar-Apr       Impact factor: 3.685

  7 in total
  4 in total

1.  Updating federal standards for toxicants: n-Hexane as the model.

Authors:  H Babich; D L Davis; R Adler
Journal:  Environ Monit Assess       Date:  1982-09       Impact factor: 2.513

2.  The background of mitochondrial DNA haplogroup J increases the sensitivity of Leber's hereditary optic neuropathy cells to 2,5-hexanedione toxicity.

Authors:  Anna Ghelli; Anna Maria Porcelli; Claudia Zanna; Sara Vidoni; Stefano Mattioli; Anna Barbieri; Luisa Iommarini; Maria Pala; Alessandro Achilli; Antonio Torroni; Michela Rugolo; Valerio Carelli
Journal:  PLoS One       Date:  2009-11-19       Impact factor: 3.240

3.  Structure and function of the somatosensory system: a neurotoxicological perspective.

Authors:  J C Arezzo; H H Schaumburg; P S Spencer
Journal:  Environ Health Perspect       Date:  1982-04       Impact factor: 9.031

4.  Early disruption of nerve mitochondrial and myelin lipid homeostasis in obesity-induced diabetes.

Authors:  Juan P Palavicini; Juan Chen; Chunyan Wang; Jianing Wang; Chao Qin; Eric Baeuerle; Xinming Wang; Jung A Woo; David E Kang; Nicolas Musi; Jeffrey L Dupree; Xianlin Han
Journal:  JCI Insight       Date:  2020-11-05
  4 in total

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