Literature DB >> 6310925

Morphometric evaluation of degenerative and regenerative changes in isoniazid-induced neuropathy.

C L Chua, A Ohnishi, J Tateishi, Y Kuroiwa.   

Abstract

Morphometric studies of the pathologic changes were carried out on the peripheral nerves, spinal roots, and different levels of the Goll's tract in rats given isoniazid and killed 1, 2, 3, 4, 5, 6, 7, 14, and 30 days after intoxication. In teased fiber preparations, axonal degeneration was the main change present, and this was seen as early as day 2 in the peroneal and distal sural nerves. The frequency of myelinated fibers showing axonal degeneration was higher in the distal than the proximal sural nerve, and in the ventral than the dorsal root. In the group of rats killed on 5, 6, 7, and 14 days, a significant decrease of the myelinated fiber density was observed in the distal and proximal sural nerves, ventral root, and at the third cervical level of the Goll's tract. The degree of fiber degeneration was more severe in the distal than in the proximal sural nerve and in the third cervical than the fifth thoracic level of the Goll's tract. Preferential decrease of large myelinated fibers was noted in all the affected nerves. No definite abnormalities, however, were seen in nerve cells of the 6th lumbar spinal ganglia and anterior horn cells of the lumbar spinal cord on light microscopy. On 30 days, regeneration at varying degrees was discerned in all the affected nerves with significant increase of small myelinated fibers, particularly in the ventral root. The findings indicate that both centrally and peripherally directed myelinated axons are more affected in the distal than in the proximal segments while the neuronal cell bodies are spared. The spatio-temporal evolution of this pattern of change is compatible with the concept of the "dying back" process or central-peripheral distal axonopathy.

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Year:  1983        PMID: 6310925     DOI: 10.1007/bf00691865

Source DB:  PubMed          Journal:  Acta Neuropathol        ISSN: 0001-6322            Impact factor:   17.088


  30 in total

1.  Ultrastructure and biochemistry of myelin after isoniazid-induced nerve degeneration in rats.

Authors:  C P Sea; R G Peterson
Journal:  Exp Neurol       Date:  1975-08       Impact factor: 5.330

2.  ULTRASTRUCTURAL STUDIES OF INH-INDUCED NEUROPATHY IN RATS. 3. REPAIR AND REGENERATION.

Authors:  W W SCHLAEPFER; H HAGER
Journal:  Am J Pathol       Date:  1964-10       Impact factor: 4.307

3.  Isoniazid neuropathy in man: quantitative electron microscope study.

Authors:  J Ochoa
Journal:  Brain       Date:  1970       Impact factor: 13.501

4.  Accumulation of organelles at the ends of interrupted axons.

Authors:  J Zelená; L Lubińska; E Gutmann
Journal:  Z Zellforsch Mikrosk Anat       Date:  1968

Review 5.  The significance of the "dying back" process in experimental and human neurological disease.

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

6.  Myoneural changes in experimental isoniazid neuropathy. Electrophysiological and histological study.

Authors:  J Hildebrand; A Joffroy; C Coërs
Journal:  Arch Neurol       Date:  1968-07

7.  Morphometric evaluation of primary sensory neurons in experimental p-bromophenylacetylurea intoxication.

Authors:  A Ohnishi; M Ikeda
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

8.  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

9.  Lead neuropathy. 1) Morphometry, nerve conduction, and choline acetyltransferase transport: new finding of endoneurial edema associated with segmental demyelination.

Authors:  A Ohnishi; K Schilling; W S Brimijoin; E H Lambert; V F Fairbanks; P J Dyck
Journal:  J Neuropathol Exp Neurol       Date:  1977-05       Impact factor: 3.685

10.  Transient, focal accumulation of axonal mitochondria during the early stages of wallerian degeneration.

Authors:  H D WEBSTER
Journal:  J Cell Biol       Date:  1962-02       Impact factor: 10.539

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  3 in total

1.  Ethylene oxide induces central-peripheral distal axonal degeneration of the lumbar primary neurones in rats.

Authors:  A Ohnishi; N Inoue; T Yamamoto; Y Murai; H Hori; M Koga; I Tanaka; T Akiyama
Journal:  Br J Ind Med       Date:  1985-06

2.  Axonal degeneration distal to the site of accumulation of vesicular profiles in the myelinated fiber axon in experimental isoniazid neuropathy.

Authors:  A Ohnishi; C L Chua; Y Kuroiwa
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

3.  Ethylene oxide polyneuropathy: clinical follow-up study with morphometric and electron microscopic findings in a sural nerve biopsy.

Authors:  J M Schröder; M Hoheneck; J Weis; H Deist
Journal:  J Neurol       Date:  1985       Impact factor: 4.849

  3 in total

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