Literature DB >> 3407392

Study of axonal dystrophy. III. Posterior funiculus and posterior column of ageing and old rats.

K Fujisawa1.   

Abstract

Axonal dystrophy in normal ageing can be studied in experimental animals. Primary sensory neurones show two different kinds of change with ageing, i.e. axonal dystrophy and axonal atrophy (degeneration). This paper reports the chronology and topography of these two processes in relation to growth and involution of these neurones throughout the lifespan of the rats used in this study. Axonal spheroids preferentially form at presynaptic terminal regions in many of the collaterals of central branches of the axons, i.e. in the posterior funiculus nuclei, posterior column and posterior funiculus. Axonal dystrophy in normal ageing is essentially a morbid process restricted to the terminal parts of the axon. It shows little tendency to expand retrogradely along the axon. Evidence is presented that spheroids in posterior funiculus also derive from terminal axons. Preference is also noted in the lumbosacral rather than cervical neurons, and in longer (posterior funiculus nuclei) rather than shorter (posterior column) collaterals. Quantitative study of myelinated fibres in posterior funiculus shows that they increase in number until middle age (400 days) of the animals, before beginning to decline. On the other hand, axonal atrophy begins to appear early in small numbers, and increases in numbers with age. Atrophy involves the whole length of the axon within the posterior funiculus from the start, suggesting, therefore, that it does not belong to a dying-back process. It is noteworthy that the main development of axonal dystrophy lies in the earlier half of the animals' life, while that of axonal atrophy lies in the latter half. This fact adds to the evidence that axonal dystrophy, as far as in normal ageing is concerned, is more related to the positive side of neuronal activity, e.g. one form of growth abnormality of axon.

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Year:  1988        PMID: 3407392     DOI: 10.1007/bf00688095

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


  19 in total

1.  AN ELECTRON MICROSCOPIC STUDY OF DYSTROPHIC AXONS IN THE GRACILE AND CUNEATE NUCLEI OF VITAMIN E-DEFICIENT RATS.

Authors:  P LAMPERT; J M BLUMBERG; A PENTSCHEW
Journal:  J Neuropathol Exp Neurol       Date:  1964-01       Impact factor: 3.685

2.  [Late infantile form of Hallervorden-Spatz disease. II. Histochemical findings; discussion on nosology].

Authors:  F SEITELBERGER; H GROSS
Journal:  Dtsch Z Nervenheilkd       Date:  1957

Review 3.  General neuropathology of degenerative processes of the nervous system.

Authors:  F Seitelberger
Journal:  Neurosci Res (N Y)       Date:  1969

4.  Comparative neuropathology of ageing. Studies on the brains of 47 species of vertebrates.

Authors:  A D Dayan
Journal:  Brain       Date:  1971       Impact factor: 13.501

5.  A quantitative study of morphological changes accompanying the initiation and progress of myelin production in the dorsal funiculus of the rat spinal cord.

Authors:  M A Matthews; D Duncan
Journal:  J Comp Neurol       Date:  1971-05       Impact factor: 3.215

Review 6.  [Neuroaxonal dystrophies].

Authors:  K Jellinger
Journal:  Verh Dtsch Ges Pathol       Date:  1968

7.  Neuroaxonal dystrophy in man: character and natural history.

Authors:  K Jellinger; A Jirásek
Journal:  Acta Neuropathol       Date:  1971       Impact factor: 17.088

8.  Study of axonal dystrophy. I. Pathology of the neuropil of the gracile and the cuneate nuclei in ageing and old rats: a stereological study.

Authors:  K Fujisawa; H Shiraki
Journal:  Neuropathol Appl Neurobiol       Date:  1978 Jan-Feb       Impact factor: 8.090

9.  [The Hallervorden-Spatz Disease].

Authors:  F Seitelberger
Journal:  Nervenarzt       Date:  1966-11       Impact factor: 1.214

10.  Axonal dystrophy in the gracile nucleus in children and young adults. Reappraisal of the incidence and associated diseases.

Authors:  J H Sung; A R Mastri; S H Park
Journal:  J Neuropathol Exp Neurol       Date:  1981-01       Impact factor: 3.685

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  4 in total

Review 1.  Regulation of neurotrophin signaling in aging sensory and motoneurons: dissipation of target support?

Authors:  B Ulfhake; E Bergman; E Edstrom; B T Fundin; H Johnson; S Kullberg; Y Ming
Journal:  Mol Neurobiol       Date:  2000-06       Impact factor: 5.590

2.  Disruption of fibroblast growth factor receptor signaling in nonmyelinating Schwann cells causes sensory axonal neuropathy and impairment of thermal pain sensitivity.

Authors:  Miki Furusho; Jeffrey L Dupree; Melissa Bryant; Rashmi Bansal
Journal:  J Neurosci       Date:  2009-02-11       Impact factor: 6.167

3.  Ultrastructural changes in the gracile nucleus of the rat after sciatic nerve transection.

Authors:  J K Persson; H Aldskogius; J Arvidsson; A Holmberg
Journal:  Anat Embryol (Berl)       Date:  1991

4.  Calcitonin gene-related peptide- and substance P-immunoreactive axons in the nucleus gracilis of the rat with special reference to axonal dystrophy: light and electron microscopic observations.

Authors:  K Fujiwara; S Y Baek; T Arakawa; K Kobayashi; H Takagi
Journal:  Acta Neuropathol       Date:  1995       Impact factor: 17.088

  4 in total

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