Literature DB >> 683455

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

K Fujisawa, H Shiraki.   

Abstract

The changes with age in the neuropil of the gracile and the cuneate nuclei of rats were studied using stereological techniques, in relation to the occurrence of axonal dystrophy. The following were found: (1) significant difference in the volume fraction of presynaptic boutons between the gracile and the cuneate nuclei throughout the whole life span (17% and 13% respectively at 100 days of age); (2) progressive decrease in the volume fraction (34% decrease in the gracile nucleus between 100 and 800 days of age) and in the numerical density of presynaptic boutons, the decline being evident as soon as the animals reached maturity and before axonal dystrophy became manifest; (3) significant differences in the volume fractions of dendrites and of nerve cell bodies between the two nuclei throughout the whole life span of the animals, both being greater in the cuneate than in the gracile nucleus; an age-related decrease in the volume fraction of dendrites was also suspected in the gracile nucleus; (4) progressive increase in the volume fraction of fibrous astrocytic processes (from 3% at 100 days to 10.5% at 800 days in the gracile nucleus); (5) the above described age-related changes of presynaptic boutons and fibrous astrocytic processes were significant only in the gracile nucleus, not in the cuneate. The loss of boutons in ageing gracile nuclei was partially reflected in the appearance of degenerating nerve fibres in ageing gracile tract in the rostral cervical cord. Involutional loss of boutons and dystrophic formation of spheroids both appear and progress closely related in time and space. It was suggested that this set of changes can be understood as one integrated whole in which axonal dystrophy may represent only one side of the coin. The question of the causal mechanisms of axonal dystrophy still remains unanswered.

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Year:  1978        PMID: 683455     DOI: 10.1111/j.1365-2990.1978.tb00525.x

Source DB:  PubMed          Journal:  Neuropathol Appl Neurobiol        ISSN: 0305-1846            Impact factor:   8.090


  10 in total

1.  Caudate nucleus pathology in Parkinson's disease: ultrastructural and biochemical findings in biopsy material.

Authors:  B Lach; D Grimes; B Benoit; A Minkiewicz-Janda
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

2.  Spheroids and altered axons in the spinal gray matter of the normal cat. An electron-microscopic study.

Authors:  K Saito
Journal:  Acta Neuropathol       Date:  1980       Impact factor: 17.088

3.  Axonal degeneration of ascending sensory neurons in gracile axonal dystrophy mutant mouse.

Authors:  T Kikuchi; M Mukoyama; K Yamazaki; H Moriya
Journal:  Acta Neuropathol       Date:  1990       Impact factor: 17.088

4.  Developmental abnormalities of neuronal structure and function in prenatal mice lacking the prader-willi syndrome gene necdin.

Authors:  Silvia Pagliardini; Jun Ren; Rachel Wevrick; John J Greer
Journal:  Am J Pathol       Date:  2005-07       Impact factor: 4.307

5.  Effects of chronic vitamin E deficiency on the nervous system of the rat.

Authors:  J Towfighi
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

6.  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

7.  Local cerebral glucose utilization in the brain of old, learning impaired rats.

Authors:  A Wree; C Kaever; B Birgel; A Schleicher; E Horvath; K Zilles
Journal:  Histochemistry       Date:  1991

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

Authors:  K Fujisawa
Journal:  Acta Neuropathol       Date:  1988       Impact factor: 17.088

9.  Mannoside storage and axonal dystrophy in sensory neurones of swainsonine-treated rats: morphogenesis of lesions.

Authors:  C R Huxtable; P R Dorling
Journal:  Acta Neuropathol       Date:  1985       Impact factor: 17.088

10.  Ultrastructure of 6-aminonicotinamide (6-AN)-induced lesions in the central nervous system of rats. III. Alterations of the spinal gray matter lesion with aging.

Authors:  N Horita; T Ishii; Y Izumiyama
Journal:  Acta Neuropathol       Date:  1981       Impact factor: 17.088

  10 in total

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