Literature DB >> 1471472

A morphometric and immunohistochemical study of the vestibular nuclear complex in bovine spongiform encephalopathy.

M Jeffrey1, W G Halliday, C M Goodsir.   

Abstract

A morphometric and immunohistochemical study of the vestibular nuclear complex was performed on five bovine spongiform encephalopathy (BSE) and five control cow brains. Neurons of the lateral and superior vestibular nuclei were counted at 500-microns intervals in 10-microns-thick sections, using an image analysis system comprising a projection microscope and digitising pad linked to a computer. A bimodal distribution of neuron diameters was recognised in the brains of normal cattle. One population of neurons had a mean diameter of 30 microns and the other had a mean diameter of 60 microns. The vestibular nuclei from BSE cattle had an approximately 50% reduction in total numbers of neurons when compared with controls (P < 0.01). Cattle which were clinically diseased longer had the fewest number of neurons preserved. Diminished numbers of neurons were detected throughout the area studied and affected neurons of all diameters. Immunohistochemical staining for synaptophysin, a protein present in synapses throughout the CNS, showed no significant reduction in axon terminals synapsing with vestibular neurons, including vacuolated neurons of BSE brains, when controls and BSE brains were compared. This suggests that de-afferentation of neurons is not the cause of neuronal loss. Prion protein was detected in the neuropil of the vestibular nuclear complex of BSE brains but not control brains. These studies show that previously unsuspected neuronal loss is a significant feature of BSE.

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Year:  1992        PMID: 1471472     DOI: 10.1007/bf00227742

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


  29 in total

1.  A novel progressive spongiform encephalopathy in cattle.

Authors:  G A Wells; A C Scott; C T Johnson; R F Gunning; R D Hancock; M Jeffrey; M Dawson; R Bradley
Journal:  Vet Rec       Date:  1987-10-31       Impact factor: 2.695

2.  Subacute spongiform encephalopathy (Creutzfeldt-Jakob disease). The nature and progression of spongiform change.

Authors:  C L Masters; E P Richardson
Journal:  Brain       Date:  1978-06       Impact factor: 13.501

3.  The sequential development of the brain lesion of scrapie in three strains of mice.

Authors:  H Fraser; A G Dickinson
Journal:  J Comp Pathol       Date:  1968-07       Impact factor: 1.311

4.  The lateral vestibular nucleus of the rat, with a note on its dorsal extension into the cerebellum.

Authors:  K M Shamboul
Journal:  J Anat       Date:  1979-08       Impact factor: 2.610

5.  Replication of the scrapie agent in hamster brain precedes neuronal vacuolation.

Authors:  J R Baringer; K A Bowman; S B Prusiner
Journal:  J Neuropathol Exp Neurol       Date:  1983-09       Impact factor: 3.685

6.  Serial studies on the development of cerebral amyloidosis and vacuolar degeneration in murine scrapie.

Authors:  M E Bruce
Journal:  J Comp Pathol       Date:  1981-10       Impact factor: 1.311

Review 7.  Creutzfeldt-Jakob disease and scrapie prions.

Authors:  S B Prusiner
Journal:  Alzheimer Dis Assoc Disord       Date:  1989 Spring-Summer       Impact factor: 2.703

8.  Serial ultrastructural study of experimental Creutzfeldt-Jacob disease in guinea pigs.

Authors:  J H Kim; E E Manuelidis
Journal:  Acta Neuropathol       Date:  1986       Impact factor: 17.088

9.  Agent replication dynamics in a long incubation period model of mouse scrapie.

Authors:  M E Bruce
Journal:  J Gen Virol       Date:  1985-12       Impact factor: 3.891

10.  Transmissible mink encephalopathy. Reduced spongiform degeneration in aged mink of the Chediak-Higashi genotype.

Authors:  R F Marsh; J C Sipe; S S Morse; R P Hanson
Journal:  Lab Invest       Date:  1976-04       Impact factor: 5.662

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  3 in total

1.  Hydrated autoclave pretreatment enhancement of prion protein immunoreactivity in formalin-fixed bovine spongiform encephalopathy-affected brain.

Authors:  M Haritani; Y I Spencer; G A Wells
Journal:  Acta Neuropathol       Date:  1994       Impact factor: 17.088

2.  A Drosophila model of GSS syndrome suggests defects in active zones are responsible for pathogenesis of GSS syndrome.

Authors:  Jin-Kyu Choi; Yong-Chul Jeon; Dae-Weon Lee; Jae-Min Oh; Hyun-Pil Lee; Byung-Hoon Jeong; Richard I Carp; Young Ho Koh; Yong-Sun Kim
Journal:  Hum Mol Genet       Date:  2010-09-09       Impact factor: 6.150

3.  Ultrastructural features of spongiform encephalopathy transmitted to mice from three species of bovidae.

Authors:  M Jeffrey; J R Scott; A Williams; H Fraser
Journal:  Acta Neuropathol       Date:  1992       Impact factor: 17.088

  3 in total

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