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  • Astrocytes  (1)
  • Cortical capillaries  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 61 (1983), S. 76-80 
    ISSN: 1432-0533
    Keywords: Alzheimer's disease ; Fibrous astrocytes ; Cortical capillaries ; GFAP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In four patients with Alzheimer's disease (AD), one patient with senile dementia of Alzheimer's type (SDAT) and five age-matched controls, occipital cortex, frontal cortex, and hippocampus were evaluated for the distribution of fibrous astrocytes (FA), using peroxidase-anti-peroxidase for glial fibrillary acidic protein (GFAP). FA, neuronal cells, neurofibrillary tangles (NFT), and senile plaques (SP) have been quantified in the occipital cortex. In AD and SDAT there was a significant increase in the number of FA in the molecular layer as well as in the other layers of the cortex. No correlation was found between the increase in FA and the number of neurons, NFT or SP. The GFAP positivity was most pronounced around small blood vessels. Electron-microscopic studies of four cortical biopsies of AD revealed dense perivascular gliosis in 48.8% of the capillaries examined as opposed to 17.8% of capillaries in three controls without dementia. The significance of increased perivascular gliosis in AD and SDAT is unknown. It may be related to a defect in the blood-brain barrier.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 77 (1989), S. 507-513 
    ISSN: 1432-0533
    Keywords: Aging ; Astrocytes ; Glial fibrillary acidic protein ; Nude mice ; PAS-positive granules
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Morphometric glial fibrillary acidic protein (GFAP) studies of the brains of 11 old (18–29 months) female, outbred athymic mice demonstrated astrocytic gliosis (increase in GFAP-positive astrocytes; GFAP-PA) in all mice with a consistent distribution pattern. Specific areas such as the central white matter, hippocampus, diencephalon, gray matter at the floor of the 4th ventricle, and posterior colliculi showed the change most conspicuously, revealing GFAP-PA both interstitially and perivascularly. There was no apparent demyelination in the affected white matter. In addition, there was an increase in GFAP-PA in the external limiting membrane surrounding the diencephalon and base of brain stem, but only to a minor degree over the cerebral hemispheres. The cerebral and cerebellar cortices and hypothalamus showed no significant increase. In contrast, all of the 2-month-old control animals showed only minor amounts of GFAP-PA, seen in the external limiting membrane and a trace in the cerebral white matter. The present data suggest that astroglial sclerotic change in various regions of the brain is an important morphological expression of cerebral aging. In view of the lack of other demonstrable histological changes (i.e., silver and amyloid stains were negative) or significant atrophy, the cause of the observed gliosis in BALB/c mice might represent a genuine aging change. As an incidental finding, aggregates of PAS-positive granules were noted in the Ammon's horn of most old animals, while none were seen in the young controls.
    Type of Medium: Electronic Resource
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