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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 53 (1981), S. 7-14 
    ISSN: 1432-0533
    Keywords: Synapse ; Locus ceruleus ; Parkinson's disease ; Alzheimer's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary We have studied the synaptic ultrastructure in human autopsy material from the locus ceruleus, an important noradrenergic center. Ten cases of Alzheimer's disease, ten cases of Parkinson's disease, and ten control brains were examined. Only a few differences in synaptic morphology between the three groups were found. Multiple symmetrical and asymmetrical contacts on medium-sized dendrites were characteristically present. Axosomatic synapses were also common. In Alzheimer's disease axosomatic synapses on nerve cell perikarya containing neurofibrillary tangles, and in Parkinson's disease on perikarya containing Lewy bodies, could be demonstrated. Dendritic spines were rare, but the control group had structures interpreted as “minispines”. In agreement with studies in the rat, cat, and rabbit, no spine apparatus was present, but in contrast to those studies no somatic spines were identified. Rare axoaxonic synapses were found in the control group. Vesicle content was often pleomorphic with flattened vesicles. Large dense core vesicles were present in variable numbers in nerve cell processes, and large accumulations of such vesicles were seen in two thirds of our cases, most abundant in the Alzheimer's and Parkinson's disease groups. Such terminals may be aminergic, perhaps serotonergic, and may be a normal component of the locus ceruleus. Their greater abundance in Alzheimer's and Parkinson's disease may be due to accumulation of the amines in afferent terminals, which have been deprived of their postsynaptic connections due to the degenerative disease process.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Acta neuropathologica 34 (1976), S. 183-197 
    ISSN: 1432-0533
    Keywords: Lewy body ; Electron microscopy ; Parkinsonism ; Dense core vesicles ; Catecholamines ; Mitochondrial inclusions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The Lewy body, a characteristic nerve cell inclusion in idiopathic parkinsonism, was examined by electron microscopy in the stellate ganglion, obtained from 9 patients at autopsy. Three main forms of Lewy bodies or Lewy body-related structures were demonstrated: A. Rare filamentous Lewy bodies, similar to Lewy bodies in the central nervous system. B. Granular Lewy bodies in nerve cell processes. C. Abnormal nerve cell processes, filled with heterogenous material. Large dense core vesicles were prominent in the last 2 forms. None of these abnormalities were found in 2 control groups consisting of 9 parkinsonism cases without central nervous system Lewy bodies, and 17 cases without parkinsonism. The filamentous Lewy body (type A) was found in the perikaryon and was surrounded by neuromelanin, whereas the other forms (type B and C) were seen in nerve cell processes. Mitochondrial inclusions, present mainly, but not exclusively, in neuromelanin-containing cells, were not related to Lewy body formation or to parkinsonism.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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