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  • Huntington's disease  (2)
  • Gangliosides  (1)
  • Mannitol  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of neural transmission 69 (1987), S. 153-160 
    ISSN: 1435-1463
    Keywords: Somatostatin ; Huntington's disease ; post mortem
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Size exclusion high performance liquid chromatography of post mortem human putamen samples revealed three somatostatin-immunoreactive peaks. The two major peaks cochromatographed with synthetic somatostatin-14 and somatostatin-28, respectively whereas the presumed somatostatin precursor preceded these peaks. In 11 samples obtained post mortem from patients suffering from Huntington's Disease somatostatin-like immunoreactivity was increased by about 55 % in the mean. This increase was mainly due to increases in somatostatin-14 and-to a minor extent-of somatostatin-28, whereas the presumed precursor was not significantly changed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Gangliosides ; Striatum ; Kainic acid lesion ; Huntington's disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Ganglioside and DNA levels were estimated in the striatum of rats 10 days and 6 weeks after lesioning by intrastriatal injection of kainic acid. There was a moderate, 21–24% decrease of the ganglioside concentration per unit protein on the side of the lesion, which can be ascribed to the loss of the intrinsic striatal neurons following the injection of kainic acid. On the other hand, there was a 131 and 60% increase of DNA per unit protein in the kainate injected side 10 days and 6 weeks after the lesions, respectively; these changes apparently reflected the gliotic reaction brought about by the neurotoxin. Qualitatively similar findings — a decrease of ganglioside and an increase of DNA levels per unit protein — were also found in the brain of patients with Huntington's disease; however, as compared with the corresponding control material, the decrease of the ganglioside concentration was more pronounced in the striatum of Huntington's disease (by 38% in the caudate nucleus and by 46% in the putamen) than in the kainate lesioned rat striatum. This difference could be due to the different proportions of the intrinsic and extrinsic neuronal plasma membranes in the striatum of the two species; however, the possibility of a more generalized affection of neuronal plasma membranes in Huntington's disease may also be envisaged.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Regulatory Peptides 26 (1989), S. 215-223 
    ISSN: 0167-0115
    Keywords: Brain ; Brain edema ; Calcitonin gene-related peptide ; Epilepsy ; Kainic acid ; Mannitol
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Medicine
    Type of Medium: Electronic Resource
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