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  • 1
    ISSN: 1432-0533
    Keywords: Cell death ; Ischemia ; Hippocampus ; Induced tolerance ; Protein synthesis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Following brief cerebral ischemia, tolerance to subsequent ischemia is induced in the hippocampal neurons. In this experiment, recovery of protein synthesis was investigated autoradiographically in gerbils with induced tolerance. The animals were subjected to single forebrain ischemia for 5 min (5-min ischemia group) or 2 min (2-min ischemia group). To observe the effect of tolerance acquisition, double forebrain ischemia (double ischemia group), 2-min ischemia followed by 5-min ischema was induced 2 days later. At various recircultion periods (90 min, 6 h, 1 day, and 4 days following ischemia), animals received a single dose of Lxxx-[2,3-3H]valine. In the 5-min ischemia group, protein synthesis in the CA1 sector was severely suppressed during the period from 90 min to 1 day of recirculation and never returned to the normal level even at 4 day of recirculation. In the 2-min ischemia group, protein synthesis recovered gradually and returned to near normal at 4 days of recirculation. On the other hand, in the double ischemia group, recovery of protein synthesis in the CA1 sector was rapid. At 1 day of recirculation, protein synthesis returned to near normal. Protein synthesis in the CA2 sector was inhibited during the 4 days of recirculation in this group. The present study revealed an early recovery of protein synthesis in the hippocampal CA1 neurons in the gerbil with induced tolerance. We suggest that recovery of protein synthesis is essential for the survival of neurons exposed to transient ischemia.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-7373
    Keywords: PCAF ; glioma ; mutations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The PCAF gene encodes the p300/CBP-Associated Factor (PCAF), a histone acetyltransferase, which regulates p53 by acetylation of Lys320 in the C-terminal portion of p53. While the p53 gene is one of the most frequently mutated tumor suppressor genes in human tumors, such mutations occur in only 30% of astrocytic tumors. Since PCAF can regulate p53 activity, abrogation of PCAF function by PCAF gene mutation could be an alternate mechanism to inactivate the p53 pathway in tumors lacking p53 mutations. To test this hypothesis, we determined the nucleotide sequence of the entire PCAF coding region in 37 astrocytic tumors (17 glioblastomas, 10 anaplastic astrocytomas, 7 low-grade astrocytomas, and 3 pilocytic astrocytomas). We detected two single-nucleotide alterations that represented non-deleterious polymorphisms (GAG 〉 GAA Glu103Glu, AAT 〉 AGT Asn386Ser) but no obvious functional mutations. Moreover, the frequency of the Asn386Ser allele that contained Ser386 in glioma patients was not statistically different from its frequency in individuals without disease, and no significant association was observed between the PCAF polymorphisms and the presence or absence of p53 mutations in the tumors. We conclude that the PCAF gene is not mutated during the development of the astrocytic tumors studied here.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Neurosurgical review 8 (1985), S. 15-25 
    ISSN: 1437-2320
    Keywords: Arteriovenous malformation ; brain tumour ; cerebrovascular occlusive disorder ; Moya moya disease
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Dynamic computed tomography (CT) scanning was performed on five normal subjects, 38 patients with cerebrovascular disorder, and 20 patients with brain tumours. It consisted of performing six rapid sequential scans after intravenous bolus injection of iodinated contrast medium. By gamma variate fit technique, five features (corrected first moment, area, peak, time to peak, and per cent terminal height) were obtained from a time-density curve in a region of interest. We compared these features in one side of the brain with those in the corresponding contralateral side and tried to get information about cerebral perfusion. These results showed that by this technique we are able to detect arterial occlusions or Moya moya diseases non-invasively and know earlier and more clearly the re-establishment of circulation in the occluded arteries and of extravasation of contrast medium in ischaemic regions than by conventional CT scanning. In arteriovenous malformations, serial images of dynamic CT scanning demonstrated the anatomical details of the nidus, and the afferent and efferent vessels. We can also identify an exact extent of tumoral invasion of the brain in patients with malignant brain tumor.
    Type of Medium: Electronic Resource
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