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  • 1990-1994  (2)
  • 1980-1984  (1)
  • 1930-1934
  • Life and Medical Sciences  (2)
  • GABA transmission  (1)
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  • 1990-1994  (2)
  • 1980-1984  (1)
  • 1930-1934
Year
  • 1
    ISSN: 1432-2072
    Keywords: HPNS ; Primates ; Abecarnil ; GABA transmission ; EEG ; Behavioural observations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract The neurophysiological interactions between the high pressure neurological syndrome (HPNS) and a newβ carboline, abecarnil, were studied in the nonhuman primatePapio anubis. Abecarnil is a partial agonist at the benzodiazepine site on the GABA/benzodiazepine receptor. Six animals were exposed on two occasions to pressures of 91 ATA in an environment of helium and oxygen. One exposure was pretreated with a total dose of abecarnil 1.0 mg/kg, the other with an equivalent volume of vehicle. Treatment with abecarnil prevented the severe signs of HPNS occurring between 51 and 91 ATA. Onset pressures of the various signs were unaffected. Some signs, e.g. myoclonus, became more frequent when abecarnil was used. A residual protective effect of abecarnil was present 4 weeks after the dose was given, active at pressures less than 71 ATA. Changes with pressure in the EEG were recorded primarily from the frontal cortex, but were also present in the parietal and occipital areas of the left cortex. Amplitude and frequency spectra were calculated and changes with pressure in the four conventional wavebands, plus two others, analysed. The most striking change was the prevention by abecarnil of the pressure-induced 100% increase in alpha wave amplitude in the frontal region. It is concluded that modulation of GABA transmission is important in controlling the expression of HPNS.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal of Morphology 177 (1983), S. 277-299 
    ISSN: 0362-2525
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: The morphology of neurons in the ventral basal complex (VBC) of the adult opossum (Didelphis virginiana) is described from thick coronal brain sections, using Golgi-, horseradish peroxidase (HRP)-, and Nissl-staining methods. Soma cross-sectional area, dendritic field shape, and the number of appendages (spines) in a defined major branch zone (MBZ) are quantified and statistically analyzed. Results indicate that neurons in opossum VBC have relatively large cell bodies, dendrites which branch in a tufted pattern, and numerous dendritic appendages. These neurons are designated as relay cells because of (1) their tufted dendritic branch patterns, considered characteristic of thalamic relay cells (Ramon-Moliner, '62), and (2) the similarity of their soma sizes with HRP-labeled somata after somatosensory cortical injections. Neurons with traditionally described interneuron morphology do not appear to be present in the VBC of this animal, and, in this respect, the neuronal morphology of opossum VBC is similar to that in rat (McAllister and Wells, '81).Based on statistical analysis of the structural features observed, the presumed relay cells in opossum VBC do not show significant differences in morphology, and consequently are not subdivided into classes. Opossum VBC neurons are recognized as forming a single category in which broad and continuous variations in morphology are indicated. Recognition of a singular class of relay cell is consistent with descriptions for rat and cat VBC (Scheibel and Scheibel, '66), but at variance with a previous report for the primate Galago VBC (Pearson and Haines, '80) subdividing thalamic relay cells into Types I, II, and intermediate categories.
    Additional Material: 15 Ill.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 0021-9541
    Keywords: Life and Medical Sciences ; Cell & Developmental Biology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Medicine
    Notes: We have applied a multiple isotope dilution technique to examine junctional permeability of human umbilical vein endothelial cells (HUVEC) in vitro. Primary cultures were grown to confluence on porous Cytodex-3 microcarrier beads, packed into 0.3 ml columns (3 × 106 cells) and perfused at varying flow rates (0.3-1.2 ml/min) with HEPES-buffered Tyrodes solution containing unlabeled cyanocobalamin, insulin, and albumin. Columns were challenged periodically with mixtures of radioactive tracers of different molecular size. Permeability to 22Na+, [57Co]cyanocobalamin (1.3 kD), [125l]insulin (6 kD) or [125l]albumin (66 kD) was assessed relative to [131l]lgG (160 kD, impermeant reference tracer) by comparing column elution profiles. Although the single passage extraction of [125l]albumin by beads alone approximated 40%, the presence of confluent HUVEC rendered these beads effectively impermeable to albumin. High junctional extractions were measured for cyanocobalamin (0.79 ± 0.02, n = 28) and insulin (0.51 ± 0.05, n = 14) in cultures perfused at 0.3-0.4 ml/min, and tracer extraction decreased as perfusion rates increased. Permeability coefficients for cyanocobalamin (9.66 × 10-5 cm/s) and insulin (4.18 × 10-5 cm/s) increased significantly during perfusion with thrombin (10 U/ml) or cytochalasin D (1 μg/ml), whereas permeability to albumin (0.39 × 10-5 cm/s) remained unchanges. Morphological studies, using the glycocalyx stain ruthenium red, revealed that thrombin or cytochalasin D increased the penetration of the stain into junctions between endothelial cells.
    Additional Material: 7 Ill.
    Type of Medium: Electronic Resource
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