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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 23 (1974), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— Previous suggestions that the K+-dependent uptake of chloride by mammalian cerebral cortex is localized to cortical astrocytes has been investigated in two lines of neural cells in tissue culture. Hamster astrocytes and mouse neuroblastoma cells were each cultured on small glass cover slips in Eagle's (astrocytes) or Dulbecco's (neuroblastoma) supplemented media. At 48 h, cultures were incubated at 37°C for 1–60 min in the presence of 36Cl plus [3H]inulin (as a measure of extracellular space). In media containing approximately 140 mm chloride, the rate of uptake of 36Cl by the astrocytes was a function of the concentration of K+ (range 5–54 mm) in the medium, and the uptake was characterized by saturation kinetics and an apparent Km of 38·5 mm. The uptake was temperature and apparently energy dependent, significantly inhibited by 5 or 10 mm Br-, I-, SCN- or ClO4-, and competitively inhibited by 10 mm acetazolamide (Ki= 27·1 mm). None of these characteristics were observed with neuroblastoma cultures studied under similar conditions. In chloride-free media, the cellular K/Na ratio of the astrocytes shifted from the usual value of 4·55 to a value of 0·29, the culture medium became more alkaline than normal, and the cells spontaneously sloughed from the cover slips but remained normally viable. Our observations are the first to provide direct support for previous suggestions that there is a mediated, K+-dependent coupled cation, chloride and fluid uptake by mammalian cerebrocortical glia and that this uptake is an enzymatically catalysed process. The observations have been discussed in terms of a presumed central role for astrocytes in modulating the external ionic milieu of the neurons they surround and in terms of implications for epilepsy, stroke and cortical edema.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— Previously reported interspecies correlations of cerebral cortical oxygen consumption (as a function of average species body weight) and of cerebral cortical chloride content and acetylcholinesterase activity (as functions of average species brain weight) were confirmed by selected repetitions of the determinations and were further validated by inclusion of data from samples of cerebral cortex of the fin whale (Balaenoptera physalus) and the sperm whale (Physeter catodon). Despite the fact that the samples of whale brain were obtained at 15–22 h after death and were preserved only by simply freezing on dry ice, no evidence of significant postmortem autolysis was obtained by examination of gangliosides, myelin basic proteins, acidic and amide residues of total isolated proteins, and lipid composition of cerebral cortical samples. The chloride content of whale cerebral cortex was 65.1 (± 12) μequiv./g, and the activity of acetylcholinesterase was 0.78 (± 0.28) μmol of acetylthiocholine hydrolysed min-1 g-1, with no differences in these values between the two species. The two interspecies correlations yielded regression curves with calculated slopes for chloride of +9.07 (± 0.37) and for acetylcholinesterase of -0–204 (± 0.006), each correlating significantly as functions of species brain weight at P 〈 0.001. Under optimal conditions of slow freezing and thawing of cerebral cortical slices equilibrated with 15 % (v/v) glycerol, oxygen consumption by the slices was only 50 per cent of the rate exhibited by fresh (unfrozen) slices. Despite the suboptimal conditions of freezing and thawing of the large (〉 200 g) samples of whale (and beef) brain, subsequently prepared slices of whale cerebral cortex respired at a rate of 20.6 (± 1.8) μmol of O2 taken up h-1 g-1, also 50 per cent of the value of 40.7 predicted by extrapolation for fresh (unfrozen) slices. When plotted as a function of species body weight, the data for oxygen consumption by previously frozen cortical slices paralleled the regression curve for fresh slices previously characterized by the expression, R = 5.4 W-0.1. The data obtained for the two species of great whales (brain weights, 6800–7800 g; body weights, 3–53 ± 104 kg) served to ‘anchor’ with more certainty the upper limits of the three interspecies correlations re-examined here and thus provided a better basis for predicting by extrapolation normal values for human cerebral cortex.
    Type of Medium: Electronic Resource
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  • 3
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— The question of a constant density of glial cells in mammalian cerebral cortex regardless of species was examined by surveying the cortical activities of two enzymes primarily localized to dial cells. The cortical activity of butyrylcholinesterase (EC 3.1.1.8) was essentially constant at a rate of approx. 0.1 μmol of butyrylthiocholine hydrolysed min-1 g-1 over the range of species from rat (brain wt., 1.6 g) to fin whale and sperm whale (brain wt., 6800 and 7800 g, respectively). Over the same range the activity of cortical acetylcholinesterase, a neuronal enzyme, decreases by a factor of 7. Thus, butyrylcholinesterase ranged from 〈 2 per cent (in small rodent brains) to approximately 10 per cent (in whale brain) of the cortical acetylcholinesterase activity. The cortical activity of carbonic anhydrase (EC 4.2.1.1) was constant at a rate of 6.2 (± 0.25) μmol of CO2 evolved min-1 g-1 over the range of species from guinea-pig (brain wt., 4.75 g) to fin whale (brain wt., 6800 g). These data obtained by assaying the dehydration reaction were confirmed by limited assays of the esterase activity of the enzyme (with p-nitrophenylacetate as substrate) and agreed with limited, previously reported data for the hydration reaction. Thus, the circumstantial evidence strongly favoured a relative constancy of cortical glial cell density regardless of species.The rates of anaerobic glycolysis in the cerebral cortex of various species were also investigated. For six species from mouse (brain wt., 0.4 g) to beef (brain wt., 380 g) cortical anaerobic glycolysis varied only slightly in the range of 50–62 μmol of CO2 evolved h-1 g-l, whereas cortical oxygen consumption for the same range of species decreased by a factor of 3. Previously frozen samples of beef cortex glycolysed at 35 per Cent of the rate of fresh (unfrozen) samples. Since identical rates were obtained for previously frozen samples of fin whale cerebral cortex, we concluded that the relative constancy of cortical anaerobic glycolysis could be extended to the range from mouse to whale and that this aspect of cortical metabolism is probably primarily glial in localization. Some implications of the latter conclusion for the proposed role of astrocytes as modulators of neuronal activity have been discussed.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 27 (1976), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1106
    Keywords: Cerebral cortexin vitro andin vivo ; Chloride transport ; Primate ; Cortical edema
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. The swelling of intact primate cerebral cortex perfused under isosmotic conditionsin vivo, like swelling of slices of mammalian cerebral cortex incubatedin vitro, is a linear function of the concentration of K+ in the extracellular fluid over the range 20–120 mM. 2. The simultaneous presence of the Cl− ion is required for the development of K+-dependent swelling of cerebral cortex under various experimental conditionsin vivo andin vitro. 3. The maintenance of previously established K+-dependent swelling of cerebral cortex bothin vitro andin vivo requires the relative concentrations of both K+ and Cl− in the extracellular fluid to remain constant. A reduction in the concentration of either ion is associated with an absolute loss of fluid of swelling of cerebral cortex. 4. The content of Cl− in cerebral cortex is a function of the magnitude of K+-dependent swelling even though the concentration of Cl− in the extracellular fluid is maintained constant. 5. The mechanism of swelling in primate cerebral cortex following cerebral circulatory arrest is discussed in the light of the experimental findings, as a model of the type of brain injury encountered in massive clinical stroke.
    Type of Medium: Electronic Resource
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