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  • 1
    Electronic Resource
    Electronic Resource
    Oxford UK : Blackwell Science Ltd.
    Journal of neurochemistry 72 (1999), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract : The concentration of glucose in the brain's extracellularfluid remains controversial, with recent estimates and measurements rangingfrom 0.35 to 3.3 mM. In the present experiments, we used the methodof zero-net-flux microdialysis to determine glucose concentration in thehippocampal extracellular fluid of awake, freely moving rats. In addition, thepoint of zero-net-flux was measured across variations in flow rate to confirmthat the results for glucose measurement were robust to such variations. In3-month-old male Sprague-Dawley rats, the concentration of glucose in thehippocampal extracellular fluid was found to be 1.00 ± 0.05mM, which did not vary with changes in flow rate. Three-month-old and24-month-old Fischer-344 rats both showed a significantly higher hippocampalextracellular fluid glucose concentration, at 1.24 ± 0.07 and 1.21± 0.04 mM, respectively ; there was no significant differencebetween the two age groups. The present data demonstrate variation inextracellular brain glucose concentration between rat strains. When takentogether with previous data showing a striatal extracellular glucoseconcentration on the order of 0.5 mM, the data also demonstratevariation in extracellular glucose between brain regions. Traditional modelsof brain glucose transport and distribution, in which extracellularconcentration is assumed to be constant, may require revision.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Annals of the New York Academy of Sciences 771 (1995), S. 0 
    ISSN: 1749-6632
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Natural Sciences in General
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Psychopharmacology 96 (1988), S. 417-420 
    ISSN: 1432-2072
    Keywords: Memory ; Amnesia ; Scopolamine ; Glucose ; Epinephrine ; Arecoline ; Aging
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Numerous studies suggest that age-related declines in memory storage are related to impairment of central cholinergic systems. Scopolamine, a muscarinic cholinergic antagonist, has been used with young humans and other animal species as a model of the cognitive impairment that often accompanies normal and pathological aging. The present study examined whether amnesia induced by scopolamine could be counteracted in mice by arecoline, a cholinergic agonist, or by other drugs, epinephrine or glucose, which have been found to enhance memory in aged rodents and humans. Young mice were administered scopolamine (3 mg/kg, IP) or saline prior to training on an inhibitory avoidance apparatus. Immediately after training, animals received injections of epinephrine (0.01, 0.05, 0.1, and 0.2 mg/kg), glucose (10, 100, and 250 mg/kg), arecoline (0.5, 1, 2, 5, 10, and 20 mg/kg), or saline. The results indicate that pre-training scopolamine reliably impaired retention assessed in test trials 48 h after training. This impairment was not attentuated by any post-training dose of arecoline; however, immediate post-training injections of both epinephrine (at 0.05 mg/kg) and glucose (at 100 mg/kg) significantly reduced the amnesia. Neither of these drugs was effective if injections were delayed by 1 h after training. These results support the value of scopolamine as a model of age-related memory impairments, but suggest further that these memory deficits may be particularly susceptible to attenuation with non-cholinergic treatments.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1432-2072
    Keywords: Memory ; Acetylcholine ; Opiates ; Tremors ; Locomotor activity ; Naloxone ; Scopolamine ; Physostigmine ; Morphine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract Peripheral glucose administration enhances memory in rodents and humans. Recent findings suggest that glucose may affect behavior, in part, by augmenting central cholinergic functions and by attenuating central opiate functions. The present experiments examined interactions between an opiate antagonist, naloxone, and cholinergic agents to determine whether the effects would parallel those found with glucose. Three behavioral measures were assessed: tremors, hyperactivity, and spontaneous alternation. Naloxone (1 mg/kg) significantly augmented tremors elicited by physostigmine (0.3 mg/kg). Naloxone (1 mg/kg) also attenuated increases in locomotor activity and impairments in spontaneous alternation performance elicited by scopolamine (1 and 3 mg/kg for activity and alternation measures, respectively). Thus, across three diverse measures, naloxone produced effects similar to those previously reported for glucose. These findings are consistent with the hypothesis that release of cholinergic activity from opiate inhibition may contribute to glucose effects on behavior.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-2072
    Keywords: Amphetamine ; Memory storage processes ; Avoidance training ; Retrograde memory enhancement ; Retrograde amnesia
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Abstract These experiments examined the effects of d-amphetamine on retention of one-trial inhibitory (passive) avoidance training in mice. Water-deprived mice were pretrained to lick from a water spout at the end of a darkened compartment. Footschock was administered during licking after 4, 6, or 7 days of pretraining. Retention performance (latency to lick) was measured 24 h after training. The effects on memory of posttraining amphetamine varied not only with amphetamine dose but also with the amount of pretraining. In animals pretraining for 7 days, 0.3 and 1.0 mg/kg but not 0.03, 0.1, or 3.0 mg/kg posttraining amphetamine significantly enhanced later retention performance. In mice pretrained for 6 days, 1 mg/kg amphetamine also enhanced retention performance. However, in mice pretrained for only 4 days, 1 mg/kg amphetamine impaired later retention performance. These results are consistent with the view that posttraining treatments may affect memory storage processes by interacting with training-related arousal levels.
    Type of Medium: Electronic Resource
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