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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 45 (1985), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: When rat brain synaptosomes were incubated for 10 min at 37°C, basal accumulation of adenosine in the medium was 66 pmol/mg of protein. An elevated K+ level (24 mM) evoked an additional accumulation of 200 pmol/mg of protein, and 50 μM veratridine evoked 583 pmol of adenosine accumulation/mg of protein. K+- and veratridine-evoked accumulation of adenosine did not arise from microsomal or mitochondrial contaminants of the synaptosomal preparation, because purified microsomes and mitochondria did not exhibit evoked accumulation of adenosine in the medium. K+-evoked accumulation of extrasynaptosomal adenosine was Ca2+-dependent, whereas veratridine-evoked accumulation of adenosine was increased in Ca2+-free medium. In the presence of α,β-methylene ADP and GMP, which inhibit ecto-5′-nucleotidase, conversion of added ATP and AMP to adenosine was inhibited by 90% in synaptosomal suspensions. However, inhibition of ecto-5′-nucleotidase only reduced basal extrasynaptosomal accumulation of adenosine by 74%, veratridine-evoked accumulation of adenosine by 46%, and K+-evoked accumulation by 33%. Most of the basal accumulation of extrasynaptosomal adenosine appears to be derived from released nucleotide, probably ATP, but about half of the veratridine-evoked accumulation of adenosine and most of the K+-evoked accumulation may arise from adenosine released in its own right, rather than from a released nucleotide.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 60 (1993), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract: Morphine-induced release of adenosine from the spinal cord is believed to contribute to spinal antinociception. Although this release is Ca2+ dependent, little is known of the nature of this dependence. In this study, the effects of the dihydropyridine L-type Ca2+ channel agonist Bay K 8644 and the antagonist nifedipine, the N-type Ca2+ channel antagonist ω-conotoxin, and ruthenium red, a blocker of Ca2+ influx induced by capsaicin, on release of adenosine evoked by morphine were determined. The effect of partial depolarization with a minimally effective concentration of K+ on morphine-evoked release of adenosine also was examined. Morphine 10−5-10−4M produced a dose-dependent enhancement of adenosine release from dorsal spinal cord synaptosomes. Following the addition of 6 mM K+ (total K+ concentration of 10.7 mM), 10−6M morphine also enhanced release, and an additional component of action at 10−8M was revealed. Release was Ca2+-dependent as it was not observed in the absence of Ca2+ and presence of EGTA. Bay K 8644 (10 nM) and nifedipine (100 nM) had no effect on the release of adenosine evoked by morphine, but ω-conotoxin (100 nM) markedly reduced such release in both the absence and the presence of the additional 6 mM K+. Morphine-evoked adenosine release was not altered in the presence of a partially effective dose of capsaicin, nor by ruthenium red. These results indicate that morphine can stimulate two distinct phases of adenosine release from the spinal cord (nanomolar and micromolar), and that both phases of release are due to Ca2+ entry via ω-conotoxin-sensitive N-type Ca2+ channels.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 29 (1977), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— —The effects of brief exposures of rat brain synaptosomes to veratridine, gramicidin D and valinomycin on noradrenaline uptake were investigated. All three drugs inhibited the Na+-dependent component of noradrenaline uptake by synaptosomes. These effects were independent of extracellular Ca2 + concentrations, indicating that the reductions were not due to the release of newly accumulated noradrenaline.Gramicidin D reduced the Vmax for noradrenaline uptake, whereas veratridine and valinomycin reduced the Vmax and also increased the Vm for uptake.Most of these findings can be explained on the basis of the effects that these drugs have on the inward-directed electrochemical gradients for Na+ across synaptosomal membranes, although, in the cases of veratridine and valinomycin, the elevated Km's suggest that an impairment of noradrenaline binding to its carriers might also be involved.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 30 (1978), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: A technique was developed which permitted the release of ATP from synaptosomes by elevated extracellular K+ or by veratridine to be directly and continuously monitored. The released ATP interacted with firefly luciferin and luciferase in the incubation medium to produce light which could be detected by a photomultiplier. The assay system was specific for ATP, in that similar concentrations of adenosine, AMP or ADP did not produce chemiluminescence. Moreover, the maximum peak of light emission correlated linearly with the concentrations of ATP present in the medium, so that semiquantitative estimates of ATP release could be made.Elevating the extracellular K+ concentration produced a graded release of ATP from synaptosomes. Rb+ also released ATP but Na+, Li+ and choline did not. The response to elevated K+ was not blocked by tetrodotoxin (TTX), indicating that this effect was not mediated by the opening of Na+-channels in synaptosomal membranes.Veratridine (50 μM) caused a graded release of ATP which was larger and more prolonged than that caused by elevated K+. The release of ATP by veratridine was blocked by TTX indicating that the opening of Na+-channels was involved. Neither veratridine nor elevated K+ released ATP from microsomal or mitochondrial fractions, showing that the release of ATP probably did not originate from microsomal, vesicular or mitochondrial contaminants of the synaptosomal preparation.Release of ATP by elevated K+ was diminished in a medium lacking CaCl+ or when EGTA was added to chelate Ca2+. In contrast, release by veratridine appeared to be augmented in Ca2+-free media or in the presence of EGTA.The K+-induced release of ATP, which is Ca2+ dependent, closely resembles the exocytotic release of putative neurotransmitters from presynaptic nerve-terminals. On the other hand, the apparent lack of a Ca2+ requirement for veratridine's action suggests that this process could originate from other sites, or involve mechanisms other than conventional neurotransmitter release processes.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 24 (1975), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: –The effects of divalent cations on the initial rates of noradrenaline uptake by synaptosomes were determined using Millipore filtration to terminate the reaction. The removal of either Ca2+ or Mg2+ from the incubation medium had no effect on uptake, but when both Ca2+ and Mg2+ were removed, uptake was reduced. Uptake was also diminished when Ca2+ was absent and 1 mm-EGTA added to the medium. It appeared that Ca2+ was required for optimal uptake but that Mg2+ could partially substitute for Ca2+ in this regard. The reduction in the rate of uptake when both Ca2+0 and Mg2+ were absent could be rapidly and completely reversed by restoring Ca2+, Mg2+, or both Ca2+ and Mg2+ to the incubation medium. Of the divalent cations tested, Ca2+ and Mg2+, but not Mn2+, supported noradrenaline uptake. When the kinetics of uptake were examined, it was found that removing both Ca2+ and Mg2+ from the medium resulted in a reduction of the Vmax for noradrenaline uptake. It is apparent from these results that, in addition to facilitating the release of noradrenaline from noradrenergic terminals, Ca2+ may also play a role in the uptake of noradrenaline by presynaptic nerve-endings in the CNS.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 28 (1977), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— The effects of brief exposures of a number of depolarizing agents on 24Na+ influx and on the Na+, K+ and ATP contents of synaptosomes were studied using a Millipore filtration technique to terminate the reaction. When synaptosomes were incubated in normal medium, there was a rapid influx of 24Na+ and a gain in Na’contents; neither the 24Na+ influx nor the Na+ gain were blocked by tetrodotoxin suggesting that this Na+ entry did not involve Na+-channels.Veratridine markedly increased the rate of 24Na+ influx into synaptosomes and also increased the Na+ content and decreased the K+ content of synaptosomes within the first 10s of exposure. The normal ion contents were reversed by 1 min. The effects of veratridine on Na+ influx and on synaptosomal ion contents were prevented by tetrodotoxin and required Na+ in the medium.The ionophores gramicidin D and valinomycin also rapidly reversed the Na+ and K+ contents of synaptosomes, but these effects could not be blocked by tetrodotoxin. The reducing effect of gramicidin D on synaptosomal K+ content required Na’in the medium, whereas valinomycin caused a fall in the K+ content of synaptosomes in a Na+-free medium.Veratridine and gramicidin D, at concentrations known to reverse the synaptosomal ion contents, did not affect synaptosomal ATP levels. In contrast, valinomycin and NaCN caused an abrupt fall in synaptosomal ATP levels.The above findings suggest that veratridine quickly alters synaptosomal Na+ and K+ contents by opening Na +-channels in the presynaptic membrane, and provide direct evidence for the existence of Na+-channels in synaptosomes. In contrast, gramicidin D and valinomycin appear to act independently of Na +-channels, possibly by their ionophoric effects and, in the case of valinomycin, by diminishing synaptosomal ATP contents and hence diminishing Na+-pump activity.The rapid reversals of Na+ and K+ contents by these drugs could affect the resting membrane potentials, Na+-Ca2+ exchange across the synaptosomal membrane, and the release, synthesis and uptake of neurotransmitters by synaptosomes.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 18 (1971), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— 〈list xml:id="l1" style="custom"〉1The passive permeability of synaptosomes to ions was measured by a light-scattering technique. Synaptosomes were freely permeable to acetate, HCO3_, SCN−and NH4+ and were impermeable to choline and SO42-.2Gramicidin D selectively increased the permeability of synaptosomes to Na+ and K+ ions.3The relative permeabilities of Na+, K+ and Cl−, measured in the presence of a number of more permeant counter-ions, was in the ratio 1:19:12. These values are discussed in terms of the source of the resting potential.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Journal of neurochemistry 17 (1970), S. 0 
    ISSN: 1471-4159
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: Abstract— (1) Swelling of synaptosomes was measured spectrophotometrically by recording changes in extinction at 520 nm.(2) Synaptosomes behaved as osmometers in NaCl solutions. When the tonicity of the medium was changed, synaptosome volume changed in accordance with Boyle and van't Hoff's Law. These changes were reversed on restoring the tonicity of the medium.(3) The rate at which a solute entered the synaptosome was determined from the rate of swelling in the presence of that solute. Permeability of synaptosomes to non-electrolytes was in the order glucose ≪ glycerol 〈 thiourea = formamide 〈 propylene glycol = dimethylsulphoxide.(4) Synaptosomes were freely permeable to ammonium and acetate ions and impermeable to Ca2+, Mg2+, PO42−, SO42− and oxalate ions.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] A survey of Ethiopia's Middle Awash Valley in 1981 yielded new and significant archaeological, palaeontological, geological and geochronological results. Included in the new discoveries are hominid fossils from the Pliocene which show primitive cranial anatomy and a femur adapted to ...
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 376 (1995), S. 559-559 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] WOLDEGABRIEL ET AL. REPLY - Our first published chronological assessment was made on the basis of stratigraphy, structural relationships, biochronology, 40Ar/39Ar dating and palaeomagnetic data3. Regional dip, coupled with stratigraphic and structural coherence, indicated that the Aramis strata ...
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