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   <subfield code="a">10.1007/BF00168742</subfield>
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   <subfield code="a">Adenosine but not an adenine nucleotide mediates tonic purinergic inhibition, as well as inhibition by glutamate, of noradrenaline release in rabbit brain cortex slices</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Ivar von Kügelgen, Leni Späth, Klaus Starke]</subfield>
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   <subfield code="a">Summary: A possible contribution of adenine nucleotides to the endogenous purinergic, A1-receptor-mediated inhibition of noradrenaline release was studied in rabbit occipito-parietal cortex slices. The slices were preincubated with [3H]-noradrenaline and then superfused and stimulated electrically, in most experiments by trains of 6 pulses/100 Hz. A few experiments were carried out in rat occipito-parietal cortex slices. The A1-purinoceptor antagonist 8-cyclopentyl-1,3-dipropylxanthine (DPCPX; 1-100 nmol/l) as well as the enzyme adenosine deaminase (0.1-10 U/ml) increased the electrically evoked overflow of tritiated compounds. The maximal increase was by about 85% for both DPCPX and adenosine deaminase. The increases obtained with maximally effective concentrations of DPCPX and adenosine deaminase were not additive. The α1-adrenoceptor-selective agonist methoxamine (10 but not 1 μmol/l) reduced the evoked overflow. Its effect was antagonized by yohimbine 1 μmol/l but then not attenuated further by DPCPX100 nmol/l.L-Glutamate (300 μmol/l-2.3 mmol/l) also reduced the evoked overflow of tritium. Its effect was not changed by yohimbine 1 μmol/l but greatly, and to the same extent, attenuated by DPCPX 100 μmol/l and adenosine deaminase 3 U/ml. Neither the N-methyl-D-aspartate (NMDA) receptor antagonist dizocilpine nor omission of Mg++ changed the inhibition by glutamate. Glutamate did not alter the basal efflux of tritium from rabbit cortex slices under any experimental condition. In contrast, glutamate (100 μmol/l and 1 μmol/l) caused an immediate, marked and transient acceleration of tritium outflow from rat occipitoparietal cortex slices (medium without Mg++). It is concluded that adenosine but not an adenine nucleotide mediates the tonic purinergic presynaptic inhibition of noradrenaline release in rabbit brain cortex. The marked degree of disinhibition by DPCPX and adenosine deaminase underscores the potential physiological role of this inhibition. The purinergic inhibitory tone is reinforced by glutamate, indicating that glutamate releases adenyl compounds in rabbit brain cortex. Again adenosine but not an adenine nucleotide mediates the indirect inhibition by glutamate of the release of noradrenaline. The noradrenaline-releasing effect that glutamate exerts in rat occipito-parietal cortex does not occur in rabbit occipito-parietal cortex. Methoxamine depresses the release of noradrenaline in rabbit brain cortex directly at presynaptic α2-adrenoceptors rather than by release of purines.</subfield>
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   <subfield code="a">Springer-Verlag, 1992</subfield>
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   <subfield code="a">Presynaptic adenosine A1-receptors</subfield>
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   <subfield code="a">Adenine nucleotides</subfield>
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   <subfield code="a">Noradrenaline release</subfield>
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   <subfield code="a">Rabbit brain cortex</subfield>
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   <subfield code="a">von Kügelgen</subfield>
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   <subfield code="u">Pharmakologisches Institut, Hermann-Herder-Strasse 5, W 7800, Freiburg i. Br., Federal Republic of Germany</subfield>
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   <subfield code="t">Naunyn-Schmiedeberg's Archives of Pharmacology</subfield>
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