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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 338 (1988), S. 250-255 
    ISSN: 1432-1912
    Keywords: Rat nucleus accumbens ; Rat nucleus caudatusputamen ; Acetylcholine release ; Dopamine receptors
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Experiments in slices of rat nucleus accumbens were carried out in order to investigate whether the release of acetylcholine in this tissue is modulated through dopamine receptors. The slices were preincubated with 3H-choline and then superfused and stimulated electrically twice for 2 min each at a frequency of 3 Hz. The electrically evoked overflow of tritium averaged 2.9–3.9% of the tritium content of the tissue in the various groups. The D2-selective agonist quinpirole (0.01–1 μmol/l) reduced the evoked overflow of tritium by maximally 56%, an effect antagonized by the D2-selective antagonist (−)-sulpiride (1 μmol/l). The D1-selective agonist 2,3,4,5-tetrahydro-7,8-dihydroxy-1-phenyl-1H-3-benzazepine (SKF 38393) caused a slight decrease only at the high concentration of 10 μmol/l. (−)-Sulpiride (0.1–10 μmol/l) moderately increased the evoked overflow of tritium when given alone. The dopamine uptake inhibitor nomifensine (10 μmol/l) caused a decrease, and in its presence the increase produced by (−)-sulpiride became much more marked, amounting to maximally 149%. (+)-Sulpiride (0.1–1 μmol/l) failed to change the evoked overflow of tritium in the presence of nomifensine. The dopamine-releasing agent (±)-amphetamine (1 μmol/l) also reduced the evoked overflow, an effect abolished by (−)-sulpiride. Finally, bretylium (1 mmol/l), which blocks the release of dopamine, increased the evoked overflow. (−)-Sulpiride (1 μmol/l) lost its facilitatory effect in slices treated with bretylium. We conclude that the release of acetylcholine in rat nucleus accumbens, like its release in the nucleus caudatusputamen, is modulated through dopamine D2-receptors. The receptors are activated by endogenous dopamine under the conditions of these experiments.
    Type of Medium: Electronic Resource
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