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  • 1
    Digitale Medien
    Digitale Medien
    [s.l.] : Nature Publishing Group
    Nature 271 (1978), S. 559-561 
    ISSN: 1476-4687
    Quelle: Nature Archives 1869 - 2009
    Thema: Biologie , Chemie und Pharmazie , Medizin , Allgemeine Naturwissenschaft , Physik
    Notizen: [Auszug] Male rats of 150 to 200 g were killed by decapitation. Slices of 0.3 mm thickness were obtained from the rat corpus striatum and occipital cerebral cortex with a Mcllwain tissue chopper. The slices were transferred to the incubation medium in an open lucite cylinder with a nylon mesh fitted to the ...
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 306 (1979), S. 161-168 
    ISSN: 1432-1912
    Schlagwort(e): Noradrenaline ; GABA ; Tyramine ; Rat occipital cortex ; Cat nictitating membrane
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The effects of GABA were studied on the release of 3H-noradrenaline (3H-NA) evoked by potassium or by tyramine from slices of the rat occipital cortex and on the release of 3H-NA elicited by nerve stimulation from the cat nictitating membrane. GABA (30–1000μM) facilitated the potassium-evoked release of 3H-NA in a concentration dependent manner. This facilitatory effect was not antagonized by bicuculline (1–100 μM) or by picrotoxin (1–100 μM). Exposure to the GABA agonist muscimol (1–100 μM) did not affect either the spontaneous or the potassium-evoked release of 3H-NA. The facilitatory effect of GABA on the release of 3H-NA elicited by potassium was observed when the occipital cortex slices were exposed to 20 mM K+ during 1 min. When depolarization was induced by 35 mM K+ exposure to GABA failed to enhance the release of the neurotransmitter. GABA 300 μM did not affect the release of the labelled neurotransmitter evoked by exposure to tyramine 0.6 μM. In the cat nictitating membrane prelabelled with 3H-NA, the stimulation evoked release of the labelled neurotransmitter was not affected by GABA (10–300 μM). In conclusion, GABA has a facilitatory effect on the calcium-dependent, potassium evoked release of 3H-NA when the depolarization is of moderate degree. This effect of GABA appears to be selective for the central nervous system.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 311 (1980), S. 45-52 
    ISSN: 1432-1912
    Schlagwort(e): Monoamine oxidase inhibition Dopamine release ; Amphetamine ; Potassium depolarization ; Corpus striatum ; Substantia nigra
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The effects of monoamine oxidase inhibition on the release of 3H-dopamine induced by exposure to amphetamine or to potassium were studied in the corpus striatum and in the substantia nigra of the rat using identical in vitro experimental conditions. Marked differences between the two areas of the dopaminergic neurone were found. In the corpus striatum, release of 3H-dopamine was observed during exposure to low concentrations of amphetamine, while considerably higher concentrations of amphetamine were required to elicit 3H-dopamine release from the substantia nigra. The difference in the effects of amphetamine on the release of 3H-dopamine from the substantia nigra and the rat corpus striatum was observed independently of whether monoamine oxidase activity was intact or inhibited by pargyline. Exposure to potassium was also more effective in inducing 3H-dopamine release from the striatum than from the substantia nigra, but the difference was less pronounced than that observed for amphetamine. Since inhibition of monoamine oxidase by pargyline results in changes in the proportions of vesicular and axoplasmic dopamine, conclusions about the in vivo effects of amphetamine on dopaminergic neurotrans-mission should not be based on in vitro studies in which the enzyme is inhibited. In addition, in vitro studies on dopamine release by nerve depolarization should be carried out under the physiological conditions in which monoamine oxidase is not inhibited by drugs.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 320 (1982), S. 26-33 
    ISSN: 1432-1912
    Schlagwort(e): Convulsions ; Noradrenaline release ; Cerebral cortex ; Brain stem ; MOPEG levels ; Quaking mice
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The Quaking mouse is a genetically determined model of convulsive disorders. We investigated the modulation of noradrenergic neurotransmission through α2-adrenoceptors in the occipital cortex and the brain stem of this mutant. The endogenous levels of noradrenaline were similar in the cerebral cortex of the Quaking mice and their corresponding controls, while a significant increase of endogenous noradrenaline was found in the brain stem of the mutants. The rate of disappearance of noradrenaline in the cerebral cortex and the brain stem after injection of FLA 63 was identical in control and Quaking mice. The calciumdependent electrically evoked overflow of 3H-noradrenaline from slices of occipital cortex was inhibited by clonidine and enhanced by yohimbine in Quaking as well as in normal mice. The negative feed-back mechanism mediated by presynaptic α2-adrenoceptors operates to a similar extent in both strains of mice. In contrast to the occipital cortex, in the brain stem, the amount of neurotransmitter released by electrical stimulation was significantly increased in Quaking mice when compared with the controls. However, in the brain stem, the negative feed-back regulation of noradrenaline release operates to a similar extent in both strains of mice. When the endogenous levels of MOPEG were determined in the brain stem, they were found to be significantly higher in the Quaking mice when compared to the controls. The results suggest that an increase in noradrenergic neurotransmission in the brain stem, rather than in the cerebral cortex, could contribute to the behavioural abnormalities exhibited by the Quaking mice.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 322 (1983), S. 322-324 
    ISSN: 1432-1912
    Schlagwort(e): Corpus striatum ; (+)-Amphetamine ; Acetylcholine
    Quelle: Springer Online Journal Archives 1860-2000
    Thema: Medizin
    Notizen: Summary The electrically evoked, calcium-dependent release of 3H-acetylcholine from slices of rat striatum was inhibited in a concentration-dependent manner by (+)-amphetamine (0.2–20 μM). This inhibitory effect of (+)-amphetamine was unaffected by depletion of the endogenous stores, of dopamine by pretreatment with rescrpine (5 mg/kg, 24h). However, the combined treatment of reserpine with α-methyl-p-tyrosine (300 mg/kg) or NSD 1015 (100 mg/kg) reduced significantly these inhibitory effects of (+)-amphetamine. Similar results were obtained after chronic 6-hydroxydopamine lesions of the corpus striatum. The inhibition of 3H-acetylcholine release by (+)-amphetamine in rats pretreated with reserpine was potentiated in the presence of 10 μM pargyline. These results support the view that the inhibitory effects of (+)-amphetamine on the electrically-evoked release of 3H-acetylcholine are mediated by dopamine released from a special pool of newly synthetized transmitter rather than through a direct action on an amphetamine recognition site or receptor.
    Materialart: Digitale Medien
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