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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 76 (1998), S. 459-460 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Cardiovascular drug reviews 4 (1986), S. 0 
    ISSN: 1527-3466
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of molecular medicine 75 (1997), S. 75-76 
    ISSN: 1432-1440
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 283 (1974), S. 409-418 
    ISSN: 1432-1912
    Keywords: Dopamine ; Pentobarbital ; Halothane ; Haloperidol ; Depolarization ; Axotomy ; Turnover ; Feedback
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The synthesis of dopamine was determined as the accumulation of Dopa after Dopa decarboxylase inhibition. The release of dopamine was determined as the disappearance of the amine after treatment with the tyrosine hydroxylase inhibitor α-methyltyrosine. These processes were not significantly changed in the rat brain by pentobarbital sodium anaesthesia or by 10 min halothane anaesthesia. The accelerations of the dopamine synthesis and release after treatment with haloperidol were markedly reduced during pentobarbital, but not halothane anaesthesia. Anaesthesia with pentobarbital did not affect the increased synthesis and release of dopamine observed when the dopaminergic nerve terminals were depolarized by local treatment with KCl. The increases in dopamine synthesis and concentration after axotomy were similar whether the operation was performed during pentobarbital or halothane anaesthesia. It is suggested that the selective reduction of the haloperidol-induced effects by pentobarbital may be due to interference with a neuronal feedback loop.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-1912
    Keywords: Dopamine ; Axotomy ; Gammahydroxybutyric Acid ; Receptor Activity ; Amphetamine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The influence of blockade or stimulation of dopamine (DA) receptors on the selective increase in brain DA seen after axotomy or injection of gammahydroxybutyric acid (sodium form, 1.5 g/kg i.p.) was studied in rats. The increases were not changed after blockade of the DA receptors by haloperidol but were slightly reduced after stimulation of these receptors by apomorphine. Since pretreatment with haloperidol counteracted this effect of apomorphine, a diminished stimulation of DA receptors may partially be responsible for the increase in brain DA seen when the nerve impulse flow has been blocked in the DA neurones by axotomy or treatment with gammahydroxybutyric acid. The NA content was usually somewhat lowered on the lesioned side and this reduction was not changed after treatment with haloperidol, apomorphine or amphetamine. The increase in brain DA usually observed after axotomy was not found when the rats were also treated with reserpine and nialamide. This effect indicates that the negative feed-back of cytoplasmic DA on the DA synthesis operates also in the absence of nerve impulses. Injection of amphetamine before or after axotomy or treatment with gammahydroxybytyric acid markedly inhibited the increase in brain DA, probably due to release of newly synthesized DA.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 279 (1973), S. 89-92 
    ISSN: 1432-1912
    Keywords: Gammahydroxybutyric Acid ; GABA ; Substantia nigra ; Inhibition ; Dopamine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Injections of gammahydroxybutyric acid or gammaaminobutyric acid (GABA), but not betahydroxybutyric acid or carnitine, into the substantia nigra induced increases in brain dopamine of rats. No effect was found after injections into the neostriatum. The noradrenaline in the forebrain was unchanged after all the treatments. Gammahydroxybutyric acid may act by directly or indirectly mimicking an inhibitory GABA mechanism on the dopamine cells in the substantia nigra.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Naunyn-Schmiedeberg's archives of pharmacology 278 (1973), S. 347-361 
    ISSN: 1432-1912
    Keywords: Dopamine ; Noradrenaline ; Nerve Impulses ; Hemisection ; Gammaydroxybutyric Acid
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Both a unilateral, frontal section of the brain at the level of the caudal hypothalamus (hemisection) and systemic treatment with gammahydroxybutyric acid (GHBA, sodium form, 1.5 g/kg i.p.) increased the dopamine (DA) in the rat forebrain by about 70% in 1 h. Both procedures also markedly decelerated the α-methyltyrosine-induced DA disappearance. The brain noradrenaline was significantly lowered after the hemisection, but was not influenced by the treatment with GHBA given either alone or in combination with α-methyltyrosine. Intrastriatal injections of 25% KCl did not change the normal DA content significantly but prevented the increase in DA observed after hemisection or treatment with GHBA, probably due to a depolarization of the DA nerve terminals. Such a treatment with KCl also rapidly released the DA accumulated after hemisection. These effects were not seen after 20% NaCl. The same increase in forebrain DA, as produced by hemisection or treatment with GHBA, was also seen after injections of 25% KCl into the substantia nigra or injections of tetrodotoxin into the neostriatum. To judge from the turning of rats, unilateral injections of 25% KCl into the neostriatum depolarized the cells in this area, whereas stimulation of the DA receptors hyperpolarized them. The increases in brain DA described may be due to an inhibition of the nerve impulse flow to the DA nerve terminals.
    Type of Medium: Electronic Resource
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  • 8
    Book
    Book
    Berlin :Akad.-Verl.,
    Title: ¬Die¬ Wissenschaft geht ins Netz /; 21.2009
    Contributer: Stock, Günter
    Publisher: Berlin :Akad.-Verl.,
    Year of publication: 2009
    Pages: 81 S. : , Ill.
    Series Statement: Gegenworte 21.2009
    Type of Medium: Book
    Language: German
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