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  • Blackwell Publishing Ltd  (3)
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  • 1
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 10 (1983), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. The influence of FLA-63 on pentobarbitone-induced sleep was studied in young chicks and adult rats.2. FLA-63 produced a time-dependent biphasic effect on the gross behaviour of chicks and rats; an initial sedation followed by behavioural excitation.3. The behavioural effects of FLA-63 were associated with an initial EEG synchronization prior to an increased activity of the EMG of the neck muscle and desynchronization of the EEG of the hyperstriatum, optic tectum and pontine reticular formation of the chick. Similarly, in rats, the EEG of the frontal cortex, optic lobe and pontine reticular formation was desynchronized while the EMG activity of the neck muscle was enhanced by FLA-63.4. FLA-63 delayed the onset and shortened the duration of pentobarbitone sleep.5. Pentobarbitone-induced EEG synchronization and decreased EMG activity in chicks was antagonized by FLA-63.6. Dopamine-induced antagonism of pentobarbitone sleep was potentiated by FLA-63 in chicks.7. Levodopa antagonized pentobarbitone-induced sleep in rats and this effect was potentiated by FLA-63.8. FLA-63 potentiated levodopa-induced desynchronization of the EEG of the frontal cortex, optic lobe and pontine reticular formation of the rat.9. Haloperidol antagonized the effect of FLA-63 on pentobarbitone-induced sleep in both rats and chicks.10. Noradrenaline induced behavioural sleep in young chicks dose-dependently; this effect was antagonized by phentolamine. In the rat, phentolamine shortened pentobarbitone sleeping time but did not significantly influence the effects of FLA-63 on pentobarbitone sleep.11. Those results suggest that an increased dopamine neurotransmission may be associated with the mechanism of wakefulness in chicks and rats.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 6 (1979), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. 6-Hydroxydopamine, injected intraperitoneally in rats and chicks, did not induce spontaneous seizures but produced significant alterations in the threshold to electroshock seizure in chicks; the particular effects were dose-dependent and time-dependent.2. Administration of 6-hydroxydopamine to 3 day old chicks and rats in the first and third days after birth resulted in an increase in the proportion exhibiting tonic seizure with electroshock when tested after 10–12 weeks.3. When 6-hydroxydopamine was injected intraperitoneally into adult rats and cocks, there was no significant alteration in seizure threshold.4. The results suggest that 6-hydroxydopamine penetrates the central nervous system of young chicks and rats and that adrenergic mechanisms are probably involved in modulating seizure mechanisms in both the chick and rat.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Oxford, UK : Blackwell Publishing Ltd
    Clinical and experimental pharmacology and physiology 7 (1980), S. 0 
    ISSN: 1440-1681
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Medicine
    Notes: 1. The influence of dopamine, levodopa and apomorphine on sleep produced by pentobarbitone was studied in 1-14 day old chicks.2. Pentobarbitone-induced sleep was associated with synchronization of the electroencephalogram (EEG) of the hyperstriatum, optic tectum and pontine reticular formation.3. Dopamine desynchronized the EEG and antagonized pentobarbitone-induced EEG synchronization.4. High doses of dopamine produced a delayed sleep which was potentiated by pimozide and antagonized by adrenoreceptor blocking agents.5. Dopamine, levodopa and apomorphine delayed the onset and shortened the duration of pentobarbitone-induced sleep; apomorphine was the most potent.6. Pimozide prolonged the duration of pentobarbitone-induced sleep, but had less effect when dopamine was also given.
    Type of Medium: Electronic Resource
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