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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 41 (1981), S. 346-357 
    ISSN: 1432-1106
    Keywords: Rat ; Tryptophan deprivation ; Sleep circadian rhythm ; Serotonin metabolism
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. A long-term (up to 16 weeks) tryp-tophan (TRP)-free diet was administered to chronically implanted adult rats in order to study the effects of a sustained reduction of endogenous brain serotonin (5-HT) levels on the sleep-waking cycle. Twentyfour hours polygraphic recordings were made either periodically on an EEG apparatus, or uninterruptedly over 50 days by a frequency analyser. Quantitative changes in wakefulness (W), slow wave sleep (SWS) and paradoxical sleep (PS), as well as the number and duration of these episodes, were studied over 24 h, with a dark period (DP) and a light period (LP). Biochemical changes in 5-HT metabolism were measured in both plasma and brain. 2. Under control conditions, the percentage of W was twice as great in DP as in LP, while the quantities of SWS and PS were twice as high in LP as in DP. Surprisingly, in spite of a decrease of about 50% in brain 5-HT under TRP-deprived conditions, no dramatic changes were observed in the qualitative or quantitative aspects of W, SWS or PS. The only electrocorticographic (ECoG) change was a disappearance of sleep spindles, which became total after 14 weeks. During the first month, there was a 7% increase in W accompanied by a 6% decrease in SWS and a 5–9% reduction in PS. Later, W and SWS returned to their control values, while the PS deficit persisted throughout the TRP-deprivation period. Despite the absence of severe quantitative disturbances over 24 h, an internal reorganization of the sleep cycle took place. This new balance, established after 2 months, was characterized by a tendency toward an equal distribution of the stages in DP and LP, resulting in the disappearance of the sleep circadian rhythm. 3. Our results are compared with those of other authors who lowered the endogenous 5-HT levels by various means, including ‘acute’ or partial TRP-deprivation. The present findings suggest that adaptive cerebral mechanisms are able to compensate for the disturbances in 5-HT metabolism, in structures responsible for W and SWS. They indicate that the neurohumoral processes underlying sleep circadian rhythm in the rat are serotoninergic and/or noradrenergic.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 48 (1982), S. 137-143 
    ISSN: 1432-1106
    Keywords: GABA uptake ; Radioautography ; Ultrastructure ; Oculomotor nucleus ; Cat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The uptake of tritiated γ-aminobutyric acid (3H-GABA) in the oculomotor nucleus of the cat was studied, using light and electron microscopic examination of radioautograms after intracerebral in vivo administration of the amino-acid. A glial uptake by oligodendrocytes was seen together with a neuronal uptake of the tracer in a certain type of axon terminals found in synaptic contact with both dendrites and soma, some of them exhibiting all the ultrastructural features of motoneurons. Previous neurochemical, electrophysiological and immunocytochemical studies indicate that GABA might well be the inhibitory neurotransmitter in the vestibuloocular reflex arc. The present results show that a morphological substrate exists for the presumed postsynaptic GABAergic inhibition of ocular motoneurons, at least in the oculomotor nucleus of the cat.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    European archives of psychiatry and clinical neuroscience 209 (1967), S. 462-473 
    ISSN: 1433-8491
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Zusammenfassung 1. Mit der vonPlas u.Naquet beschriebenen Ableitungsmethodik wird die Wirkung von Benzodiazepinen (Valium und Mogadan) auf corticale und tiefe Hirnstrukturen der Katze untersucht. 2. Beide Substanzen erzeugen einemonorhythmische Synchronisation der raschen EEG-Frequenzen (Zunahme der Amplitude schneller EEG-Wellen bei unveränderter Frequenz). Rasche Frequenzen überlagern auch die Aktivitäten des Hippocampus und sehr hohe Spindeln bis zu 400 μV erscheinen im Bereich der Amygdala (latero-basaler Kern). 3. Die Weckreaktion über dem Gyrus cruciatus, supra-sylvius und ectosylvius durch Stimulierung der Formatio reticulariswird verkürzt, die Rhythmen sind langsamer und von größerer Amplitude. Mogadan und Valium wirken unterschiedlich auf „waxing and waning“ der rekrutierten Antwort: Mogadan blockiert die Spindeln, während sie unter Valium immer noch zu erhalten sind, wenn man die Reizschwelle erhöht. 4. Die spezifischen und unspezifischen Reaktionspotentiale (evoked potentials) im optischen System auf Lichtblitze und in der Formatio reticularis mesencephalis nach elektrischer Reizung des Ischiadicus oder der Formatio reticularis bulbaris zeigen eineVerlängerung der Latenzzeit und eine Verminderung der Amplitude, jedoch keine komplette Blockterung. Die durch Reizung der Amygdala hervorgerufenen Nachentladungen erfahren eine Veränderung der Form, eine Verkürzung und besonders eine Verminderung der Ausbreitung. Mogadan erhöht die Cardiazolschwelle um das Neunfache, Valium auf das Siebenfache. 5. Der unter Mogadan im chronischen Versuch beobachteteSchlaf unterscheidet sich durch die Abwesenheit der sonst vorhandenen langsamen Spindeln, während die raschen Spindeln über 16/sec unverändert bleiben.Während des paradoxen Schlafes vermindern sich die Augenbewegungen bis zum Verschwinden. 6. Wir vermuten, daß Mogadan und Valium die Erregungsausbreitungen in polysynaptischen Relais verzögern und langsame neuronale Synchronisationenhemmen. Die antiepileptische Wirkung auf Epilepsieformen mit hypersynchronen Paroxysmen und langsamen EEG-Wellen (petit-mal, Absencen) könnte damit zusammenhängen.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1573-7381
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary GABA-immunoreactive neuronal elements were detected in the stratum griseum superficiale or superficial gray layer of the rat superior colliculus in an electron microscopic study, using postembedding immunocytochemistry with protein A-gold as a marker. In addition to neuronal somata, two types of GABA-immunoreactive neuronal processes were observed. Numerous profiles of axon terminals (1 μm in diameter) with clear round or pleomorphic synaptic vesicles and mitochondria were found to establish mostly symmetrical synaptic contacts with GABA-immunonegative dendrites of various diameters. Some axosomatic synapses could also be observed. The gold particle density in this axon terminal compartment was between seven and 13 times the background level. The stratum griseum superficiale also included GABA-immunoreactive dendrites, some of which contained clear synaptic vesicles. These dendritic profiles always formed the presynaptic component of dendrodendritic synaptic contacts. The density of the gold particles in the dendritic compartment, taken as a whole, was between three and 13 times the background level. Furthermore, the relationship between the GABA-immunoreactive neuronal elements and degenerating retinal nerve endings identified in the left stratum griseum superficiale following enucleation of the right eye was investigated after a 7-day survival period. The profiles of degenerating retinal nerve endings (0.7 μm in diameter) were found to be devoid of any specific labelling. Most of the retinal boutons established axodendritic synapses of the asymmetrical type with an immunonegative dendrite, which was also contacted in some cases by a GABA-immunopositive axon terminal. Other retinal endings were presynaptic to GABA-immunopositive dendritic profiles with synaptic vesicles, some of which were found to contact in turn an unlabelled dendrite, thereby completing serial synaptic relationships. More rarely, retinal endings formed the presynaptic component of possible axoaxonic synapses with GABA-positive terminals presumed to be axonic in nature. It can be concluded that the retinal input to the superficial gray layer often converges with a GABAergic axonal input on a dendritic target, the neurotransmitter specificity of which is unknown. In other cases, retinal terminals synaptically contact GABA-immunolabelled conventional and presynaptic dendrites and probably also some axon terminals; this might provide an anatomical substrate for the control of GABA release from these GABAergic processes. These results indicate that transmitter GABA plays an important role in retinocollicular transmission.
    Type of Medium: Electronic Resource
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