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  • 1
    ISSN: 1432-0878
    Keywords: Bulbospinal indoleamine neurons (rat) ; 5,6- and 5,7-DHT ; De- and regeneration ; Fluorescence microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary In an attempt to determine the conditions which permit central 5-HT neurons to respond to a chemical injury of their axons by sprouting and regeneration, the pattern and time-course of recovery of 5-HT concentrations and regrowth of bulbospinal 5-HT axons were evaluated in rats subjected to intraventricular treatment with either 75 μg 5,6- or 150 μg 5,7-DHT. While 5,6-DHT treatment is followed by a significant recovery of 5-HT concentrations in the telodiencephalon, brainstem and upper part of the spinal cord within 3 months, there is no significant restoration of the severely depleted 5-HT levels in the telodiencephalon and spinal cord, and only limited recovery in 5-HT content of the brainstem preparation after 5,7-DHT. These differences conform to the observation of widespread and effective regrowth and regeneration of the bulbospinal 5-HT neurons in the 5,6-DHT treated lower brainstem and upper spinal cord but restricted and localized sprouting efforts in the 5,7-DHT treated lower medulla oblongata. This could be explained by a cell body near lesion of the non-terminal indoleamine axons by 5,7-DHT which results in a late retrograde, irreversible degeneration of most of the indoleamine pericarya from group B1 and many of group B3. It is concluded that the preservation of a critical length of the main axon and part of its collaterals is necessary for the neuron's survival, and that the individual pattern of the neuropil architecture of brain centres which are invaded by the axonal sprouts may significantly influence their growth characteristics and thus either favour or impede their chance to reestablish connections with their original effector. Aberrant, localized, intense sprouting of drug-damaged axons may in itself reflect the need of the neuron—deprived of most of its axonal tree—to reestablish its original total axonal length by multiple branching.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-0878
    Keywords: Intestine, Lampetra fluviatilis ; Serotonin-, dopamine-, noradrenaline-containing neurons ; Identification by histochemistry ; Electron microscopy ; Biochemistry
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Monoamine-containing neurons in the gut of Lampetra fluviatilis are characterized by histochemical, electron microscopical and biochemical methods. Strongly yellow fluorescent, probably serotonin-containing intrinsic neurons are found along the entire length of the intestine. Their processes aggregate to form large bundles of mainly non-terminal axons, constituting a subepithelial fibre plexus. This subepithelial, ganglion cell comprising plexus is connected to a wide-meshed subserosal plexus which has ganglion cells of different size and few varicose, single axons. Intermingled with both plexus there occur — in the anterior and middle but not in the preanal portion of the lamprey intestine — scattered green fluorescent intrinsic perikarya, emanating faintly green fluorescent, poorly varicosed axons. The formaldehyde-induced neuronal fluorophores conform to serotonin (yellow fluorescent compound), noradrenaline, and dopamine (green fluorescent substance), as revealed in microspectrofluorimetric recordings. The electron microscopical analysis of the yellow fluorescent intrinsic neurons in the terminal hindgut shows nerve cell pericarya and axons equipped with a typical population of occasional small granular and many large granular vesicles (750–1600 Å). The number and opacity of cores of the small and the osmiophilia of the cores of the large granular vesicles are significantly increased following short-term treatment with 5,6-dihydroxytryptamine. Long-term treatment with 5,6- or 5,7-dihydroxytryptamine provokes severe signs of ultrastructure impairment and eventual degeneration in the supposed serotonin-containing axons, besides indications of piling-up of organelles in the non-terminal axons due to arrest of axonal transport. Chromatography of acid extracts from the lamprey intestine, gills and kidney reveals the presence of serotonin (besides another unidentified indoleamine) and dopamine and noradrenaline in the gut, but only dopamine in the brain. The detection of serotonin, noradrenaline and dopamine in the lamprey gut is confirmed by chemical determinations. The occurrence of intrinsic serotonin-, noradrenaline- and dopamine-containing neurons in the gut of Lampetra fluviatilis deviates from the established pattern of innervation of the vertebrate intestine and is considered to be a remnant of an autonomic innervation principle common in invertebrates.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 135 (1972), S. 399-414 
    ISSN: 1432-0878
    Keywords: Rat CNS ; Indoleamine containing neurons ; Chemically induced damage ; 5,7-Dihydroxytryptamine ; Drug induced behavioral alterations
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Intraventricular injections of moderate doses (25–75μg) of 5,7-dihydroxytryptamine (5,7-DHT) into the left lateral ventricle of ether anaesthetized rats cause pronounced damage to CNS indoleamine axons, reflected by accumulations of large amounts of serotonin in distorted, heavily swollen axons, so called indoleamine droplet fibres. Larger doses (100, 150 or 300 μg) provoke a piling up of catecholamines in drug affected preterminal catecholamine containing fibres besides extensive lesioning of indoleamine axons. 5,7-DHT condenses with formaldehyde to form a light yellow fluorescent compound. Uptake and accumulation of 5,7-DHT into indoleamine terminals and axons—as revealed in short term experiments—provides a means of mapping of indoleamine neurons in the rat brain. Following the application of 5,7-DHT (25–150 μg), rats develop characteristic behavioural disturbances, as e.g. increased sensitivity to sensory stimulation, and a failure to habituate to repeatedly applied sensory stimuli, and bizarre social behaviour, i.e. repeated fighting attacks in an unusual upright posture. These alterations resemble those observed after 5,6-DHT and may be indicative of a deprivation of the brain from functional serotonin. 5,7-DHT is considered to be an important, additional tool for the investigation of serotonin neurons and problems of serotonin transmission in the mammalian brain.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Cell & tissue research 147 (1974), S. 285-292 
    ISSN: 1432-0878
    Keywords: Median eminence ; Rat ; Serotonin terminals ; 5,6- and 5,7-Dihydroxytryptamine ; Chemical degeneration
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Electron microscopical evidence for the existence of an important serotonergic input to the rat median eminence is presented. This evidence is based on the demonstration of degenerating nerve terminals in the external layer of the rat median eminence following the application of 5,6-dihydroxytryptamine or 5,7-dihydroxytryptamine, drugs known to exert more or less selective toxic effects on central serotonin neurons. The finding of a serotonergic innervation of the median eminence in mammals has important implications for 5-hydroxytryptamine as a modulator of synthesis and/or release of hypothalamic, hypophysiotropic hormones.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-0878
    Keywords: Indoleamine containing nerve terminals ; Chemically induced degeneration ; 5,6-dihydroxytryptamine ; Rat brain
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary 5,6-dihydroxytryptamine (5,6-DHT) has been found to induce a substantial degree of “chemical degeneration” of indoleamine containing nerve terminals in the rat brain following a single intraventricular injection of 75 μg 5,6-DHT per animal. The disintegration of varicose terminal portions of serotonin containing neurons is reflected 1. by a loss of yellow fluorescent varicosities in certain defined parts of the rat CNS, despite a mild inhibition of the serotonin catabolizing enzyme monoamine oxidase with nialamide in the pretreated animals, 2. by a significant drop of the chemically measurable 5-hydroxytryptamine content in nearly all parts of the rat brain and spinal cord, 3. by the appearance of highly, orange or brownish fluorescent axons provided with numerous unusually large, distorted and intensely fluorescent swellings (“droplets”), resembling proximal stumps of mechanically severed indoleamine containing axons, 4. a temporary increase in the amount of indoleamine fluorophores stored in some neuronal pericarya, and 5. the electron microscopical demonstration of degenerating synaptic swellings of unmyelinated axons at all sites investigated. The selectivity of the effect of 5,6-DHT on indoleamine neurons is indicated by the absence of similar signs of injury in catecholamine containing neurons of the rat CNS.
    Type of Medium: Electronic Resource
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