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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 18 (1973), S. 446-463 
    ISSN: 1432-1106
    Keywords: Cerebellum ; Vestibular ; Spinocerebellar ; Purkinje ; Deiters
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The organization of the cerebellar, vestibular and spinal inputs to the lateral and medial vestibulospinal tract (LVST and MVST) cells was studied in anaesthetized rabbits. Synaptic actions of these inputs were determined by recording postsynaptic potentials intracellularly and also unit spike discharges extracellularly from a number of LVST and MVST cells. As reported previously in cats, inhibition was evoked very frequently from the vermal cortex of the cerebellar anterior lobe and less frequently from that of the posterior lobe. However, no such inhibition was derived from the flocculus. The cerebellar inhibition was exerted upon both LVST and MVST cells, whether they received monosynaptic activation from the primary vestibular afferents (second-order) or not and whether they conducted impulses fast or slowly. However, the inhibition was frequently absent in “slow” “second-order” MVST cells. The vast majority of LVST and MVST cells received an excitatory input from the spinocerebellar afferents ascending the funiculus posterolateralis. This input was particularly prominent from the upper cervical cord. The spinal excitation thus obtained occurred in close connection with the cerebellar inhibition. Hence, it appears that the cerebellar vermis receives the spinal signals that drive LVST and MVST cells and in turn sends out inhibitory signals to adjust the reflex activity in these cells.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1432-1106
    Keywords: Inferior olive ; Cerebellum ; Flocculus ; Rabbit ; Eye movement
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary After the dorsal cap and adjacent ventrolateral outgrowth regions of the inferior olive had been chronically destroyed in the rabbits, the eye movements evoked by local stimulation of the flocculus were reduced in amplitude and reversed in direction, indicating that the inhibition by flocculus Purkinje cells of vestibulo-ocular relay neurons could no longer be actuated by the stimulation.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 4 (1968), S. 310-320 
    ISSN: 1432-1106
    Keywords: Deiters neurones ; Cerebellum ; Inhibitory zone ; Cats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary By recording intracellularly from Deiters neurones of cats, there was a survey of those cerebellar areas that, when stimulated, produced inhibitory postsynaptic potentials (IPSPs) monosynaptically in Deiters neurones. The monosynaptic inhibitory area expanded longitudinally mainly along the ipsilateral vermal cortex of the anterior lobe. The ipsilateral cortex of the posterior lobe was also effective in inhibiting Deiters neurones though less prominently than the anterior lobe. The inhibitory fibers could be stimulated in the white matter of the cerebellum, predominantly in the ipsilateral side at rostral regions of nuclei fastigii and interpositus. It was further shown that the monosynaptic inhibition from the anterior and posterior lobes occurs chiefly in the dorsal portion of Deiters nucleus. Since in both the cerebellum and Deiters nucleus the spatial pattern of distribution of the inhibitory fibers conforms to that of the corticovestibular fibers as histologically defined, the experimental findings are in accord with the hypothesis that the cerebellar Purkinje cells are inhibitory in nature.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 6 (1968), S. 247-264 
    ISSN: 1432-1106
    Keywords: Deiters neurones ; Disinhibition ; Cerebellum ; Cats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Following the stimulation of cerebellar cortex, a slow depolarization developed in the neurones which were impaled with microelectrodes in the dorsal portion of the nucleus of Deiters. Characteristically, it was produced bilaterally from a wide area of the culmen and, with double shock stimulation at brief intervals, showed a marked potentiation, often in association with a later depression. After repetitive stimulation of the cerebellar cortex the slow depolarization was prolonged for a period of many seconds. Even stimulation of the spinal cord caused similar depolarization. By intracellular injection of currents and ions, the depolarization was shown to be disinhibition, i. e., removal of background inhibition. Accordingly, it was confirmed that there was a steady production of IPSPs in dorsal Deiters neurones, which diminished during the phase of disinhibition. As the possible source of these background IPSPs, the Purkinje cell axons within the nucleus of Deiters were found to be discharging rhythmically at a rate of 20–90/sec, and in fact they were depressed very effectively after cerebellar stimulation. At the same time, volleys along Purkinje cell axons produced by a testing cerebellar stimulation also were diminished, indicating a depression in the excitability of Purkinje cells.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 281 (1989), S. 254-259 
    ISSN: 1432-069X
    Keywords: Innermost cell layer ; Tonofilaments ; Huxley's cells ; Henle's cells ; Anagen hair follicles ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary To elucidate the biologic roles and further cytologic characteristics of the innermost cell (IMC) layer of the outer root sheath (ORS), human anagen hair follicles were ultrastructurally examined. In the lower follicle, the transeversely running tonofilaments in the inner side of the cytoplasm of the IMCs showed a massive accumulation, facing the keratinized part of a Huxley's cell protruding through a Henle's pore. In a rare instance, a spindle-shaped cell was seen between the IMC layer and the keratinized Henle's layer. At the lower isthmus portion, some of the IMCs containing a large number of tonofilaments showed a partial degeneration of the inner side of the cytoplasm. More distally, intercellular spaces between the keratinized IMCs and keratinized Henle's cells were partly dilated and contained amorphous substances. It is suggested that the IMCs in the lower follicle may play a role to support and cover the inner hair structures, tightly as hoops of a barrel. In the isthmus portion, the IMCs may loosely support and guide the keratinized Henle's cells undergoing degeneration.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 284 (1992), S. 290-296 
    ISSN: 1432-069X
    Keywords: Cepharanthine ; Minoxidil ; Culture ; Hair cells ; Electron microscopy
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The effects of cepharanthine and minoxidil on proliferation, differentiation and keratinization of cultured cells from the murine hair apparatus were examined electron microscopically. Both cepharanthine and minoxidil stimulated cell proliferation and delayed initiation of differentiation and keratinization of the cultured cells. On day 6, most control cells (87%) cultured in a 0.03 mM calcium medium without cepharanthine and minoxidil were differentiated into several subpopulations corresponding to those of in vivo cell layers of the hair apparatus, while most of the cells cultured with cepharanthine (71%) or minoxidil (70%) were still immature. On day 13, the number of degenerated cells increased (63%) in the control culture, whereas in the culture treated with cepharanthine or minoxidil, cell degeneration scarcely occurred (5% and 8%, respectively). Differentiated cells having tonofilaments were often observed in the cepharanthine- and minoxidil-treated cultures (76% and 72%, respectively). Elevation of extracellular calcium up to 1.0 mM induced keratinization (34%) in the control culture on day 6, while no keratinized cells were observed in the cepharanthine- or minoxidil-treated culture. On day 13 keratinization similarly occurred in the cultures with cepharanthine (30%) or minoxidil (48%). These results show that both cepharanthine and minoxidil may directly influence proliferation, differentiation and keratinization of cultured cells from the hair apparatus.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Archives of dermatological research 282 (1990), S. 402-407 
    ISSN: 1432-069X
    Keywords: Electron microscopy ; Culture ; Hair cells ; Growth ; Differentiation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The cultured hair cells from 4-day-old C3H mice were studied by electron microscopy. The hair roots isolated from the skin by collagenase digestion were dispersed into a cell suspension by treatment with a mixture of trypsin and ethylenediaminetetraacetate. The cells were cultured in MCDB-153 (a medium containing seven growth factors) for 1, 3, 6 or 13 days. The number of cultured cells on day 3 was twice that on day 1, and stayed at the same level until day 13. By electron microscopy, some of the cells cultured for 1 day were seen to be undifferentiated and others already showed differentiation into various hair structures. Such differentiated cells disappeared on day 3 and most of the cells cultured for 3 days were undifferentiated. Cells cultured for 6 days were differentiated showing inner root sheath cell, hair cortical cell and medulla cell structures. The characteristics of these cultured cells corresponded well to those of in vivo cells of the hair tissues from the back skin of 7-day-old C3H mice. On day 13 degeneration occurred in the cultured cells. In none of these cultures were mesenchymal cells, such as fibroblasts, found. The present electron microscopic study reveals that immature cells obtained from mouse hair tissues proliferate in vitro and differentiate into several subpopulations corresponding to those of in vivo cell layers of hair tissues. The present culture technique may be useful for studies of hair cell growth and differentiation.
    Type of Medium: Electronic Resource
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