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  • Vestibular  (7)
  • Inhibition  (4)
  • Cats  (3)
  • Electron microscopy  (3)
  • 1
    Electronic Resource
    Electronic Resource
    Effects of cepharanthine and minoxidil on proliferation, differentiation and keratinization of cultured cells from the murine hair apparatus (1992)
    Springer
    Archives of dermatological research 284 (1992), S. 290-296 
    Details
    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
    URL: http://dx.doi.org/10.1007/BF00372583
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  • 2
    Electronic Resource
    Electronic Resource
    Biologic roles of the innermost cell layer of the outer root sheath in human anagen hair follicle: further electron microscopic study (1989)
    Springer
    Archives of dermatological research 281 (1989), S. 254-259 
    Details
    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
    URL: http://dx.doi.org/10.1007/BF00431059
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  • 3
    Electronic Resource
    Electronic Resource
    Inhibitory control of intracerebellar nuclei by the Purkinje cell axons (1970)
    Springer
    Experimental brain research 10 (1970), S. 64-80 
    Details
    ISSN: 1432-1106
    Keywords: Intracerebellar nuclei ; Purkinje cells ; Inhibition ; Excitation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In anaesthetized cats, synaptic events in cerebellar nuclei neurones were investigated with intracellular microelectrode techniques. These cells were identified by their antidromic activation along their axons and/or by their location in histological sections. In the cells of lateral nucleus IPSPs were induced monosynaptically during stimulation of the overlying hemispheral cortex of the cerebellum. In the cells of nuclei interpositus and fastigii, similar IPSPs were produced from the paravermal and vermal cortices, respectively. The postulate that the Purkinje cells exert an inhibitory action upon their target neurones thus applies not only to Deiters neurones, as previously proposed, but also to cells in the cerebellar nuclei. Stimulation of the cerebellar afferents at the inferior olive, the pontine nucleus and the lateral reticular nucleus produced EPSPs in cerebellar nuclei cells with relatively brief latencies, probably through axon collaterals of these afferents. The EPSPs were followed by IPSPs and slow depolarizations of disinhibitory nature, which, as studied previously in Deiters neurones, might be caused respectively by activation and subsequent depression of Purkinje cells through the cerebellar intracortical mechanisms.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00340519
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  • 4
    Electronic Resource
    Electronic Resource
    Cerebellar-evoked disinhibition in dorsal deiters neurones (1968)
    Springer
    Experimental brain research 6 (1968), S. 247-264 
    Details
    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
    URL: http://dx.doi.org/10.1007/BF00235127
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  • 5
    Electronic Resource
    Electronic Resource
    Inhibitory interaction between the vestibulo-ocular reflexes arising from semicircular canals of rabbits (1976)
    Springer
    Experimental brain research 26 (1976), S. 89-103 
    Details
    ISSN: 1432-1106
    Keywords: Vestibular ; Oculomotor ; Canal ; Inhibition ; Rabbit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In anesthetized albino rabbits, electric pulse stimulation was applied to ampullary branches of the vestibular nerve. Reflex discharges evoked from a canal in an extraocular muscle were depressed very effectively by conditioning stimulation at a certain other canal. The present systematic survey revealed that this reflex depression occurred specifically in 3 combinations of conditioning and testing canals; 1. anterior and posterior canals of the same side; 2. anterior and posterior canals of the opposite sides; and 3. horizontal canals of the two sides. Occurrence of postsynaptic inhibition in oculomotor neurons, on the other hand, was indicated by appearance of slow muscle potentials in extraocular muscles. It was confirmed that this motoneuronal inhibition did not contribute to the reflex depression in the above combination (1). Even in combinations (2) and (3), the accompanying motoneuronal inhibition was eliminated by adjusting intensities of canal stimuli or by severing its pathway in the medulla, or it was discriminated from the reflex depression by their different latencies and time courses. Hence, it was concluded that the reflex depression was attributable, at least largely, to non-motoneuronal inhibition, presumably postsynaptic inhibition at relay neurons for vestibulo-ocular reflexes. Slow muscle potentials evoked from a canal were also used as testing responses, but their depression could not be detected after conditioning at other canals.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00235251
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  • 6
    Electronic Resource
    Electronic Resource
    Cerebellar inhibitory control of the vestibulo-ocular reflex investigated in rabbit IIIrd nucleus (1972)
    Springer
    Experimental brain research 14 (1972), S. 511-526 
    Details
    ISSN: 1432-1106
    Keywords: Vestibular ; IIIrd nucleus ; Flocculus ; Inhibition ; Picrotoxin
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary In anaesthetized rabbits, the vestibulo-ocular reflex was evoked by electric stimulation of VIIIth nerve and was observed by recording postsynaptic potentials and relevant field potentials in Illrd nucleus. The electric stimulation of flocculus produced a prominent inhibition of the vestibulo-ocular reflex in both the inhibitory component relayed by the superior vestibular nucleus and the excitatory component mediated by the brachium conjunctivum. The excitatory component mediated by the medial vestibular nucleus appeared to be free of the flocculus inhibition. The flocculus inhibition was blocked very effectively by systemic injection of picrotoxin. That the flocculus inhibitory action is due to monosynaptic postsynaptic inhibition of secondary vestibular neurones was demonstrated by direct stimulation of, and also by recording from, the superior nucleus. Recording from the superior nucleus was also performed in anaesthetized cats. All of these above results indicate that Purkinje cells in flocculus projecting to vestibular and cerebellar nuclei cells have inhibitory synaptic action. Flocculus stimulation produced also an excitatory effect upon vestibular nuclei neurones. However, this effect could be attributed to intracerebellar activation of the primary vestibular fibers which pass into the flocculus.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00236593
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  • 7
    Electronic Resource
    Electronic Resource
    The origin of cerebellar-induced inhibition of Deiters neurones II. Temporal correlation between the trans-synaptic activation of Purkinje cells and the inhibition of Deiters neurones (1966)
    Springer
    Experimental brain research 2 (1966), S. 350-364 
    Details
    ISSN: 1432-1106
    Keywords: Deiters neurones ; Inhibition ; Climbing fibre responses ; Inferior olive
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Intracellular recording with microelectrodes has been employed to reveal the causal relationship between the trans-synaptic activation of cerebellar Purkinje cells and the postsynaptic inhibition of Deiters neurones. Cerebellar stimulation produced in Deiters neurones not only monosynaptic IPSPs with latency of 0.9–1.5 msec, but also the delayed IPSPs at 1.5–9 msec. Correspondng to the latter, Purkinje cells were found to be activated orthodromically with the characteristic climbing fibre responses (CFRs), the latency varying from 0.8 up to 10 msec. On the other hand, stimulation of the inferior olive first induced EPSPs in Deiters neurones, presumably monosynaptically, then with a short delay of less than a millisecond CRFs in Purkinje cells of the anterior lobe, which in turn were succeeded by IPSPs in Deiters neurones after a further delay of a millisecond. Spinal stimulation activated the inferior olive trans-synaptically and thereby produced CFRs in Purkinje cells and a sequence of EPSPs and IPSPs in Deiters neurones. Close correlation between these spinal-induced events in both neurone species was further indicated by the concurrence of their fluctuations in intensity, these fluctuations being characteristic of the spino-olivary transmission mechanism. These results strongly support the postulate that the cerebellar Purkinje cells are inhibitory in their action upon Deiters neurones.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00234780
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  • 8
    Electronic Resource
    Electronic Resource
    Cerebellar control of the vestibulospinal tract cells in rabbit (1973)
    Springer
    Experimental brain research 18 (1973), S. 446-463 
    Details
    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
    URL: http://dx.doi.org/10.1007/BF00234131
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  • 9
    Electronic Resource
    Electronic Resource
    Postsynaptic influences on the vestibular non-deiters nuclei from primary vestibular nerve (1969)
    Springer
    Experimental brain research 8 (1969), S. 190-200 
    Details
    ISSN: 1432-1106
    Keywords: Vestibular ; EPSP ; IPSP
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Neurones in the descending, medial and superior vestibular nuclei of the cats were explored with intracellular microelectrodes. Cerebellar- and spinal-projecting neurones were identified by their antidromic invasion from the region of fastigial nuclei and from the second cervical segment, respectively, and the others by their location. The central actions of the primary vestibular impulses upon these non-Deiters vestibular nuclei neurones were investigated by using electric stimulation of the ipsilateral vestibular nerve. Many of these cells received excitatory postsynaptic potentials (EPSPs) monosynaptically, similar to those evoked in the ventral Deiters neurones, as described elsewhere, except that the unitary EPSPs are often larger. Some cells received only polysynaptic EPSPs or IPSPs and a few cells were not influenced at all.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00234539
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  • 10
    Electronic Resource
    Electronic Resource
    Axon reflex activation of Deiters neurones from the cerebellar cortex through collaterals of the cerebellar afferents (1969)
    Springer
    Experimental brain research 8 (1969), S. 249-268 
    Details
    ISSN: 1432-1106
    Keywords: Axon reflex ; Deiters neurones ; Cerebellar afferents ; Cats
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary When recording intracellularly from cat's Deiters neurones, stimulation of the anterior lobe of the cerebellar cortex produced excitatory postsynaptic potentials (EPSPs) monosynaptically, in addition to the inhibitory ones (IPSPs) that were identified previously as being produced via Purkinje cell axons. The EPSPs were induced bilaterally from a wide area of the anterior and posterior lobes of the cerebellum, in contrast to the IPSPs that were evoked only ipsilaterally, mainly from the vermal cortex. The latency of the EPSPs was slightly, but significantly, shorter than that of the IPSPs. The presynaptic impulses responsible for these EPSPs were represented by the discrete field potentials and also by unit spikes of individual fibres. The pathway for these EPSPs and presynaptic impulses was pursued by testing their interference, in the manner of impulse collision and refractoriness, with those induced from various spots within or outside the cerebellum. It is found that the excitatory fibres for Deiters neurones extend transversely, and probably longitudinally too, over the culmen and pass out of the cerebellum through cerebellar peduncles. The major portion of them appears to originate from the medulla and a minority from the spinal cord. It is postulated that cerebellar afferents from these structures have synapses with Deiters neurones via their collateral branches, through which a kind of axon reflex occurs to Deiters neurones during stimulation of the cerebellar cortex.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00234252
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