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  • 1985-1989  (19)
  • 1965-1969  (11)
  • 1960-1964
  • 1955-1959
  • 1890-1899
  • 1820-1829
  • Purkinje cells
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 179 (1989), S. 257-267 
    ISSN: 1432-0568
    Keywords: Cerebellum ; Purkinje cells ; Golgi cells ; SRIF ; Peptides ; Plasticity ; Immunofluorescence
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The distribution of somatostatin-immunoreactive (SOM-IR) elements in the cerebellar cortex of the rat has been studied at different stages of postnatal development (from birth to day 30) and in adult animals using immunohistochemistry. The results showed that in vermis of new born animals there are three main groups of SOM-IR structures within the cortex which subsequently spread along the Purkinje cell layer. In addition, both in the vermis and in the lateral lobes, numerous more evenly distributed SOM-positive cells and fibers could be seen. SOM-IR Golgi cells, Purkinje cells and climbing fibers could then be recognized during the subsequent developmental stages. In the vermal zone, SOM-IR Purkinje cells formed patches, which seemed to be part of a sagittal columnar or band-like organization. This was most obvious between days 5 and 21 of postnatal development. Subsequently there was a reduction in the number of immunoreactive Purkinje cells but a patchy disposition remained. In addition high numbers of SOM-IR Purkinje and Golgi cells and also climbing fibers were identified in the flocculus and paraflocculus at all stages of development studied, and they were also seen in the adult rats in these regions. In the lateral lobes expression of SOM-like immunoreactivity (LI) decreased and almost completely disappeared in adult animals. The present results demonstrate that a SOM or a SOM-LI peptide can be transiently detected in many Purkinje and Golgi cells in the cerebellar cortex, suggesting a role in events related to developmental processes. However, in some regions and structures SOM-LI can be seen also in adult animals.
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  • 2
    ISSN: 1432-0878
    Keywords: Cerebellum ; Purkinje cells ; Ectopia ; GABA ; Immunohistochemistry ; Rat (Wistar)
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Intensely stained cells are found in the cerebellar white matter of the vermis and paravermis in adult rats after immunoreaction with an immune serum raised against glutamic acid decarboxylase (GAD). The cells are similar in size to cortical Purkinje cells and three times the size of Golgi cells of the internal granule layer, and have a thick immunopositive cell process emerging from a welldefined cytoplasmic cone. In the cytoplasm, immunoprecipitates are more dense around the nucleus as in normally located Purkinje cells. The morphological appearance of the immunopositive cells suggests that they may be ectopically located Purkinje cells. The soma of the ectopic Purkinje cells is contacted by a few darkly stained terminal boutons. Data indicate that, in spite of the different cellular environment, ectopic Purkinje cells can develop not only the typical morphological pattern already described but also other intrinsic features, such as their typical inhibitory neurotransmitter.
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  • 3
    ISSN: 1432-0568
    Keywords: Taurine ; Immunocytochemistry ; Quantification ; Electron microscopy ; Cerebellum ; Purkinje cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Ultrathin sections of plastic-embedded rat cerebella were incubated with an antiserum against conjugated taurine and subsequently treated with a secondary antibody coupled to colloidal gold. The density of gold particles in various cellular profiles was calculated with the assistance of a computer. In the cerebellar cortex the highest density was found in the somata, dendrites, and dendritic spines of the Purkinje cells, supporting parallel light-microscopical observations in postembedding stained semithin sections from the same tissue blocks. The remaining profiles could be divided into three groups according to their immunolabelling intensity, in descending order: 1) somata and processes of granule and Golgi cells; 2) somata and processes of stellate, basket, and glial cells, and 3) mossy fiber terminals. In a representative experiment, the structures in the first and second groups showed gold particle densities in the range of 19–25%, and 4–11%, respectively, of that in the Purkinje cell somata (values corrected for background) whereas the particle density in the mossy fiber terminals was not significantly above background level. In the cerebellar nuclei, taurine-like immunoreactivity was concentrated in terminals that typically established symmetric or intermediate type contacts with weakly labelled dendrites and cell bodies. These terminals, which shared the ultrastructural features of Purkinje cell terminals, showed an average gold particle density that was about 60% higher than that of the Purkinje somata. For specificity control, ultrathin sections containing a series of different amino acid conjugates were incubated in the same drops of sera as the tissue sections. The highly selective labelling of the taurine conjugate indicated that the distribution of gold particles in the tissue was not confounded by crossreactivity with GABA, glutamate or other common amino acids but adequately reflected the distribution of fixed taurine. For additional control of specificity, the taurine antiserum was applied to the soluble fraction of a rat brain extract separated by thin layer chromatography. In this system the taurine antiserum stained a single spot that comigrated with free taurine. The present results suggest that all cell types and processes in the rat cerebellum (with the exception of the mossy fiber terminals) contain taurine. However, the concentration of taurine appears to vary considerably among the different cell types and may also differ between different parts of the same neuron.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 70 (1988), S. 477-484 
    ISSN: 1432-1106
    Keywords: Transplantation ; Cerebellum ; Migration ; Purkinje cells ; Granule cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Cerebellar primordia of different ages (embryonic days of 14 to 20) were transplanted into cerebella of normal syngeneic adult rats (Fischer 344). After 1–12 months (mostly 5–6 months), the host brains were examined by light and electron microscopy. In about 80% of our successful experiments, grafted Purkinje and/or granule cells migrated into the host molecular layer. Some granule cells migrated down along host Bergmann glia, reminiscent of their normal developmental migration route. Other granule cells migrated along astroglial processes that ensheathed capillary walls. Some grafted Purkinje cells were also located ectopically in the host molecular layer. They were identified as graft origins autoradiographically. This migration seemed to be encouraged under conditions where the subjacent host Purkinje cells had been lost. Where the grafted Purkinje cells were located on top of the host molecular layer, their primary dendrites faced vertically downwards into the host molecular layer. However, the position of the apical poles of migrated Purkinje cell bodies in the deeper aspect of the molecular layer varied considerably, suggesting that the orientation of the Purkinje cell dendrites is probably determined by the availability of afferent fibers. Thus, the present study has demonstrated that Purkinje and granule cells can migrate from embryonic cerebellar grafts into the molecular layer of the normal, adult host rat cerebellum.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 70 (1988), S. 134-144 
    ISSN: 1432-1106
    Keywords: Alert monkey ; Flocculus ; ‘Gaze velocity’ ; Purkinje cells ; Eye movements ; Sinusoidal optokinetic stimulation
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Activity of single units was recorded in the flocculus of alert, behaving monkeys during sinusoidal optokinetic (0.02–5.0 Hz), constant velocity optokinetic, vestibular and visual-vestibular conflict stimulation. The maximal stimulus velocity for sinusoidal optokinetic stimulation at different frequencies was 40 deg/s or less (at frequencies above 1 Hz). For an amplitude series at 0.2 Hz, stimulus velocity was varied between ±10 to ±80 deg/s. In one trained monkey activity was also investigated during smooth pursuit eye movements and suppression of the vestibulo-ocular reflex by visual fixation (VOR-supp.). Only neurons which responded to 0.2 Hz (±40 deg/s) optokinetic stimulation were included in the study. 2. The majority of neurons (44 out of 59) were type I Purkinje cells (PCs), which increased their simple spike activity during optokinetic cylinder rotation to the ipsilateral recording side. The responses during other, vestibular related, paradigms allowed all these neurons to be classified as so called ‘gaze velocity’ PCs. Three type II PCs were encountered, which responded similarly, but were only weakly modulated. 3. All type I PCs were modulated at frequencies of sinusoidal optokinetic stimulation between 0.05 and 2.5 Hz. PC's showed little or no modulation at 0.03 and 0.02 Hz. About half of the PC's still responded at 5.0 Hz. 4. Relative to eye velocity, the PC activity had a phase advance of about 30 deg between 0.1 and 2 Hz. It became larger at lower, and smaller at higher, frequencies. Eye velocity related sensitivity (imp/s/deg/s) was small at low stimulus frequencies and increased monotonically, on average from 0.16 at 0.02 Hz to 2.0 at 3.3 Hz. 5. Ten (out of 12) mossy fiber related input neurons were classified as visual neurons, since their activity could be related to the amount of retinal slip in all conditions. Neurons were clearly modulated at sinusoidal optokinetic stimulation up to 5 Hz. One input neuron, investigated during sinusoidal OKN, smooth pursuit eye movements, VOR and VOR-supp., behaved qualitatively like a ‘gaze velocity’ PC. The remaining input neuron encoded eye velocity at 0.2 Hz optokinetic, vestibular and visual-vestibular conflict stimulation. 6. The results show that during sinusoidal and constant velocity optokinetic stimulation ‘gaze velocity’ PC's do not encode eye velocity and/or eye acceleration. 7. The vestibular nuclei-flocculus complementary hypothesis (Waespe and Henn 1981) can explain PC responses to a large extent. However, a direct comparison shows that at low frequencies (particularly around 0.05 Hz) the complementary responses of most ‘velocity storage’ encoding vestibular nuclei neurons and floccular PC's appears insufficient to account fully for the oculomotor response.
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  • 6
    ISSN: 1432-1106
    Keywords: Taurine ; GABA ; Colocalization ; Cerebellum ; Purkinje cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The distributions of taurine-like and GABA-like immunoreactivities in the rat cerebellum were compared by analysis of consecutive semithin and ultrathin sections, postembedding labeled with the peroxidase-antiperoxidase technique or with an indirect immunogold procedure, respectively. Taurine-like immunoreactivity was selectively enriched in Purkinje cell bodies, dendrites and spines, and boutons in the cerebellar nuclei exhibiting ultrastructural features typical of Purkinje cell terminals. The stellate and basket cell bodies and terminals were very weakly labeled. A computer assisted quantitative assessment of the net immunogold labeling revealed that the mean gold particle density in the Purkinje cell terminals was about 70% higher than that in the Purkinje cell dendrites, and about 14 times higher than that in the stellate/basket cell terminals in the molecular layer. Stellate, basket and Purkinje cell terminals emerged as intensely immunoreactive in adjacent sections processed with an antiserum against conjugated GABA. These findings indicate, contrary to recent electrophysiological data, that GABA is a more likely transmitter candidate than taurine in the stellate cells. The apparent colocalization of GABA and taurine in the terminals of Purkinje cells raises the possibility that these terminals are capable of releasing two different inhibitory amino acids.
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  • 7
    ISSN: 1432-0878
    Keywords: Cerebellum ; Energy metabolism ; Neurons ; Glial cells ; Purkinje cells ; Rat, Sprague-Dawley
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Recent reports have revealed that certain neurons do not survive in vitro in the presence of glucose, which is the primary substrate and exclusive source of energy in the brain. But these neurons can survive in the presence of low-molecular-weight agents such as pyruvate, which are supplied by glial cells (Selak et al. 1984). To test whether this result also holds true in vivo, we investigated the distribution of hexokinase, lipoic dehydrogenase, β-hydroxybutyrate dehydrogenase, and glucose-6-phosphate dehydrogenase activities in the developing rat cerebellum. Hexokinase activity was relatively higher in glial cells than in neurons. After postnatal day 8, the activity of hexokinase could hardly be detected in Purkinje cells, whereas it was highest in Bergmann glial cells. Purkinje cells were the only type of neuron with high levels of lipoic dehydrogenase at all ages tested. β-Hydroxybutylate dehydrogenase activity was also high in Purkinje cells, especially in those from young rats. Relatively high glucose-6-phosphate dehydrogenase activity was demonstrated in basket and stellate cells from adult brain. Thus, it appears that, in vivo, certain neurons utilize relatively little glucose, and it is indeed possible that glial cells may supply some substance(s) other than glucose, for example pyruvate, as the primary source of energy.
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  • 8
    Electronic Resource
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    Springer
    Bulletin of experimental biology and medicine 105 (1988), S. 108-111 
    ISSN: 1573-8221
    Keywords: clinical death ; brain ; Purkinje cells ; nucleolus ; rat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
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  • 9
    ISSN: 1432-0533
    Keywords: Granular layer ; Cerebellum ; Purkinje cells ; Golgi method
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Purkinje cells, impregnated with the rapid Golgi method, in a patient with primary degeneration of the granular layer showed abnormal orientation of the perikaryon and dendrites, reduction in size of the dendritic arbor, absence of spiny branchlets, and large numbers of stubby spines and hypertrophic spines on secondary dendritic branches; stubby spines and thorn-like formations were seldom observed on the primary dendrites and perikaryon of some Purkinje cells. These findings are similar to those described in the cerebellum of the homozygous weaver mutant mouse and in the cerebella of experimentally induced agranular phenocopies, thus suggesting that similar plastic changes occur in human and animal Purkinje cells as a result of the absence of parallel fibres input in early developmental stages. In addition, Purkinje cells in this patient showed club-shaped deformities in the distal region of primary dendrites, which were filled with radially oriented, short dendrites covered with stubby spines and hypertrophic spines. These latter structures appear to be fully impregnated asteroid bodies observed in paraffin sections.
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  • 10
    Electronic Resource
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    Springer
    Cellular and molecular life sciences 43 (1987), S. 927-928 
    ISSN: 1420-9071
    Keywords: Purkinje cells ; cerebellar ontogeny ; giant mitochondria ; reptiles
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
    Notes: Summary Giant mitochondria were observed in the perikarya and dendrites of Purkinje cells in the developing cerebellar cortex of the lizardGallotia galloti at sevral stages previous to hatching. Such mitochondria are absent from the adult cerebellum.
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  • 11
    ISSN: 1432-1106
    Keywords: Cerebellar cortex ; Cerebellar nuclei ; Vermis ; Sagittal zones ; Purkinje cells ; Olivocerebellar zones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The present study is an investigation of the efferent pathways from Purkinje cells within particular sagittal zones of the vermal region of the cat cerebellar cortex. A combined electrophysiological/ autoradiographic technique was used, in which a small volume (10–120 nl) of 3H-leucine was injected into the centre of a chosen cortical zone after the mediolateral extent of the zone had been delimited electrophysiologically on the basis of its climbing fibre input. Study of the uptake and orthograde transport of labelled material by the Purkinje cells showed that the smallest injections gave rise to injection sites which were restricted to a single zone and to terminal labelling which was very reproducible between cases. Larger injections usually resulted in spread of labelled material to neighbouring zones but the resultant distribution of terminal labelling was nevertheless consistent with that arising from smaller injections. The x zone, which receives climbing fibre input transmitted from the ipsilateral forelimb via a dorsal funiculus spino-olivo-cerebellar pathway (DF-SOCP), was found to project to the junctional region between nucleus fastigius and nucleus interpositus posterior (NIP). The b zone, which lies laterally in the vermis and receives climbing fibre input transmitted from both forelimbs (and both hindlimbs) via a slower conducting SOCP, was found to project, not to the cerebellar nuclei proper, but to the ipsilateral lateral vestibular nucleus. The projection of the third zone within the vermis, the a zone, was not examined but it is generally agreed that this zone projects mainly to nucleus fastigius.
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  • 12
    ISSN: 1432-1106
    Keywords: Cerebellar cortex ; Cerebellar nuclei ; Sagittal zones ; Purkinje cells ; Olivocerebellar zones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The present study examines the projection to the cerebellar nuclei of Purkinje cells in particular sagittal zones within the intermediate region of the cerebellar cortex. The boundaries between the zones were delimited electrophysiologically on the basis of their climbing fibre input so that a small volume (10–120 nl) of 3H-leucine could be injected into the centre of a chosen zone. The subsequent uptake and orthograde transport of labelled material by the Purkinje cells was studied autoradiographically. It was found that the smallest injections resulted in injection sites restricted to a single cortical zone and extremely reproducible results could be obtained using such a combined electrophysiological/autoradiographic technique. Larger injections sometimes spread to a neighbouring zone but the resultant terminal labelling within the deep nuclei was invariably consistent with the results obtained from smaller injections. The c1 and c3 olivocerebellar zones, which are known to receive climbing fibre input transmitted from the ipsilateral forelimb via a dorsal funiculus spino-olivo-cerebellar pathway (DF-SOCP), were found to project to partially overlapping regions within nucleus interpositus anterior (NIA). No projection to nucleus interpositus posterior (NIP) was demonstrated for either zone. No distinction could be seen between the terminal fields for the medial and lateral halves of the c1 zone which are, however, known to receive their climbing fibre input from quite separate regions within the inferior olive. The c2 zone, which was delimited on the basis of its climbing fibre input which is transmitted from both forelimbs via a lateral funiculus SOCP, was found to project exclusively to interpositus posterior. The hemispheral d1 zone was found to project to the transitional region where interpositus anterior and the dentate nucleus adjoin.
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  • 13
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 67 (1987), S. 533-542 
    ISSN: 1432-1106
    Keywords: Cerebellum ; Inferior olive ; Purkinje cells ; Interposito-olivary neurones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The activity of cerebellar Purkinje cells and interpositus neurones was recorded during and after periods of high frequency (2.5–7.5 Hz) climbing fibre activation in barbiturate-anaesthetized cats. 1. During the high frequency conditioning stimulation, the Purkinje cell simple spike (SS) firing was initially silenced in all zones studied. After a few seconds, the SS reappeared and the frequency increased to well above that of the control level after approximately 10 s. Thereafter, the SS rate started to decline so that, after 15–20 s, the Purkinje cells fired no more SS. This SS silence lasted up to 60 s, whether or not the stimulation was continued. 2. The Purkinje cells responded with a complex spike (CS) to every stimulus. If the high-frequency stimulation lasted for at least 15 s, the spontaneous CS discharge of the Purkinje cells in the c1, c2, and c3 zones was suppressed after the conditioning stimulation had ended. This suppression lasted for approximately the same length of time as the SS silence. In the b zone, however, no CS suppression was observed. 3. Interpositus neurones displayed an increased discharge rate after periods of conditioning stimulation, thus displaying a mirror image of the Purkinje cell SS firing. 4. The behaviour of the neurones agrees well with the behaviour predicted by an hypothesis of the olivo-cerebello-olivary loop (Andersson and Hesslow 1987). 5. The results suggest that the cerebello-olivary projection is topographically organized and matches the microzonal organization in the olivo-cerebellar projection.
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  • 14
    Electronic Resource
    Electronic Resource
    Springer
    Anatomy and embryology 173 (1986), S. 371-376 
    ISSN: 1432-0568
    Keywords: Motilin-like immunoreactivity ; RIA ; HPLC ; Cat ; Intestine ; Rat ; Cerebellum ; Purkinje cells ; Dendrites ; Neocortex ; Pyramidal cells ; Hippocampus
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Motilin was demonstrated by the immunoperoxidase technique in endocrine cells of the gastrointestinal tract using several specific antisera. Motilin-like immunoreactivity could only be demonstrated with one of these antisera and was observed in Purkinje cells and dendrites of the cerebellum, in pyramidal cells and dendrites of the cerebral cortex and in dendrites of the CA3 field of the hippocampus of the rat. Very low motilin-like immunoreactivity was found in cerebellum as well as in cerebral cortex using radioimmunoassay. However, using reverse phase liquid chromatography combined with UV-detection and radioimmunoassay, no peak of a peptide corresponding to synthetic motilin was detectable in rat cerebellar extracts, in contrast to findings in rat duodenum. The results do not suggest that motilin is an intrinsic neuroactive substance of the cerebellum.
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  • 15
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    Springer
    Acta neuropathologica 69 (1986), S. 220-226 
    ISSN: 1432-0533
    Keywords: Brindled mouse ; Kinky hair disease ; Heterozygotes ; Purkinje cells ; Mitochondria
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The brindled mutation is an X-linked neurological mutation in mice. Male mice hemizygous for the brindled gene have metabolic defects homologous with kinky hair disease in humans. Neuropathologically, the mutation is characterized by extensive neuronal degeneration associated with pronounced mitochondrial changes in cerebral cortex and abnormal arborization of Purkinje cell dendrites, which are most pronounced in the rostral vermis or anterior lobules. In the cerebellum of female mice heterozygous for brindled gene, Purkinje cells with abnormal dendritic arborization and with unusually enlarged mitochondria were also observed. Morphological changes in affected Purkinje cells in young heterozygotes were similar to those of young hemizygotes. However, in older heterozygotes, the changes were far less conspicuous, indicating the presence of some extrinsic factor(s) to compensate expression of the mutant gene in heterozygous brains.
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  • 16
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    Springer
    Bulletin of experimental biology and medicine 102 (1986), S. 1437-1439 
    ISSN: 1573-8221
    Keywords: cerebellum ; Purkinje cells ; nucleolus ; clinical death
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
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  • 17
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    Springer
    Experimental brain research 57 (1985), S. 370-380 
    ISSN: 1432-1106
    Keywords: Inferior olive ; Purkinje cells ; Efferent cerebellar neurones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Cerebellar units were recorded extracellularly in rats before and after an intraveinous injection of 3-acetylpyridine destroying selectively the IO. All the Purkinje cells show a loss of the complex discharge between 2 h 15 min and 2 h 45 min after treatment. This time, called the “critical period” corresponds to the degeneration of the neurons of the inferior olive as revealed by the decrease of their metabolic activity. The simple spikes of the Purkinje cells increase their discharge frequency soon after the climbing fibers cease firing. On the contrary the firing frequency of the inhibitory interneurons does not show significant changes after degeneration of the inferior olive. The efferent cerebellar neurons, including cells of the cerebellar and vestibular nuclei receiving the axon terminals of the Purkinje cells, decrease their discharge rate up to thirty times during and after the critical period. It is demonstrated that this effect is due to the increased inhibitory activity of the Purkinje cells deafferented from the climbing fibers, whereas the deafferentation of the efferent cerebellar neurones from the collaterals of the olivary cells has little impact.
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  • 18
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    Experimental brain research 61 (1985), S. 186-193 
    ISSN: 1432-1106
    Keywords: Plasma membrane ; Intramembrane particles ; Cerebellum ; Purkinje cells ; Dendritic spines ; Trophic factors ; Axonal transport
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Destruction of the inferior olivary nucleus in the rat by thermocoagulation results in the degeneration of climbing fibers in the cerebellar cortex. Under these conditions the plasma membrane of Purkinje cells was selectively affected at the level of the spines on large dendrites (LD spines), the postsynaptic targets for climbing fibers. The number of small (〈 10 nm) non-junctional intramembrane particles (IMP) was significantly decreased in E-faces during the first 3 days following the lesion (47% of control IMP values). Later, the number of IMPs progressively recovered to reach 67% of the control IMP values 1 month following the lesion. IMP numbers in the P-face and in the postsynaptic junctional aggregates of the E-face were unaffected by destruction of climbing fibers. Following injection of colchicine into the inferior olivary nucleus, a treatment that inhibits axonal transport in climbing fibers, a selective decrease in IMP numbers on the E-faces of LD spines was also found. The maximal decrease was found during the first 10 days after injection (48% of control values), and then the number of IMPs gradually increased to reach control values by 90 days post-injection. In the case of colchicine treatment also, the reduction in the number of IMPs affected selectively a class of non-junctional small IMPs, less than 10 nm in diameter. These data show that there is a similar selective modification in the membrane structure of Purkinje cells, not only following destruction of climbing fibers by thermocoagulation, but also following inhibition of axonal flow in climbing fibers by colchicine injection. The results are consistent with the hypothesis that Purkinje cell membrane structure is modulated by the presence of a trophic factor(s) associated with climbing fibers.
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  • 19
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    Bulletin of experimental biology and medicine 100 (1985), S. 1592-1595 
    ISSN: 1573-8221
    Keywords: dark cells ; Purkinje cells ; protein and caloric deficiency ; rehabilitation ; carnitine
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Medicine
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  • 20
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    Experimental brain research 9 (1969), S. 1-15 
    ISSN: 1432-1106
    Keywords: Frog cerebellum ; Purkinje cells ; Climbing fibers ; Mossy fibers ; Vestibular efferents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary The relationships between the frog vestibular afferents and the cerebellum as well as the efferent vestibular system, have been studied by electron microscopy and Nauta degeneration technique. The primary vestibular fibers were found to have synaptic boutons in both the granular and the molecular layers of the cerebellar marginal zone. In the granular layer synaptic contacts are made with the granule cell dendrites while the molecular layer projection is directed to the main dendrites of the Purkinje cells in a manner similar to that of the climbing fibers. As for the efferent system, the vestibular receptor cells of the macula saccularis are contacted by vesicle-filled boutons which terminate synaptically in relation to a submembranous sac within the cell. The efferent fibers contain neurofilaments and a few neurotubules. Following lesions at different sites, it was found that all the above fibers and boutons degenerated after a) vestibular nerve section, and that b) most of them were lost when the brain stem was hemisected above the vestibular nerve. On the other hand, brain stem sectioning above the Vth nerve produced degeneration of 35% of these boutons while cerebellar undercutting produced 20% degeneration. The Nauta technique shows that following cerebellar undercutting a small efferent bundle leaves the ventral caudal side of the nerve. These findings demonstrate the existence of a cerebello-vestibular efferent system originating most possibly from the auricular lobe Purkinje cells.
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  • 21
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    Experimental brain research 8 (1969), S. 327-345 
    ISSN: 1432-1106
    Keywords: Cerebellar unit responses ; Purkinje cells ; Click response ; Mossy fibers ; Surface negativities ; Firing patterns
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Unit activities evoked by auditory stimulation in the cerebellar cortex have been studied in the encéphale isolé cat. Poststimulus-time histograms (PSTH) of 1/sec, click-evoked unit discharges have different response patterns with respect to the onset and time course of unit firing. 2. Units have been classified as type I and type II responses based on their preferred firing time relative to the first surface-negative component (N1) of the click evoked folial response. 3. Laminar analysis of the click evoked slow activity centered on an 8–12 msec negative wave in the molecular layer that corresponded with the N1 surface component. An earlier, sharp, negative-positive sequence was found at depths approaching and deep within the granule cell layer. 4. Units considered to be Purkinje cells based on antidromic stimulation or the appearance of typical climbing fiber responses (CFR's) were found exclusively within the type II unit category. Non-identified click units, including various types of cortical interneurons, were found to be either type I or type II units. 5. Evidence that cerebellar click responses are mediated predominately by mossy fiber afferents derives in part from the inhibitory effect of local folial conditioning stimulation upon N1 waves. In addition, the irregular, recurrent CFR's found in click responsive Purkinje cells were temporally unrelated to the acoustic stimulus. Thus click responses in these units appeared to be initiated by mossy fiber activity.
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  • 22
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    Experimental brain research 3 (1967), S. 1-11 
    ISSN: 1432-1106
    Keywords: Delayed coincidences ; Purkinje cells ; Frog
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary A particular correlation technique was used in order to analyse the “spontaneous” electrical activity of neurons in the frog's brain, and an electronic device was constructed for analysis of available data. On the basis of the correlograms obtained, two simple models of the net in the neighbourhood of the neuron studied are suggested as explanations for the observed regularities in the spike trains.
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  • 23
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    Experimental brain research 3 (1967), S. 58-80 
    ISSN: 1432-1106
    Keywords: Mossy fibres ; Cerebellar cortex ; Golgi cells ; Granule cells ; Purkinje cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Potential fields and unitary spikes in the cat cerebellar cortex were generated specifically by mossy fibre volleys and recorded by means of microelectrodes. The mossy fibres were excited by trans-folial (T. F.) stimulation which was compared with juxtafastigial (J.F.) stimulation. Both were conditioned by local stimuli of parallel fibres. 2. In the granular layer, an incoming mossy fibre volley evoked a small diphasic potential (P1 N1) and about 0.4 msec later a second negative wave (N2) due to the excitatory synaptic current generated by synapses of mossy fibres with granule cells and Golgi cells. In the typical configuration the N2 wave usually had a superimposed double spike potential, which is due to impulses discharged first by Golgi cells and then, about 0.5 msec later, by granule cells. 3. The transmission of impulses along the perpendicular axons of the granule cells and thence along the parallel fibres gave the fairly sharp positive potential (P2) in the granular layer, and simultaneously the negative wave (N3) in the molecular layer. The parallel fibre impulses, in turn, synaptically excited and so evoked local responses and action potentials in the dendrites of Purkinje and other cells, which aided in the production of the latter part of the N3 wave. 4. The impulses in the Purkinje cell dendrites propagate into the granular layer via the Purkinje cell somata and axons so producing the negative wave (N4) in the Purkinje and the granular layer. 5. The late and prolonged positive wave (P3) may be attributable to the deep active sources produced by postsynaptic inhibition of Purkinje cells and of granule cells by basket and Golgi cells respectively. 6. There has been good correlation between the physiological findings and the anatomical structures of the various types of cells and the synaptic connections, even to the synapses of mossy fibres on Golgi cell dendrites that have been recently described by HÁmori and SzentÁgothai.
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  • 24
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    Experimental brain research 3 (1967), S. 81-94 
    ISSN: 1432-1106
    Keywords: Cerebellar inhibition ; Golgi cells ; Basket cells ; Purkinje cells ; Granule cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. There has been a comparative study of two kinds of inhibition in the cerebellar cortex: basket cell inhibition of Purkinje cells; and Golgi cell inhibition of granule cells. These inhibitory actions were assayed by the degree of inhibition of the potential waves that juxta-fastigial (J.F.) stimulation evoked in the granular or molecular layers: basket cell inhibition by the N1 wave generated by antidromic invasion of Purkinje cells; and Golgi cell inhibition of the N3 or P2 waves evoked by the mossy fibre volley in the molecular and granular layers respectively. 2. The Golgi cell inhibition produced by a parallel fibre volley (LOC stimulation) extended transversely for no more than 200 μ on either side of the narrow beam of the excited parallel fibres, whereas the spread of basket cell inhibition was much larger — to as far as 1 mm. 3. When activated by the on-beam LOC stimulation, the Golgi cell and the basket cell inhibition showed much the same threshold of the stimulation. The off-beam LOC stimulation produced only the basket cell inhibition which is in conformity with the different transverse distributions described in (2) above. 4. When evoked by J. F. or trans-folial (T. F.) stimulation, the Golgi cell inhibition had a much lower threshold than the basket cell inhibition. It is suggested that in part at least this is attributable to the direct synaptic connection from mossy fibres to Golgi cells. 5. The Golgi cell inhibition elicited by the LOC stimulation showed a relatively short time course, the maximum being attained by about 10 msec, after which there was an approximately exponential decrease so that the total duration was only about 100 msec. On the other hand, the basket cell inhibition had a much slower time course, maximum being attained at a latency of 20 to 40 msec, the total duration being even in excess of 200 msec. Suggestions are made with respect to the factors responsible for the slow time course of the basket cell inhibition.
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  • 25
    ISSN: 1432-1106
    Keywords: Purkinje cells ; Deiters neurones ; Inhibitory synapses ; GABA
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1.Various drugs were applied intravenously or into the fourth ventricle and their effects upon the inhibition exerted by Purkinje cell axons were appraised by both extra- and intracellular recording from Deiters neurones. Strychnine, picrotoxin, pentamethylenetetrazol, β-methyl-β-ethylglutarimide, noradrenaline, dopamine, dibenamine and nethalide did not affect this inhibition. 2.γ-aminobutyric acid (GABA) and inhibitors of GABA transaminase were applied iontophoretically into the vicinity of Deiters neurones through an outer barrel of coaxial electrodes, the effects being observed either intra- or extracellularly through an inner barrel. 3. GABA depressed both inhibitory and excitatory postsynaptic potentials and often blocked the spike potentials, while it increased the membrane conductance. 4. GABA also produced a membrane hyperpolarization of 3–8 mV. Concomitantly both the spike potential and after-depolarization increased in amplitude and the after-hyperpolarization decreased. 5. In a few cases hydroxylamine but not amino-oxyacetic acid potentiated the inhibition, there being an increase in the inhibitory postsynaptic potentials thereby induced. 6. These effects were considered in connection with the possibility that GABA acts as a natural transmitter.
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  • 26
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    Experimental brain research 4 (1967), S. 97-113 
    ISSN: 1432-1106
    Keywords: Cerebellum ; Cerebellar synaptology ; Purkinje cells ; Synapses
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary An attempt at distinction between excitatory and inhibitory synapses is made in the cat cerebellum. The former are assumed to contain spheroid vesicles (S-type) of average diameter of 500 Å, while the latter flattened vesicles (F-type) of smaller size than the former. The elongation index (the ratio of the length of major versus minor axis of the vesicles) of S-type synaptic vesicles was about 1.2, while that of the F-type was more than 1.7. Parallel fibers of granule cells make S-type synaptic contacts (en-passant type or crossing-over synapse) mostly on the spines of the smaller branchlets of Purkinje cells. Climbing fibers make also S-type synapses on the smaller spines with short necks of the larger dendrites of Purkinje cells, but not frequently on the direct surface of them. It must be emphasized that almost no F-type synapse has been recognized which makes synaptic contacts directly on the spine of any type. It makes synaptic contacts usually on the direct surface of dendrites of Purkinje cells. Basket cell axons embrace directly the somas of the Purkinje cells. Their synaptic contacts were always of F-type and of en-passant character. The hypothesis is proposed that excitatory (E-type) synapses can be identified with synapses of S-type, whereas inhibitory (I-type) synapses would correspond to the F-type terminals.
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  • 27
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    Experimental brain research 2 (1966), S. 18-34 
    ISSN: 1432-1106
    Keywords: Cerebellum ; Parallel fibres ; Basket cells ; Purkinje cells
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Stimulation through concentric electrodes on the surface of a wide cerebellar folium was employed to set up a parallel fibre volley or beam. Serial recording of the field potential was made over a range of depths along microelectrode tracks arranged in a transverse plane across the folium in order to discover the action on Purkinje cells, both those that were on-beam for the parallel fibre volley and those at various distances off-beam. A juxta-fastigial electrode was carefully placed so that an applied stimulus could excite the axons of Purkinje cells distributed across the folium under investigation, the antidromic propagation of impulses thus obtained being utilized to test the effect of parallel fibre volleys upon Purkinje cells. 2. The observations were in accord with the two actions that a parallel fibre volley would be expected to exert on Purkinje cells: a direct excitatory action by the synapses made by parallel fibres with the spines of the Purkinje cell dendrites; an inhibitory action mediated by the stellate and basket cells that themselves are directly excited by the parallel fibre volley. 3. The excitatory synaptic action would result in the two types of responses that were restricted to the narrow zone and superficial location of the parallel fibre volley: active sinks formed by this excitatory synaptic action on the superficial dendrites of Purkinje cells would account for the observed depth profile of extra-cellular slow potentials, a superficial negative wave reversing to a deeper positive wave formed by passive sources on deeper dendrites; superficial synaptic excitation would also account for the facilitation of the propagation of antidromic impulses into the superficial dendrites. 4. The inhibitory synaptic action would result in the two types of responses that were widely dispersed transversely and in depth, far beyond the traject of the parallel fibre volley: a slow positive potential wave with a maximum at a depth usually of 300–400 μ; an inhibitory action on the antidromic invasion of Purkinje cells. The transverse profiles of these two presumed indices of inhibitory action on Purkinje cells apparently revealed that a basket cell may give inhibitory synapses up to 1000 μ laterally from the location of its soma and dendrites. 5. A description is given of the variants in the transverse profiles of the deeper positive waves and of inhibitory actions of a parallel fibre volley that presumably are mediated by basket cells and also by the superficial stellate cells. These physiological findings are correlated with the histologically determined distribution of synapses from a basket cell onto Purkinje cells.
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  • 28
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    Experimental brain research 1 (1966), S. 17-39 
    ISSN: 1432-1106
    Keywords: Parallel fibres ; Purkinje cells ; Cerebellum ; Cat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. When electrical stimuli were applied to the surface of a cerebellar folium by a local electrode (LOC), there was a propagated potential wave along the folium with a triphasic (positive-negative-positive) configuration. 2. Investigations by microelectrode recording established that this wave is produced by impulses propagating for at least 3 mm and at about 0.3 m/sec along a narrow superficial band or “beam” of parallel fibres. As expected from this interpretation, there was an absolutely refractory period of less than 1 msec and impulse annihilation by collision. 3. Complications occurred from the potential wave forms resulting from the excitation of mossy fibres by spreading of the applied LOC stimulus. These complications have been eliminated by chronically deafferenting the cerebellum. 4. When recording within the beam of excited parallel fibres there was a slow negative wave of about 20 msec duration, and deep and lateral thereto, there was a slow positive wave of approximately the same time course. 5. These potential fields were expressed in serial profile plots and in potential contour diagrams and shown to be explicable by the excitatory and inhibitory synaptic action on Purkinje cells: excitatory depolarizing synapses of parallel fibre impulses on the dendrites; and hyperpolarizing inhibitory synapses of stellate and basket cells respectively on the dendrites and somata. The active excitatory synapses would be strictly on the parallel fibre beam and the inhibitory concentrated deep and lateral thereto, which is in conformity with the axonal distributions of those basket and stellate cells that would be excited by the parallel fibre beam. 6. Complex problems were involved in interpretation of slow potentials produced by a second LOC stimulus at brief stimulus intervals and up to 50 msec: there was a potentiation of the slow negative wave, and often depression of the positive wave deep and lateral to the excited beam of parallel fibres. 7. Often the LOC stimulus evoked impulse discharge from the Purkinje cells, these discharges being inhibited by a preceding LOC stimulus.
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  • 29
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    Experimental brain research 1 (1966), S. 161-183 
    ISSN: 1432-1106
    Keywords: Cerebellum ; Purkinje cells ; Intracellular recording ; Postsynaptic potentials
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Intracellular recording from Purkinje cells has been employed in investigating the excitatory and inhibitory synaptic action that is exerted on these cells by the mossy fibre input into the cerebellum. 2. These synaptic actions are evoked not directly by the mossy fibres, but probably always through granule cells and their axons, the parallel fibres. The intracellular records conform with the anatomical evidence that the parallel fibres directly exert a powerful synaptic excitatory action on Purkinje cells, and that the inhibitory pathway occurs via an inhibitory interneurone — a basket cell or a stellate cell. Direct stimulation of parallel fibres gives intracellular potentials closely resembling those produced by deep stimulation of mossy fibres. 3. As would be expected, direct stimulation of parallel fibres produces an EPSP with a latency 1 to 2 msec briefer than the IPSP. The IPSP has a duration usually in excess of 100 msec. The EPSP appears to be briefer, though its superposition on the IPSP greatly reduces its apparent duration. Neutralization of the IPSP by appropriate membrane polarization or by intracellular chloride injection reveals an EPSP duration of up to 50 msec. 4. The IPSP is typically affected by polarizing currents; reduced and even inverted by hyperpolarizing currents, and increased by depolarizing currents. The IPSP is converted to a depolarizing response by excess of intracellular chloride. It must therefore be generated by an increased ionic permeability of the inhibitory subsynaptic membrane, chloride ions being importantly concerned. 5. Often small irregular IPSPs can be observed occurring spontaneously, and they react to polarizing currents and to chloride injections in a manner identical to the evoked IPSPs. It is concluded that they are generated by the spontaneous discharges of basket cells. 6. A brief account is given of various spontaneous rhythmic responses of impaled Purkinje cells, and of the effect of synaptic inhibitory action upon them. 7. There is a general discussion of these findings in relation to the various neural pathways and neural mechanisms that have been postulated in the light of the preceding investigations.
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  • 30
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    Experimental brain research 2 (1966), S. 330-349 
    ISSN: 1432-1106
    Keywords: Deiters neurones ; IPSP ; Monosynaptic ; Purkinje cells ; Inhibitory neurones
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary During stimulation of the anterior lobe of the cerebellum, postsynaptic potentials were recorded intracellularly from ipsilateral Deiters neurones of the cat. In the majority of examined cells, the inhibitory postsynapic potentials were induced with short latency; 1.06 msec on the average from lobule III or IV. The latency was longer (1.23 msec) when the lobule V was stimulated, while it was shorter (0.86 msec) from the juxtafastigial region. It follows that the IPSP was produced via a monosynaptic pathway at a conduction velocity of 15 to 20 m/sec. Recording of the extracellular field potentials and focal stimulation within and around Deiters' nucleus further indicated that the inhibitory impulses propagated out of the cerebellum along a remarkable bundle of fibres which terminated within Deiters' nucleus. These results are all explicable by assuming that the cerebellar Purkinje cells are inhibitory in nature and so produce IPSPs monosynaptically in Deiters neurones via the long corticofugal fibres. Monosynaptic EPSPs were also detected in some Deiters neurones. They are considered to be mediated by the other pathways formed of axon collaterals of the cerebellar afferents.
    Type of Medium: Electronic Resource
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