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  • 1965-1969  (7)
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  • 1966  (7)
  • Cat  (4)
  • Purkinje cells  (4)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    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.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 2 (1966), S. 247-260 
    ISSN: 1432-1106
    Keywords: Synaptic excitation ; Hippocampus ; Pyramidal cells ; Dendritic activation ; Cat ; Rabbit
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary Following selective activation of four afferent paths that terminate exclusively on dendrites, only a small proportion of pyramidal cells in the hippocampal fields CA1 and CA3 discharged impulses. Following a single afferent volley, an EPSP was never observed even in cells synaptically excited. On tetanic stimulation (about 10/sec), a large EPSP developed, but this was not a prerequisite for an action potential. Studies of the extracellular field potentials corresponding to the EPSP and the population spike potential, indicated that the EPSP was generated across the dendritic membrane and that the spike was initiated in the neighbouring part of the dendritic tree, propagating from there along the thicker dendrites towards the soma. This conduction had an average velocity of 0.4m/sec, and, presumably, a relatively low safety factor. In certain cases, the intrasomatic electrode recorded small all-or-nothing spikes which presumably were generated in the dendritic tree. These small spikes (D-spikes) invaded the soma only if assisted by some additional depolarization, for example by frequency potentiation of excitatory synapses. The results indicate two functional types of pyramidal dendrites, the conducting and the synaptic type.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 1 (1966), S. 1-16 
    ISSN: 1432-1106
    Keywords: Inhibitory interneurones ; Cerebellum ; Cat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Notes: Summary 1. Extracellular microelectrode recording has been employed to study the responses of three types of interneurones in the cat cerebellar cortex: basket cells, superficial stellate cells and Golgi cells. The large unitary spike potentials of single cells were sharply localized and presumably were generated by impulse discharges from the cell somata. The characteristics of their responses described below sharply distinguished them from Purkinje cells. 2. The parallel fibre volleys generated by surface stimulation of a folium evoked brief repetitive discharges that were graded in respect of frequency and number. Maximum responses had as many as 10 impulses at an initial frequency of 500/sec. 3. At brief test intervals there was facilitation of the response to a second parallel fibre volley; at about 50 msec it passed over to depression for over 500 msec. 4. Stimulation deep in the cerebellum in the region of the fastigial nucleus (juxta-fastigial, J.F.) evoked by synaptic action a single or double discharge, presumably by the mossy fibre-granule cell-parallel fibre path, but climbing fibre stimulation from the inferior olive also usually had a weak excitatory action evoking never more than one impulse. 5. J.F. stimulation also had an inhibitory action on the repetitive discharge evoked by a parallel fibre volley. Possibly this is due to the inhibitory action of impulses in Purkinje cell axon collaterals. 6. There was a slow (7–30/sec) and rather irregular background discharge from all interneurones. The inhibitory actions of parallel fibre and J.F. stimulation silenced this discharge for some hundreds of milliseconds, probably by Golgi cell inhibition of a background mossy fibre input into granule cells. 7. All these various features were displayed by cells at depths from 180 to 500 μ; hence it was concluded that superficial stellate, basket and Golgi cells have similar properties, discrimination being possible only by depth, the respective depth ranges being superficial to 250μ, 250μ to 400μ, and deeper than 400μ.
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    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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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Experimental brain research 1 (1966), S. 48-64 
    ISSN: 1432-1106
    Keywords: Spontaneous post-synaptic potentials (EPSPs, IPSPs) ; Motor cortex ; Cat
    Source: Springer Online Journal Archives 1860-2000
    Topics: Medicine
    Description / Table of Contents: Zusammenfassung 1. Im motorischen Cortex von ausgewachsenen Katzen (mittlere Nembutalnarkose) wurden spontane postsynaptische Potentiale (PSP) mit intrazellulären Mikroelektroden untersucht. Die spontanen EPSP wurden mit ausgelösten EPSP nach schwachen Reizen in spezifischen (VL) und unspezifischen (CM) Thalamuskernen verglichen. 2. Spontane EPSP treten entweder einzeln oder gruppiert auf. spontane IPSP sind seltener und machen nur 3–10% aller spontanen PSP aus. Die kleinsten EPSP haben eine Amplitude von 150–200 μV, daneben kommen kleinere, flache Schwankungen des Membranpotentials vor. Die mittlere Amplitude von spontanen EPSP liegt bei 0.7 mV. Amplitudenhistogramme spontaner EPSP unterscheiden sich nicht wesentlich von solchen, die durch schwache CM- oder VL-Reize ausgelöst sind. 3. Die Anstiegssteilheit von spontanen EPSP liegt zwischen 2 und 15 msec. Es besteht keine konstante Beziehung zwischen Amplitude und Anstiegssteilheit. Der Potentialabfall ist annähernd exponentiell, die Zeitkonstante liegt zwischen 8 und 12 msec und ist damit etwas länger als die passive Neuronzeitkonstante (8.5±2.2 msec nach Creutzfeldt u. Mitarb., 1964b). Es bestehen keine konstanten Unterschiede der Zeitverläufe von spontanen, durch VL- oder CM-Reiz ausgelösten EPSP-Einheiten. 4. Die Intervallhistogramme von spontanen EPSP sind verschieden je nach dem, ob alle Intervalle oder nur Perioden mit sporadischer, nicht-gruppierter Aktivität ausgezählt werden. Nicht gruppierte EPSP haben längere mittlere Intervalle (70–80 msec). 5. Nach überschwelligen Thalamusreizserien ist sowohl die spontane als auch die reizinduzierte PSP-aktivität vermindert. Es kann jedoch nicht entschieden werden, inwieweit corticale und inwieweit thalamische Mechanismen für diese post-tetanische Depression verantwortlich sind. 6. Während reversibler Deafferentierung des Cortex durch K+-depolarisation afferenter Fasern und im chronisch isolierten Cortex finden sich keine spontanen PSP mehr, obwohl EPSP und IPSP am isolierten Cortex durch epicorticale Reize noch ausgelöst werden können. 7. Aus den Befunden wird geschlossen, daß die beobachteten PSP durch afferente und collaterale Faseraktivität ausgelöst sind. Für echte „Miniaturpotentiale” entsprechend Beobachtungen an Muskelendplatten findet sich kein Anhalt. Insofern repräsentiert das „synaptische Rauschen” corticaler Zellen die konvergierende Afferenz dieser Zellen und kann nicht als echtes „spontanes Rauschen” angesehen werden.
    Notes: Summary Spontaneous post-synaptic potentials (PSP's) of neurones of the motor cortex are analysed (intracellular recording, Nembutal anesthesia, cats). Distinct EPSP's either appear grouped or more sporadically distributed. Spontaneous EPSP's only represent about 3–10% of all spontaneous PSP's. The mean amplitude of EPSP's is about 0.7 mV. The smallest EPSP's have an amplitude of 150–200 μV, smaller slow fluctuations of the membrane potential (MP) are seen occasionally. Amplitude histograms of spontaneous EPSP's are similar to those of evoked EPSP units following weak thalamic stimulation. — The rising time of spontaneous EPSP's varies between 2 and 15 msec. and is not correlated with the peak amplitude. The decay is almost exponential, the time constant is between 8 and 12msec., thus being slightly higher than the neurone time constant of cortical pyramidal cells (8.5±2.2 msec. Creutzfeldt et al., 1964b). No consistant differences in time course and amplitude of “EPSP units” after VL and CM thalamic stimulation and of spontaneous EPSP's was found. Cortical and thalamic components of post-tetanic depression of spontaneous and evoked PSP activity cannot be distinguished. Interval histograms are different whether all EPSP's during sporadic and grouped activity or whether only sporadically appearing EPSP's are counted. Non-grouped EPSP's show longer mean intervals (between 70 and 80 msec.). — During reversible deafferentation with K+-depolarization of afferent fibers and in the chronically isolated cortex no spontaneous EPSP's or IPSP's are found eventhough membrane fluctuations of cells in the latter preparation may sometimes be difficult to distinguish from real EPSP's. In the chronically isolated cortex, EPSP's and IPSP's can still be elicited by epicortical stimulation. — From these findings it is concluded that the observed spontaneous PSP's represent “unit” EPSP's and IPSP's due to afferent and collateral fiber activity and that no true miniature potentials due to spontaneous liberation of transmitter substance can be recorded. Thus, the “synaptic noise” of cortical neurones represents convergent activity on these cells and consequently cannot be considered as true “spontaneous noise”.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    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.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    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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