Literature DB >> 458677

Activity patterns of cerebellar cortical neurones and climbing fibre afferents in the awake cat.

D M Armstrong, J A Rawson.   

Abstract

1. Glass-insulated tungsten micro-electrodes were used to record from single neurones in the intermediate zone of the cerebellar cortex of cats in a state of quiet wakefulness. 2. Two hundred and seventy Purkinje (P) cells were recorded extracellularly, 95% of which displayed an irregular tonic discharge at rates between 19 and 95/s (over-all mean 44/s), including complex spikes (c.s.) which occurred at 1.0--2.5/s )over-all mean 1.5/s). The remaining cells discharged c.s. at the usual rate but only one or two simple spikes (s.s.) per minute. C.s. of spike plus wavelet and of multi-spiked type were present in approximately equal numbers of cells. 3. Presumed climbing fibre-e.p.s.p.s were recorded from fifty-six P cells and occurred both singly and in groups of two to six e.p.s.p.s at an intra-group frequency of about 500/s. The cells giving rise to the c.f.s therefore discharge propagated impulses both singly and in short bursts as previously reported for anesthetized animals. A single e.p.s.p. can give rise to more than one spike in the multi-spiked type of c.s., and probably to a complete c.s. event. 4. Following spontaneous c.s. the interval to the next s.s. varied from 8 to 600 ms. There was an inverse correlation between duration of the post-c.s. interval and the rate at which s.s. were discharged in the preceding 100 ms. The duration exceeded the mean s.s. interval provided s.s. rate was less than 40--50/s, and the post-c.s. interval would then constitute a real interruption of s.s. discharge. 5. When the superficial radial (s.r.) nerves were stimulated with single shocks too weak to produce a behavioural response changes in discharge pattern were detected in eighty-eight of 151 P cells tested. The initial responses were almost always excitatory and consisted in seventy-two cells of a c.s., in eleven of a c.s. preceded by a brief increase in s.s. and in two cases of a s.s. discharge alone. The spino-olivo-cerebellar paths responsible for the c.s. showed transmission characteristics similar to those reported for animals anaesthetized with barbiturates. 6. C.s. were readily evoked by tapping or squeezing the forepaws. 7. Excitatory responses to nerve stimulation were usually followed by a depression of the tonic s.s. discharge. Its duration ranged widely in different cells (from 10 to 500 ms) and it would coincide with equally variable periods of facilitation previously seen in neurones of nucleus interpositus. It is therefore likely that such facilitations of the cerebellar nuclear cells result at least in part from reductions in the tonic inhibitory input from the P cells. 8. Thirty-six units were classes as 'probable cortical interneurones'. They discharged more regularly, at rates between 9 and 28/s. Twenty such units (56%) responded to s.r. stimulation with a brief excitation not usually followed by any pronounced depression.

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Year:  1979        PMID: 458677      PMCID: PMC1281378          DOI: 10.1113/jphysiol.1979.sp012745

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  32 in total

1.  Changes of simple and complex spike activity of cerebellar purkinje cells with sleep and waking.

Authors:  N Mano
Journal:  Science       Date:  1970-12-18       Impact factor: 47.728

2.  Discharge of Purkinje and cerebellar nuclear neurons during rapidly alternating arm movements in the monkey.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1968-09       Impact factor: 2.714

3.  Discharge properties of Purkinje cells recorded on single and double microelectrodes.

Authors:  C C Bell; R J Grimm
Journal:  J Neurophysiol       Date:  1969-11       Impact factor: 2.714

4.  Activity of dendrites of single Purkinje cells and its relationship to so-called inactivation response in rabbit cerebellum.

Authors:  Y Fujita
Journal:  J Neurophysiol       Date:  1968-03       Impact factor: 2.714

5.  Spontaneous firing of cerebellar Purkinje cells in decerebrate and barbiturate anesthetized cats.

Authors:  J T Murphy; N H Sabah
Journal:  Brain Res       Date:  1970-02-03       Impact factor: 3.252

6.  Functional relationship among neurons of the cerebellar cortex in the absence of anesthesia.

Authors:  J R Bloedel; W J Roberts
Journal:  J Neurophysiol       Date:  1969-01       Impact factor: 2.714

7.  A spinocerebellar climbing fibre path activated by the flexor reflex afferents from all four limbs.

Authors:  B Larson; S Miller; O Oscarsson
Journal:  J Physiol       Date:  1969-08       Impact factor: 5.182

8.  Termination and functional organization of the dorsal spino-olivocerebellar path.

Authors:  O Oscarsson
Journal:  J Physiol       Date:  1969-01       Impact factor: 5.182

9.  Discharge of cerebellar neurons related to two maintained postures and two prompt movements. II. Purkinje cell output and input.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1970-07       Impact factor: 2.714

10.  The excitatory synaptic action of climbing fibres on the Purkinje cells of the cerebellum.

Authors:  J C Eccles; R Llinás; K Sasaki
Journal:  J Physiol       Date:  1966-01       Impact factor: 5.182

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  105 in total

1.  Simulations of cerebellar motor learning: computational analysis of plasticity at the mossy fiber to deep nucleus synapse.

Authors:  J F Medina; M D Mauk
Journal:  J Neurosci       Date:  1999-08-15       Impact factor: 6.167

2.  Membrane potential bistability is controlled by the hyperpolarization-activated current I(H) in rat cerebellar Purkinje neurons in vitro.

Authors:  Stephen R Williams; Soren R Christensen; Greg J Stuart; Michael Häusser
Journal:  J Physiol       Date:  2002-03-01       Impact factor: 5.182

3.  Activity-dependent recruitment of extrasynaptic NMDA receptor activation at an AMPA receptor-only synapse.

Authors:  Beverley A Clark; Stuart G Cull-Candy
Journal:  J Neurosci       Date:  2002-06-01       Impact factor: 6.167

4.  Coexistence of excitatory and inhibitory GABA synapses in the cerebellar interneuron network.

Authors:  Joël Chavas; Alain Marty
Journal:  J Neurosci       Date:  2003-03-15       Impact factor: 6.167

5.  Persistent changes in spontaneous firing of Purkinje neurons triggered by the nitric oxide signaling cascade.

Authors:  Spencer L Smith; Thomas S Otis
Journal:  J Neurosci       Date:  2003-01-15       Impact factor: 6.167

6.  Distinct contributions of small and large conductance Ca2+-activated K+ channels to rat Purkinje neuron function.

Authors:  Jeremy R Edgerton; Peter H Reinhart
Journal:  J Physiol       Date:  2003-02-07       Impact factor: 5.182

7.  Abnormal Purkinje cell activity in vivo in experimental allergic encephalomyelitis.

Authors:  Carl Y Saab; Matthew J Craner; Yuko Kataoka; Stephen G Waxman
Journal:  Exp Brain Res       Date:  2004-04-29       Impact factor: 1.972

8.  A biophysical model of synaptic delay learning and temporal pattern recognition in a cerebellar Purkinje cell.

Authors:  Volker Steuber; David Willshaw
Journal:  J Comput Neurosci       Date:  2004 Sep-Oct       Impact factor: 1.621

9.  Lobule-specific membrane excitability of cerebellar Purkinje cells.

Authors:  Chang-Hee Kim; Seung-Ha Oh; Jun Ho Lee; Sun O Chang; Jun Kim; Sang Jeong Kim
Journal:  J Physiol       Date:  2011-11-14       Impact factor: 5.182

10.  Mechanisms of synchronous activity in cerebellar Purkinje cells.

Authors:  Andrew K Wise; Nadia L Cerminara; Dilwyn E Marple-Horvat; Richard Apps
Journal:  J Physiol       Date:  2010-05-04       Impact factor: 5.182

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