Literature DB >> 4702148

Cutaneous convergence on to the climbing fibre input to cerebellar Purkynĕ cells.

R Leicht, M J Rowe, R F Schmidt.   

Abstract

1. In cats anaesthetized with Nembutal, the cutaneous receptive fields of individual cerebellar climbing fibres were assessed by recording the climbing fibre responses of single Purkyne cells following controlled mechanical stimulation (air jets, vibration, taps, pressure) of the foot pads of all four limbs and of the hairy skin of the limbs and the body.2. Three major types of cutaneous receptive fields of individual climbing fibres were recognized: (a) restricted fields generally confined to the distal areas of one limb only; (b) circumscribed fields on the distal areas of two to four limbs (discontinuous fields); and (c) widespread continuous fields extending over all or almost all of the body surface. A fourth group appears to receive cutaneous inputs from one limb and sensory input from deeper structures in other limbs.3. Thresholds for tapping of the foot pads were often quite low (< 100 mum indentation), and there was no noticeable difference in the distribution of thresholds between the climbing fibres having restricted or more widespread cutaneous receptive fields. Similarly, the latencies of climbing fibre responses evoked by vibration and tapping were in the same ranges for climbing fibres with receptive fields restricted to one limb only and for those having more widespread fields.4. In regard to location in the anterior lobe of the cerebellum it was found that those climbing fibres receiving inputs only from the ipsilateral forelimb projected to Purkyne cells located almost entirely in lobule V, whereas all other climbing fibres with restricted or more widespread receptive fields projected to Purkyne cells distributed widely within lobules II to V.

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Year:  1973        PMID: 4702148      PMCID: PMC1331242          DOI: 10.1113/jphysiol.1973.sp010102

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


  19 in total

1.  Spinal cord afferents: functional organization and inhibitory control.

Authors:  R F Schmidt
Journal:  UCLA Forum Med Sci       Date:  1969

2.  Responses of single units in the inferior olive to stimulation of the limb nerves, peripheral skin receptors, cerebellum, caudate nucleus and motor cortex.

Authors:  E M Sedgwick; T D Williams
Journal:  J Physiol       Date:  1967-04       Impact factor: 5.182

3.  Analysis of electrical potentials evoked in the cerebellar anterior lobe by stimulation of hindlimb and forelimb nerves.

Authors:  J C Eccles; L Provini; P Strata; H Táboríková
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

4.  Topographical investigations on the climbing fiber inputs from forelimb and hindlimb afferents to the cerebellar anterior lobe.

Authors:  J C Eccles; L Provini; P Strata; H Táboríková
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

5.  Mossy and climbing fibre organization on the anterior lobe of the cerebellum activated by forelimb and hindlimb areas of the sensorimotor cortex.

Authors:  L Provini; S Redman; P Strata
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

6.  Single unit responses and the total afferent outflow from the cat's foot pad upon mechanical stimulation.

Authors:  W Jänig; R F Schmidt; M Zimmermann
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

7.  Afferent volleys in limb nerves influencing impulse discharges in cerebellar cortex. II. In Purkynĕ cells.

Authors:  J C Eccles; D S Faber; J T Murphy; N H Sabah; H Táboríková
Journal:  Exp Brain Res       Date:  1971-07-26       Impact factor: 1.972

8.  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

9.  Excitability measurements at the central terminals of single mechano-receptor afferents during slow potential changes.

Authors:  R F Schmidt; J Senges; M Zimmermann
Journal:  Exp Brain Res       Date:  1967       Impact factor: 1.972

10.  Somatosensory receptive fields of single units in cat cerebellar cortex.

Authors:  W T Thach
Journal:  J Neurophysiol       Date:  1967-07       Impact factor: 2.714

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  22 in total

1.  Organization of climbing fibre projections to the cerebellar cortex from trigeminal cutaneous afferents and from the SI face area of the cerebral cortex in the cat.

Authors:  T S Miles; M Wiesendanger
Journal:  J Physiol       Date:  1975-02       Impact factor: 5.182

2.  Climbing fibre inputs to cerebellar Purkinje cells from trigeminal cutaneous afferents and the SI face area of the cerebral cortex in the cat.

Authors:  T S Miles; M Wiesendanger
Journal:  J Physiol       Date:  1975-02       Impact factor: 5.182

3.  Changes in excitability of ascending and descending inputs to cerebellar climbing fibers during locomotion.

Authors:  Joanne Pardoe; Stephen A Edgley; Trevor Drew; Richard Apps
Journal:  J Neurosci       Date:  2004-03-17       Impact factor: 6.167

4.  Neuronal activity in the lateral vestibular nucleus of the cat. V. Topographical distribution of inhibitory effects mediated by the spino-olivocerebellar pathway.

Authors:  G ten Bruggencate; H Scherer; R Teichmann
Journal:  Pflugers Arch       Date:  1975-11-28       Impact factor: 3.657

5.  Inhibition of cuneate neurones: its afferent source and influence on dynamically sensitive "tactile" neurones.

Authors:  E Bystrzycka; B S NAil; M Rowe
Journal:  J Physiol       Date:  1977-06       Impact factor: 5.182

6.  Cutaneous receptive fields of cerebellar Purkynĕ cells of unanesthetized cats.

Authors:  E Hiss; R Leicht; R F Schmidt
Journal:  Exp Brain Res       Date:  1977-03-30       Impact factor: 1.972

7.  Climbing fibres projecting to cat cerebellar anterior lobe activated by cutaneous A and C fibres.

Authors:  C F Ekerot; P Gustavsson; O Oscarsson; J Schouenborg
Journal:  J Physiol       Date:  1987-05       Impact factor: 5.182

8.  Stimulation of cat cutaneous nociceptive C fibres causing tonic and synchronous activity in climbing fibres.

Authors:  C F Ekerot; O Oscarsson; J Schouenborg
Journal:  J Physiol       Date:  1987-05       Impact factor: 5.182

9.  Cerebellar unit responses of the mossy fibre system to passive movements in the decerebrate cat. I. Responses to static parameters.

Authors:  F P Kolb; F J Rubia; E Bauswein
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

10.  Input from trigeminal cutaneous afferents to neurones of the inferior olive in rats.

Authors:  J R Cook; M Wiesendanger
Journal:  Exp Brain Res       Date:  1976-09-24       Impact factor: 1.972

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