Literature DB >> 1816375

Topography and nociceptive receptive fields of climbing fibres projecting to the cerebellar anterior lobe in the cat.

C F Ekerot1, M Garwicz, J Schouenborg.   

Abstract

1. The cutaneous receptive fields of 225 climbing fibres projecting to the forelimb area of the C3 zone in the cerebellar anterior lobe were mapped in the pentobarbitone-anaesthetized cat. Responses in climbing fibres were recorded as complex spikes in Purkinje cells. 2. A detailed topographical organization of the nociceptive climbing fibre input to the C3 zone was found. In the medial C3 zone climbing fibres with receptive fields covering proximal and/or lateral parts of the forelimb projected most medially. Climbing fibres with receptive fields located more medially on the forelimb projected successively more laterally. The sequence of receptive fields found in the lateral C3 zone was roughly the reverse of that in the medial C3 zone. Climbing fibres with receptive fields restricted to the digits projected preferentially to the caudal part of the forelimb area, whereas those with receptive fields covering both proximal and ventral areas of the forearm projected to more rostral parts. 3. The representation of the forelimb was uneven. Receptive fields with a focus on the digits or along the lateral side of the forearm dominated. 4. The proximal borders of the receptive fields were located close to joints. The area from which maximal responses were evoked was usually located eccentrically within the receptive field. Based on spatial characteristics the receptive fields could be divided into eight classes, which in turn were tentatively divided into subclasses. Similar subclasses of receptive fields were found in different cats. This classification was further supported by the results of a quantitative analysis of eighty-nine climbing fibres. The receptive fields of these climbing fibres were mapped with standardized noxious stimulation. 5. Climbing fibres terminating within sagittal strips (width, 100-300 microns; length, greater than 1 mm) had receptive fields which belonged to the same subclass. There were commonly abrupt changes in receptive fields between such microzones. Most classes of receptive fields were found in both the medial and the lateral parts of the C3 zone. However, receptive fields with a focus on the ventral side of either the metacarpals, the wrist or the forearm were found only in the medial part of the C3 zone. Furthermore, the class of receptive fields restricted to the lateral side of the upper arm and shoulder was only found in the lateral part of the C3 zone. 6. In the discussion, it is proposed that climbing fibres projecting to each microzone carry information from spinal multireceptive reflex arcs acting on a single muscle or a group of synergistic muscles.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1991        PMID: 1816375      PMCID: PMC1180197          DOI: 10.1113/jphysiol.1991.sp018750

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


  22 in total

1.  Functional significance of projection from the cerebellar nuclei to the motor cortex in the cat.

Authors:  H Asanuma; R W Hunsperger
Journal:  Brain Res       Date:  1975-11-07       Impact factor: 3.252

2.  The postsynaptic dorsal column pathway mediates cutaneous nociceptive information to cerebellar climbing fibres in the cat.

Authors:  C F Ekerot; M Garwicz; J Schouenborg
Journal:  J Physiol       Date:  1991-09       Impact factor: 5.182

3.  Long-lasting neuronal activity in rat dorsal horn evoked by impulses in cutaneous C fibres during noxious mechanical stimulation.

Authors:  J Schouenborg; A Dickenson
Journal:  Brain Res       Date:  1988-01-26       Impact factor: 3.252

4.  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

5.  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

6.  Functional organization of long, second-order afferents in the dorsal funiculus.

Authors:  N Uddenberg
Journal:  Exp Brain Res       Date:  1968       Impact factor: 1.972

7.  The cerebellar corticonuclear projection from lobule Vb/c of the cat anterior lobe: a combined electrophysiological and autoradiographic study. I. Projections from the intermediate region.

Authors:  J R Trott; D M Armstrong
Journal:  Exp Brain Res       Date:  1987       Impact factor: 1.972

8.  The density, distribution and topographical organization of spinocervical tract neurones in the cat.

Authors:  A G Brown; R E Fyffe; R Noble; P K Rose; P J Snow
Journal:  J Physiol       Date:  1980-03       Impact factor: 5.182

9.  Form and function of dorsal horn neurones with axons ascending the dorsal columns in cat.

Authors:  A G Brown; R E Fyffe
Journal:  J Physiol       Date:  1981-12       Impact factor: 5.182

10.  Input-output relations of the red nucleus in the cat.

Authors:  C Ghez
Journal:  Brain Res       Date:  1975-11-07       Impact factor: 3.252

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  45 in total

1.  Common principles of sensory encoding in spinal reflex modules and cerebellar climbing fibres.

Authors:  Martin Garwicz; Anders Levinsson; Jens Schouenborg
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

2.  The entire trajectories of single olivocerebellar axons in the cerebellar cortex and their contribution to Cerebellar compartmentalization.

Authors:  I Sugihara; H S Wu; Y Shinoda
Journal:  J Neurosci       Date:  2001-10-01       Impact factor: 6.167

3.  Sensorimotor mapping of the human cerebellum: fMRI evidence of somatotopic organization.

Authors:  W Grodd; E Hülsmann; M Lotze; D Wildgruber; M Erb
Journal:  Hum Brain Mapp       Date:  2001-06       Impact factor: 5.038

4.  Central regulation of cerebellar climbing fibre input during motor learning.

Authors:  Richard Apps; Stephen Lee
Journal:  J Physiol       Date:  2002-05-15       Impact factor: 5.182

Review 5.  Parallel fiber receptive fields: a key to understanding cerebellar operation and learning.

Authors:  Carl-Fredrik Ekerot; Henrik Jörntell
Journal:  Cerebellum       Date:  2003       Impact factor: 3.847

6.  Spinal sensorimotor transformation: relation between cutaneous somatotopy and a reflex network.

Authors:  Anders Levinsson; Hans Holmberg; Jonas Broman; Mengliang Zhang; Jens Schouenborg
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

7.  Gating of transmission in climbing fibre paths to cerebellar cortical C1 and C3 zones in the rostral paramedian lobule during locomotion in the cat.

Authors:  R Apps; S Lee
Journal:  J Physiol       Date:  1999-05-01       Impact factor: 5.182

8.  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

9.  Molecular, topographic, and functional organization of the cerebellar cortex: a study with combined aldolase C and olivocerebellar labeling.

Authors:  Izumi Sugihara; Yoshikazu Shinoda
Journal:  J Neurosci       Date:  2004-10-06       Impact factor: 6.167

10.  Functional organization of climbing fibre projection to the cerebellar anterior lobe of the rat.

Authors:  H Jörntell; C Ekerot; M Garwicz; X L Luo
Journal:  J Physiol       Date:  2000-01-15       Impact factor: 5.182

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