Skip to main content
The Journal of Physiology logoLink to The Journal of Physiology
. 1991 Sep;441:257–274. doi: 10.1113/jphysiol.1991.sp018750

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

C F Ekerot 1, M Garwicz 1, J Schouenborg 1
PMCID: PMC1180197  PMID: 1816375

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)

Full text

PDF
257

Images in this article

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Andersson G., Oscarsson O. Climbing fiber microzones in cerebellar vermis and their projection to different groups of cells in the lateral vestibular nucleus. Exp Brain Res. 1978 Aug 15;32(4):565–579. doi: 10.1007/BF00239553. [DOI] [PubMed] [Google Scholar]
  2. Andersson G., Oscarsson O. Projections to lateral vestibular nucleus from cerebellar climbing fiber zones. Exp Brain Res. 1978 Aug 15;32(4):549–564. doi: 10.1007/BF00239552. [DOI] [PubMed] [Google Scholar]
  3. Angaut-Petit D. The dorsal column system: II. Functional properties and bulbar relay of the postsynaptic fibres of the cat's fasciculus gracilis. Exp Brain Res. 1975 May 22;22(5):471–493. doi: 10.1007/BF00237349. [DOI] [PubMed] [Google Scholar]
  4. Asanuma H., Hunsperger R. W. Functional significance of projection from the cerebellar nuclei to the motor cortex in the cat. Brain Res. 1975 Nov 7;98(1):73–92. doi: 10.1016/0006-8993(75)90510-7. [DOI] [PubMed] [Google Scholar]
  5. Bennett G. J., Nishikawa N., Lu G. W., Hoffert M. J., Dubner R. The morphology of dorsal column postsynaptic spinomedullary neurons in the cat. J Comp Neurol. 1984 Apr 20;224(4):568–578. doi: 10.1002/cne.902240406. [DOI] [PubMed] [Google Scholar]
  6. Brown A. G., Brown P. B., Fyffe R. E., Pubols L. M. Receptive field organization and response properties of spinal neurones with axons ascending the dorsal columns in the cat. J Physiol. 1983 Apr;337:575–588. doi: 10.1113/jphysiol.1983.sp014643. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Brown A. G., Fyffe R. E. Form and function of dorsal horn neurones with axons ascending the dorsal columns in cat. J Physiol. 1981 Dec;321:31–47. doi: 10.1113/jphysiol.1981.sp013970. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Brown A. G., Fyffe R. E., Noble R., Rose P. K., Snow P. J. The density, distribution and topographical organization of spinocervical tract neurones in the cat. J Physiol. 1980 Mar;300:409–428. doi: 10.1113/jphysiol.1980.sp013169. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Ekerot C. F., Garwicz M., Schouenborg J. The postsynaptic dorsal column pathway mediates cutaneous nociceptive information to cerebellar climbing fibres in the cat. J Physiol. 1991 Sep;441:275–284. doi: 10.1113/jphysiol.1991.sp018751. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Ekerot C. F., Gustavsson P., Oscarsson O., Schouenborg J. Climbing fibres projecting to cat cerebellar anterior lobe activated by cutaneous A and C fibres. J Physiol. 1987 May;386:529–538. doi: 10.1113/jphysiol.1987.sp016549. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Ekerot C. F., Larson B. Branching of olivary axons to innervate pairs of sagittal zones in the cerebellar anterior lobe of the cat. Exp Brain Res. 1982;48(2):185–198. doi: 10.1007/BF00237214. [DOI] [PubMed] [Google Scholar]
  12. Ekerot C. F., Larson B. The dorsal spino-olivocerebellar system in the cat. I. Functional organization and termination in the anterior lobe. Exp Brain Res. 1979 Jul 2;36(2):201–217. doi: 10.1007/BF00238905. [DOI] [PubMed] [Google Scholar]
  13. Ekerot C. F., Larson B. The dorsal spino-olivocerebellar system in the cat. II. Somatotopical organization. Exp Brain Res. 1979 Jul 2;36(2):219–232. doi: 10.1007/BF00238906. [DOI] [PubMed] [Google Scholar]
  14. Ekerot C. F., Oscarsson O., Schouenborg J. Stimulation of cat cutaneous nociceptive C fibres causing tonic and synchronous activity in climbing fibres. J Physiol. 1987 May;386:539–546. doi: 10.1113/jphysiol.1987.sp016550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  15. Ghez C. Input-output relations of the red nucleus in the cat. Brain Res. 1975 Nov 7;98(1):93–308. doi: 10.1016/0006-8993(75)90511-9. [DOI] [PubMed] [Google Scholar]
  16. Giuffrida R., Li Volsi G., Pantò M. R., Perciavalle V., Sapienza S., Urbano A. Single muscle organization of interposito-rubral projections. Exp Brain Res. 1980;39(3):261–267. doi: 10.1007/BF00237115. [DOI] [PubMed] [Google Scholar]
  17. Lu G. W., Bennett G. J., Nishikawa N., Hoffert M. J., Dubner R. Extra- and intracellular recordings from dorsal column postsynaptic spinomedullary neurons in the cat. Exp Neurol. 1983 Nov;82(2):456–477. doi: 10.1016/0014-4886(83)90417-x. [DOI] [PubMed] [Google Scholar]
  18. Rispal-Padel L., Cicirata F., Pons C. Cerebellar nuclear topography of simple and synergistic movements in the alert baboon (Papio papio). Exp Brain Res. 1982;47(3):365–380. doi: 10.1007/BF00239355. [DOI] [PubMed] [Google Scholar]
  19. Schouenborg J., Dickenson A. Long-lasting neuronal activity in rat dorsal horn evoked by impulses in cutaneous C fibres during noxious mechanical stimulation. Brain Res. 1988 Jan 26;439(1-2):56–63. doi: 10.1016/0006-8993(88)91461-8. [DOI] [PubMed] [Google Scholar]
  20. Schouenborg J., Kalliomäki J. Functional organization of the nociceptive withdrawal reflexes. I. Activation of hindlimb muscles in the rat. Exp Brain Res. 1990;83(1):67–78. doi: 10.1007/BF00232194. [DOI] [PubMed] [Google Scholar]
  21. Trott J. R., Armstrong D. M. 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. Exp Brain Res. 1987;66(2):318–338. doi: 10.1007/BF00243308. [DOI] [PubMed] [Google Scholar]
  22. Uddenberg N. Functional organization of long, second-order afferents in the dorsal funiculus. Exp Brain Res. 1968;4(4):377–382. doi: 10.1007/BF00235702. [DOI] [PubMed] [Google Scholar]

Articles from The Journal of Physiology are provided here courtesy of The Physiological Society

RESOURCES