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The cerebellar corticonuclear and nucleocortical projections in the cat as studied with anterograde and retrograde transport of horseradish peroxidase

IV. The paraflocculus

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Summary

The cerebellar parafloccular corticonuclear and nucleocortical connections were studied in the cat by means of anterograde and retrograde transport of horseradish peroxidase.

Previous investigations have given evidence that the cortex of the paraflocculus can be subdivided into three zones. These zones are recognized as C2, D1 and D2. The material presented is compatible with the findings from previous reports with other methods that each of these zones sends its Purkinje axons to separate regions within the cerebellar nuclei. These terminal fields are the lateral part of nucleus interpositus posterior (the alleged nuclear zone C2) and the dentate nucleus and its transition area with nucleus interpositus anterior (the supposed nuclear D zones). The parafloccular corticonuclear fibres appear to terminate along a continuous mediolateral band extending from the NL through the NL-NIA transition area into the lateral NIP. This observation is in concordance with our previous findings concerning the termination of the cerebellar corticonuclear fibres (Dietrichs and Walberg 1979, 1980; Dietrichs 1981). Within the NL and NL-NIA transition area the Purkinje axons from the ventral paraflocculus terminate ventral to those from the dorsal paraflocculus.

The nucleocortical projection shows the same zonal arrangement as the corticonuclear connection, indicating the presence of a corticonuclear-nucleocortical reciprocity.

The findings are discussed with reference to previous studies on the parafloccular corticonuclear and nucleocortical connections, and some comments are made concerning the cerebellar zonal subdivision of this cortical area.

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References

  • Armstrong DM, Schild RF (1978) An investigation of the cerebellar corticonuclear projection in the rat using an autoradiographic tracing method. II. Projections from the hemisphere. Brain Res 141: 235–249

    Google Scholar 

  • Brodal A, Courville J (1973) Cerebellar corticonuclear projection in the cat. Crus II. An experimental study with silver methods. Brain Res 50: 1–23

    Google Scholar 

  • Brodal A, Kawamura K (1980) Olivocerebellar projection. A review. Adv Anat Embryol Cell Biol 64: 1–140

    Google Scholar 

  • Courville J, Faraco-Cantin F (1980) Topography of the olivocerebellar projection. An experimental study in the cat with an autoradiographic tracing method. In: Courville J, de Montigny C, Lamarc Y (eds) The inferior olivary nucleus. Anatomy and physiology. Raven Press, New York, pp 235–277

    Google Scholar 

  • Dietrichs E (1981) The cerebellar corticonuclear and nucleocortical projections in the cat as studied with anterograde and retrograde transport of horseradish peroxidase. III. The anterior lobe. Anat Embryol (Berl) (in press)

  • Dietrichs E, Walberg F (1979) The cerebellar corticonuclear and nucleocortical projections in the cat as studied with anterograde and retrograde transport of horseradish peroxidase. I. The paramedian lobule. Anat Embryol (Berl) 158: 13–39

    Google Scholar 

  • Dietrichs E, Walberg F (1980) The cerebellar corticonuclear and nucleocortical projections in the cat as studied with anterograde and retrograde transport of horseradish peroxidase. II. Lobulus simplex, crus I and II. Anat Embryol (Berl) 161: 83–103

    Google Scholar 

  • Dietrichs E, Walberg F (1981) The cerebellar nucleo-olivary projection in the cat. Anat Embryol (Berl) 162: 51–67

    Google Scholar 

  • Dietrichs E, Walberg F, Nordby T (1981) On retro- and anterograde transport of horseradish peroxidase in the pontocerebellar fibers as studied with the Mesulam TMB technique. Brain Res 204: 179–183

    Google Scholar 

  • Dow RS (1936) The fiber connections of the posterior parts of the cerebellum in the cat and rat. J Comp Neurol 63: 527–548

    Google Scholar 

  • Gould BB (1979) The organization of afferents to the cerebellar cortex in the cat. Projection from the deep cerebellar nuclei. J Comp Neurol 184: 27–42

    Google Scholar 

  • Gould BB (1980) Organization of afferents from the brain stem nuclei to the cerebellar cortex in the cat. Adv Anat Embryol Cell Biol 62: 1–79

    Google Scholar 

  • Gould BB, Graybiel A (1976) Afferents to the cerebellar cortex in the cat. Evidence for an intrinsic pathway leading from the deep nuclei to the cortex. Brain Res 110: 601–611

    Google Scholar 

  • Graham RC, Karnovsky MJ (1966) The early stages of absorption of injected horseradish peroxidase in the proximal tubule of mouse kidney. Ultrastructural cytochemistry by a new technique. J Histochem Cytochem 14: 291–302

    Google Scholar 

  • Groenewegen HJ, Voogd J, Freedman SL (1979) The parasagittal zonation within the olivocerebellar projection. II. Climbing fiber distribution in the intermediate and hemispheric parts of cat cerebellum. J Comp Neurol 183: 551–602

    Google Scholar 

  • Haines DE (1978a) Cerebellar corticonuclear-nucleocortical topography. A study of the tree shrew (Tupaia) paraflocculus. Anat Rec 190: 411

    Google Scholar 

  • Haines DE (1978b) Contralateral nucleocortical cells of the paraflocculus of tree shrew (Tupaia glis). Neurosci Lett 8: 183–190

    Google Scholar 

  • Haines DE, Pearson JC (1979) Cerebellar corticonuclear-nucleocortical topography. A study of the tree shrew (Tupaia) paraflocculus. J Comp Neurol 187: 745–758

    Google Scholar 

  • Haines DE, Whitworth RH (1978) Cerebellar cortical efferent fibers of the paraflocculus of tree shrew (Tupaia glis). J Comp Neurol 182: 137–150

    Google Scholar 

  • Hoddevik GH, Brodal A (1977) The olivocerebellar projection studied with the method of retrograde axonal transport of horseradish peroxidase. V. The projections to the flocculonodular lobe and the paraflocculus in the rabbit. J Comp Neurol 176: 269–280

    Google Scholar 

  • Kawamura K, Hashikawa T (1979) Olivocerebellar projections in the cat studied by means of anterograde axonal transport of labeled amino acids as tracers. Neuroscience 4: 1615–1633

    Google Scholar 

  • Larsell O (1970) The comparative anatomy and histology of the cerebellum from monotremes through apes (Jansen J, ed). The University of Minnesota Press, Minneapolis

    Google Scholar 

  • Mesulam M-M (1978) Tetramethyl benzidine for horseradish peroxidase neurohistochemistry. A non-carcinogenic blue reaction-product with superior sensitivity for visualizing neural afferents and efferents. J Histochem Cytochem 26: 106–117

    CAS  PubMed  Google Scholar 

  • Oscarsson O (1980) Functional organization of olivary projection to the cerebellar anterior lobe. In: Courville J, de Montigny C, Lamarc Y (eds) The inferior olivary nucleus. Anatomy and physiology. Raven Press, New York, pp 279–289

    Google Scholar 

  • Tolbert DL, Bantli H, Bloedel JR (1978) Organizational features of the cat and monkey cerebellar nucleocortical projection. J Comp Neurol 182: 39–56

    Google Scholar 

  • Voogd J (1964) The cerebellum of the cat. Structure and fibre connexions. Thesis, Van Gorcum, Assen

    Google Scholar 

  • Voogd J (1969) The importance of fiber connections in the comparative anatomy of the mammalian cerebellum. In: Llinás R (ed) Neurobiology of cerebellar evolution and development. American Medical Association, Chicago, pp 493–514

    Google Scholar 

  • Voogd J, Bigaré F (1980) Topographical distribution of olivary and corticonuclear fibers in the cerebellum: A review. In: Courville J, de Montigny C, Lamarc Y (eds) The inferior olivary nucleus. Anatomy and physiology. Raven Press, New York, pp 207–234

    Google Scholar 

  • Walberg F, Kotchabhakdi N, Hoddevik GH (1979) The olivocerebellar projections to the flocculus and paraflocculus in the cat, compared to those in the rabbit. A study using horseradish peroxidase as a tracer. Brain Res 161: 389–398

    Google Scholar 

  • Walberg F, Nordby T, Dietrichs E (1980) A note on the anterograde transport of horseradish peroxidase within the olivocerebellar fibres. Exp Brain Res 40: 233–236

    Google Scholar 

  • Yamamoto M (1979) Topographical representation in rabbit cerebellar flocculus for various afferent inputs from the brainstem investigated by means of retrograde axonal transport of horseradish peroxidase. Neurosci Lett 12: 29–34

    Google Scholar 

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Dietrichs, E. The cerebellar corticonuclear and nucleocortical projections in the cat as studied with anterograde and retrograde transport of horseradish peroxidase. Exp Brain Res 44, 235–242 (1981). https://doi.org/10.1007/BF00236560

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  • DOI: https://doi.org/10.1007/BF00236560

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