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Routes of entry into the cerebellum of spinocerebellar axons from the lower part of the spinal cord

An experimental anatomical study in the cat

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Summary

Among the newly discovered spinocerebellar cell groups, those at lumbar and more caudal levels of the cat's spinal cord were studied with regard to which of the two cerebellar peduncles, the restiform body or the superior cerebellar peduncle, is used by their axons. Bilateral injections with horseradish peroxidase were made into either of the anterior lobe or the posterior cerebellar termination area for spinocerebellar fibers, following unilateral transections of either the superior cerebellar peduncle or the restiform body, combined with low contralateral transections of the lateral and ventral funiculi. Following transection of the superior cerebellar peduncle, labeled neurons were found ipsilateral to the transection in the column of Clarke and in laminae IV–VI at L 3–L 7. Contralaterally, labeled neurons were found in the ventromedial nucleus and lamina VIII of the ventral horn in the sacro-coccygeal segments and in the medial part of lamina VII at L 6 and more caudal levels. All these neurons were regarded as sending their axons through the restiform body. Following transection of the restiform body, labeled neurons were found in the following areas contralateral to the transection: the dorsolateral nucleus of the L 3–L 6 segments, the lateral part of lamina VII at L 3–L 5/6, the medial part of lamina VII in L 6 and more caudal segments, and the ventrolateral nucleus of L 4–L 5. Ipsilaterally, labeled neurons were found in lamina VIII at L 4–L 6. All these neurons were regarded as sending their axons through the superior cerebellar peduncle. In addition to new information about the peduncular routes of spinocerebellar neurons, the study has given confirming evidence as to the crossing conditions for different spinocerebellar cell groups. The findings should be useful in future studies on the organization of the spinocerebellar systems.

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Abbreviations

BC:

brachium conjunctivum

BP:

brachium pontis

C:

cuneate nucleus

CC:

column of Clarke

DL:

dorsolateral nucleus

DSCT:

dorsal spinocerebellar tract

G:

gracile nucleus

lam:

lamina

lat:

lateral

LRN:

lateral reticular nucleus

LVN:

lateral vestibular nucleus

med:

medial

N.d.:

nucleus dentatus

N.f.:

nucleus fastigii

N.i.:

nucleus interpositus

p:

pyramidal tract

p. ant.:

pars anterior (of the paramedian lobule)

p. copul.:

pars copularis (of the paramedian lobule)

pfl. d:

dorsal paraflocculus

pmd:

paramedian lobule

p. post.:

pars posterior (of the paramedian lobule)

RB:

restiform body

SCP:

superior cerebellar peduncle

SVN:

spinal vestibular nucleus

VL:

ventrolateral nucleus

VM:

ventromedial nucleus

VSCT:

ventral spinocerebellar tract

I-X:

(on cerebellar diagrams) cerebellar lobules according to Larsell (1953)

IV–IX:

(on spinal cord diagrams), laminae according to Rexed (1954)

V (on brainstem diagrams):

trigeminal nucleus

VI (on brainstem diagram):

abducens nucleus

XII (on brainstem diagrams):

hypoglossal nucleus

References

  • Aldskogius H, Grant G, Wiksten B (1976) Cells of origin of spinocerebellar fibers from the lower lumbar spinal cord in the kitten. Anat Rec 185: 342–343

    Google Scholar 

  • Aoyama M, Hongo T, Kudo N (1973) An uncrossed ascending tract originating from below Clarke's column and conveying group I impulses from the hindlimb muscles in the cat. Brain Res 62: 237–241

    Google Scholar 

  • Brodal A (1981) Neurological Anatomy, 3rd edn. Oxford University Press, New York

    Google Scholar 

  • Burke RE, Lundberg A, Weight F (1968) Gower's tract and spinal border cells. Acta Physiol Scand 74: 16A

  • Burke RE, Lundberg A, Weight F (1971) Spinal border cell origin of the ventral spinocerebellar tract. Exp Brain Res 12: 283–294

    Google Scholar 

  • Busch HFM (1961) An anatomical analysis of the white matter in the brain stem of the cat. Van Gorcum and Comp NV, Assen

    Google Scholar 

  • Cooper S, Sherrington CS (1940) Gower's tract and spinal bordercells. Brain 63: 123–134

    Google Scholar 

  • Cummings JF, Petras JM (1977) The origin of spinocerebellar pathways. I. The nucleus cervicalis centralis of the cranial cervical spinal cord. J Comp Neurol 173: 655–692

    Google Scholar 

  • Edgley SA, Gallimore CM (1988) The morphology and projections of dorsal horn spinocerebellar tract neurons in the cat. J Physiol (Lond) 397: 99–111

    Google Scholar 

  • Edgley SA, Jankowska E (1988) Information processed by dorsal horn spinocerebellar tract neurons in the cat. J Physiol (Lond) 397: 81–97

    Google Scholar 

  • Grant G (1962) Spinal course and somatotopically localized termination of the spinocerebellar tracts. An experimental study in the cat. Acta Physiol Scand [Suppl] 56: 193

    Google Scholar 

  • Grant G, Wiksten B, Berkley KJ, Aldskogius H (1982) The location of cerebellar-projecting neurons within the lumbosacral spinal cord in the cat. An anatomical study with HRP and retrograde chromatolysis. J Comp Neurol 204: 336–348

    Google Scholar 

  • Hirai N, Hongo T, Kudo N, Yamaguchi T (1976) Heterogeneous composition of the spinocerebellar tract originating from the cervical enlargement in the cat. Brain Res 109: 387–391

    Google Scholar 

  • Hirai N, Hongo T, Sasaki S (1984) A physiological study of identification, axonal course and cerebellar projection of spinocerebellar tract cells in the central cervical nucleus of the cat. Exp Brain Res 55: 272–285

    Google Scholar 

  • Hongo T, Okada Y, Sato M (1967) Corticofugal influences on transmission to the dorsal spinocerebellar tract from hindlimb primary afferents. Exp Brain Res 3: 135–149

    Google Scholar 

  • Jankowska E, Lindström S (1970) Morphological identification of physiologically defined neurons in the cat spinal cord. Brain Res 20: 323–326

    Google Scholar 

  • Johansson H, Silfvenius H (1977a) Axon-collateral activation by dorsal spinocerebellar tract fibers of group I relay cells of nucleus z in the cat medulla oblongata. J Physiol (Lond) 265: 341–369

    Google Scholar 

  • Johansson H, Silfvenius H (1977b) Connections from large, ipsilateral hind limb muscle and skin afferents to the rostral main cuneate nucleus and to the nucleus x region in the cat. J Physiol (Lond) 265: 395–428

    Google Scholar 

  • Lafleur J, Delean J, Poirier LJ (1974) Physiopathology of the cerebellum in the monkey. Part I. Origin of cerebellar afferent nervous fibers from the spinal cord and brain stem. J Neurol Sci 22: 471–490

    Google Scholar 

  • Larsell O (1953) Cerebellum of cat and monkey. J Comp Neurol 99: 135–200

    Google Scholar 

  • Matsushita M, Hosoya Y (1979) Cells of origin of the spinocerebellar tract in the rat. Studied with the method of retrograde transport of horseradish peroxidase. Brain Res 173: 185–200

    Google Scholar 

  • Matsushita M, Hosoya Y (1982) Projections to lobules III to V of the anterior lobe in the cat, as studied by retrograde transport of horseradish peroxidase. J Comp Neurol 208: 127–143

    Google Scholar 

  • Matsushita M, Ikeda M (1975) The central cervical nucleus as cell origin of a spinocerebellar tract arising from the cervical cord: a study in the cat using horseradish peroxidase. Brain Res 100: 412–417

    Google Scholar 

  • Matsushita M, Ikeda M (1979) Spinocerebellar tract neurons projecting to lobule VIII and the paramedian lobule of the cerebellar cortex in the cat. A study by the retrograde horseradish peroxidase technique. In: Ito M, Tsukahara N, Kubota K, Yagi K (eds) Integrative control functions of the brain, Vol 2. Kodansha-Elsevier, Tokyo-Amsterdam, pp 168–170

    Google Scholar 

  • Matsushita M, Ikeda M (1980) Spinocerebellar projections to the vermis of the posterior lobe and the paramedian lobule in the cat, as studied by retrograde transport of horseradish peroxidase. J Comp Neurol 192: 143–162

    Google Scholar 

  • Matsushita M, Ikeda M (1987) Spinocerebellar projections from the cervical enlargement in the cat, as studied by anterograde transport of wheat germ agglutinin-horseradish peroxidase. J Comp Neurol 263: 223–240

    Google Scholar 

  • Matsushita M, Okado N (1981) Spinocerebellar projections to lobules I and II of the anterior lobe in the cat, as studied by retrograde transport of horseradish peroxidase. J Comp Neurol 197: 411–424

    Google Scholar 

  • Matsushita M, Hosoya Y, Ikeda M (1979) Anatomical organization of the spinocerebellar system in the cat as studied by retrograde transport of horseradish peroxidase. J Comp Neurol 184: 81–106

    Google Scholar 

  • Mesulam MM (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, Uddenberg N (1964) Identification of a spinocerebellar tract activated from forelimb afferents in the cat. Acta Physiol Scand 62: 125–136

    Google Scholar 

  • Petras JM (1977) Spinocerebellar neurons in the rhesus monkey. Brain Res 130: 146–151

    Google Scholar 

  • Petras JM, Cummings JF (1977) The origin of spinocerebellar pathways. II. The nucleus centrobasalis of the cervical enlargement and the nucleus dorsalis of the thoracolumbar spinal cord. J Comp Neurol 173: 693–716

    Google Scholar 

  • Pompeiano O, Brodal A (1957) Spino-vestibular fibers in the cat. An experimental study. J Comp Neurol 108: 353–382

    Google Scholar 

  • Randić M, Myslinski NR, Gordon JH (1976) Spinal localization of neurons receiving inputs from cutaneous afferents in the cat hindlimb. Brain Res 105: 573–577

    Google Scholar 

  • Rexed B (1954) A cytoarchitectonic atlas of the spinal cord in the cat. J Comp Neurol 100: 297–379

    Google Scholar 

  • Snyder RL, Fall RLM, Mehler WR (1978) A comparative study of the neurons of origin of the spinocerebellar afferents in the rat, cat and squirrel monkey — based on the retrograde transport of horseradish peroxidase. J Comp Neurol 181: 833–852

    Google Scholar 

  • Sprague JM (1950) Cells of the ventral spinocerebellar tract. Anat Rec 106: 289–290

    Google Scholar 

  • Sprague JM (1953) Spinal “border cells” and their role in postural mechanism (Schiff-Sherrington phenomenon). J Neurophysiol 16: 464–474

    Google Scholar 

  • Tapper DN, Mann MD, Brown PB, Cogdell B (1975) Cells of origin of the cutaneous subdivision of the dorsal spinocerebellar tract. Brain Res 85: 59–63

    Google Scholar 

  • Verhaart WJC (1964) A stereotactic atlas of the brain stem of the cat. Van Gorcum and Comp NV, Assen

    Google Scholar 

  • Voogd J (1964) The cerebellum of the cat. Van Gorcum and Comp NV, Assen

    Google Scholar 

  • Wiberg M, Blomqvist A (1984) The spinomesencephalic tract in the cat: its cells of origin and termination pattern as demonstrated by the intraaxonal transport method. Brain Res 291: 1–18

    Google Scholar 

  • Wiksten B (1975) The central cervical nucleus — a source of spinocerebellar fibers demonstrated by retrograde transport of horseradish peroxidase. Neurosci Lett 1: 81–84

    Google Scholar 

  • Wiksten B (1979a) The central cervical nucleus in the cat. II. The cerebellar connections studied with retrograde transport of horseradish peroxidase. Exp Brain Res 36: 155–173

    Google Scholar 

  • Wiksten B (1979b) The central cervical nucleus in the cat. III. The cerebellar connections studied with anterograde transport of 3H-leucine. Exp Brain Res 36: 175–189

    Google Scholar 

  • Wiksten B (1985) Retrograde HRP study of neurons in the cervical enlargement projecting to the cerebellum in the cat. Exp Brain Res 58: 95–101

    Google Scholar 

  • Wiksten B (1987) Further studies on the fiber connections of the central cervical nucleus in the cat. Exp Brain Res 67: 284–290

    Google Scholar 

  • Xu Q, Grant G (1988) Collateral projections of neurons from the lower part of the spinal cord to anterior and posterior cerebellar termination areas. A retrograde fluorescent double labeling study in the cat. Exp Brain Res 72: 562–576

    Google Scholar 

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On leave from Capital Institute of Medicine, Beijing, The People's Republic of China

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Grant, G., Xu, Q. Routes of entry into the cerebellum of spinocerebellar axons from the lower part of the spinal cord. Exp Brain Res 72, 543–561 (1988). https://doi.org/10.1007/BF00250600

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  • DOI: https://doi.org/10.1007/BF00250600

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