Literature DB >> 6468566

The distribution and origin of the ipsilateral descending limb of the brachium conjunctivum. An autoradiographic and horseradish peroxidase study in the rat.

W Woodson, P Angaut.   

Abstract

The distribution, organization and origin of the ipsilateral descending limb of the Brachium Conjunctivum (B.C.), have been studied in the rat by using anterograde and retrograde tracing techniques. After injections of tritiated leucine/proline into the lateral cerebellar nucleus, covering both its medial part, corresponding to the dorsolateral hump (DLH) of Goodman et al. (1963) and its lateral part, (designated here as the lateral dentate, LD), and the neighboring interposed nucleus (NI), emerging fibres are numerous and leave laterally from the B.C. On the contrary, injections restricted to LD reveal very few such fibers. Within the lateral parvocellular reticular formation (LPRF) terminal labelling is heavy, and moderate to sparse within the adjacent trigeminal complex. Rostro-caudally, silver grain accumulation within the LPRF extends from the level of the motor trigeminal nucleus (VM) to the pyramidal decussation, exhibiting a cephalocaudal decrease of grain density. Within the trigeminal complex, labelling occurs in the caudal VM, the dorsal portion of the principal sensory nucleus, and within and around the trigeminal spinalis oralis. In addition, the area surrounding the VM (in part corresponding to the supratrigeminal region of Lorente de Nó 1922, 1933) is moderately labelled. After injections of HRP into various levels of the ipsilateral descending B.C.'s projection field, retrogradely labelled cells are numerous within the DLH. A slightly lesser amount of labelled cells are found in the lateral half of the NI, primarily concerning the nucleus interpositus posterior. Within the LD, only a few labelled cells are observed: these are mainly restricted to the dorsal portion at rostral levels of the nucleus. The results obtained by both the anterograde and retrograde studies suggest an absence of a topographic organization within this descending B.C. component. The possible functional meaning of these results is discussed.

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Year:  1984        PMID: 6468566     DOI: 10.1007/bf00237454

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  32 in total

1.  PATTERNS OF LOCALIZATION IN THE CEREBELLAR CORTICONUCLEAR PROJECTIONS OF ALBINO RAT.

Authors:  D C GOODMAN; R E HALLETT; R B WELCH
Journal:  J Comp Neurol       Date:  1963-08       Impact factor: 3.215

2.  Descending division of the brachium conjunctivum in the cat a cerebello-reticular system.

Authors:  M B CARPENTER; H R NOVA
Journal:  J Comp Neurol       Date:  1960-06       Impact factor: 3.215

3.  Efferent pathways from the deep cerebellar nuclei of the cat.

Authors:  R E McMASTERS; G V RUSSELL
Journal:  J Comp Neurol       Date:  1958-10       Impact factor: 3.215

4.  Trigeminal projections to cerebellar tactile areas in the rat-origin mainly from n. interpolaris and n. principalis.

Authors:  C R Watson; R C Switzer
Journal:  Neurosci Lett       Date:  1978-11       Impact factor: 3.046

5.  The nucleus corporis pontobulbaris of the North American opossum.

Authors:  G F Martin; M Linauts; J M Walker
Journal:  J Comp Neurol       Date:  1977-10-01       Impact factor: 3.215

6.  Direct fastigiospinal fibers in the cat.

Authors:  K Fukushima; B W Peterson; Y Uchino; J D Coulter; V J Wilson
Journal:  Brain Res       Date:  1977-05-13       Impact factor: 3.252

7.  Lingually induced inhibition of masseteric motoneurones.

Authors:  L J Goldberg; Y Nakamura
Journal:  Experientia       Date:  1968-04-15

8.  The projection of the "vestibulocerebellum" onto the vestibular nuclei in the cat.

Authors:  P Angaut; A Brodal
Journal:  Arch Ital Biol       Date:  1967-11       Impact factor: 1.000

9.  The cerebellopontine system in the rat. I. Autoradiographic studies.

Authors:  C B Watt; G A Mihailoff
Journal:  J Comp Neurol       Date:  1983-04-10       Impact factor: 3.215

10.  Cerebello-olivary projections in the rat. An autoradiographic study.

Authors:  P Anguat; F Cicirata
Journal:  Brain Behav Evol       Date:  1982       Impact factor: 1.808

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  5 in total

1.  Tactile responses in the granule cell layer of cerebellar folium crus IIa of freely behaving rats.

Authors:  M J Hartmann; J M Bower
Journal:  J Neurosci       Date:  2001-05-15       Impact factor: 6.167

2.  Bilateral representation in the deep cerebellar nuclei.

Authors:  Demetris S Soteropoulos; Stuart N Baker
Journal:  J Physiol       Date:  2008-01-10       Impact factor: 5.182

3.  The fiber projections from the dentate nucleus to the reticular formation of the brain stem in the rabbit.

Authors:  Z W Tang; K Q Zhang; S Q Zhang
Journal:  Anat Embryol (Berl)       Date:  1987

4.  Dorsolateral pontine tegmentum and the classically conditioned nictitating membrane response: analysis of CR-related single-unit activity.

Authors:  J E Desmond; J W Moore
Journal:  Exp Brain Res       Date:  1986       Impact factor: 1.972

5.  Effects of muscimol inactivation of the cerebellar interposed-dentate nuclear complex on the performance of the nictitating membrane response in the rabbit.

Authors:  V Bracha; M L Webster; N K Winters; K B Irwin; J R Bloedel
Journal:  Exp Brain Res       Date:  1994       Impact factor: 1.972

  5 in total

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