The DOI matches its Crossref record; 96 of the 96 references it cites were found in a registry or an index.
Afferent and efferent connections of the oculomotor region of the fastigial nucleus in the macaque monkey
Abstract
Afferent and efferent connections of the fastigial oculomotor region (FOR) were studied in macaque monkeys by using axonal transport of wheat germ agglutinin conjugated horseradish peroxidase (WGA‐HRP). When injected HRP is confined to the FOR, retrogradely labeled cells appear in lobules VIc and VII of the ipsilateral vermis and in group b of the contralateral medial accessory olive (MAO). In reference to the maps of topographical organization, the extent of the effective site in the fastigial nucleus (FN) could be assessed from the distributions of labeled Purkinje cells (P cells) in the vermis and labeled olivary neurons in the MAO. In contrast to the unilateral nature of the P‐cell and climbing‐fiber projections, those from the other brainstem regions to the FOR were bilateral. Following the injection of HRP into the FOR, the largest number of retrogradely labeled cells appeared in the pontine nuclei. Although the number of labeled cells was greater on the contralateral side in both the peduncular and dorsomedial pontine nuclei (DMPN), the number on each side was virtually identical in the dorsolateral pontine nucleus (DLPN). In the nucleus reticularis tegmenti pontis(NRTP), labeled cells were located only in its medial and dorsolateral portions bilaterally. In the vestibular complex, labeled cells appeared in the superior (SVN), medial (MVN), and inferior vestibular nuclei (IVN) bilaterally. The lateral vestibular nucleus (LVN), including y group and the ventrolateral vestibular nucleus, were free of labeled cells. Labeled cells appeared also in the perihypoglossal nucleus (PHN) bilaterally. In the pontine raphe (PR) and paramedian pontine reticular formation (PPRF), labeled cells appeared bilaterally in the caudal third of the area between the oculomotor and abducens nuclei. Labeled cells appeared also in the mesencephalic and medullary reticular formation. Tracing of anterogradely labeled axons demonstrated that most fibers from the FOR decussated within the cerebellum and entered the brainstem via the contralateral uncinate fasciculus. Some crossed fibers ascended with the contralateral brachium conjunctivum and terminated in the midbrain tegmentum. A small contingent of fibers advanced further to the thalamus. In the mesodiencephalic junction, labeled terminals were found contralaterally in the rostral interstitial nucleus of medial longitudinal fasciculus (riMLF) and a medial portion of Forel's H Field. They appeared also in the central mesencephalic reticular formation (cMRF), the periaqueductal gray (PAG), the posterior commissure nucleus, and the superior colliculus. The oculomotor and trochlear nuclei, the red nucleus, and the interstitial nucleus of Cajal were free of labeled terminals. The projections from the FOR to the vestibular complex were bilateral and were mainly to the ventral portions of the LVN and IVN. The ipsilateral fibers emerged with the juxtarestiform body. The PHN, the SVN, and the MVN were free of terminals. Crossed fibers arising from the FOR terminated in a caudal portion of the PR, the PPRF, the DMPN, the NRTP, and the dorsomedial portion of the medullary reticular formation (DMRF). Labeled terminals in the DMRF were also found on the ipsilateral side, although the contralateral side was predominant. When the HRP injection involved a fastigial area rostral to the FOR, labeled terminals appeared also in the PHN, SVN, MVN, and DLPN of the contralateral side.
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Citations
Cites
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Effects of Lesions of the Oculomotor Vermis on Eye Movements in Primate: Saccades
Takagi, M., Zee, D. S., & Tamargo, R. J. (1998) · Journal of Neurophysiology · doi:10.1152/jn.1998.80.4.1911 · Cited by 373
Present concepts of oculomotor organization
Büttner, U., & Büttner-Ennever, J. A. (2006) · Progress in Brain Research · doi:10.1016/s0079-6123(05)51001-x · Cited by 272
Functional localization in the cerebellum
Glickstein, M., Sultan, F., & Voogd, J. (2011) · Cortex · doi:10.1016/j.cortex.2009.09.001 · Cited by 194
Cerebellar contributions to adaptive control of saccades in humans
Xu-Wilson, M., Chen-Harris, H., Zee, D. S., & Shadmehr, R. (2009) · The Journal of Neuroscience · doi:10.1523/jneurosci.3115-09.2009 · Cited by 190
The role of cerebellar circuitry alterations in the pathophysiology of autism spectrum disorders
Mosconi, M. W., Wang, Z., Schmitt, L. M., Tsai, P., & Sweeney, J. A. (2015) · Frontiers in Neuroscience · doi:10.3389/fnins.2015.00296 · Cited by 112
Metadata
- Authors
- Noda, H., Sugita, S., & Ikeda, Y.
- Venue
- Journal of Comparative Neurology
- Publisher
- Wiley
- Published
- 1990-12-08
- Volume
- 302
- Issue
- 2
- Pages
- 330-348
- ISSN
- 0021-9967 (ISSN-L)
- 1096-9861
- OpenAlex
- W2006465350
- Cited by
- 317
- References
- 96
- FWCI
- 3.47
- Type
- journal article
- Language
- en
- Open access
- closed
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- Noda, H., Sugita, S., & Ikeda, Y. (1990). Afferent and efferent connections of the oculomotor region of the fastigial nucleus in the macaque monkey. Journal of Comparative Neurology. https://doi.org/10.1002/cne.903020211
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