Literature DB >> 8714648

Anatomy and physiology of the primate interstitial nucleus of Cajal I. efferent projections.

T Kokkoroyannis1, C A Scudder, C D Balaban, S M Highstein, A K Moschovakis.   

Abstract

1. The efferent projections of the interstitial nucleus of Cajal (NIC) were studied in the squirrel monkey after iontophoretic injections of biocytin and Phaseolus Vulgaris leucoagglutinin into the NIC. To ensure the proper placement of the tracer, the same pipettes were used to extracellularly record the discharge pattern of NIC neurons. 2. Three projection systems of the NIC were distinguished: commissural (through the posterior commissure), descending, and ascending. 3. The posterior commissure system gave rise to dense terminal fields in the contralateral NIC, the oculomotor nucleus, and the trochlear nucleus. 4. The descending system of NIC projections deployed dense terminal fields in the ipsilateral gigantocellular reticular formation and the paramedian reticular formation of the pons, as well as in the ventromedial and commissural nuclei of the first two spinal cervical segments. It also gave rise to moderate or weak terminal fields in the vestibular complex, the nucleus prepositus hypoglossi, the inferior olive, and the magnocellular reticular formation, as well as cell groups scattered along the paramedian tracts in the pons and the pontine and medullary raphe. 5. The ascending system of NIC projections gave rise to dense terminal fields in the ipsilateral mesencephalic reticular formation and the zona incerta as well as moderate or weak terminal fields in the ipsilateral centromedian and parafascicular thalamic nuclei. It also provided dense bilateral labeling of the rostral interstitial nucleus of the medial longitudinal fasciculus and the fields of Forel, and moderate or weak bilateral labeling of the mediodorsal, central medial, and central lateral nuclei of the thalamus. 6. Models of saccade generation that rely on feedback from the velocity-to-position integrators and include the superior colliculus in their local feedback loop are contradicted because no fibers originating from the NIC traveled to the superior colliculus to deploy terminal fields. 7. Consistent with its morphological and functional diversity, these data indicate that the primate NIC sends signals to a multitude of targets implicated in the control of eye and head movements.

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Year:  1996        PMID: 8714648     DOI: 10.1152/jn.1996.75.2.725

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  24 in total

1.  Influence of orbital eye position on vertical saccades in progressive supranuclear palsy.

Authors:  Rosalyn Schneider; Athena L Chen; Susan A King; David E Riley; Steven A Gunzler; Michael W Devereaux; R John Leigh
Journal:  Ann N Y Acad Sci       Date:  2011-09       Impact factor: 5.691

Review 2.  Imaging correlates of neural control of ocular movements.

Authors:  Mohit Agarwal; John L Ulmer; Tushar Chandra; Andrew P Klein; Leighton P Mark; Suyash Mohan
Journal:  Eur Radiol       Date:  2015-09-22       Impact factor: 5.315

3.  Oscillatory head movements in cervical dystonia: Dystonia, tremor, or both?

Authors:  Aasef G Shaikh; David S Zee; H A Jinnah
Journal:  Mov Disord       Date:  2015-04-16       Impact factor: 10.338

4.  Immunoreactivity for calcium-binding proteins defines subregions of the vestibular nuclear complex of the cat.

Authors:  Joan S Baizer; James F Baker
Journal:  Exp Brain Res       Date:  2005-01-21       Impact factor: 1.972

5.  Eye position modulates the electromyographic responses of neck muscles to electrical stimulation of the superior colliculus in the alert cat.

Authors:  K Hadjidimitrakis; A K Moschovakis; Y Dalezios; A Grantyn
Journal:  Exp Brain Res       Date:  2006-11-08       Impact factor: 1.972

6.  Corticobasal degeneration with TDP-43 pathology presenting with progressive supranuclear palsy syndrome: a distinct clinicopathologic subtype.

Authors:  Shunsuke Koga; Naomi Kouri; Ronald L Walton; Mark T W Ebbert; Keith A Josephs; Irene Litvan; Neill Graff-Radford; J Eric Ahlskog; Ryan J Uitti; Jay A van Gerpen; Bradley F Boeve; Adam Parks; Owen A Ross; Dennis W Dickson
Journal:  Acta Neuropathol       Date:  2018-06-20       Impact factor: 17.088

Review 7.  Synaptic control of motoneuronal excitability.

Authors:  J C Rekling; G D Funk; D A Bayliss; X W Dong; J L Feldman
Journal:  Physiol Rev       Date:  2000-04       Impact factor: 37.312

8.  Physiology of midbrain head movement neurons in cervical dystonia.

Authors:  Alexey Sedov; Valentin Popov; Vladimir Shabalov; Svetlana Raeva; H A Jinnah; Aasef G Shaikh
Journal:  Mov Disord       Date:  2017-02-20       Impact factor: 10.338

9.  Truncal contrapulsion in pretectal syndrome.

Authors:  Jae-Hyeok Heo; Ji Soo Kim; Kyung-Bok Lee; Keun-Hwa Jung; Hyun-Kyung Kim; Sung-Hun Kim; Jae-Kyu Roh
Journal:  J Clin Neurol       Date:  2006-03-20       Impact factor: 3.077

10.  Vertical eye movement-related type II neurons with downward on-directions in the vestibular nucleus in alert cats.

Authors:  Masatoshi Niwa; Sohei Chimoto; Yoshiki Iwamoto; Kaoru Yoshida
Journal:  Exp Brain Res       Date:  2004-01-13       Impact factor: 1.972

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