Literature DB >> 8836230

Anatomy and physiology of saccadic long-lead burst neurons recorded in the alert squirrel monkey. II. Pontine neurons.

C A Scudder1, A K Moschovakis, A B Karabelas, S M Highstein.   

Abstract

1. The discharge patterns and axonal projections of saccadic long-lead burst neurons (LLBNs) with somata in the pontine reticular formation were studied in alert squirrel monkeys with the use of the method of intraaxonal recording and horseradish peroxidase injection. 2. The largest population of stained neurons were afferents to the cerebellum. They originated in the dorsomedial nucleus reticularis tegmenti pontis (NRTP) including its dorsal cell group (N = 5), the preabducens intrafascicular nucleus (N = 5), and the raphe pontis (N = 1). Axons of all neurons coursed under NRTP and entered brachium pontis without having synapsed in the brain stem. Three axons sent collaterals to the floccular lobe, but other more distant targets of these and the other cerebellar afferents could not be determined. Movement fields of these neurons were intermediate between vectorial and directional types. 3. Four neurons had their somata in nucleus reticularis pontis oralis and terminations in the brain stem reticular formation. Each neuron was different, but all terminated in the region containing excitatory burst neurons, and most terminated in the region containing inhibitory burst neurons. Other targets include nucleus reticularis pontis oralis and caudalis, NRTP, raphe interpositus, and the spinal cord. Discharge patterns included both vectorial and directional types. 4. Two reticulospinal neurons had large multipolar somata either just rostral or ventral to the abducens nucleus. These neurons also projected to the medullary reticular formation, caudal nucleus prepositus hypoglossi, and dorsal and ventral paramedian reticular nucleus. 5. The functional implications of the connections of these LLBNs and those reported in the companion paper are extensively discussed. The fact that the efferents of the superior colliculus target the regions containing medium-lead saccadic burst neurons confirms the role of the colliculus in saccade generation. However, the finding that many other neurons project to these regions and the finding that superior colliculus efferents project more heavily to areas containing reticulospinal neurons argue for a diminished role of the superior colliculus in saccade generation but an augmented role in head movement control.

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Year:  1996        PMID: 8836230     DOI: 10.1152/jn.1996.76.1.353

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


  17 in total

1.  Discharge of monkey nucleus reticularis tegmenti pontis neurons changes during saccade adaptation.

Authors:  N Takeichi; C R S Kaneko; A F Fuchs
Journal:  J Neurophysiol       Date:  2005-05-25       Impact factor: 2.714

2.  Saccade-related, long-lead burst neurons in the monkey rostral pons.

Authors:  Chris R S Kaneko
Journal:  J Neurophysiol       Date:  2005-10-19       Impact factor: 2.714

3.  Kinematics and eye-head coordination of gaze shifts evoked from different sites in the superior colliculus of the cat.

Authors:  Alain Guillaume; Denis Pélisson
Journal:  J Physiol       Date:  2006-10-05       Impact factor: 5.182

4.  Effect of pharmacological inactivation of nucleus reticularis tegmenti pontis on saccadic eye movements in the monkey.

Authors:  Chris R S Kaneko; Albert F Fuchs
Journal:  J Neurophysiol       Date:  2006-02-08       Impact factor: 2.714

5.  Dissociation of eye and head components of gaze shifts by stimulation of the omnipause neuron region.

Authors:  Neeraj J Gandhi; David L Sparks
Journal:  J Neurophysiol       Date:  2007-05-09       Impact factor: 2.714

6.  Activity of long-lead burst neurons in pontine reticular formation during head-unrestrained gaze shifts.

Authors:  Mark M G Walton; Edward G Freedman
Journal:  J Neurophysiol       Date:  2013-10-30       Impact factor: 2.714

7.  Coordination of eye and head components of movements evoked by stimulation of the paramedian pontine reticular formation.

Authors:  Neeraj J Gandhi; Ellen J Barton; David L Sparks
Journal:  Exp Brain Res       Date:  2008-05-06       Impact factor: 1.972

8.  Saccades evoked in response to electrical stimulation of the posterior bank of the arcuate sulcus.

Authors:  E Neromyliotis; A K Moschovakis
Journal:  Exp Brain Res       Date:  2017-06-20       Impact factor: 1.972

9.  Disassociation between brain activation and executive function in fragile X premutation females.

Authors:  Annie L Shelton; Kim Cornish; Meaghan Clough; Sanuji Gajamange; Scott Kolbe; Joanne Fielding
Journal:  Hum Brain Mapp       Date:  2016-10-14       Impact factor: 5.038

10.  Response suppression deficits in treatment-naïve first-episode patients with schizophrenia, psychotic bipolar disorder and psychotic major depression.

Authors:  Margret S H Harris; James L Reilly; Michael E Thase; Matcheri S Keshavan; John A Sweeney
Journal:  Psychiatry Res       Date:  2009-11-10       Impact factor: 3.222

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