Literature DB >> 16308353

Neurones associated with saccade metrics in the monkey central mesencephalic reticular formation.

Jason A Cromer1, David M Waitzman.   

Abstract

Neurones in the central mesencephalic reticular formation (cMRF) begin to discharge prior to saccades. These long lead burst neurones interact with major oculomotor centres including the superior colliculus (SC) and the paramedian pontine reticular formation (PPRF). Three different functions have been proposed for neurones in the cMRF: (1) to carry eye velocity signals that provide efference copy information to the SC (feedback), (2) to provide duration signals from the omnipause neurones to the SC (feedback), or (3) to participate in the transformation from the spatial encoding of a target selection signal in the SC into the temporal pattern of discharge used to drive the excitatory burst neurones in the pons (feed-forward). According to each respective proposal, specific predictions about cMRF neuronal discharge have been formulated. Individual neurones should: (1) encode instantaneous eye velocity, (2) burst specifically in relation to saccade duration but not to other saccade metrics, or (3) have a spectrum of weak to strong correlations to saccade dynamics. To determine if cMRF neurones could subserve these multiple oculomotor roles, we examined neuronal activity in relation to a variety of saccade metrics including amplitude, velocity and duration. We found separate groups of cMRF neurones that have the characteristics predicted by each of the proposed models. We also identified a number of subgroups for which no specific model prediction had previously been established. We found that we could accurately predict the neuronal firing pattern during one type of saccade behaviour (visually guided) using the activity during an alternative behaviour with different saccade metrics (memory guided saccades). We suggest that this evidence of a close relationship of cMRF neuronal discharge to individual saccade metrics supports the hypothesis that the cMRF participates in multiple saccade control pathways carrying saccade amplitude, velocity and duration information within the brainstem.

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Year:  2005        PMID: 16308353      PMCID: PMC1479872          DOI: 10.1113/jphysiol.2005.096834

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  45 in total

1.  Direct and indirect preoculomotor pathways of the brainstem: an autoradiographic study of the pontine reticular formation in the cat.

Authors:  A M Graybiel
Journal:  J Comp Neurol       Date:  1977-09-01       Impact factor: 3.215

2.  Population coding of saccadic eye movements by neurons in the superior colliculus.

Authors:  C Lee; W H Rohrer; D L Sparks
Journal:  Nature       Date:  1988-03-24       Impact factor: 49.962

3.  Structure-function relationships in the primate superior colliculus. I. Morphological classification of efferent neurons.

Authors:  A K Moschovakis; A B Karabelas; S M Highstein
Journal:  J Neurophysiol       Date:  1988-07       Impact factor: 2.714

4.  Spatio-temporal recoding of rapid eye movement signals in the monkey paramedian pontine reticular formation (PPRF).

Authors:  K Hepp; V Henn
Journal:  Exp Brain Res       Date:  1983       Impact factor: 1.972

5.  Projections from the superior colliculus to a region of the central mesencephalic reticular formation (cMRF) associated with horizontal saccadic eye movements.

Authors:  B Cohen; J A Büttner-Ennever
Journal:  Exp Brain Res       Date:  1984       Impact factor: 1.972

6.  Efferent projections of the cat oculomotor reticular omnipause neuron region: an autoradiographic study.

Authors:  T P Langer; C R Kaneko
Journal:  J Comp Neurol       Date:  1983-07-01       Impact factor: 3.215

7.  Visuomotor deficits following ablation of monkey superior colliculus.

Authors:  J E Albano; M Mishkin; L E Westbrook; R H Wurtz
Journal:  J Neurophysiol       Date:  1982-08       Impact factor: 2.714

8.  Natural and drug-induced variations of velocity and duration of human saccadic eye movements: evidence for a control of the neural pulse generator by local feedback.

Authors:  R Jürgens; W Becker; H H Kornhuber
Journal:  Biol Cybern       Date:  1981       Impact factor: 2.086

9.  A quantitative method of computer analysis of spike train data collected from behaving animals.

Authors:  J M MacPherson; J W Aldridge
Journal:  Brain Res       Date:  1979-10-12       Impact factor: 3.252

10.  Deficits in eye movements following frontal eye-field and superior colliculus ablations.

Authors:  P H Schiller; S D True; J L Conway
Journal:  J Neurophysiol       Date:  1980-12       Impact factor: 2.714

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  23 in total

Review 1.  The central mesencephalic reticular formation: its role in space-time coordinated saccadic eye movements.

Authors:  Werner M Graf; Gabriella Ugolini
Journal:  J Physiol       Date:  2006-01-05       Impact factor: 5.182

2.  Anatomical evidence for interconnections between the central mesencephalic reticular formation and cervical spinal cord in the cat and macaque.

Authors:  Susan Warren; David M Waitzman; Paul J May
Journal:  Anat Rec (Hoboken)       Date:  2008-02       Impact factor: 2.064

3.  Anatomical evidence that the superior colliculus controls saccades through central mesencephalic reticular formation gating of omnipause neuron activity.

Authors:  Niping Wang; Eddie Perkins; Lan Zhou; Susan Warren; Paul J May
Journal:  J Neurosci       Date:  2013-10-09       Impact factor: 6.167

4.  The feedback circuit connecting the central mesencephalic reticular formation and the superior colliculus in the macaque monkey: tectal connections.

Authors:  Lan Zhou; Susan Warren; Paul J May
Journal:  Exp Brain Res       Date:  2008-06-14       Impact factor: 1.972

5.  Cerebellar control of saccade dynamics: contribution of the fastigial oculomotor region.

Authors:  Julie Quinet; Laurent Goffart
Journal:  J Neurophysiol       Date:  2015-03-04       Impact factor: 2.714

6.  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

7.  Neural control of rapid binocular eye movements: Saccade-vergence burst neurons.

Authors:  Julie Quinet; Kevin Schultz; Paul J May; Paul D Gamlin
Journal:  Proc Natl Acad Sci U S A       Date:  2020-11-02       Impact factor: 11.205

8.  A central mesencephalic reticular formation projection to the supraoculomotor area in macaque monkeys.

Authors:  Martin O Bohlen; Susan Warren; Paul J May
Journal:  Brain Struct Funct       Date:  2015-04-10       Impact factor: 3.270

9.  A central mesencephalic reticular formation projection to the Edinger-Westphal nuclei.

Authors:  Paul J May; Susan Warren; Martin O Bohlen; Miriam Barnerssoi; Anja K E Horn
Journal:  Brain Struct Funct       Date:  2015-11-28       Impact factor: 3.270

10.  The macaque midbrain reticular formation sends side-specific feedback to the superior colliculus.

Authors:  Niping Wang; Susan Warren; Paul J May
Journal:  Exp Brain Res       Date:  2009-11-26       Impact factor: 1.972

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