Literature DB >> 18835656

Neurophysiology and neuroanatomy of reflexive and volitional saccades: evidence from studies of humans.

Jennifer E McDowell1, Kara A Dyckman, Benjamin P Austin, Brett A Clementz.   

Abstract

This review provides a summary of the contributions made by human functional neuroimaging studies to the understanding of neural correlates of saccadic control. The generation of simple visually guided saccades (redirections of gaze to a visual stimulus or pro-saccades) and more complex volitional saccades require similar basic neural circuitry with additional neural regions supporting requisite higher level processes. The saccadic system has been studied extensively in non-human (e.g., single-unit recordings) and human (e.g., lesions and neuroimaging) primates. Considerable knowledge of this system's functional neuroanatomy makes it useful for investigating models of cognitive control. The network involved in pro-saccade generation (by definition largely exogenously-driven) includes subcortical (striatum, thalamus, superior colliculus, and cerebellar vermis) and cortical (primary visual, extrastriate, and parietal cortices, and frontal and supplementary eye fields) structures. Activation in these regions is also observed during endogenously-driven voluntary saccades (e.g., anti-saccades, ocular motor delayed response or memory saccades, predictive tracking tasks and anticipatory saccades, and saccade sequencing), all of which require complex cognitive processes like inhibition and working memory. These additional requirements are supported by changes in neural activity in basic saccade circuitry and by recruitment of additional neural regions (such as prefrontal and anterior cingulate cortices). Activity in visual cortex is modulated as a function of task demands and may predict the type of saccade to be generated, perhaps via top-down control mechanisms. Neuroimaging studies suggest two foci of activation within FEF - medial and lateral - which may correspond to volitional and reflexive demands, respectively. Future research on saccade control could usefully (i) delineate important anatomical subdivisions that underlie functional differences, (ii) evaluate functional connectivity of anatomical regions supporting saccade generation using methods such as ICA and structural equation modeling, (iii) investigate how context affects behavior and brain activity, and (iv) use multi-modal neuroimaging to maximize spatial and temporal resolution.

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Year:  2008        PMID: 18835656      PMCID: PMC2614688          DOI: 10.1016/j.bandc.2008.08.016

Source DB:  PubMed          Journal:  Brain Cogn        ISSN: 0278-2626            Impact factor:   2.310


  247 in total

1.  Frontal eye field activity preceding aurally guided saccades.

Authors:  G S Russo; C J Bruce
Journal:  J Neurophysiol       Date:  1994-03       Impact factor: 2.714

2.  Role of the human anterior cingulate cortex in the control of oculomotor, manual, and speech responses: a positron emission tomography study.

Authors:  T Paus; M Petrides; A C Evans; E Meyer
Journal:  J Neurophysiol       Date:  1993-08       Impact factor: 2.714

3.  Principal component analysis learning algorithms: a neurobiological analysis.

Authors:  K J Friston; C D Frith; R S Frackowiak
Journal:  Proc Biol Sci       Date:  1993-10-22       Impact factor: 5.349

4.  Role of the left and right supplementary motor areas in memory-guided saccade sequences.

Authors:  B Gaymard; S Rivaud; C Pierrot-Deseilligny
Journal:  Ann Neurol       Date:  1993-09       Impact factor: 10.422

Review 5.  The basal ganglia and adaptive motor control.

Authors:  A M Graybiel; T Aosaki; A W Flaherty; M Kimura
Journal:  Science       Date:  1994-09-23       Impact factor: 47.728

Review 6.  The supplementary motor area in the cerebral cortex.

Authors:  J Tanji
Journal:  Neurosci Res       Date:  1994-05       Impact factor: 3.304

7.  Cortical control of saccades and fixation in man. A PET study.

Authors:  T J Anderson; I H Jenkins; D J Brooks; M B Hawken; R S Frackowiak; C Kennard
Journal:  Brain       Date:  1994-10       Impact factor: 13.501

8.  Normal and pathological saccadic dysmetria.

Authors:  K Bötzel; K Rottach; U Büttner
Journal:  Brain       Date:  1993-04       Impact factor: 13.501

9.  Prefrontal neuronal activity in rhesus monkeys performing a delayed anti-saccade task.

Authors:  S Funahashi; M V Chafee; P S Goldman-Rakic
Journal:  Nature       Date:  1993-10-21       Impact factor: 49.962

10.  Horizontal eye movement disorders after posterior vermis infarctions.

Authors:  K Vahedi; S Rivaud; P Amarenco; C Pierrot-Deseilligny
Journal:  J Neurol Neurosurg Psychiatry       Date:  1995-01       Impact factor: 10.154

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  128 in total

1.  Effects of anti-saccade training with neck flexion on eye movement performance, presaccadic potentials and prefrontal hemodynamics in the elderly.

Authors:  Naoe Kiyota; Katsuo Fujiwara
Journal:  Eur J Appl Physiol       Date:  2010-08-14       Impact factor: 3.078

2.  Cognitive correlates of anti-saccade task performance.

Authors:  Christoph Klein; Reinhold Rauh; Monica Biscaldi
Journal:  Exp Brain Res       Date:  2010-05-09       Impact factor: 1.972

3.  Antisaccade performance in schizophrenia patients, their first-degree biological relatives, and community comparison subjects: data from the COGS study.

Authors:  Allen D Radant; Dorcas J Dobie; Monica E Calkins; Ann Olincy; David L Braff; Kristin S Cadenhead; Robert Freedman; Michael F Green; Tiffany A Greenwood; Raquel E Gur; Ruben C Gur; Gregory A Light; Sean P Meichle; Steve P Millard; Jim Mintz; Keith H Nuechterlein; Nicholas J Schork; Larry J Seidman; Larry J Siever; Jeremy M Silverman; William S Stone; Neal R Swerdlow; Ming T Tsuang; Bruce I Turetsky; Debby W Tsuang
Journal:  Psychophysiology       Date:  2010-04-05       Impact factor: 4.016

4.  Saccadic preparation in the frontal eye field is modulated by distinct trial history effects as revealed by magnetoencephalography.

Authors:  Adrian K C Lee; Matti S Hämäläinen; Kara A Dyckman; Jason J S Barton; Dara S Manoach
Journal:  Cereb Cortex       Date:  2010-06-03       Impact factor: 5.357

5.  Vector inversion diminishes the online control of antisaccades.

Authors:  Matthew Heath; Jeffrey Weiler; Kendall Marriott; Timothy N Welsh
Journal:  Exp Brain Res       Date:  2011-01-06       Impact factor: 1.972

6.  Preparatory activations across a distributed cortical network determine production of express saccades in humans.

Authors:  Jordan P Hamm; Kara A Dyckman; Lauren E Ethridge; Jennifer E McDowell; Brett A Clementz
Journal:  J Neurosci       Date:  2010-05-26       Impact factor: 6.167

7.  The neural network of saccadic foreknowledge.

Authors:  Sarah Bär; Martinus Hauf; Jason J S Barton; Mathias Abegg
Journal:  Exp Brain Res       Date:  2016-02       Impact factor: 1.972

8.  Pre-cue fronto-occipital alpha phase and distributed cortical oscillations predict failures of cognitive control.

Authors:  Jordan P Hamm; Kara A Dyckman; Jennifer E McDowell; Brett A Clementz
Journal:  J Neurosci       Date:  2012-05-16       Impact factor: 6.167

9.  Anomalous use of context during task preparation in schizophrenia: a magnetoencephalography study.

Authors:  Dara S Manoach; Adrian K C Lee; Matti S Hämäläinen; Kara A Dyckman; Jesse S Friedman; Mark Vangel; Donald C Goff; Jason J S Barton
Journal:  Biol Psychiatry       Date:  2013-02-04       Impact factor: 13.382

Review 10.  The tell-tale tasks: a review of saccadic research in psychiatric patient populations.

Authors:  Diane C Gooding; Michele A Basso
Journal:  Brain Cogn       Date:  2008-10-23       Impact factor: 2.310

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