Literature DB >> 8410157

Fixation cells in monkey superior colliculus. I. Characteristics of cell discharge.

D P Munoz1, R H Wurtz.   

Abstract

1. We studied the role of the superior colliculus (SC) in the control of visual fixation by recording from cells in the rostral pole of the SC in awake monkeys that were trained to perform fixation and saccade tasks. 2. We identified a subset of neurons in three monkeys that we refer to as fixation cells. These cells increased their tonic discharge rate when the monkey actively fixated a visible target spot to obtain a reward. This sustained activity persisted when the visual stimulation of the target spot was momentarily removed but the monkey was required to continue fixation. 3. The fixation cells were in the rostral pole of the SC. As the electrode descended through the SC, we encountered visual cells with foveal and parafoveal receptive fields most superficially, saccade-related burst cells with parafoveal movement fields below these visual cells, and fixation cells below the burst cells. From this sequence in depth, the fixation cells appeared to be centered in the deeper reaches of the intermediate layers, and this was confirmed by small marking lesions identified histologically. 4. During saccades, the tonically active fixation cells showed a pause in their rate of discharge. The duration of this pause was correlated to the duration of the saccade. Many cells did not decrease their discharge rate for small-amplitude contraversive saccades. 5. The saccade-related pause in fixation cell discharge always began before the onset of the saccade. The mean time from pause onset to saccade onset for contraversive saccades and ipsiversive saccades was 36.2 and 33.0 ms, respectively. Most fixation cells were reactivated before the end of contraversive saccades. The mean time from saccade terminatioN to pause end was -2.6 ms for contraversive saccades and 9.9 ms for ipsiversive saccades. The end of the saccade-related pause in fixation cell discharge was more tightly correlated to saccade termination, than pause onset was to saccade onset. 6. After the saccade-related pause in discharge, many fixation cells showed an increased discharge rate exceeding that before the pause. This increased postsaccadic discharge rate persisted for several hundred milliseconds. 7. The discharge rate of fixation cells was not consistently altered when the monkey actively fixated targets requiring different orbital positions. 8. Fixation cells discharged during smooth pursuit eye movements as they did during fixation. They maintained a steady tonic discharge during pursuit at different speeds and in different directions, provided the monkey looked at the moving target.(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1993        PMID: 8410157     DOI: 10.1152/jn.1993.70.2.559

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


  142 in total

1.  The oculomotor distractor effect in normal and hemianopic vision.

Authors:  R Walker; S Mannan; D Maurer; A L Pambakian; C Kennard
Journal:  Proc Biol Sci       Date:  2000-03-07       Impact factor: 5.349

2.  Role of primate superior colliculus in preparation and execution of anti-saccades and pro-saccades.

Authors:  S Everling; M C Dorris; R M Klein; D P Munoz
Journal:  J Neurosci       Date:  1999-04-01       Impact factor: 6.167

3.  Recognition Memory in Marmoset and Macaque Monkeys: A Comparison of Active Vision.

Authors:  Samuel U Nummela; Michael J Jutras; John T Wixted; Elizabeth A Buffalo; Cory T Miller
Journal:  J Cogn Neurosci       Date:  2018-12-04       Impact factor: 3.225

4.  The timing of sequences of saccades in visual search.

Authors:  E M Van Loon; I Th C Hooge; A V Van den Berg
Journal:  Proc Biol Sci       Date:  2002-08-07       Impact factor: 5.349

5.  Active eye fixation performance in 940 young men: effects of IQ, schizotypy, anxiety and depression.

Authors:  N Smyrnis; E Kattoulas; I Evdokimidis; N C Stefanis; D Avramopoulos; G Pantes; C Theleritis; C N Stefanis
Journal:  Exp Brain Res       Date:  2003-12-19       Impact factor: 1.972

6.  Selectivity of macaque ventral intraparietal area (area VIP) for smooth pursuit eye movements.

Authors:  Anja Schlack; Klaus-Peter Hoffmann; Frank Bremmer
Journal:  J Physiol       Date:  2003-06-25       Impact factor: 5.182

Review 7.  The neural selection and control of saccades by the frontal eye field.

Authors:  Jeffrey D Schall
Journal:  Philos Trans R Soc Lond B Biol Sci       Date:  2002-08-29       Impact factor: 6.237

8.  Temporal interactions of air-puff-evoked blinks and saccadic eye movements: insights into motor preparation.

Authors:  Neeraj J Gandhi; Desiree K Bonadonna
Journal:  J Neurophysiol       Date:  2004-10-06       Impact factor: 2.714

9.  Control of fixation and saccades during an anti-saccade task: an investigation in humans with chronic lesions of oculomotor cortex.

Authors:  Liana Machado; Robert D Rafal
Journal:  Exp Brain Res       Date:  2003-12-18       Impact factor: 1.972

10.  Effects of lesions of the human posterior thalamus on ocular fixation during voluntary and visually triggered saccades.

Authors:  R Rafal; M McGrath; L Machado; J Hindle
Journal:  J Neurol Neurosurg Psychiatry       Date:  2004-11       Impact factor: 10.154

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