Literature DB >> 7931519

Neural activity in cortical area MST of alert monkey during ocular following responses.

K Kawano1, M Shidara, Y Watanabe, S Yamane.   

Abstract

1. We studied response properties of neurons in the superior temporal sulcus (STS) of behaving monkeys that discharged during brief, sudden movements of a large-field visual stimulus, eliciting ocular following. Most neurons responded to movements of a large-field visual stimulus with directional selectivity, preferring high stimulus speeds. Neurons were mostly recorded in the medial superior temporal area (MST) (187/250) and the middle temporal area (MT) (57/250). Further response properties were studied in the MST neurons. 2. Response latencies were measured when a large-field random dot pattern was moved in the preferred direction and preferred speed for each neuron. Eighty percent (120/150) of the neurons were activated < 50 ms after the onset of the stimulus motion. In most cases (89%, 134/150), increased firing rates started before the eye movements, with 59% (88/150) starting > 10 ms before the eye movements. 3. The relationship between the latency of neuronal responses and that of eye movements was studied in 59 neurons by changing the stimulus speed systematically (10-160 degrees/s). The latencies of both neuronal and ocular responses decreased as stimulus speed increased. As a result, the time difference between the response latencies for neuronal and ocular responses varied little with changes in stimulus speed. 4. Blurring of the random dot pattern, by interposing a sheet of ground glass, increased the latency of both neuronal responses and eye movements. 5. With the use of a check pattern instead of random dots, both neuronal and ocular responses began to decrease rapidly when the temporal frequency of the visual stimulus exceeded 20 Hz. At 40 Hz the neurons showed a distinctive burst-and-pause firing pattern, and the eye movements showed signs of oscillation. 6. The response properties of the MST neurons during ocular following were similar to those of the dorsolateral pontine nucleus (DLPN) neurons, reported previously. Our results indicate that the MST neurons may provide visual information to the DLPN neurons and may play a role in eliciting ocular following. 7. Responses during smooth-pursuit eye movement were studied in 55 MST neurons. Each of these neurons responded to the moving large-field visual stimulus, which elicited ocular following, and 40 of these neurons were activated during smooth pursuit in the dark. Response latencies during smooth pursuit were long in those neurons having different directional preferences during smooth pursuit and ocular following but were short for those having the same directional preferences during smooth pursuit and ocular following.(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1994        PMID: 7931519     DOI: 10.1152/jn.1994.71.6.2305

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


  50 in total

1.  The timing of response onset and offset in macaque visual neurons.

Authors:  Wyeth Bair; James R Cavanaugh; Matthew A Smith; J Anthony Movshon
Journal:  J Neurosci       Date:  2002-04-15       Impact factor: 6.167

2.  Parallel motion processing for the initiation of short-latency ocular following in humans.

Authors:  Guillaume S Masson; Eric Castet
Journal:  J Neurosci       Date:  2002-06-15       Impact factor: 6.167

3.  Short-latency ocular following in humans is dependent on absolute (rather than relative) binocular disparity.

Authors:  D-S Yang; F A Miles
Journal:  Vision Res       Date:  2003-06       Impact factor: 1.886

4.  Temporospatial properties of the effects of bottom-up attention on smooth pursuit initiation in humans.

Authors:  Kouki Hashimoto; Kazuyo Suehiro; Kenji Kawano
Journal:  Exp Brain Res       Date:  2003-12-19       Impact factor: 1.972

5.  Early behavior of optokinetic responses elicited by transparent motion stimuli during depth-based attention.

Authors:  Masaki Maruyama; Tetsuo Kobayashi; Takusige Katsura; Shinya Kuriki
Journal:  Exp Brain Res       Date:  2003-06-13       Impact factor: 1.972

6.  A rapid and precise on-response in posterior parietal cortex.

Authors:  James W Bisley; B Suresh Krishna; Michael E Goldberg
Journal:  J Neurosci       Date:  2004-02-25       Impact factor: 6.167

7.  Neuronal variability of MSTd neurons changes differentially with eye movement and visually related variables.

Authors:  Lukas Brostek; Ulrich Büttner; Michael J Mustari; Stefan Glasauer
Journal:  Cereb Cortex       Date:  2012-07-06       Impact factor: 5.357

8.  The initial ocular following responses elicited by apparent-motion stimuli: reversal by inter-stimulus intervals.

Authors:  B M Sheliga; K J Chen; E J FitzGibbon; F A Miles
Journal:  Vision Res       Date:  2005-10-18       Impact factor: 1.886

Review 9.  Initial ocular following in humans depends critically on the fourier components of the motion stimulus.

Authors:  K J Chen; B M Sheliga; E J Fitzgibbon; F A Miles
Journal:  Ann N Y Acad Sci       Date:  2005-04       Impact factor: 5.691

10.  Predictive smooth pursuit of complex two-dimensional trajectories in monkey: component interactions.

Authors:  R E Kettner; H C Leung; B W Peterson
Journal:  Exp Brain Res       Date:  1996-03       Impact factor: 1.972

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