Literature DB >> 10997582

The effect of disparity on the very earliest ocular following responses and the initial neuronal activity in monkey cortical area MST.

A Takemura1, Y Inoue, K Kawano.   

Abstract

Movement of the visual scene evokes tracking movement with the eyes (ocular following response, OFR) at short latency (Miles, F.A., Kawano, K., Optican, L.M., 1986. Short-latency ocular following responses of monkey. I. Dependence on temporospatial properties of visual input. J. Neurophysiol. 56, 1321-1354). We examined the effect of binocular disparity on the initial OFR. The dependence of the OFR on horizontal disparity steps was studied in three monkeys (Macaca fuscata), and the associated unit discharges in the medial superior temporal area (MST) were studied in two of these. Based on the changes in eye position over the period 50-83 ms (measured from stimulus onset), the initial OFR showed clear dependence on the disparity imposed during the preceding centering saccade. The disparity tuning curves were S-shaped with a peak at a small crossed disparity and a trough at uncrossed disparities. Based on the changes in discharge rate over the period 40-73 ms (measured from stimulus onset), almost all OFR-related MST neurons (80/83, 96.4%) showed significant dependence on the disparity step (Student's t-test, P < 0.05). The early neuronal responses of the majority of units (41/75, 55%) had disparity tuning curves resembling those for the OFR, which peaked at small crossed disparities. These findings suggest that the neurons in the MST contain information on binocular disparity in their short-latency discharges, and are involved in the neural basis of the OFR's dependence on horizontal disparity.

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Year:  2000        PMID: 10997582     DOI: 10.1016/s0168-0102(00)00149-8

Source DB:  PubMed          Journal:  Neurosci Res        ISSN: 0168-0102            Impact factor:   3.304


  8 in total

1.  Neuronal responses in MST reflect the post-saccadic enhancement of short-latency ocular following responses.

Authors:  Aya Takemura; Kenji Kawano
Journal:  Exp Brain Res       Date:  2006-06-29       Impact factor: 1.972

2.  Deficits in short-latency tracking eye movements after chemical lesions in monkey cortical areas MT and MST.

Authors:  Aya Takemura; Yumi Murata; Kenji Kawano; F A Miles
Journal:  J Neurosci       Date:  2007-01-17       Impact factor: 6.167

3.  Spatial summation properties of the human ocular following response (OFR): evidence for nonlinearities due to local and global inhibitory interactions.

Authors:  B M Sheliga; E J Fitzgibbon; F A Miles
Journal:  Vision Res       Date:  2008-07-07       Impact factor: 1.886

4.  The effects of prolonged viewing of motion on short-latency ocular following responses.

Authors:  Masakatsu Taki; Kenichiro Miura; Hiromitsu Tabata; Yasuo Hisa; Kenji Kawano
Journal:  Exp Brain Res       Date:  2009-03-24       Impact factor: 1.972

5.  Macaque monkeys show reversed ocular following responses to two-frame-motion stimulus presented with inter-stimulus intervals.

Authors:  Aya Takemura; Junya Matsumoto; Ryota Hashimoto; Kenji Kawano; Kenichiro Miura
Journal:  J Comput Neurosci       Date:  2020-07-17       Impact factor: 1.621

6.  Binocular disparity tuning and visual-vestibular congruency of multisensory neurons in macaque parietal cortex.

Authors:  Yun Yang; Sheng Liu; Syed A Chowdhury; Gregory C DeAngelis; Dora E Angelaki
Journal:  J Neurosci       Date:  2011-12-07       Impact factor: 6.167

7.  Ocular following responses of monkeys to the competing motions of two sinusoidal gratings.

Authors:  K Matsuura; K Miura; M Taki; H Tabata; N Inaba; K Kawano; F A Miles
Journal:  Neurosci Res       Date:  2008-01-31       Impact factor: 3.304

8.  Neural activity in the dorsal medial superior temporal area of monkeys represents retinal error during adaptive motor learning.

Authors:  Aya Takemura; Tomoyo Ofuji; Kenichiro Miura; Kenji Kawano
Journal:  Sci Rep       Date:  2017-01-19       Impact factor: 4.379

  8 in total

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