Literature DB >> 1578251

Neural activity in dorsolateral pontine nucleus of alert monkey during ocular following responses.

K Kawano1, M Shidara, S Yamane.   

Abstract

1. Movements of the visual scene evoke short-latency ocular following responses. To study the neural mediation of the ocular following responses, we investigated neurons in the dorsolateral pontine nucleus (DLPN) of behaving monkeys. The neurons discharged during brief, sudden movements of a large-field visual stimulus, eliciting ocular following. Most of them (100/112) responded to movements of a large-field visual stimulus with directional selectivity. 2. Response amplitude was measured in two components of the neural response: an initial transient component and a late sustained component. Most direction-selective DLPN neurons showed their strongest responses at high stimulus speeds (80-160 degrees/s), whether their response components were initial (63/87, 72%) or sustained (63/87, 72%). The average firing rates of 87 DLPN neurons increased as a linear function of the logarithm of stimulus speed up to 40 degrees/s for both initial and sustained responses. 3. Not only the magnitude but also the latency of the neural and ocular responses were dependent on stimulus speed. The latencies of both neural and ocular responses were inversely related to the stimulus speed. As a result, the time difference between the response latencies for neural and ocular responses did not vary much with changes of stimulus speed. 4. Response latency was measured when a large-field random dot pattern was moved in the preferred direction and at the preferred speed of each neuron. Seventy-three percent (56/77) of the neurons were activated less than 50 ms after the onset of the stimulus motion. In most cases (67/77, 87%), their increase of firing rate started before the eye movements, and 34% of them (26/77) started greater than 10 ms before the eye movements. 5. Blurring of the random dot pattern by interposing a sheet of ground glass increased the latency of both neural responses and eye movements. On the other hand, the blurred images did not change the timing of the effect of blanking the visual scene on the responses of the neurons or eye movements. 6. When a check pattern was used instead of random dots, both neural and ocular responses began to decrease rapidly when the temporal frequency of the visual stimulus exceeded 20 Hz. When the temporal frequency of the visual stimulus approached 40 Hz, the neurons showed a distinctive burst-and-pause firing pattern. The eye movements recorded at the same time showed signs of oscillation, and their temporal patterns were closely correlated to those of the firing rate.(ABSTRACT TRUNCATED AT 400 WORDS)

Mesh:

Year:  1992        PMID: 1578251     DOI: 10.1152/jn.1992.67.3.680

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


  12 in total

1.  Preparatory modulation of the gain of visuo-motor transmission for smooth pursuit in monkeys.

Authors:  Yasushi Kodaka; Kenji Kawano
Journal:  Exp Brain Res       Date:  2003-02-11       Impact factor: 1.972

2.  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

3.  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

4.  Brainstem and cerebellar fMRI-activation during horizontal and vertical optokinetic stimulation.

Authors:  Sandra Bense; Barbara Janusch; Goran Vucurevic; Thomas Bauermann; Peter Schlindwein; Thomas Brandt; Peter Stoeter; Marianne Dieterich
Journal:  Exp Brain Res       Date:  2006-04-25       Impact factor: 1.972

5.  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

6.  Role of Purkinje cells in the ventral paraflocculus in short-latency ocular following responses.

Authors:  M Shidara; K Kawano
Journal:  Exp Brain Res       Date:  1993       Impact factor: 1.972

7.  Selective defects of visual tracking in progressive supranuclear palsy (PSP): implications for mechanisms of motion vision.

Authors:  Anand C Joshi; David E Riley; Michael J Mustari; Mark L Cohen; R John Leigh
Journal:  Vision Res       Date:  2010-02-01       Impact factor: 1.886

8.  A behavioral receptive field for ocular following in monkeys: Spatial summation and its spatial frequency tuning.

Authors:  Frédéric V Barthélemy; Jérome Fleuriet; Laurent U Perrinet; Guillaume S Masson
Journal:  eNeuro       Date:  2022-06-27

9.  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

10.  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

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.