Literature DB >> 2358873

Visual responses of Purkinje cells in the cerebellar flocculus during smooth-pursuit eye movements in monkeys. II. Complex spikes.

L S Stone1, S G Lisberger.   

Abstract

1. We report the complex-spike responses of two groups of Purkinje cells (P-cells). The cell were classified according to their simple-spike firing during smooth eye movements evoked by visual and vestibular stimuli with the use of established criteria (Lisberger and Fuchs 1978; Stone and Lisberger 1990). During pursuit with the head fixed, ipsi gaze-velocity P-cells (GVP-cells) showed increased simple-spike firing when gaze moved toward the side of the recording, whereas down GVP-cells showed increased simple-spike firing when gaze moved downward. 2. During pursuit of sinusoidal target motion, the complex-spike firing rate was modulated out-of-phase with the simple-spike firing rate. Ipsi GVP-cells showed increased complex-spike firing during pursuit away from the side of the recording, and down GVP-cells showed increased complex-spike firing during upward pursuit. The strength of the complex-spike response increased as a function of the frequency of sinusoidal target motion. 3. GVP-cells showed directionally selective complex-spike responses during the initiation of pursuit to ramp target motion. Ipsi GVP-cells had increased complex-spike firing 100 ms after the onset of contralaterally directed target motion and decreased complex-spike activity after the onset of ipsilaterally directed target motion. Down GVP-cells had increased complex-spike firing 100 ms after the onset of upward target motion and decreased firing after the onset of downward target motion. As during sinusoidal target motion, each cell's simple- and complex-spike responses had the opposite directional preferences. 4. When the monkeys fixated a stationary target during a transient vestibular stimulus, the retinal slip caused by the 14-ms latency of the vestibuloocular reflex (VOR) affected the complex-spike firing rate. For ipsi GVP-cells, ipsilateral head motion caused transient contralateral image motion and an increase in complex-spike firing. The same vestibular stimulus in darkness caused an almost identical eye movement but had no effect on complex-spike firing. We conclude that complex spikes in ipsi GVP-cells are driven by contralaterally directed image motion. 5. To determine the events surrounding complex-spike firing during pursuit, we triggered averages of eye and target velocity on the occurrence of complex spikes during pursuit of sine-wave target motion. The averages revealed a transient pulse of retinal image motion that peaked approximately 100 ms before the complex spike. We conclude that complex spikes during steady-state pursuit are driven by the retinal slip associated with imperfect pursuit.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1990        PMID: 2358873     DOI: 10.1152/jn.1990.63.5.1262

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


  48 in total

1.  Visual error signals from the pretectal nucleus of the optic tract guide motor learning for smooth pursuit.

Authors:  Seiji Ono; Michael J Mustari
Journal:  J Neurophysiol       Date:  2010-05       Impact factor: 2.714

Review 2.  The great gate: control of sensory information flow to the cerebellum.

Authors:  Anna Devor
Journal:  Cerebellum       Date:  2002 Jan-Mar       Impact factor: 3.847

3.  Roles of the cerebellum in pursuit-vestibular interactions.

Authors:  Kikuro Fukushima
Journal:  Cerebellum       Date:  2003       Impact factor: 3.847

Review 4.  Pontine nuclei-mediated cerebello-cerebral interactions and its functional role.

Authors:  Soichi Nagao
Journal:  Cerebellum       Date:  2004       Impact factor: 3.847

Review 5.  What we know about the generation of nystagmus and other ocular oscillations: are we closer to identifying therapeutic targets?

Authors:  Rebecca Jane McLean; Irene Gottlob; Frank Antony Proudlock
Journal:  Curr Neurol Neurosci Rep       Date:  2012-06       Impact factor: 5.081

6.  Learning on multiple timescales in smooth pursuit eye movements.

Authors:  Yan Yang; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2010-09-08       Impact factor: 2.714

Review 7.  Activation of climbing fibers.

Authors:  Alan R Gibson; Kris M Horn; Milton Pong
Journal:  Cerebellum       Date:  2004       Impact factor: 3.847

8.  Encoding and decoding of learned smooth-pursuit eye movements in the floccular complex of the monkey cerebellum.

Authors:  Javier F Medina; Stephen G Lisberger
Journal:  J Neurophysiol       Date:  2009-07-22       Impact factor: 2.714

9.  Searching for an Internal Representation of Stimulus Kinematics in the Response of Ventral Paraflocculus Purkinje Cells.

Authors:  Pablo M Blazquez; GyuTae Kim; Tatyana A Yakusheva
Journal:  Cerebellum       Date:  2017-08       Impact factor: 3.847

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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