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J Neurophysiol (March 1, 2003). 10.1152/jn.00519.2002
Submitted on Submitted 8 July 2002; accepted in final form 12 November 2002
1Laboratory of Sensorimotor Research National Eye Institute Bethesda, Maryland 20892; 2Medical Research Council-Cognition and Brain Sciences Unit and Department of Experimental Psychology, University of Oxford, Oxford OX1-3UD, United Kingdom; 3Keck-Mahoney Institute for Brain and Cognition, Center for Neurobiology and Behavior, and Departments of Neurology and Psychiatry, Columbia University College of Physicians and Surgeons New York, 10032; and 4New York State Psychiatric Institute, New York, New York 10032
Kusunoki, Makoto and
Michael E. Goldberg.
The Time Course of Perisaccadic Receptive Field Shifts in the
Lateral Intraparietal Area of the Monkey. J. Neurophysiol. 89: 1519-1527, 2003. Neurons in the
lateral intraparietal area of the monkey (LIP) have visual receptive
fields in retinotopic coordinates when studied in a fixation task.
However, in the period immediately surrounding a saccade these
receptive fields often shift, so that a briefly flashed stimulus
outside the receptive field will drive the neurons if the eye movement
will bring the spatial location of that vanished stimulus into the
receptive field. This is equivalent to a transient shift of the retinal
receptive field. The process enables the monkey brain to process a
stimulus in a spatially accurate manner after a saccade, even though
the stimulus appeared only before the saccade. We studied the time
course of this receptive field shift by flashing a task-irrelevant
stimulus for 100 ms before, during, or after a saccade. The stimulus
could appear in receptive field as defined by the fixation before the
saccade (the current receptive field) or the receptive field as defined by the fixation after the saccade (the future receptive field). We
recorded the activity of 48 visually responsive neurons in LIP of three
hemispheres of two rhesus monkeys. We studied 45 neurons in the current
receptive field task, in which the saccade removed the stimulus from
the receptive field. Of these neurons 29/45 (64%) showed a significant
decrement of response when the stimulus appeared 250 ms or less before
the saccade, as compared with their activity during fixation. The
average response decrement was 38% for those cells showing a
significant (P < 0.05 by t-test) decrement.
We studied 39 neurons in the future receptive field task, in which the
saccade brought the spatial location of a recently vanished stimulus
into the receptive field. Of these 32/39 (82%) had a significant
response to stimuli flashed for 100 ms in the future receptive field,
even 400 ms before the saccade. Neurons never responded to stimuli
moved by the saccade from a point outside the receptive field to
another point outside the receptive field. Neurons did not necessarily
show any saccadic suppression for stimuli moved from one part of the
receptive field to another by the saccade. Stimuli flashed <250 ms
before the saccade-evoked responses in both the presaccadic and the
postsaccadic receptive fields, resulting in an increase in the
effective receptive field size, an effect that we suggest is
responsible for perisaccadic perceptual inaccuracies.
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