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Response Properties of Relay Cells in the A-laminae of the Cat's Dorsal Lateral Geniculate Nucleus After Saccades

Overview
Journal Exp Brain Res
Specialty Neurology
Date 1996 Aug 1
PMID 8871102
Citations 6
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Abstract

Responses of relay cells in the A-laminae of the dorsal lateral geniculate nucleus (LGNd) during spontaneous saccades and saccade-like visual stimulation were extracellularly recorded in awake cats. Ninety-six out of 137 cells recorded (42 X and 54 Y cells) were responsive during spontaneous saccadic eye movements. All Y cells and 67% of the X cells responded with burst activity, i.e. with either one or two activity peaks during and after saccades. Thirty-three percent of the X cells were inhibited during saccades. Excitatory peaks occurred at mean latencies of 33 ms and 31 ms for X and Y cells, respectively. Comparable burst responses were obtained when retinal image shifts similar to those during saccades were induced by external saccade-like stimulus movements. However, the latencies of excitatory peak activity were significantly longer to external stimuli than to the onsets of saccades. This indicates the existence of an eye movement-related input which activates LGNd relay cells in addition to the visual input. We propose that the pretectogeniculate projection may contribute to the responses of LGNd relay cells following saccadic eye movements via a disinhibitory input and that this input could be involved in intra- and postsaccadic modulations of the transfer of visual signals to visual cortex.

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References
1.
Noda H . Discharges of relay cells in lateral geniculate nucleus of the cat during spontaneous eye movements in light and darkness. J Physiol. 1975; 250(3):579-95. PMC: 1348394. DOI: 10.1113/jphysiol.1975.sp011071. View

2.
Sherman S, Koch C . The control of retinogeniculate transmission in the mammalian lateral geniculate nucleus. Exp Brain Res. 1986; 63(1):1-20. DOI: 10.1007/BF00235642. View

3.
Cleland B, Dubin M, LEVICK W . Sustained and transient neurones in the cat's retina and lateral geniculate nucleus. J Physiol. 1971; 217(2):473-96. PMC: 1331787. DOI: 10.1113/jphysiol.1971.sp009581. View

4.
Lal R, Friedlander M . Effect of passive eye position changes on retinogeniculate transmission in the cat. J Neurophysiol. 1990; 63(3):502-22. DOI: 10.1152/jn.1990.63.3.502. View

5.
Ilg U, Hoffmann K . Motion perception during saccades. Vision Res. 1993; 33(2):211-20. DOI: 10.1016/0042-6989(93)90159-t. View