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Richard A. Andersen
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Journal Articles
Publisher: Journals Gateway
Journal of Cognitive Neuroscience (2013) 25 (8): 1270–1283.
Published: 01 August 2013
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The ability to selectively process visual inputs and to decide between multiple movement options in an adaptive manner is critical for survival. Such decisions are known to be influenced by factors such as reward expectation and visual saliency. The dorsal pulvinar connects to a multitude of cortical areas that are involved in visuospatial memory and integrate information about upcoming eye movements with expected reward values. However, it is unclear whether the dorsal pulvinar is critically involved in spatial memory and reward-based oculomotor decision behavior. To examine this, we reversibly inactivated the dorsal portion of the pulvinar while monkeys performed a delayed memory saccade task that included choices between equally or unequally rewarded options. Pulvinar inactivation resulted in a delay of saccade initiation toward memorized contralesional targets but did not affect spatial memory. Furthermore, pulvinar inactivation caused a pronounced choice bias toward the ipsilesional hemifield when the reward value in the two hemifields was equal. However, this choice bias could be alleviated by placing a high reward target into the contralesional hemifield. The bias was less affected by the manipulation of relative visual saliency between the two competing targets. These results suggest that the dorsal pulvinar is involved in determining the behavioral desirability of movement goals while being less critical for spatial memory and reward processing.
Journal Articles
Publisher: Journals Gateway
Journal of Cognitive Neuroscience (2000) 12 (4): 601–614.
Published: 01 July 2000
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Many neurons in the posterior-parietal cortex (PPC) have saccadic responses to visual and auditory targets. The responses are modulated by eye position and head position. These findings suggest that PPC integrates multisensory inputs and may provide information about saccadic targets represented in different coordinate frames. In addition to an eye-centered output representation, PPC may also project to brain areas which contain head-centered and body-centered representations of the space. In this report, possible coordinate transformations in PPC were examined by comparing several sets of models of PPC, each having different representations in the output layer: (i) an eye-centered map only; (ii) a head-centered map only; (iii) an eye-centered map and a head-centered map; and (iv) an eye-centered map, a head-centered map, and a body-centered map. These output maps correctly encoded saccades to visual and auditory targets through training. The units in the hidden layers of the models exhibited the following properties: (1) The units had gain fields (GFs) for eye position, and also for head position if the model had a body-centered output representation; (2) As the result of the GF and the nonlinear activation function of the units, the hidden layers often employed “intermediate” coding, e.g., the hidden units coded targets partially in eye-centered coordinates and, partially, in head-centered coordinates; (3) Different types of coordinate transformations in these models were carried out by different relationships between the receptive fields (RFs) and the GFs of the hidden units; and (4) The properties of PPC neurons are in better accordance with the hidden units of the models that had multiple-output representations than the models that had only one single-output representation. In conclusion, the results show that the GF is an effective mechanism for performing coordinate transformations. The models also suggest that neurons with intermediate coding are to be expected in the process of coordinate transformations.
Journal Articles
Publisher: Journals Gateway
Journal of Cognitive Neuroscience (1989) 1 (4): 317–326.
Published: 01 October 1989
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Microstimulation of many saccadic centers in the brain produces eye movements that are not consistent with either a strictly retinal or strictly head-centered coordinate coding of eye movements. Rather, stimulation produces some features of both types of coordinate coding. Recently we demonstrated a neural network model that was trained to localize the position of visual stimuli in head-centered coordinates at the output using inputs of eye and retinal position similar to those converging on area 7a of the posterior parietal cortex of monkeys (Zipser & Andersen 1988; Andersen & Zipser 1988). Here we show that microstimulation of this trained network, achieved by fully activating single units in the middle layer, produces “saccades” that are very much like the saccades produced by stimulating the brain. The activity of the middle-layer units can be considered to code the desired location of the eyes in head-centered coordinates; however, stimulation of these units does not produce the saccades predicted by a classical head-centered coordinate coding because the location in space appears to be coded in a distributed fashion among a population of units rather than explicitly at the level of single cells.