To produce meaningful behavior, the brain must link information represented in sensory cortex to motor circuitry involved in the planning and execution of behavior. This linkage requires the integration of sensory cues across time and modality. Our research targets neurons in the association cortex of the parietal and frontal lobes, which are believed to play an essential role in working memory. These neurons discharge for several seconds before gaze is shifted to a remembered location in the visual field. Their response provides a temporal bridge between the spatial cues present in visual cortex and oculomotor circuitry. These neurons also appear to link the representation of visual motion toward a perceptual decision. We have recorded from neurons in the prefrontal cortex of two rhesus monkeys while they judged the direction of motion of a random dot display. We have studied neurons that are thought to play a role in spatial working memory and the planning of eye movements. The majority of these neurons are active when the monkey plans eye movements as a means of communicating its judgment about the direction of motion. Our findings suggest that the prefrontal and parietal cortex plays a role in both eye movement planning and visual processing. Using a reaction time paradigm, we have found that this activity arises before the monkey arrives at a judgment. This is the strongest evidence to date for a neural linkage between sensory processing and a contingent behavior. The experiments have begun to reveal the computations performed by neurons in association cortex, lending novel insight into the neurobiology of cognition and its disorders. We are optimistic that our results will lead to new understanding and treatment of such pernicious disorders as Alzheimer's disease, encephalopathy, and stroke.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Primate Research Center Grants (P51)
Project #
5P51RR000166-37
Application #
6277534
Study Section
Project Start
1998-05-01
Project End
1999-04-30
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
37
Fiscal Year
1998
Total Cost
Indirect Cost
Name
University of Washington
Department
Type
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Pham, Amelie; Carrasco, Marisa; Kiorpes, Lynne (2018) Endogenous attention improves perception in amblyopic macaques. J Vis 18:11
Zanos, Stavros; Rembado, Irene; Chen, Daofen et al. (2018) Phase-Locked Stimulation during Cortical Beta Oscillations Produces Bidirectional Synaptic Plasticity in Awake Monkeys. Curr Biol 28:2515-2526.e4
Choi, Hannah; Pasupathy, Anitha; Shea-Brown, Eric (2018) Predictive Coding in Area V4: Dynamic Shape Discrimination under Partial Occlusion. Neural Comput 30:1209-1257
Shushruth, S; Mazurek, Mark; Shadlen, Michael N (2018) Comparison of Decision-Related Signals in Sensory and Motor Preparatory Responses of Neurons in Area LIP. J Neurosci 38:6350-6365
Raghanti, Mary Ann; Edler, Melissa K; Stephenson, Alexa R et al. (2018) A neurochemical hypothesis for the origin of hominids. Proc Natl Acad Sci U S A 115:E1108-E1116
Wool, Lauren E; Crook, Joanna D; Troy, John B et al. (2018) Nonselective Wiring Accounts for Red-Green Opponency in Midget Ganglion Cells of the Primate Retina. J Neurosci 38:1520-1540
Hasegawa, Yu; Curtis, Britni; Yutuc, Vernon et al. (2018) Microbial structure and function in infant and juvenile rhesus macaques are primarily affected by age, not vaccination status. Sci Rep 8:15867
Oleskiw, Timothy D; Nowack, Amy; Pasupathy, Anitha (2018) Joint coding of shape and blur in area V4. Nat Commun 9:466
Balakrishnan, Ashwini; Goodpaster, Tracy; Randolph-Habecker, Julie et al. (2017) Analysis of ROR1 Protein Expression in Human Cancer and Normal Tissues. Clin Cancer Res 23:3061-3071
Shooner, Christopher; Hallum, Luke E; Kumbhani, Romesh D et al. (2017) Asymmetric Dichoptic Masking in Visual Cortex of Amblyopic Macaque Monkeys. J Neurosci 37:8734-8741

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