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      CONTROL OF VISUAL CORTICAL SIGNALS BY PREFRONTAL DOPAMINE

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          Abstract

          The prefrontal cortex (PFC) is thought to modulate sensory signals in posterior cortices during top-down attention 1, 2 , yet little is known about the underlying neural circuitry. Experimental and clinical evidence suggest that prefrontal dopamine plays an important role in cognitive functions 3 , acting predominantly through D1 receptors (D1Rs). Here we show that dopamine D1Rs mediate prefrontal control of signals within visual cortex. We pharmacologically altered D1R-mediated activity within the frontal eye field (FEF) of the PFC and measured its effects on the responses of neurons within visual cortex. This manipulation was sufficient to enhance the response magnitude, orientation selectivity and response reliability of neurons in area V4 to an extent comparable with the known effects of top-down attention. The observed enhancement in V4 signals was restricted to neurons with response fields (RFs) overlapping the part of visual space affected by the D1R manipulation. Altering D1R or D2R-mediated FEF activity increased saccadic target selection, but the D2R manipulation did not enhance V4 signals. Our results identify a role of D1Rs in mediating the control of visual cortical signals by the PFC and demonstrate how processing within sensory areas can be altered in mental disorders involving prefrontal dopamine.

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          Cellular basis of working memory

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            High-frequency, long-range coupling between prefrontal and visual cortex during attention.

            Electrical recordings in humans and monkeys show attentional enhancement of evoked responses and gamma synchrony in ventral stream cortical areas. Does this synchrony result from intrinsic activity in visual cortex or from inputs from other structures? Using paired recordings in the frontal eye field (FEF) and area V4, we found that attention to a stimulus in their joint receptive field leads to enhanced oscillatory coupling between the two areas, particularly at gamma frequencies. This coupling appeared to be initiated by FEF and was time-shifted by about 8 to 13 milliseconds across a range of frequencies. Considering the expected conduction and synaptic delays between the areas, this time-shifted coupling at gamma frequencies may optimize the postsynaptic impact of spikes from one area upon the other, improving cross-area communication with attention.
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              Neuroscience of attention-deficit/hyperactivity disorder: the search for endophenotypes.

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                Author and article information

                Journal
                0410462
                6011
                Nature
                Nature
                Nature
                0028-0836
                1476-4687
                30 March 2011
                15 May 2011
                16 December 2011
                : 474
                : 7351
                : 372-375
                Affiliations
                Howard Hughes Medical Institute and Department of Neurobiology, Stanford University School of Medicine, Stanford, CA 94305
                Author notes
                Correspondence to: Behrad Noudoost, Department of Neurobiology, Stanford University School of Medicine, Fairchild Bldg, 299 Campus Drive West, Stanford, CA 94305, Phone: 650.387.6739, FAX: 650.725.3958, behrad@ 123456stanford.edu
                Article
                nihpa280591
                10.1038/nature09995
                3117113
                21572439
                9c320b0c-39b3-432f-8b76-2e463926c426

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                History
                Funding
                Funded by: National Eye Institute : NEI
                Award ID: R01 EY014924-06A2 || EY
                Funded by: National Eye Institute : NEI
                Award ID: R01 EY014924-05 || EY
                Funded by: National Eye Institute : NEI
                Award ID: R01 EY014924-04 || EY
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