The long-term goal of this research is to understand the neural mechanisms underlying simple forms of visually based cognition, including visually based decision-making in particular. The projects will focus on a network of high-level brain structures that appears to translate perception of the visual world into plans for action. Prior studies indicate that this network includes cortical areas of the parietal and frontal lobes as well as midbrain structures such as the superior colliculus. A similar network of structures is present in humans, and the proposed research is thus likely to contribute directly to our developing knowledge of human vision, cognition, and their clinical disorders.
Three specific aims will be pursued during the coming grant period: 1. Electrical microstimulation techniques will be employed to test rigorously the causal role played by each candidate neural structure in visually-based decision making. 2. Combined stimulation and recording techniques will be employed to test specific hypotheses concerning the functional circuitry that connects these areas and the infromation that flows between them. 3. Electrophysiological techniques will be employed to study identify and study the neural mechanisms that compute the """"""""subjective value"""""""" that an organism places on alternative actions. Psychological and economic studies have shown that perceived value exerts an enormous influence on decisionmaking. Together the proposed experiments will provide considerable impetus toward understanding the neural mechanisms underlying a simple form of cognition. The ultimate health-related value of this work will follow from an understanding of the biological basis of mental function. Neurological and psychiatric diseases that affect mental function take a massive toll on the health and well-being of our citizenry. These diseases are particularly insidious because they slowly rob the afflicted person of normal cognitive abilities - the very essence of personal identity. Understanding how brain activity gives rise to mental function in normal subjects will undoubtedly provide a deeper understanding of what goes wrong in various disease processes, and suggest useful therapeutic approaches for such diseases.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY005603-20
Application #
6788886
Study Section
Visual Sciences B Study Section (VISB)
Program Officer
Oberdorfer, Michael
Project Start
1985-01-01
Project End
2008-07-31
Budget Start
2004-09-15
Budget End
2005-07-31
Support Year
20
Fiscal Year
2004
Total Cost
$197,017
Indirect Cost
Name
Stanford University
Department
Biology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305
Fiorillo, Christopher D; Yun, Sora R; Song, Minryung R (2013) Diversity and homogeneity in responses of midbrain dopamine neurons. J Neurosci 33:4693-709
Fiorillo, Christopher D; Song, Minryung R; Yun, Sora R (2013) Multiphasic temporal dynamics in responses of midbrain dopamine neurons to appetitive and aversive stimuli. J Neurosci 33:4710-25
Hedges, James H; Gartshteyn, Yevgeniya; Kohn, Adam et al. (2011) Dissociation of neuronal and psychophysical responses to local and global motion. Curr Biol 21:2023-8
Churchland, Mark M; Yu, Byron M; Cunningham, John P et al. (2010) Stimulus onset quenches neural variability: a widespread cortical phenomenon. Nat Neurosci 13:369-78
Cohen, Marlene R; Newsome, William T (2009) Estimates of the contribution of single neurons to perception depend on timescale and noise correlation. J Neurosci 29:6635-48
Cohen, Marlene R; Newsome, William T (2008) Context-dependent changes in functional circuitry in visual area MT. Neuron 60:162-73
Newsome, W T; Pare, E B (1988) A selective impairment of motion perception following lesions of the middle temporal visual area (MT). J Neurosci 8:2201-11