Visual and vestibular sensory cues interact to support self-movement perception and spatial orientation. We hypothesize that MSTd neurons combine visual and vestibular signals that indicate the same direction of self-movement to enhance heading perception. We further hypothesize that superimposed stimuli indicating different headings evoke neuronal responses that contribute to detecting independently moving objects. Our previous work suggests that neurons in dorsal medial superior temporal cortex (MSTd) access both visual and vestibular signals to support an integrated representation of self-movement heading direction. In addition, we have found that: 1. Responses to object motion are enhanced when superimposed on optic flow that indicates a different heading direction, implying that the object is moving independently of the observer. 2. Responses to real movement can be enhanced when combined with optic flow indicating a different heading direction, implying that the head and visual axes are not aligned in some neuron's, hi the proposed studies we will determine if MSTd combines multi-sensory and gaze signals to support veridical heading perception and detect independent visual object motion during observer self-movement. In three Specific Aims we will study cue interactions between: 1) optic flow and object motion, 2) optic flow and real movement, and 3) object motion and real movement. In all three Aims we will monitor neuronal activity and heading perception focusing on: changes in the relative directions of stimuli cueing independent visual motion, and the effects of gaze angle shifts that might alter the reference frame for observer and object motion perception. All three Aims use the same data analyses, but the interpretation of the results is unique to each, especially for visual-visual (Aim #1) and visual-vestibular (Aims 2 & 3) effects. Our objective is to determine how cortical neurons combine sensory cues about self-movement both to estimate the observer's heading direction and to detect potentially threatening independent object motion. These experiments will elucidate the neuronal mechanisms of visuospatial disorientation that we have linked to getting lost and risks of collisions in healthy older adults and patients with Alzheimer's disease.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY010287-14
Application #
7439065
Study Section
Central Visual Processing Study Section (CVP)
Program Officer
Oberdorfer, Michael
Project Start
1994-07-01
Project End
2010-06-30
Budget Start
2008-07-01
Budget End
2009-06-30
Support Year
14
Fiscal Year
2008
Total Cost
$371,129
Indirect Cost
Name
University of Rochester
Department
Neurology
Type
Schools of Dentistry
DUNS #
041294109
City
Rochester
State
NY
Country
United States
Zip Code
14627
Sato, Nobuya; Page, William K; Duffy, Charles J (2013) Task contingencies and perceptual strategies shape behavioral effects on neuronal response profiles. J Neurophysiol 109:546-56
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Fernandez, Roberto; Duffy, Charles J (2012) Early Alzheimer's disease blocks responses to accelerating self-movement. Neurobiol Aging 33:2551-60
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Kishore, Sarita; Hornick, Noah; Sato, Nobuya et al. (2012) Driving strategy alters neuronal responses to self-movement: cortical mechanisms of distracted driving. Cereb Cortex 22:201-8
Kavcic, Voyko; Vaughn, William; Duffy, Charles J (2011) Distinct visual motion processing impairments in aging and Alzheimer's disease. Vision Res 51:386-95
Yu, Chen Ping; Page, William K; Gaborski, Roger et al. (2010) Receptive field dynamics underlying MST neuronal optic flow selectivity. J Neurophysiol 103:2794-807
Sato, Nobuya; Kishore, Sarita; Page, William K et al. (2010) Cortical neurons combine visual cues about self-movement. Exp Brain Res 206:283-97
Mapstone, Mark; Duffy, Charles J (2010) Approaching objects cause confusion in patients with Alzheimer's disease regarding their direction of self-movement. Brain 133:2690-701
Dubin, Marc J; Duffy, Charles J (2009) Neuronal encoding of the distance traversed by covert shifts of spatial attention. Neuroreport 20:49-55

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