The central focus of this project is to determine how the LVOR processes otolith and oculomotor information spatially to generate the appropriate ocular response to linear motion in any direction. We quantify the LVOR during translation along arbitrary axes to determine its accuracy and stability in 3-D. A secondary question is the nature of adaptive mechanisms that maintain the various kinematic controls in the LVOR. We hypothesize that an adaptive mechanism must exist to calibrate the relationship between LVOR responses and fixation distance. Another presumably exists to calibrate the relationship between gaze and the axis of translation in order to properly govern the NO-LVOR. We have selectively identified and quantified these processes, using both optical manipulations and lesion techniques. We have recently demonstrated, in the squirrel monkey, that the AVOR can be selectively recalibrated in a single plane. This occurs when head rotations are restricted to one plane while subjects wear magnifying optics; visual-vestibular mismatch is then limited to one plane and recalibration occurs selectively in that same plane. We will expand this approach to the LVOR and canal-otolith interactions. Future work will attempt to define the points in VOR circuitry where the AVOR and LVOR share common elements. We plan to use behavioral techniques to infer convergence of function. Canal and otolith signals have been recorded in neurons in vestibular nuclei, but the relevance of these neurons to VOR performance is unknown. We hypothesize that selective adaptation of one translational LVOR might be accompanied by parallel changes in the AVOR, implying shared (convergent) elements prior to motor neurons.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
5P41RR009283-03
Application #
5225752
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1996
Total Cost
Indirect Cost
Rothkopf, Constantin A; Ballard, Dana H (2013) Modular inverse reinforcement learning for visuomotor behavior. Biol Cybern 107:477-90
Velarde, Carla; Perelstein, Elizabeth; Ressmann, Wendy et al. (2012) Independent deficits of visual word and motion processing in aging and early Alzheimer's disease. J Alzheimers Dis 31:613-21
Fernandez, Roberto; Duffy, Charles J (2012) Early Alzheimer's disease blocks responses to accelerating self-movement. Neurobiol Aging 33:2551-60
Rothkopf, Constantin A; Ballard, Dana H (2010) Credit assignment in multiple goal embodied visuomotor behavior. Front Psychol 1:173
Huxlin, Krystel R; Martin, Tim; Kelly, Kristin et al. (2009) Perceptual relearning of complex visual motion after V1 damage in humans. J Neurosci 29:3981-91
Rothkopf, Constantin A; Ballard, Dana H (2009) Image statistics at the point of gaze during human navigation. Vis Neurosci 26:81-92
Jovancevic-Misic, Jelena; Hayhoe, Mary (2009) Adaptive gaze control in natural environments. J Neurosci 29:6234-8
Kavcic, Voyko; Ni, Hongyan; Zhu, Tong et al. (2008) White matter integrity linked to functional impairments in aging and early Alzheimer's disease. Alzheimers Dement 4:381-9
Droll, Jason A; Hayhoe, Mary M; Triesch, Jochen et al. (2005) Task demands control acquisition and storage of visual information. J Exp Psychol Hum Percept Perform 31:1416-38
Bayliss, Jessica D; Inverso, Samuel A; Tentler, Aleksey (2004) Changing the P300 brain computer interface. Cyberpsychol Behav 7:694-704

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