The vestibular system is crucial in maintaining equilibrium and orientation in space. One of its major functions is the vestibulo-ocular reflex (VOR). The VOR generates compensatory rotations of the eyes during head movements in order to maintain binocular fixation on visual targets, and therefore a stable retinal image. We focus on the VOR because it is the most direct and accessible behavior from which mechanistic inferences about vestibular function can be derived. The VOR is activated by two kinds of head acceleration; angular (the AVOR), driven by the semicircular canals, and linear (the LVOR), driven by the otoliths. Linear stimuli include two forms, translational motion and tilt relative to gravity. Each drives the LVOR in specific ways. An important feature of the VOR is its ability to adaptively modify performance in response to prolonged visual-vestibular mismatch during head movements. However, this phenomenon has only been demonstrated in the AVOR. In addition, the VOR is modulated by instantaneous viewing conditions (e.g. target distance and gaze), more so in the LVOR than the AVOR. The proposed experiments will determine how canal and otolith inputs interact to generate, and adaptively maintain, behaviorally useful ocular responses during angular, linear, and complex head movements. New techniques will be employed to study the LVOR and its relationships with the AVOR and vision over a broad range of motion profiles and fixation contexts. Relationships between translational and tilt LVORs will be elucidated. Novel adaptive mechanisms will be explored and characterized. We will determine whether plasticity in the AVOR and LVOR share neural elements. Specific endorgan lesions will be employed to directly assess the origin of VOR behaviors, and to elucidate unique adaptive processes that restore function.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC001935-03
Application #
2127009
Study Section
Special Emphasis Panel (ZRG1-VISB (03))
Project Start
1993-07-01
Project End
1997-06-30
Budget Start
1995-07-01
Budget End
1996-06-30
Support Year
3
Fiscal Year
1995
Total Cost
Indirect Cost
Name
University of Rochester
Department
Neurology
Type
Schools of Dentistry
DUNS #
208469486
City
Rochester
State
NY
Country
United States
Zip Code
14627
Seidman, Scott H; Au Yong, Nicholas; Paige, Gary D (2009) The perception of translational motion: what is vestibular and what is not. Ann N Y Acad Sci 1164:222-8
Au Yong, N; Paige, G D; Seidman, S H (2007) Multiple sensory cues underlying the perception of translation and path. J Neurophysiol 97:1100-13
Barnes, G R; Paige, G D (2004) Anticipatory VOR suppression induced by visual and nonvisual stimuli in humans. J Neurophysiol 92:1501-11
Zwiers, Marcel P; Van Opstal, A John; Paige, Gary D (2003) Plasticity in human sound localization induced by compressed spatial vision. Nat Neurosci 6:175-81
Seidman, S H; Paige, G D; Tomlinson, R D et al. (2002) Linearity of canal-otolith interaction during eccentric rotation in humans. Exp Brain Res 147:29-37
Seidman, S H; Paige, G D; Tomko, D L (1999) Adaptive plasticity in the naso-occipital linear vestibulo-ocular reflex. Exp Brain Res 125:485-94
Telford, L; Seidman, S H; Paige, G D (1998) Canal-otolith interactions in the squirrel monkey vestibulo-ocular reflex and the influence of fixation distance. Exp Brain Res 118:115-25
Telford, L; Seidman, S H; Paige, G D (1997) Dynamics of squirrel monkey linear vestibuloocular reflex and interactions with fixation distance. J Neurophysiol 78:1775-90
Telford, L; Seidman, S H; Paige, G D (1996) Canal-otolith interactions driving vertical and horizontal eye movements in the squirrel monkey. Exp Brain Res 109:407-18
Seidman, S H; Telford, L; Paige, G D (1995) Vertical, horizontal, and torsional eye movement responses to head roll in the squirrel monkey. Exp Brain Res 104:218-26