The vestibulo-ocular reflex (VOR) stabilizes gaze and hence foveal images during head movements. Deficits in the VOR resulting from disease or changes in development can severely impair vision. Neural adaptation in the VOR is essential to overcome these deficits. Over the past several decades, the investigation of the VOR and its adaptation has been focused on the contributions of brainstem and cerebellar pathways. The contributions of cerebral cortex in the VOR, however, remain largely unexplored. Recent studies have demonstrated that the frontal eye field (FEF) has direct projections to brainstem VOR pathways and neurons in the subregion of the FEF linked to smooth eye movements (FEFsem) exhibit activity related to both eye movements and head movements, suggesting an important role for the FEFsem in the VOR. The objective of the proposed research is to employ single unit recording and chemical lesion approaches to study the contributions of the FEFsem in the generation and adaptation of the VOR.
The first aim i s to use single unit recording techniques to quantitatively analyze how the FEFsem neurons encode head motion in monkeys. Recently, we have developed a paradigm that induces robust short-term and long-term plasticity in the VOR that compensates for translational head movements (TVOR). A novel feature of the paradigm is that these behavioral changes are not guided by visual information but by the spatial context of the task, i.e. whether the target is stationary in space or fixed relative to the head.
The second aim i s to take advantage of this paradigm to study the role of the FEFsem neurons in the generation of the TVOR. This experiment will provide greater understanding of the FEFsem in the information processing related to the task context and in the voluntary control and adaptation of the TVOR.
The third aim i s to assess the functional significance of the FEFsem by reversibly inactivating the FEFsem and studying its effect on the generation and adaptation of the TVOR. This research will provide important knowledge for understanding the fundamental vestibular and oculomotor neurophysiology and improving the diagnosis and treatment of vestibular disorders in humans.

Agency
National Institute of Health (NIH)
Institute
National Institute on Deafness and Other Communication Disorders (NIDCD)
Type
Research Project (R01)
Project #
5R01DC005785-02
Application #
6662000
Study Section
Integrative, Functional and Cognitive Neuroscience 8 (IFCN)
Program Officer
Platt, Christopher
Project Start
2002-09-20
Project End
2007-08-31
Budget Start
2003-09-01
Budget End
2004-08-31
Support Year
2
Fiscal Year
2003
Total Cost
$296,000
Indirect Cost
Name
University of Mississippi Medical Center
Department
Otolaryngology
Type
Schools of Medicine
DUNS #
928824473
City
Jackson
State
MS
Country
United States
Zip Code
39216
Luis, L; Lehnen, N; Muñoz, E et al. (2016) Anticompensatory quick eye movements after head impulses: A peripheral vestibular sign in spontaneous nystagmus. J Vestib Res 25:267-71
Luis, Leonel; Zhu, Hong; Costa, João et al. (2014) Reply to the Commentary on Luis et al. ""Spontaneous plugging of the horizontal semicircular canal with reversible canal dysfunction and recovery of vestibular evoked myogenic potentials"". Otol Neurotol 35:379-83
Zhou, Wu; Xu, Youguo; Simpson, Ivra et al. (2007) Multiplicative computation in the vestibulo-ocular reflex (VOR). J Neurophysiol 97:2780-9
Zhu, Hong; Jordan, James R; Hardy, Steven P G et al. (2007) Linear acceleration-evoked cardiovascular responses in awake rats. J Appl Physiol 103:646-54
Zhou, Wu; Simpson, Ivra; Xu, Youguo et al. (2005) Activity-dependent modulation: a non-linearity in the unilateral vestibulo-ocular reflex pathways. Exp Brain Res 163:267-72
Zhou, Wu; Mustain, W; Simpson, I (2004) Sound-evoked vestibulo-ocular reflexes (VOR) in trained monkeys. Exp Brain Res 156:129-34
Zhou, Wu; Weldon, Patrick; Tang, Bingfeng et al. (2003) Rapid motor learning in the translational vestibulo-ocular reflex. J Neurosci 23:4288-98