Baclofen, motion sickness susceptibility and the neural basis for velocity storage.

Reduction of the dominant time constant (T(VOR)) of the angular vestibulo-ocular reflex (aVOR) by habituation is associated with a decrease in motion sickness susceptibility. Baclofen, a GABA(b) agonist, reduces the time constant of the velocity storage integrator in the aVOR in a dose-dependent manner. The high frequency aVOR gain is unaltered by baclofen. Here we demonstrate that the reduction in T(VOR) produced by oral administration of 20 mg of baclofen causes a significant reduction in motion sickness susceptibility, tested with roll while rotating (RWR). These data show that motion sickness susceptibility can be pharmacologically manipulated with a GABA(b) agonist and support our conclusion that motion sickness is generated through velocity storage. We also show how baclofen acts on velocity storage at the neural level. A vestibular-plus-saccade (VPS) neuron was recorded in the rostral medial vestibular nucleus (rMVN) of a cynomolgus monkey, an area where we postulate that velocity storage is generated. The cell had a time constant during steps of velocity that was close to that of the T(VOR). After parenteral administration of baclofen, there was a similar decrease in the time constants of the VPS neuron and the T(VOR). This is the first demonstration of the concurrence of unit and aVOR time constants before and after baclofen. The data support the hypothesis that the velocity storage integrator is generated through activity of vestibular-only (VO) and VPS neurons in rMVN and suggest that GABA(b) synapses on VO and VPS neurons are likely to be involved in the baclofen-induced reduction in motion sickness susceptibility.

[1]  R J Leigh,et al.  A HYPOTHETICAL EXPLANATION FOR PERIODIC ALTERNATING NYSTAGMUS: INSTABILITY IN THE OPTOKINETIC‐VESTIBULAR SYSTEM * , 1981, Annals of the New York Academy of Sciences.

[2]  J. Yokota,et al.  Nystagmus induced by electrical stimulation of the vestibular and prepositus hypoglossi nuclei in the monkey: evidence for site of induction of velocity storage , 2004, Experimental Brain Research.

[3]  B. Cohen,et al.  The relation of motion sickness to the spatial–temporal properties of velocity storage , 2003, Experimental Brain Research.

[4]  B Cohen,et al.  Model-based study of the human cupular time constant. , 1999, Journal of vestibular research : equilibrium & orientation.

[5]  B Cohen,et al.  Semicircular canal contributions to the three-dimensional vestibuloocular reflex: a model-based approach. , 1995, Journal of neurophysiology.

[6]  J. Peterson,et al.  Immunohistochemical distribution of protein kinase C isozymes is differentially altered in ischemic gerbil hippocampus , 1992, Brain Research.

[7]  B. Cohen,et al.  The ultrastructure of GABA-immunoreactive vestibular commissural neurons related to velocity storage in the monkey , 1999, Neuroscience.

[8]  Y. Zhang,et al.  Properties of superior vestibular nucleus neurons projecting to the cerebellar flocculus in the squirrel monkey. , 1993, Journal of neurophysiology.

[9]  Theodore Raphan,et al.  Effects of baclofen on the angular vestibulo-ocular reflex , 2006, Experimental Brain Research.

[10]  B. Cohen,et al.  Eye movements induced by ampullary nerve stimulation. , 1963, The American journal of physiology.

[11]  Theodore Raphan,et al.  The vestibulo-ocular reflex in three dimensions , 2002, Experimental Brain Research.

[12]  B Cohen,et al.  Control of Spatial Orientation of the Angular Vestibulo‐Ocular Reflex by the Nodulus and Uvula of the Vestibulocerebellum , 1999, Annals of the New York Academy of Sciences.

[13]  Theodore Raphan,et al.  Habituation and adaptation of the vestibuloocular reflex: a model of differential control by the vestibulocerebellum , 2004, Experimental Brain Research.

[14]  H. Reisine,et al.  Neural basis for eye velocity generation in the vestibular nuclei of alert monkeys during off-vertical axis rotation , 2004, Experimental Brain Research.

[15]  V. Henn,et al.  Vestibular nuclei activity during optokinetic after-nystagmus (OKAN) in the alert monkey , 1977, Experimental Brain Research.

[16]  B Cohen,et al.  Spatial Orientation of the Vestibular System a , 1992, Annals of the New York Academy of Sciences.

[17]  R. L. Nó The regulation of eye positions and movements induced by the labyrinth: Chapter I. Tonic labyrinth reflexes on the eye , 1932 .

[18]  T Raphan,et al.  Modeling the spatiotemporal organization of velocity storage in the vestibuloocular reflex by optokinetic studies. , 1991, Journal of neurophysiology.

[19]  S. Lisberger,et al.  Brain stem neurons in modified pathways for motor learning in the primate vestibulo-ocular reflex. , 1988, Science.

[20]  A Graybiel,et al.  Experimental M-131--human vestibular function. , 1973, Aerospace medicine.

[21]  B. Cohen,et al.  Velocity storage in the vestibulo-ocular reflex arc (VOR) , 1979, Experimental Brain Research.

[22]  B Cohen,et al.  Baclofen and velocity storage: a model of the effects of the drug on the vestibulo‐ocular reflex in the rhesus monkey. , 1987, The Journal of physiology.

[23]  B. Cohen,et al.  Spatial orientation of the vestibular system: dependence of optokinetic after-nystagmus on gravity. , 1991, Journal of neurophysiology.

[24]  Peter Rudge,et al.  Treatment of periodic alternating nystagmus , 1980, Annals of neurology.

[25]  B. Cohen,et al.  l-Baclofen-sensitive GABAB binding sites in the medial vestibular nucleus localized by immunocytochemistry , 1992, Brain Research.