A Computational Model of Vestibular Fluid Response to Human Body Rotation

Author(s):  
Marie-Urlima Okeke ◽  
Sonya T. Smith ◽  
Werner Graf

A computational model was developed to study the response of vestibular fluid to body motions, relating eye movement to vestibular displacement. The response in the semicircular canals (SCCs) and otolith organs were approximated as a torsional pendulum and a forced wave equation, respectively. The results of the math model were found to be consistent with results found in previous models. The results of the model will also be compared to those found experimentally using VALUS, a rotational platform updated to be used for vestibular testing.

2018 ◽  
Vol 119 (1) ◽  
pp. 73-83 ◽  
Author(s):  
Shawn D. Newlands ◽  
Ben Abbatematteo ◽  
Min Wei ◽  
Laurel H. Carney ◽  
Hongge Luan

Roughly half of all vestibular nucleus neurons without eye movement sensitivity respond to both angular rotation and linear acceleration. Linear acceleration signals arise from otolith organs, and rotation signals arise from semicircular canals. In the vestibular nerve, these signals are carried by different afferents. Vestibular nucleus neurons represent the first point of convergence for these distinct sensory signals. This study systematically evaluated how rotational and translational signals interact in single neurons in the vestibular nuclei: multisensory integration at the first opportunity for convergence between these two independent vestibular sensory signals. Single-unit recordings were made from the vestibular nuclei of awake macaques during yaw rotation, translation in the horizontal plane, and combinations of rotation and translation at different frequencies. The overall response magnitude of the combined translation and rotation was generally less than the sum of the magnitudes in responses to the stimuli applied independently. However, we found that under conditions in which the peaks of the rotational and translational responses were coincident these signals were approximately additive. With presentation of rotation and translation at different frequencies, rotation was attenuated more than translation, regardless of which was at a higher frequency. These data suggest a nonlinear interaction between these two sensory modalities in the vestibular nuclei, in which coincident peak responses are proportionally stronger than other, off-peak interactions. These results are similar to those reported for other forms of multisensory integration, such as audio-visual integration in the superior colliculus. NEW & NOTEWORTHY This is the first study to systematically explore the interaction of rotational and translational signals in the vestibular nuclei through independent manipulation. The results of this study demonstrate nonlinear integration leading to maximum response amplitude when the timing and direction of peak rotational and translational responses are coincident.


1986 ◽  
Vol 56 (4) ◽  
pp. 1147-1156 ◽  
Author(s):  
R. H. Schor ◽  
I. Suzuki ◽  
S. J. Timerick ◽  
V. J. Wilson

The responses of interneurons in the cervical spinal cord of the decerebrate cat to whole-body tilt were studied with a goal of identifying spinal elements in the production of forelimb vestibular postural reflexes. Interneurons both in the cervical enlargement and at higher levels, from which propriospinal neurons have been identified, were examined, both in animals with intact labyrinths and in animals with nonfunctional semicircular canals (canal plugged). Most cervical interneurons responding to tilt respond best to rotations in vertical planes aligned within 30 degrees of the roll plane. Two to three times as many neurons are excited by side-up roll tilt as are excited by side-down roll. In cats with intact labyrinths, most responses have dynamics proportional either to (and in phase with) the position of the animal or to a sum of position and tilt velocity. This is consistent with input from both otolith organs and semicircular canals. In animals without functioning canals, the "velocity" response is absent. In a few cells (8 out of 76), a more complex response, characterized by an increasing gain and progressive phase lag, was observed. These response dynamics characterize the forelimb reflex in canal-plugged cats and have been previously observed in vestibular neurons in such preparations.


2016 ◽  
Vol 116 (4) ◽  
pp. 1586-1591 ◽  
Author(s):  
Joanne Wang ◽  
Richard F. Lewis

Migraine is associated with enhanced motion sickness susceptibility and can cause episodic vertigo [vestibular migraine (VM)], but the mechanisms relating migraine to these vestibular symptoms remain uncertain. We tested the hypothesis that the central integration of rotational cues (from the semicircular canals) and gravitational cues (from the otolith organs) is abnormal in migraine patients. A postrotational tilt paradigm generated a conflict between canal cues (which indicate the head is rotating) and otolith cues (which indicate the head is tilted and stationary), and eye movements were measured to quantify two behaviors that are thought to minimize this conflict: suppression and reorientation of the central angular velocity signal, evidenced by attenuation (“dumping”) of the vestibuloocular reflex and shifting of the rotational axis of the vestibuloocular reflex toward the earth vertical. We found that normal and migraine subjects, but not VM patients, displayed an inverse correlation between the extent of dumping and the size of the axis shift such that the net “conflict resolution” mediated through these two mechanisms approached an optimal value and that the residual sensory conflict in VM patients (but not migraine or normal subjects) correlated with motion sickness susceptibility. Our findings suggest that the brain normally controls the dynamic and spatial characteristics of central vestibular signals to minimize intravestibular sensory conflict and that this process is disrupted in VM, which may be responsible for the enhance motion intolerance and episodic vertigo that characterize this disorder.


2004 ◽  
Vol 96 (6) ◽  
pp. 2301-2316 ◽  
Author(s):  
Richard C. Fitzpatrick ◽  
Brian L. Day

Galvanic vestibular stimulation (GVS) is a simple, safe, and specific way to elicit vestibular reflexes. Yet, despite a long history, it has only recently found popularity as a research tool and is rarely used clinically. The obstacle to advancing and exploiting GVS is that we cannot interpret the evoked responses with certainty because we do not understand how the stimulus acts as an input to the system. This paper examines the electrophysiology and anatomy of the vestibular organs and the effects of GVS on human balance control and develops a model that explains the observed balance responses. These responses are large and highly organized over all body segments and adapt to postural and balance requirements. To achieve this, neurons in the vestibular nuclei receive convergent signals from all vestibular receptors and somatosensory and cortical inputs. GVS sway responses are affected by other sources of information about balance but can appear as the sum of otolithic and semicircular canal responses. Electrophysiological studies showing similar activation of primary afferents from the otolith organs and canals and their convergence in the vestibular nuclei support this. On the basis of the morphology of the cristae and the alignment of the semicircular canals in the skull, rotational vectors calculated for every mode of GVS agree with the observed sway. However, vector summation of signals from all utricular afferents does not explain the observed sway. Thus we propose the hypothesis that the otolithic component of the balance response originates from only the pars medialis of the utricular macula.


2019 ◽  
Author(s):  
Charlotte Héricé ◽  
Shuzo Sakata

AbstractSleep is a fundamental homeostatic process within the animal kingdom. Although various brain areas and cell types are involved in the regulation of the sleep-wake cycle, it is still unclear how different pathways between neural populations contribute to its regulation. Here we address this issue by investigating the behavior of a simplified network model upon synaptic weight manipulations. Our model consists of three neural populations connected by excitatory and inhibitory synapses. Activity in each population is described by a firing-rate model, which determines the state of the network. Namely wakefulness, rapid eye movement (REM) sleep or non-REM (NREM) sleep. By systematically manipulating the synaptic weight of every pathway, we show that even this simplified model exhibits non-trivial behaviors: for example, the wake-promoting population contributes not just to the induction and maintenance of wakefulness, but also to sleep induction. Although a recurrent excitatory connection of the REM-promoting population is essential for REM sleep genesis, this recurrent connection does not necessarily contribute to the maintenance of REM sleep. The duration of NREM sleep can be shortened or extended by changes in the synaptic strength of the pathways from the NREM-promoting population. In some cases, there is an optimal range of synaptic strengths that affect a particular state, implying that the amount of manipulations, not just direction (i.e., activation or inactivation), needs to be taken into account. These results demonstrate pathway-dependent regulation of sleep dynamics and highlight the importance of systems-level quantitative approaches for sleep-wake regulatory circuits.Author SummarySleep is essential and ubiquitous across animal species. Over the past half-century, various brain areas, cell types, neurotransmitters, and neuropeptides have been identified as part of a sleep-wake regulating circuitry in the brain. However, it is less explored how individual neural pathways contribute to the sleep-wake cycle. In the present study, we investigate the behavior of a computational model by altering the strength of connections between neuronal populations. This computational model is comprised of a simple network where three neuronal populations are connected together, and the activity of each population determines the current state of the model, that is, wakefulness, rapid-eye-movement (REM) sleep or non-REM (NREM) sleep. When we alter the connection strength of each pathway, we observe that the effect of such alterations on the sleep-wake cycle is highly pathway-dependent. Our results provide further insights into the mechanisms of sleep-wake regulation, and our computational approach can complement future biological experiments.


1996 ◽  
Vol 6 (5) ◽  
pp. 319-329 ◽  
Author(s):  
Izumi Koizuka ◽  
Robert H. Schor ◽  
Joseph M. Furman

1999 ◽  
Vol 9 (5) ◽  
pp. 347-357
Author(s):  
A. Tribukait

Measurements of the subjective visual horizontal (SVH) were performed in 11 healthy test persons during an increase of the resultant gravitoinertial force vector in a large swing-out gondola centrifuge. Three levels of hypergravity (1.5g, 2.0g, 2.5g) were used, each with a duration of 4 minutes and with 1–2 minute pauses at 1.0g in between. The direction of the resultant gravitoinertial force vector was always parallel with the head and body length axis. Hence, there was no roll stimulus to the otolith organs. The swing-out of the gondola during acceleration, however, is sensed by the vertical semicircular canals as a change in roll head position, thus creating an otolith-semicircular canal conflict. After acceleration of the centrifuge there was a tilt of the SVH relative to the resultant gravitoinertial horizontal. This tilt gradually decayed during the 4-minute period of recordings. For a subgroup of seven test subjects who had completely normal ENG-recordings in 1g environment, the initial offset of SVH and the time constants for exponential decay were determined for each g level; initial offsets: 9 . 9 ∘ (1.5g), 7 . 7 ∘ (2.0g), 6 . 1 ∘ (2.5g); time constants: 89s (1.5g), 74s (2.0g), 37s (2.5g). The offset of SVH is interpreted as being the result of mainly the stimulus to the vertical semicircular canals during acceleration of the centrifuge. The slow decay, however, does not correspond to the dynamics of the semicircular canal system, and is suggested to reflect some kind of central position storage mechanism. A smaller offset and more rapid decay for the higher g loads may be explained by an increasing dominance of graviceptive input, presumably from the saccules. In conclusion, these results might suggest the role of the vertical semicircular canals as well as the sacculus in the formation of SVH. They may also have relevance with regard to the spatial disorientation problem in aviators.


2002 ◽  
Vol 11 (6) ◽  
pp. 365-370 ◽  
Author(s):  
Joseph M. Furman ◽  
Mark S. Redfern

This study assessed visual-otolith interaction in healthy older humans and compared responses from older subjects to those of younger subjects. Using off-vertical axis rotation (OVAR) to stimulate the otolith organs, eye movement responses, measured using electro-oculography, were recorded during rotation in the dark, rotation with an earth-fixed lighted visual surround, and rotation with a subject-fixed fixation target. Results indicated that older subjects, like young subjects, exhibit a modulation component that was as large during rotation with a lighted earth-fixed visual surround as that seen in the dark and a modulation component during rotation with a subject-fixed visual target that was incompletely suppressed. The modulation component was, in general, larger in the older subjects. This study confirms findings from a previous study of visual-otolith interaction in young subjects and suggests that older subjects, like young subjects, have difficulty visually suppressing the modulation component induced by off-vertical axis rotation.


1973 ◽  
Vol 59 (2) ◽  
pp. 491-521
Author(s):  
CHRISTOPHER PLATT

1. Flatfish metamorphose from a larval form that swims upright like a standard fish to an adult that lies on one side, with both eyes on the upper side, having rotated posture 90° relative to gravity and the former normal posture. Adult Citharichthys stigmaeus and Hypsopsetta guttulata were used in behavioural and physiological experiments to determine whether the postural change is a peripheral or central phenomenon. 2. Cleared and sectioned specimens verify that the otolith organs, unlike the eyes, do not rotate within the skull, and so do not maintain the normal vertebrate orientation with respect to gravity. 3. Ocular compensation to lateral tilt shows that tactile cues, vision, and the semicircular canals are inadequate to produce tilt responses, but elimination of otolith function abolishes tilt responses. The major postural role of the otolith organs is not lost. 4. Selective removal of otoliths demonstrates that the flatfish utriculus has only a minor role in tilt responses, and that the sacculus-lagena is required, unlike the situation in other vertebrates. The details of the ocular compensation responses are similar to those of standard fishes. Each sacculus lies at an angle of up to 45° when in the normal position, but unilateral loss does not change the phase of the response curve, indicating that the null response is set for a non-zero value of gravitational shear, unlike the null at zero shear to the utriculus in other vertebrates. 5. Hysteresis effects suggest a differential sensitivity between tilts near the normal and the upside-down null positions. The narrowness of the effect argues against mechanical restrictions. Possibly the vertical utriculus is useful only near the normal, as an accessory organ, like the vertical lagena in other vertebrates. 6. Neural units recorded from both eighth nerve and medulla show the expected activity properties of regular and irregular rate, tonic and phasic responses to tilt, directional dependence and ‘multi-valuedness’, as in other vertebrates. No novel response types are found, nor any distinctive ‘into-level‘ types described for some vertebrates. Vibration sensitivity is associated with irregular rate, and exclusively vibration-sensitive units are apparent only in the utriculus. The shift in functional relations of the otolith organs relative to gravity is not apparently compensated for by any major change in peripheral afferent gravistatic unit properties. 7. An increasing distinction between the null at normal and the null upside-down shown by limited data on ocular compensation in three year-classes of flatfish. A central change in vestibular function is suggested that might be dependent on experience, as is gradual compensation to a vestibular lesion. 8. Since peripheral changes are not responsible for the postural change, alternative central mechanisms are proposed, including central weighting of input, recognition of a complex input pattern, and plasticity of connexions, all of which have received some supporting evidence from these results.


2002 ◽  
Vol 88 (4) ◽  
pp. 2104-2113 ◽  
Author(s):  
Sam Musallam ◽  
R. D. Tomlinson

Angular and translational accelerations excite the semicircular canals and otolith organs, respectively. While canal afferents approximately encode head angular velocity due to the biomechanical integration performed by the canals, otolith signals have been found to approximate head translational acceleration. Because central vestibular pathways require velocity and position signals for their operation, the question has been raised as to how the integration of the otolith signals is accomplished. We recorded responses from 62 vestibular-only neurons in the vestibular nucleus of two monkeys to position transients in the naso-occipital and interaural orientations and varying directions in between. Responses to the transients were directionally asymmetric; one direction elicited a response that approximated the integral of the acceleration of the stimulus. In the opposite direction, the cells simply encoded the acceleration of the motion. We present a model that suggests that a neural integrator is not needed. Instead a neuron with a long membrane time constant and an excitatory postsynaptic potential duration that increases with the firing rate of the presynaptic cell can emulate the observed behavior.


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