[THE CONTROL OF VESTIBULARLY EXCITABLE NEURONS OF THE BRAIN STEM BY ELECTROPHORETICALLY ADMINISTERED ACETYLCHOLINE].
Explore the source record for details and available documents.
Acetylcholine↗
SEARCH · Search PubMed
Results for “Vestibular Neuronitis”
Search indexed PubMed citations on genomics, clinical trials, systematic reviews and public health. Explore titles, authors and supplied subject terms, then open the PubMed record.
Quote a phrase for an exact phrase match. Source license links do not imply unrestricted reuse.
Unbiased number of vestibular ganglion neurons in the mouse.
Vestibular sensory information from the labyrinth and otolith organs is conducted to the central nervous system exclusively via primary vestibular afferents (PVA) originating from neurons located in the vestibular ganglion (VG). In the present study, the total number of VG neurons was determined in two different wild-type mouse strains using the principles of unbiased stereological counting methods by means of the physical disector. 3316 (+/-225 SD) neurons were present in the VG of the B6CBA-strain and 3551 (+/-239 SD) in C57BL/6J-mice. Since no statistical difference was detected between the two strains, the pooled mean number was 3433 (+/-232 SD) neurons. This is the first unbiased estimate of VG neurons aimed at providing a numerical basis for comparative studies and for the impact of experimental, pharmacological and pathological conditions as well as ageing on the survival and maintenance of VG neurons.
Animals↗
Immunocytochemical detection of vitamin D-dependent calcium-binding protein (CaBP-28K) in vestibular sensory hair cells and vestibular ganglion neurones of the cat.
Vestibular sensory hair cells, afferent fibres and vestibular ganglion neurones of the cat are intensely labelled by a specific antibody to rat kidney vitamin D-dependent calcium-binding protein (CaBP-28K). Type I hair cells are more weakly CaBP immunoreactive than type II hair cells. Ganglion neurones also present a differential staining. The presence of calcium-binding protein in sensory hair cells could be of interest for the understanding of transductional mechanisms.
Animals↗
Horizontal linear and angular responses of neurons in the medial vestibular nucleus of the decerebrate cat.
Responses to linear accelerations in the earth-horizontal plane (typically provoked by tilts of the head or body) are characterized by a stimulus direction that produces the maximal excitation. Although changes in cardiovascular, sympathetic, and respiratory outflow are maximized during pitch, no collection of central vestibular neurons had been identified where pitch responses predominate. In the present study, response properties of neurons in the medial vestibular nucleus were examined in decerebrate cats placed on a turntable. Activation of otolith afferents was provided by constant velocity rotation with the turntable axis tilted 5 degrees from the vertical. Responsive neurons exhibited a sinusoidal modulation in their firing rate; the optimal excitatory stimulus direction was derived from responses to clockwise and counterclockwise rotations. Many of these neurons were also tested for input from horizontal semicircular canals using 0.5 Hz sinusoidal rotation about an earth-vertical axis. Of 22 tilt-sensitive neurons in the medial vestibular nucleus whose optimal stimulus direction was determined, 9 were best stimulated by pitch, 10 by stimuli in one of the two vertical semicircular canal planes, and 3 by roll. Of the 33 neurons in this nucleus tested for possible convergent inputs from the otolith organs and the horizontal semicircular canals, 8 responded to both the constant velocity (otolith) stimulus and to the sinusoidal rotation, 7 appeared to receive otolith, but not horizontal canal, input, while 18 had a canal, but no otolith, response. Thus, besides serving as a relay for horizontal canal signals, the medial vestibular nucleus may also be an important relay for information about orientation within the sagittal (pitch) plane.
Acceleration↗
Firing behaviour of squirrel monkey eye movement-related vestibular nucleus neurons during gaze saccades.
The firing behaviour of vestibular nucleus neurons putatively involved in producing the vestibulo-ocular reflex (VOR) was studied during active and passive head movements in squirrel monkeys. Single unit recordings were obtained from 14 position-vestibular (PV) neurons, 30 position-vestibular-pause (PVP) neurons and 9 eye-head-vestibular (EHV) neurons. Neurons were sub-classified as type I or II based on whether they were excited or inhibited during ipsilateral head rotation. Different classes of cell exhibited distinctive responses during active head movements produced during and after gaze saccades. Type I PV cells were nearly as sensitive to active head movements as they were to passive head movements during saccades. Type II PV neurons were insensitive to active head movements both during and after gaze saccades. PVP and EHV neurons were insensitive to active head movements during saccadic gaze shifts, and exhibited asymmetric sensitivity to active head movements following the gaze shift. PVP neurons were less sensitive to on-direction head movements during the VOR after gaze saccades, while EHV neurons exhibited an enhanced sensitivity to head movements in their on direction. Vestibular signals related to the passive head movement were faithfully encoded by vestibular nucleus neurons. We conclude that central VOR pathway neurons are differentially sensitive to active and passive head movements both during and after gaze saccades due primarily to an input related to head movement motor commands. The convergence of motor and sensory reafferent inputs on VOR pathways provides a mechanism for separate control of eye and head movements during and after saccadic gaze shifts.
Animals↗
Response of guinea pig vestibular nucleus neurons to clicks.
Responses of single neurons in the vestibular nuclei to clicks were studied by extracellular recording in anaesthetised guinea pigs. Eighty-four neurons in the ipsilateral vestibular nuclei were activated with an average latency of 1.75 +/- 0.30 ms, which is about 0.9 ms longer than the mean latency of activation of click-sensitive vestibular afferents to intense clicks. The threshold of clicks for evoking the response of these neurons was around 70 dB above the auditory brainstem response threshold. Earlier studies have indicated that click-sensitive vestibular afferents are tilt-sensitive and likely to originate from saccular receptors, and in the present study nine of the click-sensitive vestibular nucleus neurons were tilt-sensitive, suggesting that these central neurons receive monosynaptic input from the corresponding saccular afferents. Recording sites were marked by means of iontophoretic injection of FCF green dye; they were located in the lateral portion of the descending vestibular nucleus and the caudal and ventral regions of the lateral vestibular nucleus.
Acoustic Stimulation↗
Nonlinear characteristics of single neurons in the vestibular nuclei.
The characteristics of response of 99 vestibular nuclei neurons were investigated in the cat anesthetized with pentobarbital sodium. All neurons responded to stimulation of the horizontal semicircular canals (HSCC) with prolonged 2, 4, 6, or 8 degrees/second2 angular acceleration. Neural response was recorded utilizing the single-neuron recording technique. The vestibular neurons responded nonlinearly to stimulation of the HSCC. Specifically (1) the time required to reach the maximum response level decreased nonlinearly with an increase in stimulus magnitude (SM); (2) the maximum response level increased nonlinearly with the increase in SM: (3) the neural response to excitatory stimulus was not the mirror image of that to an inhibitory stimulus. Several existing mathematical models were simulated by utilization of the IBM Continuous System Modeling Program, account for the nonlinear response of the vestibular nuclei neurons. The nonlinearities observed in the responses may be due to (1) nonlinear behavior of the end organ, (2) the influence of the CNS including the vestibular efferent system, or (3) the inherent neural properties of the vestibular nuclei.
Acceleration↗
Quantitative study of the coexpression of Fos and N-methyl-D aspartate (NMDA) receptor subunits in otolith-related vestibular nuclear neurons of rats.
The expression of NMDA receptor subunits (NR1 and NR2A/B) was demonstrated immunocytochemically in otolith-related neurons within the vestibular nuclear complex and its subnuclei of conscious Sprague-Dawley adult rats. All experimental animals were subjected to constant velocity off-vertical axis rotation (OVAR). The rotating gravity vector during OVAR sequentially activates hair cells on all sectors of the utricular maculae; neurons so activated within the vestibular nuclei were denoted by the expression of Fos protein. Control animals, i.e., labyrinthectomized rats subjected to OVAR and normal rats that remained stationary, showed only a few sporadically scattered labeled neurons. In the brainstem of normal rats subjected to OVAR, a high density of Fos-immunoreactive (Fos-ir) neurons was found in the vestibular nuclear complex (namely, spinal vestibular nucleus, SpVe; medial vestibular nucleus, Mve; superior vestibular nucleus, SuVe) and subnuclei (namely, group x and group y), whereas a lower density was found in the lateral vestibular nucleus (LVe). A double-immunofluorescence study indicated that both NR1 and NR2A/B subunits were highly expressed in Fos-ir neurons within the vestibular nuclei. Fos/NR1 or Fos/NR2A/B double-labeled neurons constitute over three-quarters of the total number of Fos-ir neurons in SpVe, MVe, LVe, SuVe, and groups x and y. Our findings suggest that NMDA-type ionotropic glutamate receptors play a key role in the OVAR-induced neuronal activation of the vestibular nuclei, thus providing a morphological basis for further study of glutamatergic central otolith neurons and their involvement in sensorimotor regulation and autonomic functions of rats.
Animals↗
Responses of neurons of lizard's, Lacerta viridis, vestibular nuclei to electrical stimulation of the ipsi- and contralateral VIIIth nerves.
Field and intracellular potentials were recorded in the vestibular nuclei of the lizard following stimulation of the ipsi- and contralateral vestibular nerves. The field potentials induced by ipsilateral VIIIth nerve stimulation consisted of an early negative or positive-negative wave (presynaptic component) followed by a slow negativity (transsynaptic component). The spatial distribution of the field potential complex closely paralleled the extension of the vestibular nuclei. Mono- and polysynaptic EPSPs were recorded from vestibular neurons after ipsilateral VIIIth nerve stimulation. In some neurons early depolarizations preceded the EPSPs. These potentials may be elicited by electrical transmission. Often spikelike partial responses were superimposed on the EPSPs. It is assumed that these potentials represent dendritic spikes. Contralateral VIIIth nerve stimulation generated disynaptic and polysynaptic IPSPs in some neurons and EPSPs in others. The possible role of commissural inhibition in phylogeny is discussed. In a group of vestibular neurons stimulation of the ipsilateral VIIIth nerve evoked full action potentials with latencies ranging from 0.25-1.1msec. These potentials are caused by antidromic activation of neurons which send their axons to the labyrinth.
Action Potentials↗
Signal processing by vestibular nuclei neurons is dependent on the current behavioral goal.
The vestibular sensory apparatus and associated vestibular nuclei are generally thought to encode angular head velocity during our daily activities. However, in addition to direct inputs from vestibular afferents, the vestibular nuclei receive substantial projections from cortical, cerebellar, and other brainstem structures. Given this diversity of inputs, the question arises: How are the responses of vestibular nuclei neurons to head velocity modified by these additional inputs during naturally occurring behaviors? Here we have focused on the signal processing done by two specific classes of neurons in the vestibular nuclei: (1) position-vestibular-pause (PVP) neurons that mediate the vestibulo-ocular reflex (VOR), and (2) vestibular-only (VO) neurons that are thought to mediate, at least in part, the vestibulo-collic reflex (VCR). We first characterized neuronal responses to passive rotation in the head-restrained condition, and then released the head to record the discharges of the same neurons during self-generated head movements. VOR interneurons (i.e., PVP neurons) faithfully transmitted head velocity signals when the animal stabilized its gaze, regardless of whether the head motion was actively or passively generated; their responses were attenuated only when the monkey's behavioral goal was to redirect its axis of gaze relative to space. In contrast, VCR interneurons (i.e., VO neurons) faithfully transmitted head velocity signals during passive head motion, but their responses were greatly (and similarly) attenuated during all behaviors (i.e., gaze shifts, gaze pursuit, gaze stabilization) during which the monkey's behavioral goal was to move its head relative to the body. To characterize the mechanism(s) that underlie this differential processing, we tested neurons during passive rotation of the head relative to the body, as well as during a task in which a monkey actively "drove" both its head and body together in space. We conclude that neither passive activation of neck proprioceptors nor knowledge of self-generated head-in-space motion directly mediate the observed reductions in head-velocity-related modulation. Instead, we propose that the VOR and VCR pathways use efference copies of oculomotor and neck movement commands, respectively, for the differential processing of vestibular information.
Action Potentials↗
Spontaneous synaptic activity in chick vestibular nucleus neurons during the perinatal period.
The principal cells of the chick tangential nucleus are second-order vestibular neurons involved in the vestibuloocular and vestibulocollic reflexes. The spontaneous synaptic activity of morphologically identified principal cells was characterized in brain slices from 1-day-old hatchlings (H1) using whole-cell voltage-clamp recordings and Cs-gluconate pipet solution. The frequency was 1.45 Hz for spontaneous excitatory postsynaptic currents (sEPSCs) and 1.47 Hz for spontaneous inhibitory postsynaptic currents (sIPSCs). Using specific neurotransmitter receptor antagonists, all of the sEPSCs were identified as AMPA receptor-mediated events, whereas 56% of the sIPSCs were glycine and 44% were GABA(A) receptor-mediated events. On exposure to TTX, the frequency of EPSCs decreased by 68%, while the frequency of IPSCs decreased by 33%, indicating greater EPSC dependency on presynaptic action potentials. These data on spontaneous synaptic activity at H1 were compared with those obtained in previous studies of 16-day old embryos (E16). After birth, the spontaneous synaptic activity exhibited increased EPSC frequency, increased ratio for excitatory to inhibitory events, increased percentage of TTX-dependent EPSCs, and faster kinetics. In addition, the ratio for glycine/GABA receptor-mediated events increased significantly. Altogether, these data indicate that at hatching spontaneous synaptic activity of vestibular nucleus neurons in brain slices of the chick tangential nucleus undergoes appreciable changes, with increased frequency of EPSCs and glycinergic activity playing more important roles compared with the late-term chick embryo when GABAergic activity prevailed. The definition of this developmental pattern of synaptic activity in vestibular nucleus neurons should contribute to understanding how vestibular reflex activity is established in the hatchling chick.
Afferent Pathways↗
Responses of vestibular nucleus neurons to tilt following chronic bilateral removal of vestibular inputs.
Recordings were made from the vestibular nuclei of decerebrate cats that had undergone a combined bilateral labyrinthectomy and vestibular neurectomy 49-103 days previously and allowed to recover. Responses of neurons were recorded to tilts in multiple vertical planes at frequencies ranging from 0.05 to 1 Hz and amplitudes up to 15 degrees. Many spontaneously active neurons were present in the vestibular nuclei; the mean firing rate of these cells was 43 +/- 5 (SEM) spikes/s. The spontaneous firing of the neurons was irregular: the coefficient of variation was 0.86 +/- 0.14. The firing of 27% of the neurons was modulated by tilt. The plane of tilt that elicited the maximal response was typically within 25 degrees of pitch. The response gain was approximately 1 spikes/s/degree across stimulus frequencies. The response phase was near stimulus position at low frequencies, and lagged position slightly at higher frequencies (average of 35 +/- 9 degrees at 0.5 Hz). The source of the inputs eliciting modulation of vestibular nucleus activity during tilt in animals lacking vestibular inputs is unknown, but could include receptors in the trunk or limbs. These findings show that activation of vestibular nucleus neurons during vertical rotations is not exclusively the result of labyrinthine inputs, and suggest that limb and trunk inputs may play an important role in graviception and modulating vestibular-elicited reflexes.
Animals↗
In vitro electrophysiological study of spontaneous activity in neonatal mouse vestibular ganglion neurons during development.
Spontaneous discharges from vestibular ganglion neurons have been studied in mice between 0 and 10 days in freshly isolated in vitro preparations. The vestibular ganglion neurons were electrophysiologically active at birth with irregular activities. From the 3rd day. the activities could be divided into irregular and regular discharging units based on the coefficient of variation of their interspike intervals. This study provides two criteria for maturation of vestibular activities: a decreasing number of irregular units with age and an increase of the spontaneous discharge frequencies.
Action Potentials↗
Static and dynamic membrane properties of lateral vestibular nucleus neurons in guinea pig brain stem slices.
In vitro intracellular recordings of central vestibular neurons have been restricted so far to the medial vestibular nucleus (MVN). We performed intracellular recordings of large Deiters' neurons in the lateral vestibular nucleus (LVN) to determine their static and dynamic membrane properties, and compare them with those of type A and type B neurons identified in the MVN. Unlike MVN neurons (MVNn), the giant-size LVN neurons (LVNn) form a homogeneous population of cells characterized by sharp spikes, a low-amplitude, biphasic after-hyperpolarization like type B MVNn, but also an A-like rectification like type A MVNn. In accordance with their lower membrane resistance, the sensitivity of LVNn to current injection was lower than that of MVNn over a large range of frequencies. The main difference between LVNn and MVNn was that the Bode plots showing the sensitivity of LVNn as a function of stimulation frequency were flatter than those of MVNn, and displayed a weaker resonance. Furthermore, most LVNn did not show a gradual decrease of their firing rate modulation in the frequency range where it was observed in MVNn. LVNn synchronized their firing with the depolarizing phase of high-frequency sinusoidal current injections. In vivo studies have shown that the MVN would be mainly involved in gaze control, whereas the giant LVNn that project to the spinal cord are involved in the control of posture. We suggest that the difference in the membrane properties of LVNn and MVNn may reflect their specific physiological roles.
Action Potentials↗
Effects of the neurosteroid dehydroepiandrosterone sulfate on medial vestibular nucleus neurons.
Neurosteroids increase in concentration under conditions of stress and produce behavioral effects. An electrophysiological investigation was undertaken to determine whether dehydroepiandrosterone sulfate (DHEAS), a neurosteroid, influences the neuronal activity of medial vestibular nucleus (MVN) neurons in alpha-chloralose-anesthetized cats. Single neuronal activities in MVN were recorded extracellularly using a glass-insulated silver wire microelectrode attached along a seven-barreled micropipette. Each pipette was filled with DHEAS, GABA, muscimol (a GABA[A] receptor agonist) and baclofen (a GABA[B] receptor agonist), which were applied microiontophoretically to the immediate vicinity of the target neurons. The effects of these chemicals were examined on type I neurons. identified by responses to horizontal and sinusoidal rotations. Microiontophoretic application of DHEAS did not affect the spontaneous and rotation-induced firings of type I neurons, but dose-dependently blocked GABA-induced inhibitory effects on type I neurons. In addition, both muscimol- and baclofen-induced inhibitions of firing were blocked by DHEAS. These results suggest that DHEAS suppresses GABAergic inhibitory effects on MVN neurons through both GABA(A) and GABA(B) receptors, presumably resulting in disturbance of control of neuronal activity in the vestibular nucleus and consequent development of vertigo.
Animals↗
Discharge characteristics of vestibular saccade neurons in alert monkeys.
We previously described a class of neurons, located in and around the interstitial nucleus of Cajal of the cat, that discharged during vestibular stimulation and before saccades. We called these neurons vestibular saccade neurons (VSNs). In the present study, we characterized similar neurons in the monkey. These neurons discharged before vertical saccades and during vertical vestibular stimulation as well as vertical smooth pursuit. Like cat VSNs, the discharge metrics of these VSNs were poorly related to saccade metrics and showed only occasional, weak sensitivity to eye position. They discharged most intensely (on-direction) for movements that were either upward or downward, and their on-directions were consistent during pitch and pursuit but not for eye position. For saccades, the correlation coefficient of number of spikes and vertical saccade size varied from 0.08 to 0.90 with a mean of approximately 0.6. The average sensitivity (i.e., slope) of the number of spikes and vertical saccade size linear regression was 0.3 +/- 0.2 spike/deg. Average correlations between peak discharge rate and peak saccade velocity and between burst duration and saccade duration were 0.5 and 0.4; sensitivities were 0.2 +/- 0.2 spike per s per deg/s and 0.6 +/- 0.5 ms/ms, respectively. Average vestibular sensitivities during 0.5 Hz, +/-10 degrees sinusoidal pitch while the animals suppressed their vestibular ocular reflex were 0.97 spike/s per deg/s for up VSNs and 0.66 spike/s per deg/s for down VSNs. The average static position sensitivity for the population of 39 VSNs tested was 0.55 spike/s per deg. The average gain for VSNs tested during 0.5 Hz, +/-10 degrees sinusoidal smooth pursuit tracking was 1.4 spike/s per deg/s. As we could not identify analogous neurons in the region of the monkey ponto-medullary junction, we conclude that horizontal on-direction VSNs do not exist in the monkey. We discuss a possible functional role for VSNs and similar neurons described in previous studies and conclude that these neurons are most likely involved with the process of neural integration (in a mathematical sense) of velocity-coded inputs from a variety of oculomotor subsystems and are not a pivotal element in saccade generation.
Action Potentials↗
Localization and responses of neurones in the parieto-insular vestibular cortex of awake monkeys (Macaca fascicularis).
1. In four Java monkeys (Macaca fascicularis) 152 vestibular neurones were recorded in the parietal cortex located in the upper bank of the lateral sulcus near the posterior end of the insula. We called this region parieto-insular vestibular cortex (PIVC). PIVC extends about 6-8 mm in the anterior-posterior direction from the posterior part of the insula into the retroinsular region (stereotaxic co-ordinates: anterior 4-12 mm, lateral 16-19 mm and vertical 3-6 mm). 2. About two-thirds of the neurones recorded from this region responded to vestibular stimuli; the non-vestibular neurones responded predominantly to somatosensory stimulation of the neck and shoulder region. The PIVC area is a polysensory field, since almost all vestibular neurones were also activated by somatosensory and visual stimuli. Large-field optokinetic stimulation was the most effective visual stimulus. 3. With vestibular stimuli, responses to angular acceleration were dominant; steady tilt in darkness rarely led to any change in neuronal spontaneous activity. Of sixty-four neurones tested by rotation in more than one plane, fifty-four responded to excitation of semicircular canal receptors aroused by rotation in more than one of the three experimental planes (roll, yaw, pitch). Compared with vestibular brain stem units PIVC neurones discharged with a higher variability. 4. In the responses to horizontal rotation of the animal 38% type I, 53% type II and 9% type III units were recorded (classification according to Duensing & Schaefer, 1958). The gain measured with horizontal sinewave rotation was lower by a factor of about 4 in PIVC neurones as compared with the responses of vestibular neurones in the brain stem or thalamus (VPL). The phase response characteristics and the gain increase with increasing sinewave stimulus frequency, however, were in the same range as observed in neurones of the afferent vestibular system. 5. When the vestibular responses to sinusoidal rotation were tested in all three experimental planes (yaw, roll, pitch), the response strength as expressed by the amplitude of the peristimulus time histograms (PSTHs) differed for the three rotational planes. For different units the relative sensitivity to rotation in each of the three planes also differed. We concluded from this observation that different PIVC units had different optimum sensitivity planes for rotation with respect to the head co-ordinates, whereby all possible planes are represented.
Animals↗
Heterogeneous potassium conductances contribute to the diverse firing properties of postnatal mouse vestibular ganglion neurons.
How mechanical information is encoded in the vestibular periphery has not been clarified. To begin to address the issue we examined the intrinsic firing properties of postnatal mouse vestibular ganglion neurons using the whole cell, tight-seal technique in current-clamp mode. We categorized two populations of neurons based on the threshold required to evoke an action potential. Low-threshold neurons fired with an average minimum current injection of -43 pA, whereas high-threshold neurons required -176 pA. Using sine-wave stimuli, we found that the neurons were inherently tuned with best frequencies that ranged up to 40 Hz. To investigate the membrane properties that contributed to the variability in firing properties we examined the same neurons in voltage-clamp mode. High-threshold neurons had larger cell bodies and whole cell capacitances but a resting conductance density of 0.18 nS/pF, nearly identical to that of low-threshold neurons, suggesting that cell size was an important parameter determining threshold. We also found that vestibular ganglion neurons expressed a heterogeneous population of potassium conductances. TEA-sensitive conductances contributed to the position of the tuning curve in the frequency domain. A 4-AP-sensitive conductance was active at rest and hyperpolarized resting potential, limited spontaneous activity, raised threshold, and prevented repetitive firing. In response to sine-wave stimulation 4-AP-sensitive conductances prevented action potential generation at low frequencies and thus contributed to the high-pass corner of the tuning curve. The mean low-pass corner (about 29 Hz) was determined by the membrane time constant. Together these factors contributed to the sharply tuned, band-pass characteristics intrinsic to postnatal vestibular ganglion neurons.
4-Aminopyridine↗