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PubMed2000

Neck proprioceptive inputs to primate vestibular nucleus neurons.

The contribution of neck proprioceptive signals to signal processing in the vestibular nucleus was studied by recording responses of secondary horizontal canal-related neurons to neck rotation in the squirrel monkey. Responses evoked by passive neck rotation while the head was held stationary in space were compared with responses evoked by passive whole body rotation and by forced rotation of the head on the trunk. Most neurons (76%; 45/59) were sensitive to neck rotation. The nature and strength of neck proprioceptive inputs varied and usually combined linearly with vestibular inputs. In most cases (94%), the direction of the neck proprioceptive input was "antagonistic" or "reciprocal" with respect to vestibular sensitivity and, consequently, reduced the vestibular response during head-on-trunk rotation. Different types of vestibular neurons received different types of proprioceptive input. Neurons whose firing behavior was related to eye position (position-vestibular-pause neurons and position-vestibular neurons) were often sensitive to the position of the head with respect to the trunk. The sensitivity to head position was usually in the same direction as the neuron's eye position sensitivity. Non-eye-movement related neurons and eye-head-velocity neurons exhibited the strongest sensitivity to passive neck rotation and had signals that were best related to neck velocity. The results suggest that neck proprioceptive inputs play an important role in shaping the output of the primate vestibular nucleus and its contribution to posture, gaze and perception.

Animals↗
PubMed1991

Inhibition of lateral vestibular nucleus neurons by 5-hydroxytryptamine derived from the dorsal raphe nucleus.

Electrophysiological studies were performed to elucidate the effect of 5-hydroxytryptamine (5-HT) originating in the dorsal raphe nucleus (DR) on neuronal activity in the lateral vestibular nucleus (LVN) neurons, using cats anesthetized with alpha-chloralose. LVN neurons were classified into monosynaptic and polysynaptic neurons according to their responses to vestibular nerve stimulation. Conditioning stimuli applied to the DR inhibited orthodromic spikes elicited by vestibular nerve stimulation predominantly in polysynaptic neurons of the LVN. The iontophoretic application of 5-HT also inhibited orthodromic spikes of the LVN neurons. A close correlation was observed between the effects of DR conditioning stimulation and iontophoretically applied 5-HT in the same neurons. These inhibitions with both treatments were antagonized during the application of methysergide, a 5-HT antagonist. In the majority of LVN polysynaptic neurons that responded to antidromic stimulation of the ipsilateral or contralateral abducens nucleus, orthodromic spikes elicited by vestibular nerve stimulation were inhibited by DR conditioning stimulation and the iontophoretic application of 5-HT. In contrast, LVN neurons that responded to antidromic stimulation of the vestibulospinal tract were rarely affected by these treatments. These results indicate that 5-HT derived from the DR inhibits the synaptic transmission of LVN polysynaptic neurons ascending to the abducens nucleus, and suggest that 5-HT derived from the DR is involved in the regulation of the vestibulo-ocular reflex.

Abducens Nerve↗
PubMed2000

Convergence of posterior semicircular canal and saccular inputs in single vestibular nuclei neurons in cats.

Convergence between posterior canal (PC) and saccular (SAC) inputs in single vestibular nuclei neurons was investigated in decerebrated cats. Postsynaptic potentials were recorded intracellularly after selective stimulation of the SAC and PC nerves. Stimulation of either the SAC or PC nerve orthodromically activated 143 vestibular nuclei neurons. Of these, 61 (43%) were antidromically activated by stimulation of the C1-C2 junction, 14 (10%) were antidromically activated by stimulation of the oculomotor or trochlear nucleus, and 14 (10%) were antidromically activated by stimulation of both the oculomotor or trochlear nucleus and the spinal cord. Fifty-four (38%) neurons were not activated by stimulation of either or both. We named these neurons vestibulospinal (VS), vestibulo-ocular (VO), vestibulooculo-spinal (VOS) and vestibular (V) neurons, respectively. Both PC and SAC inputs converged in 47 vestibular nuclei neurons (26 VS, 2 VO, 6 VOS and 13 V neurons). Of these, 19 received monosynaptic excitatory inputs from both nerves. This input pattern was frequently seen in VS neurons. Approximately half of the convergent VS neurons descended to the spinal cord through the lateral vestibulospinal tract. The remaining half and all the convergent VOS neurons descended to the spinal cord through the medial vestibulospinal tract. Most of the convergent neurons were located in the lateral nucleus or descending nucleus.

Animals↗
PubMed2002

Convergence of limb, visceral, and vertical semicircular canal or otolith inputs onto vestibular nucleus neurons.

The major goal of this study was to determine the patterns of convergence of non-labyrinthine inputs from the limbs and viscera onto vestibular nucleus neurons receiving signals from vertical semicircular canals or otolith organs. A secondary aim was to ascertain whether the effects of non-labyrinthine inputs on the activity of vestibular nucleus neurons is affected by bilateral peripheral vestibular lesions. The majority (72%) of vestibular nucleus neurons in labyrinth-intact animals whose firing was modulated by vertical rotations responded to electrical stimulation of limb and/or visceral nerves. The activity of even more vestibular nucleus neurons (93%) was affected by limb or visceral nerve stimulation in chronically labyrinthectomized preparations. Some neurons received non-labyrinthine inputs from a variety of peripheral sources, including antagonist muscles acting at the same joint, whereas others received inputs from more limited sources. There was no apparent relationship between the spatial and dynamic properties of a neuron's responses to tilts in vertical planes and the non-labyrinthine inputs that it received. These data suggest that non-labyrinthine inputs elicited during movement will modulate the processing of information by the central vestibular system, and may contribute to the recovery of spontaneous activity of vestibular nucleus neurons following peripheral vestibular lesions. Furthermore, some vestibular nucleus neurons with non-labyrinthine inputs may be activated only during particular behaviors that elicit a specific combination of limb and visceral inputs.

Animals↗
PubMed1979

Mechanisms of compensation for vestibular deficits in the frog. I. Modification of the excitatory commissural system.

In hemilabyrinthectomized frogs excitatory responses of central vestibular neurons to electrical stimulation of the remaining vestibular nerve were recorded extra- and intracellulary at different stages (0, 3, and 60 days) after the operation. The output pattern of ipsilateral vestibular neurons sending an axon across the midline via the vestibular commissure to the deafferented nucleus did not change postoperatively. The synaptic efficacy of these commissural axons ending on partially deafferented vestibular neurons on the lesioned side increased with time. This enhanced synaptic potency was associated with a shortening in time to peak and duration and an increase in amplitude of the evoked EPSPs. As a result most vestibular neurons were readily excited by single shock stimulation of the contralateral vestibular nerve, a finding which was rarely observed in control animals. These plastic changes are explained by the assumption of reactive synaptogenesis. The consequences of this modification for the readjustment of static and dynamic vestibular reflexes are discussed.

Afferent Pathways↗
PubMed2001

Intrinsic excitability changes in vestibular nucleus neurons after unilateral deafferentation.

Two synergistic plastic mechanisms have recently been identified in rat medial vestibular nucleus (MVN) neurons during 'vestibular compensation', the behavioral recovery that follows damage to the vestibular receptors or nerve of one inner ear. Ipsi-lesional MVN neurons develop a significant increase in their intrinsic excitability, and a marked decrease in the functional efficacy of GABA(A) and GABA(B) receptors, within 4 h of unilateral vestibular deafferentation. These mechanisms presumably counteract the disfacilitation and excessive commissural inhibition of the ipsi-lesional cells after deafferentation, and thus promote the recovery of resting activity. In this study, we investigated the intrinsic membrane properties and spike firing characteristics of rostral ipsi-lesional MVN neurons in slices from animals that underwent vestibular compensation for either 24-72 h or 7-10 days. Significant changes were observed in the spontaneous in vitro discharge rate, resting membrane potentials and voltage-activated membrane conductances of type B cells, but not type A cells. There was a significant increase in the number of type B(LTS) cells compared to normal. These findings indicate that during vestibular compensation marked changes occur in ion channel expression and function selectively in type B MVN neurons. These changes are appropriate to increase the responsiveness of type B cells both to their own intrinsic pacemaker-like membrane conductances and excitatory synaptic inputs. Together with the downregulation of inhibitory receptor efficacy, this increased intrinsic excitability may be sufficient to restore the resting discharge of the deafferented neurons in vivo. These results therefore provide further evidence for synaptic and neuronal plasticity in ipsi-lesional MVN neurons during vestibular compensation.

Action Potentials↗
PubMed1991

Ultrastructure of cat superior vestibular commissural neurons.

The ultrastructure of the feline superior vestibular commissural neurons (CNs) was studied after labeling by contralateral injection of horseradish peroxidase. These small spindle-shaped cells are found in clusters oriented in a rostrocaudal, dorsoventral or lateromedial direction. The CNs have a cleft nucleus, with the majority of nerve terminals contacting the CN near the emergence of polar dendrites. Polarization of the afferent synaptic profiles suggests a bidirectional nature of inputs to CNs by the vestibular nerve, contralateral CNs, and/or cerebellar systems. One type of labeled cell does not conform to this pattern, instead resembling a vestibulo-ocular neuron. Hence, it may function as a commissural and a vestibulo-ocular neuron. Characterization of different types of synapses, based on the size and eccentricity of their synaptic vesicles, indicates a continuum rather than separate populations. Volume fraction of intracellular organelles showed a larger volume fraction percent of polyribosomes in larger cells. Since this organelle is involved with protein synthesis, this finding may indicate that larger CNs have a more extensive dendritic tree.

Adaptation, Physiological↗
PubMed1995

Vestibular responses of flocculus and vestibular nuclei neurons in mice (B6CBA). Variation of stimulus amplitude and frequency.

Vestibular nuclei (Vn) neurons and floccular Purkinje (P) cells of unanesthetized paralyzed mice (B6CBA) responding to horizontal angular acceleration in the dark (type I and type II neurons) were studied by extracellular recordings with micropipettes while varying either the frequency (and velocity) or the amplitude (and velocity) of the sinusoidal rotation, keeping the respective third parameter constant. Phase and sensitivity were analyzed by a Fourier analysis and a "best sine fitting" program. Recording sites were localized by means of small iontophoretically applied horseradish peroxidase markings. The neuronal response amplitude at fundamental frequency (determined from peristimulus time histograms) increased with the frequency and amplitude of the sinusoidal rotation for both Vn and floccular neurons (0.05-0.5 Hz; +/- 60 degrees amplitude). Stimulus frequency/response amplitude and stimulus amplitude/response amplitude curves of floccular neurons were distinctly lower in magnitude than those of Vn neurons (P < 0.01) Accordingly, the sensitivity (re velocity) curves of Vn neurons and P cells differed in magnitude significantly (decreasing slightly with increasing stimulus frequency and amplitude in Vn neurons and more or less independent of stimulus parameters in floccular P cells). Response amplitudes of type I and type II neurons did not differ from each other. Phase advance relative to head angular velocity in the midfrequency range in Vn neurons was very small, indicating a head velocity signal carried by the Vn neurons. In floccular P cells phase advance was only small at 0.1 Hz (amplitude +/- 35 degrees), but increased with augmenting frequency to 140 degrees at 0.5 Hz. With a constant stimulus frequency (0.3 Hz) and varied stimulus amplitude, phase advance was 90 degrees at +/- 20 degrees amplitude and 60 degrees amplitude. Data are shown for the first time in which both the stimulus frequency and the stimulus amplitude have been varied in the same species and in the same neurons. The results demonstrate that the single data are in general well within the range of those found in other species, but they demonstrate further that phase behavior is dependent on the stimulus paradigm. The data provide the basis for comparative studies with mutant mice.

Animals↗
PubMed1997

Three-dimensional analysis of vestibular efferent neurons innervating semicircular canals of the gerbil.

Anterograde labeling techniques were used to examine peripheral innervation patterns of vestibular efferent neurons in the crista ampullares of the gerbil. Vestibular efferent neurons were labeled by extracellular injections of biocytin or biotinylated dextran amine into the contralateral or ipsilateral dorsal subgroup of efferent cell bodies (group e) located dorsolateral to the facial nerve genu. Anterogradely labeled efferent terminal field varicosities consist mainly of boutons en passant with fewer of the terminal type. The bouton swellings are located predominately in apposition to the basolateral borders of the afferent calyces and type II hair cells, but several boutons were identified close to the hair cell apical border on both types. Three-dimensional reconstruction and morphological analysis of the terminal fields from these cells located in the sensory neuroepithelium of the anterior, horizontal, and posterior cristae were performed. We show that efferent neurons densely innervate each end organ in widespread terminal fields. Subepithelial bifurcations of parent axons were minimal, with extensive collateralization occurring after the axons penetrated the basement membrane of the neuroepithelium. Axonal branching ranged between the 6th and 27th orders and terminal field collecting area far exceeds that of the peripheral terminals of primary afferent neurons. The terminal fields of the efferent neurons display three morphologically heterogeneous types: central, peripheral, and planum. All cell types possess terminal fields displaying a high degree of anisotropy with orientations typically parallel to or within +/-45 degrees of the longitudinal axis if the crista. Terminal fields of the central and planum zones predominately project medially toward the transverse axis from the more laterally located penetration of the basement membrane by the parent axon. Peripheral zone terminal fields extend predominately toward the planum semilunatum. The innervation areas of efferent terminal fields display a trend from smallest to largest for the central, peripheral, and planum types, respectively. Neurons that innervate the central zone of the crista do not extend into the peripheral or planum regions. Conversely, those neurons with terminal fields in the peripheral or planum regions do not innervate the central zone of the sensory neuroepithelium. The central zone of the crista is innervated preferentially by efferent neurons with cell bodies located in the ipsilateral group e. The peripheral and planum zones of the crista are innervated preferentially by efferent neurons with cell bodies located in the contralateral group e. A model incorporating our anatomic observations is presented describing an ipsilateral closed-loop feedback between ipsilateral efferent neurons and the periphery and an open-loop feed-forward innervation from contralateral efferent neurons. A possible role for the vestibular efferent neurons in the modulation of semicircular canal afferent response dynamics is proposed.

Animals↗
PubMed1989

Neural correlates of horizontal vestibulo-ocular reflex cancellation during rapid eye movements in the cat.

1. The aim of the present study is to describe the behaviour of identified second-order vestibular neurones in the alert cat during eye saccades. A selection of neurones which are involved in horizontal eye movements has been made. The activity has been compared with a selected sample of abducens motoneurones recorded in the same animals. 2. Alert head-fixed cats were used for this study. Eye movements were recorded by the scleral search coil technique. Abducens motoneurones were identified by antidromic stimulation from the VIth nerve with chronically implanted electrodes. They were recorded extracellularly. 3. Second-order vestibular neurones were identified by orthodromic stimulation from the vestibular organs. They were recorded intra-axonally and injected with horseradish peroxidase after recording of their physiological characteristics. Their morphology was reconstructed from frozen sections. 4. All the recorded vestibular neurones showed various amounts of eye position sensitivity. The firing rate (F) - horizontal eye position (H) characteristics are compared for abducens and vestibular neurones. The population average values are F = 33 + 4 H for motoneurones and F = 51 + 2.4 H for vestibular neurones. 5. All recorded vestibular neurones showed an increase of discharge rate during contralateral horizontal saccades and a strong decrease or pause during ipsilateral saccades. Firing rate - horizontal eye velocity sensitivity has been calculated. 6. Results suggest a strong inhibitory input on vestibular neurones from the saccadic generator. This mechanism underlies the suppression of the vestibulo-ocular reflex during saccades. Our results suggest that in the cat, for saccades of amplitude smaller than 20 deg, there is a variable degree of suppression which is provided by a projection of excitatory bursters (EBNs) on second-order vestibular neurones through inhibitory type II neurones. 7. We also conclude from this study that the eye position sensitivity of vestibular second-order neurones is in fact a motor signal indicating a motor error, i.e. the amount of head or eye movement which remains to be done in order to align gaze on target with the eyes centred in the orbit.

Abducens Nerve↗
PubMed1985

Influence of stimulation of the visual system on the activity of vestibular nuclear neurons in the frog.

In the frog (Rana esculenta L.) we have tested the possible existence of visual inputs in the vestibular nuclei by recording the activity of second-order vestibular neurons receiving primarily horizontal canal inputs, while the visual system was stimulated by either light pulses or optokinetic stimulation; moreover, combined visuovestibular stimulation (horizontal rotatory stimulation in light) was performed and the response compared to the one obtained during vestibular stimulation alone (horizontal rotatory stimulation in dark). 42.2% of the neurons tested (38/90) responded to light pulse stimulation of the retinae by an increase of their discharge frequency of about 150%, while the other neurons (57.8%) did not. Optokinetic stimulation was completely ineffective in modulating the discharge frequency of all the neurons (98) recorded. Among 30 neurons tested during constant-velocity horizontal rotation of the turntable (2.5-10%s) in the excitatory direction, 13 units (43.3%) had a discharge rate significantly greater than the spontaneous frequency during the constant-velocity phase when the rotation was performed in light, while a few seconds after beginning of the constant-velocity phase the discharge frequency returned to its resting value when the rotation was performed in dark. Moreover, the difference between the maximum discharge frequency and the resting discharge frequency (delta F) was significantly higher in light than in dark. The behavior of the 17 other neurons (56.7%) was similar whether the rotation was performed in light or in dark. When tested to sinusoidal rotation (0.05 Hz +/- 40 degrees or 0.1 Hz +/- 30 degrees), the characteristics of the responses were different in light and in dark.(ABSTRACT TRUNCATED AT 250 WORDS)

Animals↗
PubMed2004

AMPA receptor subunit expression in chick vestibular nucleus neurons.

The principal cells of the chick tangential nucleus are vestibular nucleus neurons whose responses on vestibular nerve stimulation are abolished by glutamate receptor antagonists. Using confocal microscopy, we quantified immunolabeling for AMPA receptor subunits GluR1, GluR2, GluR2/3, and GluR4 in principal cells that were identified by the neuronal marker, microtubule-associated protein 2 (MAP2). This work was focused primarily on 9 days after hatching (H9) when the principal cells have acquired some important mature electrophysiologic properties. At H9, the principal cell bodies stained strongly with GluR2/3 and GluR4, whereas GluR1 and GluR2 produced weak signals. Moreover, GluR2/3 and GluR4 receptor subunit clusters in principal cell bodies and dendrites were localized at sites contacted by biocytin-labeled vestibular nerve terminals and synaptotagmin-labeled terminals. Developmental expression of AMPA receptor immunolabeling was studied in the principal cell bodies at embryonic day 16 (E16) and hatching (H1). At E16, labeling for GluR4 was already strong, and continued to increase at H1 and H9. In contrast, GluR2/3 labeling was weak at E16, but increased significantly at H1, and more so by H9. GluR1 and GluR2 were present at low levels at E16 and H1. From E16 to H9, overall AMPA receptor subunit expression increased steadily, with H9 showing the strongest labeling. Ultrastructural observations at E16 and H3 confirmed the presence of immunogold labeling for AMPA receptor subunits at the vestibular nerve and non-vestibular nerve synapses on the principal cell bodies. In summary, these results indicate that GluR3 and GluR4 are the major AMPA receptor subunits involved in excitatory synaptic transmission in principal cells during the perinatal period.

Age Factors↗
PubMed1990

[Vestibular efferent neurons of the guinea pig forming projections into the saccule].

The distribution of vestibular efferent neurons projecting to the saccule and efferent neurons transmitting axons to the acoustic nerve (cochlear efferent neurons) has been studied in guinea pig by comparison using the method of retrograde axonal transport of horseradish peroxidase. The saccular efferent neurons are revealed bilaterally in the subendymal granular fundus of the fourth ventricle of the brain and more laterally of the facial nerve genu, ipsilaterally in the small-celled reticular nucleus as well as in nuclei of the supraolivary complex: nucleus of lateral oliva and lateral nucleus of the trapezoid body. The cochlear efferent neurons are localized ipsilaterally in the reticular caudal nucleus of the bridge in the anteroventral cochlear nucleus and in nuclei of lateral and medial olivae. In the medial nucleus of the trapezoid body such neurons are found contralaterally. Thus, the regions of the vestibular saccular efferent neurons are partially overlapped with such of the cochlear efferent units. Possible participation of the vestibular efferent neurons of the saccule in the mechanism of the acoustic perception is discussed.

Animals↗
PubMed1995

Membrane and firing properties of avian medial vestibular nucleus neurons in vitro.

The intrinsic membrane and firing properties of medial vestibular nucleus (MVN) neurons were investigated in slices of the chick brainstem using intracellular recording and current injection. Avian MVN neurons fired spontaneous action potentials with very regular interspike intervals. The rapid repolarization of all action potentials was followed by an after-hyperpolarization. Intracellular injection of steps of hyperpolarizing current revealed both an inward rectification of the membrane potential during the step and a rebound depolarization following the offset of the step. In some neurons, the rebound depolarization resulted in bursts of action potentials. Steps of depolarizing current applied to spontaneously active neurons evoked increases in firing rate that were higher at the onset of the step than during the steady-state response. The relationship between current and firing rate was linear. The membrane and firing properties of avian MVN neurons were distributed continuously across the population of recorded neurons. These properties appear identical to those of rodent MVN neurons, suggesting that the composition and distribution of ion channels in the MVN neuronal membrane has been highly conserved across vertebrate species.

Animals↗
PubMed1998

Development of action potentials and apamin-sensitive after-potentials in mouse vestibular nucleus neurones.

The postnatal maturation of medial vestibular nucleus (MVN) neurones was examined in slices of the dorsal brainstem prepared from balb/c mice at specific stages during the first postnatal month. Using spike-shape averaging to analyse the intracellularly recorded action potentials and after-hyperpolarizations (AHPs) in each cell, all the MVN neurones recorded in the young adult (postnatal day 30; P30) mouse were shown to have either a single deep AHP (type A cells), or an early fast and a delayed slow AHP (type B cells). The relative proportions of the two subtypes were similar to those in the young adult rat. At P5, all the MVN cells recorded showed immature forms of either the type A or the type B action potential shape. Immature type A cells had broad spontaneous spikes, and the characteristic single AHP was small in amplitude. Immature type B cells had somewhat narrower spontaneous spikes that were followed by a delayed, apamin-sensitive AHP. The delayed AHP was separated from the repolarisation phase of the spike by a period of isopotentiality. Over the period P10-P15, the mean resting potentials of the MVN cells became more negative, their action potential fall-times became shorter, the single AHP in type A cells became deeper, and the early fast AHP appeared in type B cells. Until P15 cells of varying degrees of electrophysiological maturity were found in the MVN but by P30 all MVN cells recorded were typical adult type A or type B cells. Exposure to the selective blocker of SK-type Ca-activated K channels, apamin (0.3 microM), induced depolarising plateaux and burst firing in immature type B cells at rest. The duration of the apamin-induced bursts and the spike frequency during the bursts were reduced but not abolished after blockade of Ca channels in Ca-free artificial cerebrospinal fluid containing Cd2+. By contrast, in mature type B cells at rest apamin selectively abolished the delayed slow AHP but did not induce bursting activity. Apamin had no effect on the action potential shape of immature type A cells. These data show that the apamin-sensitive I(AHP) is one of the first ionic conductances to appear in type B cells, and that it plays an important role in regulating the intrinsic rhythmicity and excitability of these cells.

Action Potentials↗
PubMed2002

Convergence of ipsilateral semicircular canal inputs onto single vestibular nucleus neurons in cats.

Convergent inputs from the ipsilateral semicircular canal nerves onto single vestibular nucleus neurons were investigated in decerebrate cats using intracellular recording after selective stimulation of each ampullar nerve. One hundred and seventy-four neurons were activated by stimulating the anterior semicircular (AC) and/or posterior semicircular canal (PC) nerves. These neurons were also antidromically stimulated and classified according to the pattern of their collateral projections to the oculomotor complex and the spinal cord. Four types were found: vestibulo-ocular (VO), vestibulospinal (VS), vestibulo-oculospinal (VOS), and vestibular (V) neurons, the latter of which were not activated by stimulation of either the oculomotor complex or the spinal cord. Of 174 AC- and/or PC-activated vestibular nucleus neurons, 32 (18%) received convergent inputs from both nerves. These convergent neurons included 11 VS, 6 VOS, and 15 V neurons. We found no VO neurons with convergent input. The vast majority (82%) of AC/PC-activated VS and VOS convergent neurons received excitatory inputs from both nerves, 12% received reciprocal inputs (i.e., excitatory from one and inhibitory from the other), and the remaining neurons received inhibitory inputs from both nerves. By stimulating the horizontal semicircular (HC) and/or PC nerves, 183 neurons were activated. Of these, 44 (24%) received convergent inputs from both nerves. These convergent neurons included 19 VS, 5 VOS, 2 VO, and 18 V neurons. Approximately one-half (46%) of HC/PC-activated VS and VOS convergent neurons received excitatory inputs from both nerves and 42% received reciprocal inputs, and the remaining neurons received inhibitory inputs from both nerves. In both nerve pairs, the percentage of VS neurons was higher (AC/PC, 34%; HC/PC, 43%) than that of VOS or VO neurons. Approximately half of these convergent neurons were located in the lateral nucleus. These results suggest that, during mixed angular head accelerations, the vestibulocollic reflex may be partly accomplished by VS and VOS convergent neurons.

Afferent Pathways↗
PubMed1987

Effects of ethanol on vestibular nucleus neurons responding to sinusoidal rotation.

Effects of ethanol applied by electro-osmosis were examined on the rat vestibular nucleus neurons responding to vestibular nerve stimulation and horizontal sinusoidal rotation. Ethanol (50-150 nA) inhibited the neurons monosynaptically activated by vestibular nerve stimulation and also suppressed the activity of the type I neuron, which responded with an increase in firing on ipsilateral rotation and a decrease on contralateral rotation. However, the drug did not affect the type II neuron, which showed the opposite response to the ipsi- and contralateral rotation compared with the type I neuron. Iontophoretic application of atropine (25-50 nA) inhibited spontaneous and rotation-induced firing in both type I and II neurons. These results suggest that ethanol inhibits the type I neuron projecting to the abducens nucleus, thereby impairing the vestibulo-ocular reflex.

Action Potentials↗
PubMed1992

Activity of lateral vestibular nucleus neurons during locomotion in the decerebrate guinea pig.

The influence of locomotor activity upon neurons in the lateral vestibular nucleus was investigated in precollicularly-postmamillary decerebrate guinea pigs. Out of 95 recorded neurons, 24 were identified as vestibulospinal and 71 had no descending projections. Locomotor activity occurred either spontaneously or was prompted by electrical stimulation of the mesencephalic locomotor region. Natural vestibular stimulation was supplied by tilting the animal about its longitudinal axis. Locomotor rhythmic limb muscle activity was accompanied by an increase in the firing frequency in the vast majority of investigated neurons. The increase in frequency was observed at the beginning of ipsilateral forelimb extensor muscle activity. Only in a few non-vestibulospinal neurons was the spontaneous activity depressed during locomotion. An increase in evoked responses was observed in almost all vestibulospinal neurons and in two thirds of the neurons without descending projections. A decrease in evoked responses was observed in one quarter of non-vestibulospinal neurons. During locomotion, the mean and maximal frequencies of evoked neuronal impulse activity changed, but the phase lag of these changes was not altered significantly. The results suggest an enhancement of vestibulospinal influences during locomotion, thus providing a high level of tonus in antigravitational muscles. This is interpreted as a mechanism to ensure that equilibrium is maintained during motion in different gaits and postures.

Animals↗