Gene/Protein Disease Symptom Drug Enzyme Compound
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Query: UNIPROT:P50583 (asymmetrical)
 12,197 document(s) hit in 31,850,051 MEDLINE articles (0.00 seconds)

Vertical optokinetic nystagmus (OKN) i.e., OKN in the sagittal plane, was asymmetrical in the monkey when it was induced with animals lying on their sides in a 90 degrees roll position. In typical monkeys the slow phase velocity of downward OKN (slow phases up) increased proportionally with stimulus velocity at close to unity gain to about 60 degrees/s and saturated at about 100 degrees/s. Upward OKN (slow phases down) increased with close to unity gain only to about 40 degrees/s and saturated at about 60 degrees/s. The slow phase velocity of upward OKN was usually irregular and its frequency was lower than that of downward or horizontal OKN. Upward and downward optokinetic after-nystagmus (OKAN) were also asymmetrical. Upward OKAN was weak or absent and when present it usually saturated at 10 degrees/s. Downward OKAN was stronger, increasing with a gain of about 0.7 with regard to stimulus velocity to a saturation velocity of about 50-60 degrees/s. This was usually about 10-30 degrees/s less than the saturation velocity of horizontal OKAN. The weak or absent upward OKAN indicates that stored activity related to slow phase eye velocity contributes little to the production of upward OKN. In agreement with this, there was little or no slow rise in slow phase velocity to a steady state level during upward OKN. Instead eye velocity rose to its peak velocity at the onset of stimulation. The lack of stored velocity information is probably largely responsible for the differences in regularity, gain and frequency between upward and downward OKN. Vertical vestibular nystagmus was induced by rotating monkeys in darkness with steps of velocity about a vertical axis, while they were lying on their sides in a 90 degree roll position. The velocities of the initial upward and downward slow phases were approximately equal. Gains of the vertical VOR ranged from about 0.5 to 0.98 for stimuli up to 150 degrees/s. Despite equivalent initial gains for upward and downward nystagmus, the vertical VOR was asymmetrical in that downward nystagmus had a higher frequency and generally lasted longer than upward nystagmus. Time constants of downward nystagmus (slow phases up) were about 15 s on average and were similar to those of horizontal nystagmus. Mean time constants of upward nystagmus (slow phases down) were about 8 s. This is only slightly longer than the average time constant of afferent activity in the semicircular canal nerves induced by steps of velocity.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Vertical optokinetic nystagmus and vestibular nystagmus in the monkey: up-down asymmetry and effects of gravity. 660 54

The simple (SS) and complex spike (CS) responses of Purkinje (P-cells) and non-Purkinje (non P-cells) in the cerebellar flocculus were studied in alert pigmented rats (DA-HAN) during binocular and monocular optokinetic stimulation (OKS), vestibular stimulation and a combination of the two. Of a total of 98 P-cells whose SS discharges were activated by rotary stimulation of the horizontal canal in the dark (type I and type II P-cells), the vast majority (72%) responded to constant velocity binocular OKS that was produced by means of a horizontal shadow projector system. The remaining P-cells responded only to vestibular stimulation (19%), to OKS or to the presumed fast components of optokinetic and vestibular nystagmus (9%). The optokinetic responses of P-cells were generally bidirectional but asymmetrical, i.e., the increases in rate in one direction were larger in magnitude than decreases on opposite OKS and were synergistic with the semicircular canal input. During constant velocity OKS, the discharge of a few P-cells rose approximately exponentially, outlasted the stimulus by as much as 10-13.5s and, thus, resembled OKS responses of vestibular nucleus neurons. However, the majority exhibited a phasic-tonic response governed by a short "time constant" of from 0.5-3s. The velocity tuning curves of vestibular/OKS responding P-cells showed peak sensitivities with retinal slip velocities of 1.5-2 degrees/s. This is higher than the ca. 1 degree/s determined for other relay nuclei of the horizontal optokinetic pathway. The responses of non P-cells suggest that they originate from mossy fiber projections from vestibular, visual (optokinetic) and saccadic eye movement-related areas of the brainstem. Most of the units carried a combined vestibular and optokinetic signal. The majority showed a bidirection-selective response to OKS, and a small percentage showed unidirectional responses only. Monocular testing of P-cells revealed that most received a bidirection-selective, but asymmetrical, OKS input. Slightly more than half of these had a strongest OKS drive from the contralateral eye; the remaining units were driven most strongly by the ipsilateral eye. Unidirection-selective P-cells, driven by OKS to the ipsi- or contralateral eye, were uncommon; yet this class is common among other portions of the horizontal optokinetic system (e.g., vestibular nuclei, praepositus hypoglossi nucleus, nucleus reticularis tegmenti pontis).(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Responses of units in the rat cerebellar flocculus during optokinetic and vestibular stimulation. 660 84

1. For horizontal eye movements, previous observations led to the hypothesis that the legendary neural integrator necessary for correct gaze holding, adequate vestibuloocular reflex (VOR), and optokinetic nystagmus, was located in the region of the complex formed by the nucleus prepositus hypoglossi (NPH) and the medial vestibular nucleus (MVN). 2. The aim of the present study was to test the respective contributions of the NPH, of the rostral part of the MVN, which contains most second-order vestibular neurons, and of the central part of the MVN to the horizontal integrator. 3. An injection of muscimol was used to inactivate each of these three zones in the cat's brain. Muscimol is a gamma-aminobutyric acid (GABA) agonist. By binding to GABAA receptors, it induces a hyperpolarization of the neurons that nullifies their activity. Muscimol was injected into the brain stem of the alert cat through a micropipette by an air pressure system. 4. The search coil technique was used to record spontaneous eye movements and the VOR induced by rotating a turntable at a constant velocity. VOR was analyzed by a new method: transient analysis of vestibular nystagmus. 5. A unilateral injection of muscimol into the NPH induced a bilateral gaze-holding failure: saccades were followed by a centripetal postsaccadic drift. A vestibular imbalance was also present but it was moderate and variable. The VOR responses were distorted drastically. Through transient analysis of vestibular nystagmus, that distortion was revealed to be due more to a failure of the neural integrator than to an alteration of the vestibular input to the neural integrator. The responses to a rotation either toward the injected side or in the opposite direction were asymmetrical. The direction of that asymmetry was variable. 6. A unilateral injection of muscimol into the rostral part of the MVN caused a vestibular imbalance: in complete darkness, a nystagmus appeared, whose linear slow phases were directed toward the side of injection. 7. A unilateral injection of muscimol into the central part of the MVN induced a syndrome where a severe bilateral gaze-holding failure was combined with a vestibular imbalance. In the light, saccades were followed by a bilateral centripetal postsaccadic drift. In complete darkness, a nystagmus was observed, whose curved slow phases were directed towards the side of injection. The VOR responses were distorted drastically. Here again, that distortion was revealed by our analysis to be due more to a failure of the neural integrator than to an alteration of the vestibular input to the neural integrator.(ABSTRACT TRUNCATED AT 400 WORDS)
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PMID:Effect of muscimol microinjections into the prepositus hypoglossi and the medial vestibular nuclei on cat eye movements. 798 36