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PubMed1980

Extent of reaction capacity of the vestibulo-ocular reflex.

On theoretical grounds, a high capacity of the vestibulo-ocular reflex, compensating for head velocities above 300 degrees/s, is assumed. However, in man the maximum eye speed, induced by solely vestibular stimuli, is only 100 degrees/s. With the usual clinical tests is seems impossible to get a sufficient strength of stimulus that would correspond to a strong physiological stimulus. With a systematic investigation with fistula symptoms finally a patient was found with an ideal mechanism of release of the fistula symptom. The maximum eye speed of the compensatory phase was 315 degrees/s. In this case, the vestibular phase was quicker than the so-called rapid phase. This now proven high reaction capacity constitutes the "missing link" between the hypothetical high capacity of the systems concept and the until now measured, only limited reactions after solely vestibular stimulation. For most physiological stimuli, i.e., quick head movements, the system can act as a simple reflex organ, being a velocity transducer with linear function thus successfully maintaining ocular fixation.

Aged↗

PubMed1986

Posture testing (posturography) in the diagnosis of peripheral vestibular pathology.

In patients with peripheral vestibular deficiencies, the testing of posture or "posturography" can give specific information about any compensation obtained in the vestibulospinal reflex (VSR). We have used the statokinesimetric parameter of length in this study. Nearly 50% of the patients with unilateral vestibular hypofunction as well as those patients with paroxysmal positional vertigo (PPV) show abnormal results. These findings indicate deficient compensation at the vestibulospinal level, which is independent of any compensation already achieved at the vestibulo-ocular level. The tests used for the latter, such as positioning and rotational tests, are unable to provide information about the degree of compensation reached in the VSR. The examinations used in the different modalities of sensory interaction can show the presence of influences of ocular fixation and changes of head position. We have observed three types of deviant interaction. Our posturographic data have allowed us to assess functional situations in a more precise way. Any rehabilitation exercises used should be adapted according to these data.

Humans↗

PubMed2004

Latency of adaptive vergence eye movements induced by vergence-vestibular interaction training in monkeys.

Clear vision of objects that move in depth toward or away from an observer requires vergence eye movements. The vergence system must interact with the vestibular system to maintain the object images on the foveae of both eyes during head movement. Previous studies have shown that training with sinusoidal vergence-vestibular interaction improves the frequency response of vergence eye movements during pitch rotation: vergence eye velocity gains increase and phase-lags decrease. To further understand the changes in eye movement responses in this adaptation, we examined latencies of vergence eye movements before and after vergence-vestibular training. Two head-stabilized Japanese monkeys were rewarded for tracking a target spot moving in depth that required vergence eye movements of 10 degrees/s. This target motion was synchronized with pitch rotation at 20 degrees/s. Both target and chair moved in a trapezoidal waveform interspersed with random inter-trial intervals. Before training, pitch rotation in complete darkness without a target did not induce vergence eye movements. Mean latencies of convergence and divergence eye movements induced by vergence target motion alone were 182 and 169 ms, respectively. After training, mean latencies of convergence and divergence eye movements to a target synchronized with pitch rotation shortened to 65 and 53 ms, and vergence eye velocity gains (relative to vergence target velocity) at the normal latencies were 0.68 and 1.53, respectively. Pitch rotation alone without a target induced vergence eye movements with similar latencies after training. These results indicate that vestibular information can be used effectively to initiate vergence eye movements following vergence-vestibular training.

Adaptation, Physiological↗

PubMed2001

Representation of the visual field in the lateral intraparietal area of macaque monkeys: a quantitative receptive field analysis.

The representation of the visual field in the primate lateral intraparietal area (LIP) was examined, using a rapid, computer-driven receptive field (RF) mapping procedure. RF characteristics of single LIP neurons could thus be measured repeatedly under different behavioral conditions. Here we report data obtained using a standard ocular fixation task during which the animals were required to monitor small changes in color of the fixated target. In a first step, statistical analyses were conducted in order to establish the experimental limits of the mapping procedure on 171 LIP neurons recorded from three hemispheres of two macaque monkeys. The characteristics of the receptive fields of LIP neurons were analyzed at the single cell and at the population level. Although for many neurons the assumption of a simple two-dimensional gaussian profile with a central area of maximal excitability at the center and progressively decreasing response strength at the periphery can represent relatively accurately the spatial structure of the RF, about 19% of the cells had a markedly asymmetrical shape. At the population level, we observed, in agreement with prior studies, a systematic relation between RF size and eccentricity. However, we also found a more accentuated overrepresentation of the central visual field than had been previously reported and no marked differences between the upper and lower visual representation of space. This observation correlates with an extension of the definition of LIP from the posterior third of the lateral intraparietal sulcus to most of the middle and posterior thirds. Detailed histological analyses of the recorded hemispheres suggest that there exists, in this newly defined unitary functional cortical area, a coarse but systematic topographical organization in area LIP that supports the distinction between its dorsal and ventral regions, LIPd and LIPv, respectively. Paralleling the physiological data, the central visual field is mostly represented in the middle dorsal region and the visual periphery more ventral and posterior. An anteroposterior gradient from the lower to the upper visual field representations can also be identified. In conclusion, this study provides the basis for a reliable mapping method in awake monkeys and a reference for the organization of the properties of the visual space representation in an area LIP extended with respect to the previously described LIP and showing a relative emphasis of central visual field.

Animals↗

PubMed1975