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At least 163 records · Page 9Linked to original sources
PubMed1990

Visual and somatosensory processing in the macaque temporal cortex: the role of 'expectation'.

The somatosensory and visual properties of cells in a polymodal region of temporal cortex were studied in 4 awake behaving macaque monkeys. When stimulated passively and out of sight, cells with tactile responses were found to have very large receptive fields covering most of the body surface and an apparent lack of selectivity for size, shape or texture of the tactile stimulus. These properties are equivalent to those described for the anaesthetized preparation (Bruce et al. 1981). Our study revealed that tactile responses were influenced by the degree to which stimuli could be 'expected'. Tactile stimulation arising from active exploration of novel surfaces produced vigourous neuronal responses but equivalent stimulation of the skin arising when the monkey contacted 'expected' surfaces such as itself or items with which it had become familiar produced no responses. The responses of cells to active or passive tactile stimulation were attenuated when the monkey could see the objects causing the stimulation. For cells responsive to more than one sensory modality, visual and somatosensory responses were associated in a compatible manner. Cells responsive to the onset of touch were selective for the sight of objects moving towards the monkey, whereas cells selective for the offset of touch were responsive to the sight of movements away from the monkey.

Animals↗
PubMed1977

Extraocular proprioceptive projections to the visual cortex.

Electrical stimulation of the intraorbital part of the motor branches of extraocular muscles, where proprioceptive fibers run, evokes responses in 25% of the units of the striate cortex of the cat. The latency ranges between 25 and 40 msec. Mechanical stretch of extraocular muscles evokes multiunit responses in the striate cortex. The response is abolished by injection of xylocaine into the stretched muscle. The suppression of the response is reversible.

Afferent Pathways↗
PubMed1983

Auditory compensation of the effects of visual deprivation in the cat's superior colliculus.

Neurones in the superior colliculus of normal and visually deprived cats were analyzed for their responses to visual, auditory and somatosensory stimuli. The percentage of auditory-responsive cells throughout all layers had increased from 11% to 42% after binocular deprivation. Some auditory responses were found even in superficial layers. The number of somatosensory responses, though not systematically tested, was also higher in the visually deprived animals. Visually responsive units did not significantly decrease in number, thus resulting in an increased proportion of multisensory neurones. The vigour of auditory responses had increased after visual deprivation, while the vigour of visual responses had decreased significantly. In addition to the auditory effects of visual deprivation found, our study confirms previous findings on the visual effects of visual deprivation in the superior colliculus. Since only qualitative changes of visual responses, but no suppression of visual by non-visual activity was found, the neuronal mechanisms responsible for these changes may be different from competition as present in the visual cortex.

Acoustic Stimulation↗
PubMed1994

Sensory modality distribution in the anterior ectosylvian cortex (AEC) of cats.

Modality specificity of neuronal responses to visual, somesthetic and auditory stimuli was investigated in the anterior ectosylvian cortex (AEC) of cats, using single-unit recording techniques. Seven classes of neurons were found, and according to their responsiveness to sensory stimuli regrouped into three categories: unimodal, bimodal and trimodal. Unimodal cells that responded to only one of the three stimulus modalities formed 59% of the units; 30.2% were bimodal, in that they showed a clear increase of neuronal discharges to two of the three stimulus types; 10.8% were defined as trimodal because they responded to all three stimulus modalities. Although the different categories of cells were intermingled within the AEC, indicating a certain degree of overlap between sensory modalities, some clustering of cell types was nonetheless evident. Thus, the somatosensory responsive cells were mainly located in the anterior two-thirds of the dorsal bank of the anterior ectosylvian sulcus. Visually responsive cells were concentrated on the ventral bank of the sulcus, whereas neurons with an auditory response occupied the banks and fundus of the posterior three-quarters of the sulcus. The histological distribution and physiological properties of AEC neurons suggest that this cortical region is a higher-order associative area whose function may be to integrate information from different sensory modalities.

Acoustic Stimulation↗
PubMed1988

Cross-coupled effects of repeated vestibular and optokinetic stimulations on the dynamics of the vestibulo-ocular and optokinetic reflexes in the cat.

Cats were submitted to repeated step stimulations either vestibular or optokinetic. Regardless of which of the two stimuli was used, dynamic modifications were observed in both vestibulo-ocular response and optokinetic after-nystagmus (OKAN). The progressive changes in post-rotational nystagmus and OKAN were quantified by measuring the duration of their primary phase. A parallel evolution of these two parameters was found. When repeated unidirectional vestibular stimulations were used, the same asymmetry was induced in both vestibuloocular responses and OKAN. These results support the hypothesis that the vestibulo-ocular and the optokinetic reflex share a common velocity storage mechanism, although alternative hypotheses cannot be excluded.

Animals↗
PubMed1996

Properties of eye movements induced by activation of neck muscle proprioceptors.

BACKGROUND: We have previously reported that neck muscle vibration can induce visual illusory movements and eye movements under subdued ambient illumination in human subjects with the head and body fixed. The subjects viewed a fixation light with one eye and the other eye was covered. The eye movements were recorded with an infrared system mounted in goggles attached to the head of the subject. METHODS: In order to further examine the properties of these cervico-ocular reactions and reveal any artefacts in the eye movement recordings, we have studied (1) the effect of increasing the ambient light, which made visual illusory movements disappear, (2) the timing between the illusory movement and the eye movement in subdued light, (3) the effect of viewing the target through a pin-hole, which would reveal artefacts due to head movement, and (4) the effect of mounting the eye movement recording system on the head support, which would allow recording to the absolute eye position change. RESULTS: The results of these experiments showed no significant difference from those that were reported previously. Eye movements of about the same amplitude were induced in both eyes under all conditions, and there was no time difference in the occurrence of visual illusory movements and eye movements. CONCLUSION: The results of this study confirm that neck muscle vibration can induce eye position changes. This seems to confirm that the proprioceptive messages originating in the neck muscles are processed together with visual information of eye position in determining gaze direction.

Adult↗
PubMed1987

Comparison of color sensation in dichoptic and in normal vision.

Color vision in humans is independent over a wide range of the spectral composition of the illuminating light (Young 1807; Hering 1879). The retinex theory accounts for this color constancy by assuming that for each of the three waveband channels determined by the retinal cones a global lightness record of the scene is first computed by the visual system. The three records then serve to generate color at every point (Land 1983). Where do these computations take place? In this report a scene consisting of fourteen colored fields was viewed while one band of wavelengths enters one eye and a different band enters the other (dichoptic case) or while both bands enter both eyes (normal case) under otherwise identical conditions. The perceived color of every field is very similar in both cases although the physical stimulation of the eyes differs. It is also found that color constancy is maintained under dichoptic conditions. The results show that the cortex is crucial for the computation of color.

Adult↗
PubMed1986

Different forms of blinks and their two-stage control.

The purpose of this paper is to examine blink kinematics and the neural basis of blinks evoked reflexively by different kinds of stimuli. The kinematics of the upper lid movement and the electromyographic response of lid muscles levator palpebrae and orbicularis oculi were recorded in the rabbit during trigeminally and visually-evoked blinks. We find that there is a basic, kinematic difference between blinks. A blink in response to an airpuff is more rapidly accomplished and achieves a higher velocity than does an equal amplitude blink in response to a flash of light. The two forms of the reflex blink result from differences in the nature and timing of activity in antagonistic lid muscle motoneurons. Nevertheless, most characteristics of blink neural control are common to both reflex blinks. Most importantly, it appears that blinks are produced by two-stage neural control, an early component that is preprogrammed and a late component that is under stimulus control.

Animals↗
PubMed1980

Visual-vestibular convergence in the vestibular nuclei of the cat.

Responses from neurons of the vestibular nuclei were recorded in N2O-anaesthetized cats. Most neurons in the rostral parts of the nuclei responded to bimodal visual-vestibular stimulation, following a trapezoidal velocity profile. Both combinations of the two stimuli were tested: rotation of the animal with stationary visual field and rotation with overtaking visual field, i.e. the visual pattern running in the same direction as the turntable with twice the velocity. Some correlation of physiological data with results in corresponding psychophysical experiments were found. As a possible biological function of visual-vestibular convergence a phylogenetic solution for discrimination of body and outer world movement is discussed.

Animals↗
PubMed1984

Self-organizing mechanism for the formation of ordered neural mappings.

A model for the formation of ordered neural mappings in general, and of retinotectal connections, in particular is given. The main point came from the theory of "noise induced transitions", i.e. order may be the result of the interplay between deterministic and random interactions. An activity-dependent self-organizing mechanism is presented in terms of modifiable synapses. Simulation experiments were done not only for the normal ontogenetic development but also for the plastic behaviour of the retinotopic connections.

Animals↗
PubMed1980

Visual evoked potentials as an aid in evaluating brain dysfunction following concussional injury: an animal model.

Visual evoked potentials were recorded sequentially, using permanent epidurally implanted electrodes, before and after accelerating the heads of rabbits. The amplitude of VEP, recorded after lesioning, was diminished and recovery time was prolonged depending on the amount of acceleration and the extent of brain lesions found later in histological examinations. VEP reflected damage to the brain more precisely than EEG or somatosensory evoked potentials, thus giving values for judging the extent of lesions in patients with brain injuries.

Animals↗
PubMed1975

Effect of sensory stimulation on the potency of cataleptogens.

Pressures of up to 100 mm Hg applied to the mouse tail caused marked enhancement of the cataleptogenic potency of morphine, haloperidol and arecoline. Visual and auditory stimuli of moderate intensity also enhanced morphine catalepsy. Thus potentiation of cataleptogens by alteration of sensory input appears to be a fairly general phenomenon. The significance of these findings is discussed.

Acoustic Stimulation↗
PubMed1982

Optokinetic, vestibular, and optokinetic-vestibular responses in albino and pigmented rats.

Horizontal eye movements and neuronal activity in the vestibular nuclei and pretectum were recorded in albino and pigmented rats in response to optokinetic, vestibular (VS), combined visual-vestibular (VVS) sinusoidal stimulations. 1. VOR slow phase velocity in VS condition leads head velocity. This phase lead is smaller in albino than in pigmented rats. 2. Presence of vision (VVS) improves the phase angle of the VOR in both strains, especially at low frequencies. In pigmented rats the VOR is perfectly compensatory with respect to phase at all frequencies whereas in albinos the eye velocity still leads the head velocity. 3. There is no difference in the response characteristics of vestibular nuclear neurons (VN) to VS between albino and pigmented rats which could explain the difference in their VORs. 4. In the pigmented rat, there is a strong optokinetic input to VN which provokes a shift of the response peak towards peak head velocity. These visual-vestibular interactions at VN level are in agreement with the changes in the phase angle of the VOR. 5. In albino rat, there are no differences in the response characteristics of VN between VS and VVS, thus the decrease of the VOR phase lead observed in VVS compared to VS is due either to visual-vestibular interactions outside of the vestibular nuclei or to some general arousing effect of light. 6. Recording of responses of pretectal neurons to visual stimulation in albino rats has shown that they are activated in a phasic or tonic way by light on ("On cells") or off ("Off cells"). Contrary to the pigmented rat, pretreated neurons in albino exhibited no detectable direction specific optokinetic responses.

Animals↗
PubMed1988

The tritocerebral commissure 'dwarf' (TCD): a major GABA-immunoreactive descending interneuron in the locust.

The minor branch of the tritocerebral commissure of the locust, Locusta migratoria, contains only two axons which are from interneurons in the brain descending to the ventral cord ganglia. The smaller of these two neurons, the tritocerebral commissure dwarf (TCD), is immunoreactive to GABA, suggesting that it may be an inhibitory interneuron. We have exploited the accessibility of its axon in the commissure, first, to fill it with cobalt to define its morphology, and second, to record its input characteristics. It has a cell body and arborization of fine branches in the deutocerebrum of the brain, its axon passes contralateral through the tritocerebral commissure and it forms bilateral arborizations in the suboesophageal and three thoracic ganglia. It receives mechanosensory input from many regions of the ipsilateral body and head, and it is sensitive to illumination levels, generally showing greater spontaneous activity in the dark. It is one of the largest GABA-immunoreactive descending interneurons in the locust, suggesting it plays a prominent role in behaviour. Since it is easily accessible for physiological recording, its roles in circuits for particular components of behaviour should be amenable to investigation.

Action Potentials↗