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Results for “Spatial orientation”

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PubMed1971

Judgment of spatial orientation in patients with focal brain damage.

Thirty control and 121 brain-damaged patients with injury restricted to one hemisphere were presented with a test requiring the placing of a rod, fixed on a support by a hinged joint, in the same position as a model. Two versions of the test were given, one to be performed with the aid of vision and the other only by touch. The brain-damaged patients were subdivided into the following groups: right hemisphere patients without visual field defect (VFD): 30; right hemisphere patients with VFD: 20; left hemisphere patients without VFD: 46; left hemisphere patients with VFD: 25. The test modality did not differentially affect the performance of the groups. Both on the visually and on the tactually guided version of the test the right hemisphere group with VFD did significantly worse not only with respect to controls but also with respect to the three other braindamaged groups. The latter, in turn, were not significantly inferior to patients without cerebral damage. It appears, therefore, that when spatial perception is tested at a very basic and simple level, such as the detection of orientation in space of a rod, there is an almost complete dominance of the posterior region of the so-called minor hemisphere. This result must be contrasted with the less striking asymmetry of functions shown in more complex spatial tasks-for example, route finding, copying drawings, block designs-that are failed also by patients with damage to the left posterior area. Normal subjects reproduced the orientation of the rod on the horizontal plane with a constant error which was found to be dependent on the position of the model. Clockwise deviations were made when the model was on the left and counterclockwise deviations when the model was on the right. The constant error was present in left brain-damaged patients too, while it was not significantly different from zero in right brain-damaged patients. A systematic error was also found on the vertical plane and it consisted in the tendency to stop the rod below the level of the standard.

Brain Damage, Chronic↗

PubMed1999

Neural basis of endogenous and exogenous spatial orienting. A functional MRI study.

Whole-brain functional magnetic resonance imaging (MRI) was used to examine the neural substrates of internally (endogenous) and externally (exogenous) induced covert shifts of attention. Thirteen normal subjects performed three orienting conditions: endogenous (location of peripheral target predicted by a central arrow 80% of the time), exogenous (peripheral target preceded by noninformative central cue). Behavioral results indicated faster reaction times (RTs) for valid than for invalid trials for the endogenous condition but slower RTs for valid than for invalid trials for the exogenous condition (inhibition of return). The spatial extent and intensity of activation was greatest for the endogenous condition, consistent with the hypothesis that endogenous orienting is more effortful (less automatic) than exogenous orienting. Overall, we did not observe distinctly separable neural systems associated with the endogenous and exogenous orienting conditions. Both exogenous and endogenous orienting, but not the control condition, activated bilateral parietal and dorsal premotor regions, including the frontal eye fields. These results suggest a specific role for these regions in preparatory responding to peripheral stimuli. The right dorsolateral prefrontal cortex (BA 46) was activated selectively by the endogenous condition. This finding suggests that voluntary, but not reflexive, shifts of attention engage working memory systems.

Adult↗

PubMed1997

Audiovisual links in exogenous covert spatial orienting.

Subjects judged the elevation (up vs. down, regardless of laterality) of peripheral auditory or visual targets, following uninformative cues on either side with an intermediate elevation. Judgements were better for targets on either modality when preceded by an uninformative auditory cue on the side of the target. Experiment 2 ruled out nonattentional accounts for these spatial cuing effects. Experiment 3 found that visual cues affected elevation judgments for visual but not auditory targets. Experiment 4 confirmed that the effect on visual targets was attentional. In Experiment 5, visual cues produced spatial cuing when targets were always auditory, but saccades toward the cue may have been responsible. No such visual-to-auditory cuing effects were found in Experiment 6 when saccades were prevented, though they were present when eye movements were not monitored. These results suggest a one-way cross-modal dependence in exogenous covert orienting whereby audition influences vision, but not vice versa. Possible reasons for this asymmetry are discussed in terms of the representation of space within the brain.

Adult↗

PubMed2005

Learning spatial orientation tasks in the radial-maze and structural variation in the hippocampus in inbred mice.

In the present paper we review a series of experiments showing that heritable variations in the size of the hippocampal intra- and infrapyramidal mossy fiber (IIPMF) terminal fields correlate with performance in spatial, but not non-spatial radial-maze tasks. Experimental manipulation of the size of this projection by means of early postnatal hyperthyroidism produces the effects predicted from the correlations obtained with inbred mouse strains. Although the physiological mechanisms behind these correlations are unknown as yet, several lines of evidence indicate that these correlations are causal.

Journal Article↗

PubMed2004

Neck muscle fatigue and spatial orientation during stepping in place in humans.

Neck proprioceptive input, as elicited by muscle vibration, can produce destabilizing effects on stance and locomotion. Neck muscle fatigue produces destabilizing effects on stance, too. Our aim was to assess whether neck muscle fatigue can also perturb the orientation in space during a walking task. Direction and amplitude of the path covered during stepping in place were measured in 10 blindfolded subjects, who performed five 30-s stepping trials before and after a 5-min period of isometric dorsal neck muscle contraction against a load. Neck muscle electromyogram amplitude and median frequency during the head extensor effort were used to compute a fatigue index. Head and body kinematics were recorded by an optoelectronic system, and stepping cadence was measured by sensorized insoles. Before the contraction period, subjects normally stepped on the spot or drifted forward. After contraction, some subjects reproduced the same behavior, whereas others reduced their forward progression or even stepped backward. The former subjects showed minimal signs of fatigue and the latter ones marked signs of fatigue, as quantified by the dorsal neck electromyogram index. Head position and cadence were unaffected in either group of subjects. We argue that the abnormal fatigue-induced afferent input originating in the receptors transducing the neck muscle metabolic state can modulate the egocentric spatial reference frame. Notably, the effects of neck muscle fatigue on orientation are opposite to those produced by neck proprioception. The neck represents a complex source of inputs capable of modifying our orientation in space during a locomotor task.

Adaptation, Physiological↗

PubMed2001

Effects of grating spatial orientation on visual evoked potentials and contrast sensitivity in multiple sclerosis.

Previous studies suggest a delay of pattern visual evoked potentials (PVEPs) in multiple sclerosis (MS) depending on grating orientation. We examined a group of 14 patients with definite MS recording PVEPs to vertical and horizontal grating and analysing latency and amplitude of P60, N70 and P100 waves. We evaluated contrast sensitivity (CS) to dark and bright bars of several spatial frequencies (SF). The aim was to evaluate the diagnostic value of evoked responses and CS in revealing involvement of cortical structures. PVEPs to 1 degrees cycle/degree (c/d) vertical bars were abnormal in 25% for P60, in 32% for N70 and in 36%, for P100; in 25%, 36% and 42% respectively at 4 c/d; as regards horizontal bars at 1 c/d we found alterations of P60, N70 and P100 in 11%, 19% and 27% respectively; at 4 c/d in 19%, 27%) and 35%. CS resulted more abnormal for vertical grating, with a maximum impairment for 3.7 c/d SF. We may conclude that the use of vertical grating in clinical routine is more reliable both for PVEPs and CS testing; in addition CS can be abnormal even with normal PVEPs: this could mean an early impairment of CS and provide useful indications about a subclinical involvement of visual cortex.

Adult↗

PubMed2002

Estimating the magnitude of the sum of two magnetic fields with uncertain spatial orientations, polarizations, and/or relative phase.

A problem frequently encountered when modeling the power frequency magnetic fields, B and A, produced by two sources is the necessity of estimating the root mean square (rms) magnitude of their sum, i.e., T = /B + A/, when the rms magnitudes, B and A, of the fields are specified by the model, but not necessarily their spatial directions, polarizations, and/or relative phase. The estimator Q = sqrt [B2+A2] was proposed many years ago for this purpose. The accuracy of this estimator is characterized in this paper. If it is known that B and A are approximately linearly polarized and in phase, the maximum bias (i.e., systematic) and random errors for Q used to estimate T are 6.1 and 35%, respectively, when B = A. These errors decrease as the difference between B and A increases. The bias and random errors are, respectively, 3.2 and 26% when B = 2A or A/2 and 0.2 and 5.8% when B = 10A or A/10. If the directions, relative phase, and polarizations of the two fields are unknown, Q has maximum bias and random errors of approximately 2.6 and approximately 23%, respectively, when B = A. These errors decrease to approximately 1.5 and approximately 18% when B =2 A or A/2 and approximately 0.08 and approximately 4.0% when B = 10A or A/10. If B and A are known to be linearly polarized and collinear, but with unknown phase between them, the maximum bias and random errors are 11 and 48%, respectively, when B = A. The errors are 5.1 and 32% when B = 2A or A/2 and 0.2 and 7.0% when B = 10A or A/10. Estimators for T with zero bias can be derived, but they are more complicated and increase overall accuracy very little.

Biophysical Phenomena↗

PubMed2003

Effects of head-slaved navigation and the use of teleports on spatial orientation in virtual environments.

The type of navigation interface in a virtual environment (VE)--head slaved or indirect--determines whether or not proprioceptive feedback stimuli are present during movement. In addition, teleports can be used, which do not provide continuous movement but, rather, discontinuously displace the viewpoint over large distances. A two-part experiment was performed. The first part investigated whether head-slaved navigation provides an advantage for spatial learning in a VE. The second part investigated the role of anticipation when using teleports. The results showed that head-slaved navigation has an advantage over indirect navigation for the acquisition of spatial knowledge in a VE. Anticipating the destination of the teleport prevented disorientation after the displacement to a great extent but not completely. The time that was needed for anticipation increased if the teleport involved a rotation of the viewing direction. This research shows the potential added value of using a head-slaved navigation interface--for example, when using VE for training purposes--and provides practical guidelines for the use of teleports in VE applications.

Adolescent↗

PubMed1995

Cortical control of double-step saccades: implications for spatial orientation.

To accurately localize a visual target in space despite eye movement-induced shifts of its retinal image, the brain must take into account both its retinal location and information about current eye position or at least the preceding eye displacement. We examined this ability with respect to saccadic eye movements by applying "double-step" stimuli, where the locations of two sequentially flashed target lights have to be fixated by two successive saccades performed after their disappearance. As the 2nd saccade will not start at the spatial location from which the 2nd target was seen, a dissonance arises between its retinal coordinates and the motor coordinates of the required 2nd saccade. Nevertheless, these saccades were performed quite accurately by 32 healthy human adults. To investigate the contribution of the cerebral cortex, we recorded horizontal double-step saccades in 35 patients with focal unilateral hemispheric lesions. Whereas frontal lesions impaired temporal properties, posterior parietal lesions caused spatial dysmetria or failure of even ipsiversive 2nd saccades following contraversive 1st saccades. This reflects an inability to compensate for retinospatial dissonance by using nonretinal information (corollary discharge) about eye displacement associated with a previous saccade into the contralesional hemifield. In conclusion, the parietal cortex is crucial for spatial constancy across saccades.

Adult↗

PubMed2003

Multimodal spatial representations engaged in human parietal cortex during both saccadic and manual spatial orienting.

BACKGROUND: Recent neuroimaging studies have found that several areas of the human brain, including parietal regions, can respond multimodally. But given single-cell evidence that responses in primate parietal cortex can be motor-related, some of the human multimodal activations might reflect convergent activation of potentially motor-related areas, rather than multimodal representations of space independent of motor factors. Here we crossed sensory stimulation of different modalities (vision or touch, in left or right hemifield) with spatially directed responses to such stimulation by different effector-systems (saccadic or manual). RESULTS: The fMRI results revealed representations of contralateral space in both the posterior part of the superior parietal gyrus and the anterior intraparietal sulcus that activated independently of both sensory modality and motor response. Multimodal saccade-related or manual-related activations were found, by contrast, in different regions of parietal cortex. CONCLUSIONS: Whereas some parietal regions have specific motor functions, others are engaged during the execution of movements to the contralateral hemifield irrespective of both input modality and the type of motor effector.

Adult↗

PubMed2000

The spatial orientation of the essential amino acid residues arginine and aspartate within the alpha1beta1 integrin recognition site of collagen IV has been resolved using fluorescence resonance energy transfer.

The interaction of collagen IV with cells is mediated mainly by the integrin alpha1beta1. The recognition site has been located to a segment of the triple-helical domain 100 nm away from the N terminus of the collagen molecule. The three essential amino acid residues of the alpha1beta1 binding site, arginine alpha2(IV)461 and the two aspartate residues alpha1(IV)461, are all located on different chains. Since the spatial array of the three residues depends on the stagger of the chains within the triple helix, the stagger has been elucidated using fluorescence resonance energy transfer with phenylalanine alpha1(IV)473 and tryptophan alpha2(IV)479 as the fluorescent donor/acceptor pair. The distance R between phenylalanine and tryptophan was determined by analysis of the energy transfer efficiency, E, and the orientation factor, kappa(2). In parallel, distance R and orientation factor, kappa(2 )were also calculated from the coordinates of the triple helix. Comparison of the calculated and empirically determined values unequivocally showed the stagger to be alpha1'alpha1alpha2. This arrangement of the three alpha chains describes the conformation of the alpha1beta1 integrin recognition site, that is the distinct orientation of the side-chains of the essential residues aspartate and arginine in respect to the helix axis.

Amino Acid Sequence↗

PubMed2001

Spatial orientation in construction divers--are there associations with diving experience?

OBJECTIVE: The purpose of this work was to investigate whether or not navigation abilities are impaired in construction divers and if putative deficits can be related to MRT-verified brain lesions and/or to diving experience. METHODS: Nineteen construction divers and 19 controls matched for age, intelligence, and socioeconomic background were studied by use of a "locomotor search through" task which resembled working conditions at ground. The task incorporated a spatial working memory and a spatial reference memory component. Moreover, navigation parameters (i.e., rotational turns, distances traveled, speed of navigation) were derived from the participant's locomotor behavior, which was recorded automatically. Groups were compared by navigation performance, standard neuropsychological tests, and the number of brain lesions obtained by MRT-scans. RESULTS: Divers were widely comparable with respect to neuropsychological test scores, exploration behavior and speed of navigation during testing. Performance deficits in divers were seen in the three test trials with respect to the number of reference memory errors and navigation behavior. Only in controls were age and the number of MRI-verified lesions related to neuropsychological test performance and to maze variables, but in divers the number of lesions seemed to be related to hyperbaric exposure. CONCLUSION: Despite possible positive selection effects in long-term construction divers, these results may have implications for health care of middle-aged divers who are exposed to critical depths of more than 60 meter sea water (msw).

Adult↗

PubMed2001

Spatial orientation and balance control changes induced by altered gravitoinertial force vectors.

To better understand the mechanisms of human adaptation to rotating environments, we exposed 19 healthy subjects and 8 vestibular-deficient subjects ("abnormal"; four bilateral and four unilateral lesions) to an interaural centripetal acceleration of 1 g (resultant 45 degrees roll-tilt of 1.4 g) on a 0.8-m-radius centrifuge for periods of 90 min. The subjects sat upright (body z-axis parallel to centrifuge rotation axis) in the dark with head stationary, except during 4 min of every 10 min, when they performed head saccades toward visual targets switched on at 3- to 5-s intervals at random locations (within +/- 30 degrees) in the earth-horizontal plane. Eight of the normal subjects also performed the head saccade protocol in a stationary chair adjusted to a static roll-tilt angle of 45 degrees for 90 min (reproducing the change in orientation but not the magnitude of the gravitoinertial force on the centrifuge). Eye movements, including voluntary saccades directed along perceived earth- and head-referenced planes, were recorded before, during, and immediately after centrifugation. Postural center of pressure (COP) and multisegment body kinematics were also gathered before and within 10 min after centrifugation. Normal subjects overestimated roll-tilt during centrifugation and revealed errors in perception of head-vertical provided by directed saccades. Errors in this perceptual response tended to increase with time and became significant after approximately 30 min. Motion-sickness symptoms caused approximately 25% of normal subjects to limit their head movements during centrifugation and led three normal subjects to stop the test early. Immediately after centrifugation, subjects reported feeling tilted 10 degrees in the opposite direction, which was in agreement with the direction of their earth-referenced directed saccades. Postural COP, segmental body motion amplitude, and hip-sway frequency increased significantly after centrifugation. These postural effects were short-lived, however, with a recovery time of several postural test trials (minutes). There were also asymmetries in the direction of postcentrifugation COP and head tilt which depended on the subject's orientation during the centrifugation adaptation period (left ear or right ear out). The amount of total head movements during centrifugation correlated poorly or inversely with postcentrifugation postural stability, and the most unstable subject made no head movements. There was no decrease in postural stability after static tilt, although these subjects also reported a perceived tilt briefly after return to upright, and they also had COP asymmetries. Abnormal subjects underestimated roll-tilt during centrifugation, and their directed saccades revealed permanent spatial distortions. Bilateral abnormal subjects started out with poor postural control, but showed no postural decrements after centrifugation, while unilateral abnormal subjects had varying degrees of postural decrement, both in their everyday function and as a result of experiencing the centrifugation. In addition, three unilateral, abnormal subjects, who rode twice in opposite orientations, revealed a consistent orthogonal pattern of COP offsets after centrifugation. These results suggest that both orientation and magnitude of the gravitoinertial vector are used by the central nervous system for calibration of multiple orientation systems. A change in the background gravitoinertial force (otolith input) can rapidly initiate postural and perceptual adaptation in several sensorimotor systems, independent of a structured visual surround.

Acceleration↗

PubMed1995

Right-left confusion in Gerstmann's syndrome: a model of body centered spatial orientation.

Gerstmann's syndrome encompasses the tetrad of finger agnosia, agraphia, acalculia and right-left confusion and is associated with lesions of the dominant angular gyrus. The localizing value of this syndrome has been questioned because multiple mechanisms can account for each of the components of the syndrome. We present the case of a man who developed Gerstmann's syndrome following a focal infarct of the left angular gyrus. The patient's right-left confusion could not be accounted for by either an aphasia or a degraded body schema. A series of experiments that investigated the patient's spatial mapping system by progressively restricting the degrees of freedom for spatial rotation revealed an isolated defect in deriving the relative position of an object along the horizontal axis. Defective horizontal mapping can account for the other components of Gerstmann's syndrome because they all share a common dependency on relative horizontal positioning.

Aged↗

PubMed1992

Spatial orientation of the vestibular system.

1. A simplified three-dimensional state space model of visual vestibular interaction was formulated. Matrix and dynamical system operators representing coupling from the semicircular canals and the visual system to the velocity storage integrator were incorporated into the model. 2. It was postulated that the system matrix for a tilted position was a composition of two linear transformations of the system matrix for the upright position. One transformation modifies the eigenvalues of the system matrix while another rotates the pitch and roll eigenvectors with the head, while maintaining the yaw axis eigenvector approximately spatially invariant. Using this representation, the response characteristics of the pitch, roll, and yaw eye velocity were obtained in terms of the eigenvalues and associated eigenvectors. 3. Using OKAN data obtained from monkeys and comparing to the model predictions, the eigenvalues and eigenvectors of the system matrix were identified as a function of tilt to the side or of tilt to the prone positions, using a modification of the Marquardt algorithm. The yaw eigenvector for right-side-down tilt and for downward pitch cross-coupling was approximately 30 degrees from the spatial vertical. For the prone position, the eigenvector was computed to be approximately 20 degrees relative to the spatial vertical. For both side-down and prone positions, oblique OKN induced along eigenvector directions generated OKAN which decayed to zero along a straight line with approximately a single time constant. This was verified by a spectral analysis of the residual sequence about the straight line fit to the decaying data. The residual sequence was associated with a narrow autocorrelation function and a wide power spectrum. 4. Parameters found using the Marquardt algorithm were incorporated into the model. Diagonal matrices in a head coordinate frame were introduced to represent the direct pathway and the coupling of the visual system to the integrator. Model simulations predicted the behavior of yaw and pitch OKN and OKAN when the animal was upright, as well as the cross-coupling in the tilted position. The trajectories in velocity space were also accurately simulated. 5. There were similarities between the monkey eigenvectors and human perception of the spatial vertical. For side-down tilts and downward eye velocity cross-coupling, there was only an Aubert (A) effect. For upward eye velocity cross-coupling there were both Müller (E) and Aubert (A) effects. The mean of the eigenvectors for upward and downward eye velocities overlay human 1 x g perceptual data.(ABSTRACT TRUNCATED AT 400 WORDS)

Animals↗

PubMed1990

Patients with early Parkinson's disease are not impaired on spatial orientating of attention.

The shifting of attention to visual stimuli was studied in twenty patients with early Parkinson's disease (stage I or II as defined by the Hoehn and Yahr scale) and twenty normal controls matched for age, sex and intellectual status. Both groups were screened to exclude dementia, psychiatric disease and other neurological abnormalities. The speed of shifting attention to visual stimuli was measured using the cost and benefit paradigm. The results showed an overall increase in response latencies in patients with early Parkinson's disease compared to the Control group, but without a concomitant slowness to shift their attention toward a visual spatial target. This slowness which appears to reflect a delay in the decision-making process, regardless of the demands of the task, was independent of motor impairment, mood, intellectual status and Levodopa medication. While the Parkinson patients and normal controls showed a 38 msec benefit when the target stimulus was expected in a given location, all subjects failed to demonstrate a cost when the target stimulus was presented in an unexpected location. This may be a reflection of age. Alternatively, subjects may have learned to inhibit responses to the invalid cue.

Aged↗

PubMed1998

A spatially oriented decision does not induce consciousness in a motor task.

Visual information follows at least two branches in the human nervous system, following a common input stage: a cognitive "what" branch governs perception and experience, while a sensorimotor "how" branch handles visually guided behavior though its outputs are unconscious. The sensorimotor system is probed with an isomorphic task, requiring a 1:1 relationship between target position and motor response. The cognitive system, in contrast, is probed with a forced qualitative decision, expressed verbally, about the location of a target. Normally, the cognitive system is influenced by context-induced illusions of visual direction, while the sensorimotor system is not. Here, we inquire whether the process of making a spatially based decision is critical in forcing subjects to use the information in the cognitive system for spatial tasks. Subjects hear a tone that determines whether they jab an "X" or an "O" with the forefinger. Despite making a decision about which target to contact, the jab is not influenced by the position of a surrounding frame, indicating that choice can be handled within the context-insensitive sensorimotor system.

Adult↗

PubMed1991

Spatial orientation of the vestibular system: dependence of optokinetic after-nystagmus on gravity.

1. Monkeys received optokinetic stimulation at 60 degrees/s about their yaw (animal vertical) and pitch (animal horizontal) axes, as well as about other head-centered axes in the coronal plane. The animals were upright or tilted in right-side-down positions with regard to gravity. The stimuli induced horizontal, vertical, and oblique optokinetic nystagmus (OKN). OKN was followed by optokinetic after-nystagmus (OKAN), which was recorded in darkness. 2. When monkeys were tilted, stimulation that generated horizontal or yaw axis eye velocity during OKN induced a vertical or pitch component of slow phase velocity during OKAN. This has been designated as "cross-coupling" of OKAN. Eigenvalues and eigenvectors associated with the system generating OKAN were found as a function of tilt. They were determined by use of the Levenberg-Marquardt algorithm to minimize the mean square error between the output of a model of OKAN and the data. 3. The eigenvector associated with yaw OKAN (yaw axis eigenvector) was maintained close to the spatial vertical regardless of the angle of tilt. The eigenvector associated with pitch OKAN (pitch axis eigenvector) was always aligned with the body axis. The data indicate that velocity storage can be modeled by a piecewise linear system, the structure of which is dependent on gravity and the yaw axis eigenvector, which tends to align with gravity. 4. Yaw axis eigenvectors were also determined by giving optokinetic stimulation about head-centered axes in the coronal plane with the animal in various angles of tilt. A technique using a spectral analysis of residuals was developed to estimate whether yaw and pitch OKAN slow phase velocities decayed concurrently at the same relative rate and over the same time course. The eigenvectors determined by this method were in agreement with those obtained by analyzing OKAN elicited by yaw OKN. 5. During yaw OKN with the animal in tilted positions, the mean vector of the ensuing nystagmus was closer to the body axis than to the spatial vertical. This suggests that there is suppression of the cross-coupled pitch component during OKN. The direction of the stimulus may be utilized to suppress components of velocity storage not coincident with the direction of stimulus motion. 6. There were similarities between the monkey eigenvectors and human perception of the spatial vertical, and the mean of eigenvectors for upward and downward eye velocities overlay human 1-g perceptual data.(ABSTRACT TRUNCATED AT 400 WORDS)

Acceleration↗