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Profile view of the kidney obtained by "reverse oblique" x-ray projection was found to be useful in the spatial localization of intrarenal stones. The patient's position on the x-ray table is described, and 4 cases of patients with renal stones are illustrated.
Four subjects suffering from a unilateral peripheral paralysis of the 3rd or the 6th nerves have been studied in spatial localization tasks, with their normal eye occluded. When peripheral targets were presented in the hemifield corresponding to the paralysis, the saccadic eye movements (recorded from the normal occluded eye) were of an exaggerated amplitude. 'Staircase' oculomotor patterns, closely similar to those occurring in 'open-loop' visual stimulation, could also be observed. Our patients also presented the classical hypermetric misreaching when attempting to point by hand at visual targets in an otherwise dark room. This effect (past-pointing) was likely to be due to a monitoring of the exaggerated oculomotor signal: in one subject past-pointing disappeared when reaching at the targets on the basis of the sole retinal cues. Finally, the classically described illusory visual effects of ocular paralysis were limited to a feeling of instability during self-motion.
This experiment examines the notion that in the rat the hippocampal formation is an essential structure in the neurological representation of spatial abilities. Spatial localization by rats with different types of hippocampal damage, including bilateral electrolytic lesions, unilateral and bilateral kainic acid-induced CA3-CA4 lesions, and unilateral and bilateral colchicine-induced dentate gyrus lesions, was compared with vehicle-injected and normal control groups in the Morris water task. The task required the rats to escape from cold water by finding a submerged and hidden platform located at a fixed place within the room. The start point was varied randomly from trial to trial and there were no local cues available to indicate the position of the hidden platform. After training, the platform was moved. Escape latencies and the initial swimming headings revealed that all lesion groups, except the unilateral CA3-damaged group, were impaired at finding the platform: the dentate-damaged rats exhibited the greatest deficit. When the platform was moved the control rats swam mainly in the part of the pool that had previously contained the platform and, on finding it in the new location, they showed a marked dishabituation of rearing. None of the bilateral lesion groups showed these effects.
A new method of eliminating NMR image artifacts caused by random or sporadic motion is presented. The method uses only NMR techniques. A combination of a spatial localization method and a standard 2DFT imaging sequence is employed and consequently named SLO-MOTION. Alternatively, the sequence may be used to aid motion artifact reduction by postprocessing methods. The feasibility of the method is demonstrated on a phantom.
The use of a current-generated, inhomogeneous, surface-spoiling magnetic field gradient for enhancing magnetic resonance spatial localization, by rapidly inducing spin phase incoherence in surface lying regions of a sample is examined theoretically. A geometrically simple surface-spoiling magnetic field gradient coil design is presented and its gradient field characterized via computer simulations. Mathematical expressions describing the time dependence of net sample spin phase coherence under influence of the spoiling gradient are developed for application with homogeneous (B1) volume coils. The dependence of spoiling efficiency on the magnetogyric ratio of the nuclide under investigation and on the current driving the gradient field is described. Spoiling periods of ca 1-2 ms with driving currents of ca 0.5-1.0 A are predicted to be adequate for surface-spoiling experiments with rat, e.g., for noninvasive monitoring of liver. A companion article (W. Chen and J.J.H. Ackerman, NMR Biomed., 3, 158-165 (1990)) describes implementation of the surface-spoiling technique with multicompartment models (phantoms) and with rat in vivo.
The concept of local scale asserts that for a given class of psychophysical measurements, performance at any two visual field locations is equated by magnifying the targets by the local scale associated with each location. Local scale has been hypothesized to be equal to cortical magnification or alternatively to the linear density of receptors or ganglion cells. Here, we show that it is possible to estimate local scale without prior knowledge about the scale or its physiological basis.
Coronary stenosis results in transmurally non-uniform blood flow with the inner layers of the left ventricular wall typically suffering a more severe hypoperfusion relative to the outer layers. Coupled with numerous other transmural non-uniformities such as systolic tension development and oxygen needs, the heterogeneous blood flow distribution in the presence of coronary stenosis is expected to result in transmurally heterogeneous ischemia. All previous NMR spectroscopy studies of myocardial metabolism and bioenergetics under normal and ischemic conditions treated the organ as a homogeneous tissue. We have utilized spatially localized 31P NMR spectroscopy together with non-NMR measurements of regional blood flow to study the myocardium with transmural spatial differentiation under normal and flow-restricted conditions. 31P NMR and blood flow data obtained concurrently on each heart revealed that sustained coronary artery stenosis resulted in transmurally non-uniform ischemia which largely paralleled the hypoperfusion pattern. The reduction in creatine phosphate content (with consequent elevation of Pi) and hypoperfusion was tightly correlated in the subendocardium for flow rates less than approximately 0.7 mL/min per g wet myocardium. The high energy phosphate and Pi content of the epicardium, however, was responsive not only to the flow to this region but also to the extent of ischemia in the subendocardial layers. These results document the utility of localized NMR spectroscopy in physiologic research and suggest potential biomedical applications due to the tight correlation noted between alterations in blood flow and changes in the phosphorylated metabolite levels detected by 31P NMR.
Thin sections of deep-frozen unfixed muscle were studied in a scanning electron microscope modified for transmission imaging and equipped with a "cryostage" for vacuum compatibility of hydrated tissue. With an energy-dispersive x-ray analysis system, intracellular atomic species in the scan beam path were identified by their fluorescent x-rays and spatially localized in correlation with the electron optical image of the microstructure. Marked differences are noted between the ultrastructure of deep-frozen hydrated muscle and that of fixed dehydrated muscle. In frozen muscle, myofibrils appear to be composed of previously undescribed longitudinal structures between 400-1000 A wide ("macromyofilaments"). The usual myofilaments, mitochondria, and sarcoplasmic reticulum were not seen unless the tissue was "fixed" before examination. Fluorescent x-ray analysis of the spatial location of constituent elements clearly identified all elements heavier than Na. Intracellular Cl was relatively higher than expected.
Adiabatic pulses have been employed in spectroscopic imaging and relaxation rate measurements at 4.7 T to demonstrate the feasibility of obtaining spectroscopic data from the complete sensitive volume of a surface coil using the surface coil as a transmitter and receiver. With conventional B1 sensitive pulses, spectroscopic localization or imaging techniques, such as chemical-shift imaging, yield resonance intensities that are distorted severely as a function of space, and maximal signal is detected from a small region within the complete sensitive volume of the coil. With adiabatic pulses, however, this problem is eliminated completely. In addition, a new method of spatial localization is introduced. This method, referred to as FLAX-ISIS, is a derivative of longitudinally modulated Fourier series window and ISIS approaches and utilizes adiabatic inversion and excitation pulses. The method allows construction of localized spectra for multiple regions along the surface coil axis by postacquisition data manipulation of a single set of free induction decays. These techniques were applied to the study of the myocardium using an implanted surface coil in an instrumented closed-chest canine model and in an open-chest preparation. The results demonstrate that one-dimensional techniques are adequate for transmural detection of metabolites provided signal origin is restricted to a column perpendicular to the left ventricle wall.
The use of inhomogeneous surface-spoiling magnetic field gradients for elimination of signal from surface lying regions of a sample was theoretically examined in the companion article (W. Chen and J.J.H. Ackerman, NMR Biomed. 3, 147-157 (1990)). Using the spoiling gradient coil design described therein, this article presents experimental verification of the feasibility of such an approach to enhanced spatial localization. Single coil mode 31P NMR surface coil interrogation of both a two compartment phantom and rat in vivo are shown to provide excellent suppression of surface lying regions with minimal degradation of signal from the deep lying region of interest. Both pulse-and-collect and spin echo sequences were highly efficient in concert with spoiling gradient periods of 0.5-2 ms and driving currents of 0.5-2 A. The use of a current-generated surface spoiling gradient offers a robust means to remove surface tissue signal contributions and can be implemented with a wide range of localizing pulse sequences and imaging protocols.
In 1990 Cheatham suggested there might be a right-ear advantage for the perception of speech and music for right-handed individuals, which confirms Kinsbourne's observation of a general right-ear advantage. These findings, however, contrast with Segalowitz and Plantery's work that supports attentional bias in lateralized processing of these stimuli. The attentional bias model has also been criticized by Bryden on the basis of its circularity. At present there has not been sufficient evidence to settle this debate empirically. The author suggests that the controversy may best be resolved by disentangling the folklore surrounding spatial localization and auditory lateralization to reexamine this field in light of recent empirical findings by Bryden and by Porac, Coren, and Duncan, who inferred an inherent rightward bias to many kinds of stimulation, including auditory, in right-handed individuals. The present focus is that Cheatham's 1990 data lend themselves more readily to the rightward bias that occurs in right-handed subjects and not to previous structural or attentional models.
Visually guided, spatially oriented behavior involves an ongoing integration of signals regarding the loci of the retinal images and the position and orientation of the eye. In the strabismic this requires an altered spatial metric resulting from a functional readaptation to avoid confusion and diplopia. A comparator mechanism for evaluating these two signals is presented. A case report using "disruptive" therapeutic procedures that deliberately alter the strabismic's visual-postural control system is presented. A treatment plan for altering the anomalous binocular link, a characteristic of the well adapted strabismic, is described and related to the comparator mechanism.
To explain the veridical percept of the spatial ordering of objects and the generation of eye movements to peripheral targets, Lotze (1885 Microcosmos. Edinburgh: T. & T. Clark) proposed that there is a position label (local sign) for each retinal element. To estimate the precision of local sign information, we measured absolute localization thresholds at various eccentricities in the nasal visual field, in the complete absence of visual references. To eliminate perception of the visual surround, observers viewed a large display screen through a neutral density filter (2.0 log unit) in a dark room. The fixation target was extinguished at various times (interstimulus intervals or ISIs) prior to the onset of the test stimulus. In general, our results show that localization thresholds are proportional to the target eccentricity at all ISIs. At each eccentricity, localization thresholds are elevated after the extinction of the visual reference compared to thresholds when the reference is present. However, relative to the referenced threshold, unreferenced thresholds are elevated by a greater proportion at smaller eccentricities than at larger eccentricities. Our threshold vs ISI data can be adequately modeled on the basis of an intrinsic positional uncertainty, which increases with eccentricity, and additive and multiplicative sources of noise. The additive noise appears to reflect primarily the increasing scatter in eye position when the fixation target is extinguished. Our model's estimate of intrinsic positional uncertainty in the isoeccentric direction appears to reflect primarily the intrinsic positional uncertainty of the peripheral retina (the local sign), being very similar to cumulative cone position uncertainty and to the spacing between ON-P beta ganglion cells. In the isoeccentric direction, the estimated precision of the local sign mechanism across eccentricities is slightly better than the precision of saccadic endpoints, suggesting that noise in the motor system must also contribute to the scatter of saccadic endpoints in the isoeccentric direction. Interestingly, in the radial direction, we find a surprising similarity in our observers' positional uncertainty and the precision of saccadic endpoints.
In order to understand the regional distribution of the mechanisms which underlie localization accuracy we (1) chose a task which is known to involve localization accuracy (2) optimized stimulus parameters for ecentric loci and (3) determined how two key spatial factors which affect localization accuracy vary as a function of ecentricity. These involve Gaussian blur and Gaussian jitter. These results suggest that there are three different functions with ecentricity for the mechanisms underlying this task which we relate to the spatial properties of the retina, namely mean cone density, receptoral convergence and regularity.
Five experiments are reported in which subjects judged the movement or spatial location of a visible object that underwent a combination of real and induced (illusory) motion. When subjects attempted to reproduce the distance that the object moved by moving their unseen hands, they were more affected by the illusion than when they pointed to the object's perceived final location. Furthermore, pointing to the final location was more affected by the illusion when the hand movement began from the same position as that at which the object initially appeared, as compared with responses that began from other positions. The results suggest that people may separately encode two distinct types of spatial information: (1) information about the distance moved by an object and (2) information about the absolute spatial location of the object. Information about distance is more susceptible to the influence of an induced motion illusion, and people appear to rely differentially on the different types of spatial information, depending on features of the pointing response. The results have important implications for the mechanisms that underlie spatially oriented behavior in general.
The spatial organization of two rheumatic disease-associated epitopes and the RNA "cap" structure of the U1 small nuclear ribonucleoprotein (snRNP2) was analyzed both in situ and in vitro by two independent interference immuno-assays. Sm and RNP autoantibodies, associated with systemic lupus erythematosus and mixed connective tissue disease, respectively, were used to probe the epitope locations. The Sm epitope on the U1 snRNP structure was localized proximal to the RNP. Experiments with an anti-m7G (mRNA "cap") monoclonal antibody revealed that an in situ association of the Sm and RNP epitopes with the mRNA "cap" structure may exist. Our findings, together with previous observations by others, suggest a model for the spatial arrangement of these rheumatic disease-associated protein epitopes, and the U1 RNA within the U1 snRNP particle.
In two studies, we compared the size of the spatial discrepancies made by young, good and poor readers when locating patterns in space. In the first study, each child was asked to point to the location of a briefly displayed pattern in a 7 x 7 matrix, and the discrepancy between the target's location and the child's response was recorded. The pattern was either a shape or a letter, and the target appeared at nine distances from the middle of the display. The discrepancies made by both groups of children increased with eccentricity, but the rate of increase was significantly greater for the poor readers. The second study required that two temporally and spatially separated target patterns be located on each trial. The discrepancies between their positions and the positions specified by the children were recorded for each target as a function of its eccentricity, and the results for both targets were similar to those obtained in the first study. That is, the discrepancies made by both groups of children increased with eccentricity, but the rate of increase was significantly greater for the poor readers. It was argued that the results of both studies are consistent with the hypothesis that poor readers are handicapped by a low-level processing or perceptual deficiency in the visual encoding system.
The spatial distribution of the intracellular free Ca2+ (Ca2+i) rise elicited by different stimuli in bovine adrenal chromaffin cells was examined in single fura-2-loaded cells. In response to the potent secretagogues nicotine and high K+, Ca2+i was initially localized exclusively to the entire subplasmalemmal area of the cell. In response to the ineffective secretagogues, methacholine and muscarine, the rise in Ca2+i originated only in one pole of the cell and even at the peak of the response Ca2+ was still generally restricted to this same area of the cell. These results suggest that the triggering of exocytosis from these cells requires a specific spatial distribution of Ca2+i.