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PubMed2005

Map plasticity in somatosensory cortex.

Sensory maps in neocortex are adaptively altered to reflect recent experience and learning. In somatosensory cortex, distinct patterns of sensory use or disuse elicit multiple, functionally distinct forms of map plasticity. Diverse approaches-genetics, synaptic and in vivo physiology, optical imaging, and ultrastructural analysis-suggest a distributed model in which plasticity occurs at multiple sites in the cortical circuit with multiple cellular/synaptic mechanisms and multiple likely learning rules for plasticity. This view contrasts with the classical model in which the map plasticity reflects a single Hebbian process acting at a small set of cortical synapses.

Animals↗
PubMed2005

Orientation-selective adaptation to first- and second-order patterns in human visual cortex.

Second-order textures-patterns that cannot be detected by mechanisms sensitive only to luminance changes-are ubiquitous in visual scenes, but the neuronal mechanisms mediating perception of such stimuli are not well understood. We used an adaptation protocol to measure neural activity in the human brain selective for the orientation of second-order textures. Functional MRI (fMRI) responses were measured in three subjects to presentations of first- and second-order probe gratings after adapting to a high-contrast first- or second-order grating that was either parallel or orthogonal to the probe gratings. First-order (LM) stimuli were generated by modulating the stimulus luminance. Second-order stimuli were generated by modulating the contrast (CM) or orientation (OM) of a first-order carrier. We used four combinations of adapter and probe stimuli: LM:LM, CM:CM, OM:OM, and LM:OM. The fourth condition tested for cross-modal adaptation with first-order adapter and second-order probe stimuli. Attention was diverted from the stimulus by a demanding task at fixation. Both first- and second-order stimuli elicited orientation-selective adaptation in multiple cortical visual areas, including V1, V2, V3, V3A/B, a newly identified visual area anterior to dorsal V3 that we have termed LO1, hV4, and VO1. For first-order stimuli (condition LM:LM), the adaptation was no larger in extrastriate areas than in V1, implying that the orientation-selective first-order (luminance) adaptation originated in V1. For second-order stimuli (conditions CM:CM and OM:OM), the magnitude of adaptation, relative to the absolute response magnitude, was significantly larger in VO1 (and for condition CM:CM, also in V3A/B and LO1) than in V1, suggesting that second-order stimulus orientation was extracted by additional processing after V1. There was little difference in the amplitude of adaptation between the second-order conditions. No consistent effect of adaptation was found in the cross-modal condition LM:OM, in agreement with psychophysical evidence for weak interactions between first- and second-order stimuli and computational models of separate mechanisms for first- and second-order visual processing.

Adaptation, Physiological↗
PubMed1994

Neuronal selectivities to complex object features in the ventral visual pathway of the macaque cerebral cortex.

1. To infer relative roles of cortical areas at different stages of the ventral visual pathway, we quantitatively examined visual responses of cells in V2, V4, the posterior part of the inferotemporal cortex (posterior IT), and the anterior part of the inferotemporal cortex (anterior IT), using anesthetized macaque monkeys. 2. The critical feature for the activation was first determined for each recorded cell by using a reduction method. We started from images of three-dimensional complex objects and simplified the image of effective stimuli step by step by eliminating a part of the features present in the image. The simplest feature that maximally activated the cell was determined as the critical feature. The response to the critical feature was then compared with responses of the same cell to a routine set of 32 simple stimuli, which included white and black bars of four different orientations and squares or spots of four different colors. 3. Cells that responded maximally to particular complex object features were found in posterior IT and V4 as well as in anterior IT. The cells in posterior IT and V4 were, however, different from the cells in anterior IT in that many of them responded to some extent to some simple features, that the size of the receptive field was small, and that they intermingled in single penetrations with cells that responded maximally to some simple features. The complex critical features in posterior IT and V4 varied; they consisted of complex shapes, combinations of a shape and texture, and combinations of a shape and color. 4. We suggest that local neuronal networks in V4 and posterior IT play an essential role in the formation of selective responses to complex object features.

Animals↗
PubMed1994

Population encoding of spatial frequency, orientation, and color in macaque V1.

1. We recorded local field potentials in the parafoveal representation in the primary visual cortex of anesthetized and paralyzed macaque monkeys with a multicontact electrode that provided for sampling of neural activity at 16 sites along a vertical penetration. Differential recordings at adjacent contacts were transformed into an estimate of current source density (CSD), to provide a measure of local neural activity. 2. We used m-sequence stimuli to map the region of visual space that provided input to the recording site. The local field potential recorded in macaque V1 has a population receptive field (PRF) size of approximately 2 deg2. 3. We assessed spatial tuning by the responses to two-dimensional Gaussian noise, spatially filtered to retain power only within one octave. Responses to achromatic band-limited noise stimuli revealed a prominent band-pass spatial tuning in the upper layers, but a more low-pass spatial tuning in lower layers. 4. We assessed orientation tuning by the responses to band-limited noise whose spectrum was further restricted to lie within 45 degrees wedges. The local field potential showed evidence of orientation tuning at most sites. Orientation tuning in upper and lower layers was manifest by systematic variations not only in response size but also in response dynamics. 5. We assessed chromatic tuning by the responses to isotropic band-limited noise modulated in a variety of directions in tristimulus space. Some lower-layer locations showed a nulling of response under near-isoluminant conditions. However, response dynamics in upper and lower layers depended not only on luminance contrast, but also on chromatic inputs. 6. Responses to near-isoluminant stimuli and to low-contrast luminance modulation were shifted to lower spatial frequencies. 7. We determined the extent to which various temporal frequencies in the response conveyed information concerning spatial frequency, orientation, and color under the steady-state conditions used in these studies. In each case, information is distributed in the response dynamics across a broad temporal frequency range, beginning at 4 Hz (the lowest frequency used). For spatial frequency the information rate remains significant up to at least 25 Hz. For orientation tuning and chromatic tuning, the information rate is lower overall and remains significant up to 13 Hz. In contrast, for texture discrimination, information is shifted to lower temporal frequencies.

Animals↗
PubMed1992

The effects of background pattern and contrast on prey discrimination by the praying mantis Sphodromantis lineola (Burr.).

Tethered, adult female Sphodromantis lineola (Burr.) were presented with two groups of two-dimensional stimuli (i.e., 2-D lures) against various backgrounds. Lure Group 1 comprised various black rectangles in three different size arrays: each size array included a 2, 6, or 12 mm square, respectively, several 'worm' lures of a constant width (l2, edge perpendicular to the direction of movement, 3-30 mm), but varying in length (l1, parallel to the direction of movement, 6-114 mm), and several 'antiworm' lures of a constant length but varying width. Group 1 lures were presented against patterned backgrounds of similar luminance: one natural pattern mimicking foliage and the other a random geometric pattern of rectangles. Group 2 lures comprised various configurations and combinations of black and white lures which were presented against white, black, and natural pattern backgrounds. The appetitive behaviors of approaching and striking at a lure were dependent measures indicating that a stimulus was categorized as prey. For Group 1 lures, overall response rates to lures of the same size were enhanced by the natural pattern background rather than the geometric pattern background. Against the natural pattern background, worm lures were stronger releasers of predatory behavior than antiworm lures of the same size. Lure configuration (especially for the smallest array) was masked by the geometric pattern background, although worm versus antiworm discrimination was apparent with the largest size array. For Group 2 lures, lure-to-background contrast, as well as configuration, effected prey recognition. For instance, lures with low lure-to-background contrast ratios were weaker releasers than those with high ratios, and lures that were darker (versus lighter) than the background were stronger releasers. In addition, particular stimulus properties interacted to effect lure strength. For instance, a weak or strong releaser became stronger or weaker, respectively, when a more or less, respectively, preferred releaser was super-imposed. The results also suggest that S. lineola attends preferentially to the leading edge of a moving stimulus. These findings are in agreement with predatory behavior of praying mantises in the wild.

Animals↗
PubMed1998

Deficits in complex visual perception following unilateral temporal lobectomy.

Although human temporal cortex is known to be important for short- and long-term memory, its role in visual perception is not well understood. In this study, we compared the performance of three patients with unilateral temporal lobectomies to that of normal controls on both "simple" and "complex" visual discriminations that did not involve explicit memory components. Two types of complex tasks were tested that involved discriminations secondary to texture segmentation. These were contrasted with simple discriminations using luminance-defined stimuli. Patients showed impaired thresholds only on tasks involving texture segmentation, performing as well as controls when the targets were defined by luminance rather than texture. The minimum stimulus presentation times for threshold performance were also measured for all tasks and found to be elevated in temporal lobectomy patients relative to controls. Although the magnitude of the deficits observed was substantial, loss was equivalent in ipsi- and contra-lesional regions of the visual field. Additional control experiments showed that the patients' perceptual deficits were not due, even in part, to disturbances of basic visual capacities such as acuity and contrast sensitivity. Our results indicate that temporal lobe damage disrupts complex, but not simple, visual discriminations throughout the visual field.

Case-Control Studies↗
PubMed1990

Spatial, colour and contrast response characteristics of mechanisms which mediate discrimination of pattern orientation and magnification.

We have measured response times for the detection of a single target presented against a set of reference elements which are characterised by combinations of four different stimulus parameters; colour, contrast polarity, magnification and orientation. The aim of the experiments was to determine the response characteristics of visual mechanisms which mediate target detection through the discrimination of orientation and magnification. In the first experiments, we determined sensitivity to differences in colour and contrast polarity, and show that the mechanisms responsible for the discrimination of orientation and of magnification are both selective in their responses to colour and to contrast polarity. There are, nonetheless, residual interactions between patterns of different contrast polarities and between those of different colour, and in the latter case, weak interactions persist under equiluminance conditions. In a second set of experiments, we examined the interactions between orientation and magnification. We conclude that the responses of visual mechanisms which mediate target detection through discrimination of orientation are markedly dependent on stimulus magnification whereas those which mediate detection through discrimination of magnification are, in contrast, relatively insensitive to stimulus orientation.

Adult↗
PubMed2001

Separating attention deficit hyperactivity disorder and learning disabilities in girls: a familial risk analysis.

OBJECTIVE: Familial risk analysis was used to clarify the relationship in girls between attention deficit hyperactivity disorder (ADHD) and learning disabilities in either mathematics or reading. METHOD: The authors assessed the presence of ADHD and learning disabilities in 679 first-degree relatives of three groups of index children: girls with ADHD and a comorbid learning disability, girls with ADHD but no learning disabilities, and a comparison group of girls without ADHD. RESULTS: The risk for ADHD was similarly higher in families of ADHD probands with and without learning disabilities; both groups had significantly higher rates of ADHD than did families of the comparison girls. In contrast, only among relatives of ADHD probands with a learning disability was there a higher risk for learning disabilities. A strong (although statistically nonsignificant) difference emerged that suggested at least some degree of cosegregation of ADHD and learning disabilities in family members. There was no evidence of nonrandom mating between spouses with ADHD and learning disabilities. CONCLUSIONS: These results extend previously reported findings regarding the relationship of ADHD and learning disabilities to female subjects and raise the possibility that, in girls, the relationship between ADHD and learning disabilities is due to shared familial risk factors.

Adolescent↗
PubMed2002

Ethics, data-dependent designs, and the strategy of clinical trials: time to start learning-as-we-go?

The seeds of modern clinical trials were unwittingly sown with the first use of randomization in a 1920s agricultural field experiment. The historical development of trials is briefly reviewed here, as are multifarious pressures and problems faced by those involved with clinical trials today. These challenges include recruitment difficulties, the emerging role of patient support groups, and legal threats over informed consent, to name three. Fundamentally, they reflect an overall shift towards patient-centred, individual ethics. I suggest many problems may be overcome by increased implementation of hitherto neglected, data-dependent designs for clinical trials. Over a dozen arguments against their use are countered, primarily through ethical considerations. Benefits and costs of refining clinical trials strategy are explored hypothetically under enhanced use of such 'learn-as-you-go' designs, in contrast to traditional, equal-allocation, fixed-sample-size and frequentist-based designs. These latter methods mirror crop field trials in which one cannot make scientific progress until after gathering objective data at harvest time. Some attempts to alleviate certain problems, such as Zelen randomization to boost recruitment, or over-reliance on 'large and simple trials' to detect moderate-sized treatment effects, are discussed and found inadequate. A proposal for wider discussion is made to assist the selective introduction of 'small and complex trials,' which could simultaneously expedite medical research, satisfy the concerns of regulators, statisticians, and doctors alike, and help address the growing demands of 21st-century patients.

Clinical Trials as Topic↗
PubMed2005

Do common mechanisms of adaptation mediate color discrimination and appearance? Uniform backgrounds.

Color vision is useful for detecting surface boundaries and identifying objects. Are the signals used to perform these two functions processed by common mechanisms, or has the visual system optimized its processing separately for each task? We measured the effect of mean chromaticity and luminance on color discriminability and on color appearance under well-matched stimulus conditions. In the discrimination experiments, a pedestal spot was presented in one interval and a pedestal + test in a second. Observers indicated which interval contained the test. In the appearance experiments, observers matched the appearance of test spots across a change in background. We analyzed the data using a variant of Fechner's proposal, that the rate of apparent stimulus change is proportional to visual sensitivity. We found that saturating visual response functions together with a model of adaptation that included multiplicative gain control and a subtractive term accounted for data from both tasks. This result suggests that effects of the contexts we studied on color appearance and discriminability are controlled by the same underlying mechanism.

Adaptation, Ocular↗
PubMed2005

Response saturation of monochromatic increments on intense achromatic backgrounds: implications for color-opponent organization in human vision.

We present evidence that steady achromatic adapting fields can produce response saturation in color-opponent pathways. We measured tvi (log increment threshold illuminance versus log background illuminance) functions at four test wavelengths (430, 490, 575, and 660 nm) and nine background illuminances from 4.0 to 5.6 log Td. Foveal, 2 degrees diameter, 1 s duration test stimuli were presented on a concentric, perceptually white (5128 degrees K color temperature), 7 degrees diameter, steady background. Thresholds were obtained by the method of adjustment, after which the test stimulus illuminances were increased 0.6 log unit and the subject estimated percentages of red, yellow, green, blue, and white. Average tvi slopes for two subjects were 2.06 for 430 nm, 1.6 for 490 nm, 1.11 for 575 nm and 1.34 for 660 nm, consistent with the estimated ratios of chromatic to achromatic sensitivity at the same wavelengths. Also, the percentage of white seen in the suprathreshold increments increased with increasing background illuminance despite increases in excitation purity. These findings imply that steady, intense, achromatic backgrounds can produce response saturation in color-opponent mechanisms at wavelengths across the visible spectrum. The saturation was more extreme at short wavelengths than at middle or long wavelengths, producing a tritanopic condition at the highest background illuminances. The tritanopia reduced color space to a predominately red-blue dichromacy, in agreement with previous findings. The results support a multistage opponent-color model in which precortical koniocellular and parvocellular opponent pathways interact to produce the observed red-green and yellow-blue color-opponent channels at a cortical level.

Adaptation, Ocular↗
PubMed2005

Effect of stimulus intensity on the sizes of chromatic perceptive fields.

The effects of intensity on chromatic perceptive field size were investigated along the horizontal meridian at 10 degrees temporal eccentricity by manipulating stimulus intensity from 0.3 to 3.3 log trolands. Following light adaptation, observers described the hue and saturation of monochromatic stimuli (440-660 nm, in 10 nm steps) for a series of test sizes (0.098-3 degrees) presented along the time period associated with the cone plateau of the dark-adaptation function. Perceptive field sizes of the four elemental hues (red, green, yellow, and blue) and the saturation component were estimated by three observers at each intensity level for each wavelength. In general, perceptive field sizes of blue and red are the smallest, and yellow and green are the largest. Furthermore, perceptive field sizes of all four hues decrease with increasing stimulus intensity, though the absolute change is largest for green and yellow. The decrease in size with increase in intensity cannot be completely explained in terms of saturation or rod signals and is likely, then, attributable to a cone-based mechanism.

Adaptation, Ocular↗
PubMed2006

Systems consolidation requires postlearning activation of NMDA receptors in the medial prefrontal cortex in trace eyeblink conditioning.

The importance of the hippocampus in declarative memory is limited to recently acquired memory, and remotely acquired memory is believed to be stored somewhere in the neocortex. However, it remains unknown how the memory network is reorganized from a hippocampus-dependent form into a neocortex-dependent one. We reported previously that the medial prefrontal cortex (mPFC) is important for this neocortex-dependent remote memory in rat trace eyeblink conditioning. Here, we investigate the involvement of NMDA receptors in the mPFC in this reorganization and determine the time window of their contribution using chronic infusion of an antagonist into the mPFC, specifically during the postlearning consolidation period. The rats with blockade of the mPFC NMDA receptors during the first 1 or 2 weeks after learning showed a marked impairment in memory retention measured 6 weeks after learning, but relearned normally with subsequent conditioning. In contrast, the same treatment had no effect if it was performed during the third to fourth weeks or during the first day just after learning. The specificity of NMDA receptor blockade was confirmed by the reduced long-term potentiation in the hippocampal-prefrontal pathway in these rats. These results suggest that successful establishment of remotely acquired memory requires activation of NMDA receptors in the mPFC during at least the initial week of the postlearning period. Such NMDA receptor-dependent processes may mediate the maturation of neocortical networks that underlies permanent memory storage and serve as a way to reorganize memory circuitry to the neocortex-dependent form.

Animals↗
PubMed1995

Effects of moderate dose alcohol on visual contrast sensitivity for stationary and moving targets.

OBJECTIVE: Contrast sensitivity involves distinguishing threshold luminance differences and is usually assessed using static sine-wave gratings over a range of different spatial frequencies. The purpose of this study was to determine the effects of various levels of acute alcohol intoxication on contrast sensitivity to stationary and moving sine-wave gratings. Moving gratings required the subjects to make pursuit eye movements. A secondary goal was to investigate whether any alcohol-related effects were associated with any measures of intoxication. METHOD: Male volunteers (N = 8) participated in three counterbalanced, double-blind, testing sessions (low alcohol, moderate alcohol and placebo) plus a control session with no beverage. Breath alcohol concentration and two subjective measures of intoxication were measured for each subject. Static and dynamic contrast sensitivity were determined for electronically generated sine-wave gratings that were either stationary or traveled in a circular path with a diameter of 9 cm (3.7 degrees) at 51.7 rpm, thus requiring the subject to make smooth pursuit eye movements. RESULTS: The mean blood alcohol concentration measured in the moderate alcohol condition was 0.043% and in the low alcohol condition 0.011%. Moderate dose alcohol consumption significantly impaired both static and dynamic contrast with a greater effect for moving targets. CONCLUSIONS: Objective and subjective measures of intoxication were unrelated to the alcohol-related losses in contrast sensitivity. Although most states currently prohibit driving with BACs of 0.08-0.10%, the present data indicate reliable visual impairment at approximately half of that level (.44%).

Adult↗
PubMed1994

A zoom lens before the eyes during imagery: individual differences and strange, unexpected responses.

The research examined some aspects of an hypothetical involvement of the eyes in the process of imagery and the individual differences in the modulation of the imagery-perception interaction of 59 (7 male and 52 female) undergraduate students in psychology. The subjects were asked to image with open eyes and to project, looking through a zoom lens, the "mental" image onto a white screen. While the subject was imaging, the experimenter moved the lever of the zoom lens in the direction of an hypothetical enlargement. This movement evoked different classes of responses: 46% of the subjects had a loss, even if for a short time, of the image, 37% of the subjects observed a strange and unexpected enlargement of the mental image, 7% did not observe any change in imagery, and 10% had other responses. A psychophysiological discussion concerned the strange phenomena observed in this research that have not yet been explored enough.

Adult↗
PubMed1995

Effects of cross-modal manipulations of attention on the ability of human subjects to discriminate changes in texture.

Cross-modal manipulations of attention significantly affect the detectability of tactile stimuli, but the effects on a more complex perceptual task, the discrimination of surface texture, are unknown. This study sought to examine whether attention influences the ability to discriminate a change in texture during passive touch. Twelve subjects were trained to perform two discrimination tasks: discriminating an increase in the intensity of a visual stimulus, and discriminating a change in the texture of a surface that was displaced beneath the tip of one digit. The texture change consisted of an increase in the spatial period between rectangular arrays of raised dots on Nyloprint surfaces, and for each subject an increment close to his or her discrimination threshold was employed in the experiment. Each trial began with the presentation of two baseline stimuli: A standard voltage illuminated the visual stimulus (an array of yellow light-emitting diodes (LEDs), and a standard texture (3-mm spatial period) was displaced under the tip of digit 3. For visual trials, three different increments in luminous intensity were presented, at one of three different delays following the initial presentation of the baseline stimuli. For texture trials, a single increment in spatial period was presented at one of three delays after the onset of the baseline stimuli. In any one trial, only one modality changed in intensity. The subject's task was to signal, as quickly as possible, the occurrence of the change. Instructional cues (red and green LEDs) were used to direct the subjects' attention toward the modality that changed (valid cue), to divide the subjects' attention between the visual and tactile modalities (neutral cue) as either might change, or to direct the subjects' attention toward the modality that did not change (invalid cue). Two measures of performance were employed: accuracy (percentage correct) and reaction time (speed with which the subject responded). The results indicated that cue condition significantly influenced the ability of subjects to discriminate a change in texture: Both accuracy and speed were significantly improved when subjects' attention was selectively directed toward the textured surface, as compared to when it was misdirected toward the visual modality. Performance was intermediate when attention was divided between the two modalities. The results were compared with those obtained previously in a tactile detection task using a similar attentional manipulation.(ABSTRACT TRUNCATED AT 400 WORDS)

Adult↗
PubMed2006

Exemplar similarity, study list homogeneity, and short-term perceptual recognition.

Kahana and Sekuler (2002) conducted short-term perceptual recognition experiments and modeled the data with a noisy exemplar similarity model. They found model-based evidence that list homogeneity (i.e., the degree to which exemplars on a study list are similar to one another) exerted a significant impact on recognition performance--a finding that is not predicted by standard global familiarity models. A potential limitation of their experiments is that they tested complex stimuli in which psychological similarities among exemplars may have been misspecified. Also, the relative importance of list homogeneity was not compared with that of alternative forms of parametric variation in the model. We conducted conceptual replications of their experiments, using a simpler set of stimuli in which interexemplar similarities could be more precisely measured. Extensive model-based comparisons reveal, in accord with the results of Kahana and Sekuler, strong evidence for a role of listhomogeneity on old-new recognition performance. We suggest that subjects systematically adjust their response criteria on the basis of the homogeneity of the study list items.

Attention↗