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Biomedical subjects

V C Smith

Publications and source records attributed to V C Smith.

At least 37 records · Page 2Linked to original sources

Color vision in two observers with highly biased LWS/MWS cone ratios.

Two sisters, heterozygous carriers for congenital X-linked protanopia, were diagnosed as normal trichromats by the Rayleigh match on the anomaloscope. The heterozygous state was established by molecular analysis of their visual pigment genes. The normal color match establishes that the spectral sensitivities of their long-wavelength-sensitive (LWS) and middle-wavelength-sensitive (MWS) cone visual photopigments are within normal variability. Their FM 100-hue test error scores were low, demonstrating superior chromatic discrimination. Heterochromatic flicker photometric (HEP) spectral sensitivities were like those of protanopes. The estimated LWS/MWS cone ratios from the HFP data were 0.09/1 and 0.03/1, compared with ratios in the range of 0.6/1 to 10/1 for typical normal trichromats. Measurements of chromatic grating acuity on chromatically selective backgrounds were performed to study the cone mosaic. The data were consistent with a sparsity of LWS cones. Both protan carriers showed normal spectral sensitivities for all three cone types under cone isolating chromatic adaptation and normal three-peaked curves for increment thresholds on a white pedestal. Hue estimation, run on one carrier was normal. The equilibrium yellow locus was measured in the other carrier and was in the range of normal trichromats. The data indicate that normal color vision can occur even when the LWS/MWS cone ratio is quite abnormal.

Adaptation, Ocular↗

Color appearance: neutral surrounds and spatial contrast.

The experimental data in this paper show that chromatic bars presented in alternation with equiluminant neutral-appearing bars are seen as more saturated than the same chromaticity presented as a uniform rectangle. This effect was diminished but not eliminated when test and match stimuli were presented within a slightly dimmer neutral surround. The test stimulus was a 2 x 5 degrees rectangle with a 0.7 cpd square wave grating composed of alternating equiluminant chromatic test bars and neutral bars. Asymmetric matching was used to match the test bar appearance to a uniform 2 x 5 degrees comparison rectangle. Test and comparison stimuli were presented to separate eyes in a haploscope and appeared flanking a central fixation target. Data were collected with test and inducing stimuli on the cardinal axes of color space. Test bars separated by neutral bars appeared more saturated than the comparison rectangle for both the l- and s-axis directions. Manipulation of excitation on one cardinal axis did not affect the appearance matches made for the other cardinal axis.

Adult↗

Rod inputs to macaque ganglion cells.

The strength of rod inputs to ganglion cells was assessed in the macaque retina at retinal positions within 3-15 deg eccentricity. The experimental paradigm used temporally modulated heterochromatic lights whose relative phase was varied. This paradigm provided a sensitive test to detect rod input. In parvocellular (PC) pathway cells, the gain of the cone-driven signal decreased with decrease in luminance. At 2 td a weak rod response, of a few impulses per second for 100% rod modulation, was revealed in about 60% of cells. For blue-on cells, the cone-driven response also decreased with retinal illuminance, but no rod response could be found. In magnocellular (MC) pathway cells, rod input was much more apparent. Responses became rod dominated at and below 20 td; we cannot exclude rod intrusion at higher retinal illuminances. Responsivity was maintained even at low retinal illuminances. Temporal-frequency dependent rod-cone interactions were observed in MC-pathway cells. Rod responses were of longer latency than cone responses, but there was no evidence of any difference in rod latency between parvocellular and magnocellular pathways.

Animals↗

Optical density of the human lens.

Optic disk reflectance was measured from 27 normal observers with their physiological lenses (aged 21-74 yr) and from two pseudophakic observers (aged 69 and 70 yr) with use of a Utrecht fundus reflection densitometer. Psychophysical heterochromatic flicker photometric luminance matches (10 degrees field) were obtained on the same group of the observers. A four-parameter model incorporating lens density, hemoglobin absorption, optic disk reflectance, and superficial stray light was used to fit the reflectometric data. A model incorporating lens density and the Judd revised spectral luminous-efficiency function was used to fit the psychophysical data. The lens-density spectrum used the two-factor aging model of Pokorny, et al. [Appl. Opt. 26, 1437 (1987)]. The lens density for each normal observer was estimated through a least-squares fitting procedure yielding an estimated lens age. For the reflectometric data the observer's chronological age agreed with estimated lens age with a correlation coefficient of 0.92. The reflectometric regression line underestimated chronological age by approximately 5 yr. The mean reflectance of the optic disk was 0.047 with standard error of the mean of 0.0044. Data from the pseudophakic observers were well described when corneal density was used to replace lens density. The lens density was also estimated from the psychophysical data. The observer's chronological age agreed with psychophysically estimated lens age with a correlation coefficient of 0.92. It was concluded that the in vivo lens density can be estimated from the reflectance spectrum measured off the optic disk. The reflectance spectrum of the optic disk was inferred to be close to spectrally neutral.

Adult↗

Psychophysical signatures associated with magnocellular and parvocellular pathway contrast gain.

Physiological data have revealed characteristic contrast gain and temporal integration signatures of the magnocellular (MC) and the parvocellular (PC) pathways. The goal in this study was to find psychophysical correlates of these signatures. Psychophysical forced-choice, luminance pedestal discrimination data were collected with a stimulus-surround display. A 2.05 degrees four-square stimulus array was varied from 73 to 182 trolands (Td) in a larger 115-Td surround. When the stimulus array was pulsed briefly, discrimination thresholds showed a minimum at the surround retinal illuminance, increasing in a V shape when the stimulus array was incremental or decremental to the surround. When the stimulus array was presented continuously as a steady pedestal within the constant 115-Td surround, discrimination thresholds increased monotonically with stimulus array retinal illuminance, obeying a slope of unity. Exposure duration variation showed temporal summation to extend to longer durations for the pulse increments and decrements than for the steady pedestal condition. Discrimination thresholds for pulsed medium-sized contrast steps showed the contrast pedestal paradigm showed the temporal signature of the MC pathway. Discrimination thresholds for small pedestal steps of the stimulus array from a steady pedestal showed the contrast gain signature of the MC pathway. The data suggested a difference in the spatiotemporal control of adaptation of the two pathways: The MC pathway adapted locally to the stimulus array, while the PC pathways showed little evidence of local adaptation. The experiments show that characteristic signatures of MC- and PC-pathway processing can be demonstrated by use of psychophysical procedures.

Adaptation, Physiological↗

Horizontal cells of the primate retina: cone specificity without spectral opponency.

The chromatic dimensions of human color vision have a neural basis in the retina. Ganglion cells, the output neurons of the retina, exhibit spectral opponency; they are excited by some wavelengths and inhibited by others. The hypothesis that the opponent circuitry emerges from selective connections between horizontal cell interneurons and cone photoreceptors sensitive to long, middle, and short wavelengths (L-, M-, and S-cones) was tested by physiologically and anatomically characterizing cone connections of horizontal cell mosaics in macaque monkeys. H1 horizontal cells received input only from L- and M-cones, whereas H2 horizontal cells received a strong input from S-cones and a weaker input from L- and M-cones. All cone inputs were the same sign, and both horizontal cell types lacked opponency. Despite cone type selectivity, the horizontal cell cannot be the locus of an opponent transformation in primates, including humans.

Animals↗

Increment threshold and purity discrimination spectral sensitivities of X-chromosome-linked color-defective observers.

The goal of the study was to evaluate spectral opponency in nine X-chromosome-linked color-defective observers. The tasks included increment threshold spectral sensitivity on an achromatic background, heterochromatic flicker photometry, and colorimetric purity discrimination. With a task of heterochromatic flicker photometry, the anomalous trichromatic observers showed spectral sensitivity of the corresponding dichromat. The increment threshold spectral sensitivity and colorimetric purity discrimination data were analyzed using the concept of standard cone photopigment spectral sensitivities for normal and defective vision, and a model that postulates one cone-additive and two cone-antagonistic systems. The model incorporated a shift of the peak spectral sensitivity of the long-wavelength-sensitive (LWS) pigment (for protan observers) or of the middle-wavelength-sensitive (MWS) pigment (for deutan observers). Two dichromats and two anomalous trichromats did not show clear evidence of LWS vs MWS cone antagonism. Five anomalous trichromats showed such cone antagonism. Molecular genetic analysis of the opsin genes is presented for eight of the observers.

Color Vision Defects↗

Color contrast under controlled chromatic adaptation reveals opponent rectification.

Color contrast was assessed in the equiluminant plane using asymmetric matching. Test and surround stimuli lay on cardinal axes of a cone opponent chromaticity space, (l-lw, s-sw). Matches were made as a function of both test and surround chromaticity. Some matches showed constant maximal induction consistent with retinal adaptation to the surround; others showed constant minimal induction. These matches were separated by a hiatus in which color appearance did not vary greatly with test chromaticity. The results suggest that rectified retinal spectral opponent pathways do not form a unitary chromatic opponent pathway but are subject to pathway-specific interactions.

Adaptation, Ocular↗

Cone-rod receptor spaces with illustrations that use CRT phosphor and light-emitting-diode spectra.

The purpose of the study is to characterize the excitation of the three cone types and the rods in a colorimetric system. Two representations of photoreceptor activity are developed. In the first, rod activity is characterized within a cone colorimetric system that is based on three known physical primaries. Examples are given that use color CRT phosphor spectra. We illustrate how this representation can be used to evaluate the range of chromaticities over which rod signals may intrude into color-monitor-based investigations of cone function. In the second representation, mixtures of four physical primary lights are used to manipulate the four receptor excitations independently. This method allows specification of sets of lights that isolate or silence up to three receptor classes or any combination of receptor classes. Examples are given that use spectra from four light-emitting diodes. This approach opens a field of research in which rod input to various retinal pathways can be evaluated.

Color Perception↗

Postnatal retinal development as measured by the electroretinogram in premature infants.

Light-adapted and dark-adapted electroretinograms were obtained in 27 premature infants who were screened for retinopathy of prematurity shortly after birth. Thirteen showed no retinopathy and 13 had mild to moderate retinopathy, which ranged from stage I, zone III (International Classification) to stage III, zone II. Measurements were made during the first 16 months of life. The configuration of the waveforms under both photopic and scotopic conditions changed during this period showing increased amplitudes of both the a- and the b-waves. A scotopic intensity series was performed and the b-wave amplitudes and implicit times were measured. The b-wave amplitude data were averaged for three adult control subjects, for infants without retinopathy of prematurity measured at 3-4 and at 6-7 months and for infants with retinopathy of prematurity measured at 3-4 and at 6-7 months. The Naka-Rushton function was fitted to the average data. The Rmax increased from 3 to 6 months and from 6 months to adulthood, and the Isat values decreased over this age range. The b-wave implicit times were within normal range in the 6-month data. There was no difference in Rmax or Isat for infants with and without ROP.

Adaptation, Ocular↗

Chromatic-discrimination axes, CRT phosphor spectra, and individual variation in color vision.

There is a growing use of color monitor systems in visual research and a parallel growth in the use of cone-excitation space to define stimuli and to report data. Color specification in monitor systems is accomplished by combination of the phosphor chromaticities. The effect of interobserver variation on color specification is highly dependent on the spectroradiometric properties of the primaries. We review potential sources of biologic variability and its effect on the nominal axes in a cone-excitation diagram for a color monitor system. Variation in preretinal pigment (lens and macular pigment), in the effective optical density and the spectral sensitivity of the visual photopigments, and in the cone weighting used to derive the spectral luminosity function are considered. The consequences of such biological variability are rotation and translation of the axes for a given observer relative to the nominal axes that the observer used for color specification. The importance of such rotations can be viewed within the framework of a particular experimental paradigm.

Adult↗

Mechanisms subserving temporal modulation sensitivity in silent-cone substitution.

Temporal contrast sensitivity data were collected with sine-wave-modulated lights for achromatic, chromatic, and silent-cone-substitution stimuli. Achromatic (556- and 642-nm lights in phase) and chromatic (556- and 642-nm lights in counterphase) modulation sensitivities were measured at a constant time-average retinal illuminance of 1256 trolands (Td) and chromaticity of 595 nm. These data were considered to represent isolated temporal responses of luminance and red-green chromatic channels, respectively. Silent cone substitution was achieved with counterphase modulation of the 556- and the 642-nm lights and by suitable adjustment of the modulations or the radiances of the two lights. (1) The peak modulation depth of the 642-nm light was reduced to silence the long-wavelength-sensitive (LWS) cone, and the peak modulation depth of the 556-nm light was reduced to silence the middle-wavelength-sensitive (MWS) cone. These protocols maintained the time-average retinal illuminance and chromaticity as for the control conditions. (2) The luminance of the 642-nm light was decreased to silence the LWS cone and was increased to silence the MWS cone. In this procedure the time-average retinal illuminance and chromaticity differ for the silenced-LWS-cone (1047 Td and 589.5 nm) and the silenced-MWS-cone (4358 Td and 622 nm) conditions. The response modulation of the achromatic and the chromatic channels was calculated for the silent-substitution conditions. The chromatic channel is more sensitive at low frequencies, with a transition to greater achromatic channel sensitivity near 13 Hz for the silenced-LWS-cone condition and near 6 Hz for the silenced-MWS-cone condition.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗

Responses to pulses and sinusoids in macaque ganglion cells.

The goal of the study was to compare pulse responses with sinusoidal temporal responsivity. The response of macaque ganglion cells was measured to brief luminance and chromatic pulses and to luminance or chromatic sinusoidal modulation. To make both positive and negative lobes of the pulse response visible, responses to pulses of opposite polarity were combined to yield a linearized pulse response. Tests of superposition were used to evaluate the linearized pulse response to different combinations of pulse duration and Weber contrast. A prediction of the pulse response was derived using sinusoidal responsivity functions and Fourier synthesis. For ganglion cells of the parvocellular (PC) pathway, shape and absolute amplitude of linearized pulse responses corresponded well to the predicted responses over a range of pulse durations at 0.5 and 1.0 Weber contrast for both luminance and chromatic modulation. For ganglion cells of the magnocellular (MC) pathway, shape and amplitude of the linearized pulse responses and the predicted responses corresponded when the contrast-duration product was low. This correspondence held for luminance modulation over a thousand-fold range of retinal illuminance. For contrast-duration combinations that produced a more vigorous response, over 100 imp/sec, the linearized pulse responses of MC-pathway cells became larger and time-advanced relative to the linear prediction until saturation became apparent. Incorporation of high Michelson contrast responses in the Fourier synthesis captured the timing but not the amplitude of the linearized pulse response. The data suggest that a mechanism similar to a contrast gain control acts upon MC- but not PC-pathway-cells. The data confirm that use of linear modelling to describe temporal behaviour of retinal ganglion cells is appropriate for small signals.

Animals↗

Balloon angioplasty with stent implantation in experimental coarctation of the aorta.

BACKGROUND: Balloon angioplasty of coarctation of the aorta is an effective method of treatment but is complicated by tearing of the aortic intima, formation of aneurysms, and restenosis. Stent placement at the time of balloon dilation could prevent restenosis and could also prevent progression of intimal tears to aneurysms. The purpose of this study was to evaluate the feasibility of balloon dilation and implantation of balloon-expandable stents in an experimental model of coarctation and to examine the effect of stent placement at the site of surgically created stenosis. METHODS AND RESULTS: Coarctation of the aorta was surgically produced in 11 juvenile swine. Simultaneous coarctation angioplasty and stent implantation was performed in 10 animals 34 +/- 7.8 days after surgery. Repeat catheterization was performed 59 +/- 6 days after stent implantation. Five animals underwent reexpansion of stents with subsequent follow-up catheterization. Aortic specimens were examined by light microscopy and scanning electron microscopy. Coarctation angioplasty with stent implantation was successful in all, with an increase in coarctation diameter from 46 +/- 8.5% to 90 +/- 12.2% of proximal aortic diameter (P = .0001). Systolic pressure gradient decreased from 32 +/- 19.8 to 0.5 +/- 2.8 mm Hg (P < .001). All stents were patent at follow-up catheterization, with no evidence of intraluminal thrombosis. Reexpansion in five animals increased the stent diameter from a mean of 77.4 +/- 12.1% to 93 +/- 11.0% of proximal aortic diameter (P = .02). Gross examination of aortic specimens demonstrated formation of neointima over the stent wherever the stent struts were in contact with the aortic wall. The stent occupied a subintimal position and produced minimal compression of the underlying media. Medial compression was noted immediately beneath stent struts, but there was no evidence of intimal or medial dissection. CONCLUSIONS: Balloon angioplasty with simultaneous implantation of balloon-expandable stents is effective in relieving aortic obstruction in experimental coarctation. Reexpansion of the rigid stent can be performed in an area of surgical aortotomy and coarctation without significant intimal or medial injury. Stent implantation may be useful in preventing restenosis and aneurysm formation after angioplasty of coarctation.

Angioplasty, Balloon↗

Responses of macaque ganglion cells and human observers to compound periodic waveforms.

We measured responses of macaque retinal ganglion cells to different periodic waveforms (sinusoidal, square, rapid-on and rapid-off sawtooth waveforms) for both luminance and equiluminant chromatic modulation. We analyzed the responses with a peak-to-trough detector. At low frequencies, on-center and off-center magnocellular (MC-) pathway cells showed a ten-fold higher responsivity to the rapid-on and rapid-off sawtooth respectively. Red-on (+L-M) and green-on (+M-L) parvocellular (PC-) pathway cells showed a four-fold greater responsivity to rapid red-on and rapid green-on equiluminant chromatic sawtooth waveforms respectively. At an equivalent retinal eccentricity, we measured psychophysical thresholds for luminance stimuli and chromatic stimuli. We concluded that luminance sawtooth sensitivities from psychophysics are consistent with selective detection through MC-pathway on- and off-center channels in the visual system. The differences between the compound periodic waveforms seen in the PC-pathway cell data did not occur in the psychophysics. In a second analysis, cell responses to sinusoidal modulation were used to predict the linear response to square-wave and sawtooth waveforms. PC-pathway cells showed linear temporal behavior over a wide range of contrasts, but MC-pathway cells displayed linear behavior only for low-contrast luminance modulation. Using these linear fits, we implemented a model incorporating central low-pass filtering in the MC- and PC-pathways before the peak-to-trough detector. This model captured better the time scale and relative sensitivity to periodic waveforms found in the psychophysical data.

Adult↗

Chromatic discrimination with variation in chromaticity and luminance: data and theory.

Boynton and Kambe developed a model of chromatic discrimination in which thresholds are mediated by two independent mechanisms: the short-wavelength sensitive (S-) cones (S-cone axis), and the middle-wavelength sensitive (M-) and long-wavelength sensitive (L-) cones (M/L-cone axis). In this study, we used a Maxwellian view optical system to investigate fundamental properties of the model as a function of chromaticity and luminance. We confirmed that discriminations along the S-cone axis were dependent on S-cone excitation level. However, changes in chromaticity and changes in mean luminance were not described by a single threshold-vs-radiance (TVR) template. We developed a model to account for the different effects of changing S-cone excitation by varying mean chromaticity and by varying mean luminance. M/L-cone discriminations showed a minimum at the L-cone excitation to white, indicating strong opponency. The thresholds increased with luminance approaching a Weber region and showing parallel functions for differing chromaticities. These data are fit by a model allowing retinal gain controls and spectral opponency.

Adult↗

Colorimetric purity discrimination: data and theory.

Colorimetric purity, measured as the first step from white toward the spectrum has a V-shaped function. Purity discrimination is best near 400 nm, least at 570 nm and intermediate at mid-spectrum and long wavelengths. A much flatter function occurs when colorimetric purity is measured as the first step from the spectrum toward white. In this study, we applied the formulation of chromatic discrimination thresholds measured along the S-cone and M/L-cone axis to account for chromatic discrimination in the equiluminant plane. The modeling results show that the purity step from white has a 1.6 log unit calculated range, similar to the classical data. The purity step from the spectrum is much flatter. The predicted range is dependent on the individual variance in chromatic discrimination thresholds and the luminance level. We then used psychophysical procedures to test the model's predictions. The resulting purity discrimination functions were generally in agreement with the model. Our modeling indicates that discrepant data of colorimetric purity can be explained with the context of discrimination models.

Adult↗

Comparison of thromboelastography to bleeding time and standard coagulation tests in patients after cardiopulmonary bypass.

This prospective study of 36 adult patients undergoing cardiopulmonary bypass (CPB) was conducted to determine the utility of thromboelastography (TEG) versus platelet studies (bleeding time, platelet count, mean platelet volume) and standard coagulation tests (prothrombin time, activated partial thromboplastin time, fibrinogen) to more effectively discriminate patients likely to benefit from platelet or fresh frozen plasma (FFP) transfusion. Although the sensitivities of the bleeding time (71.4%) and platelet count (100%) were similar to the TEG (71.4%), the specificity (89.3%) of the TEG was greater than that of the bleeding time (78.5%) and platelet count (53.6%). Seven patients experienced clinically significant hemorrhage; 5 (71.4%) had an abnormal TEG. Three of 8 (38%) other patients with an abnormal TEG had no abnormal bleeding. Only 2 of 27 (7.4%) patients with a normal TEG had abnormal bleeding requiring platelet or FFP transfusion. Therefore, it is suggested that post-CPB patients with a normal TEG should not receive platelet or FFP transfusions empirically. If excessive bleeding is noted in a patient with a normal TEG, this suggests a surgically correctable etiology. Data from this series suggest that patients displaying an abnormal TEG appear to be at increased risk for hemorrhage; therefore, appropriate blood product support should be initiated at the first sign of accelerated bleeding.

Adolescent↗