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Using 3-D FLASH, high resolution, very thin section T1 weighted images of the CNS, spine, and extremities can be obtained. From these single data sets, reformatted images whose resolution is equal to that of the original data set can be constructed in any desired plane. This approach may lead to the replacement of conventional T1 weighted spin echo imaging by 3-D FLASH techniques.
Flashing tomosynthesis, a procedure that consists of a recording step and a reconstruction step, facilitates the tomographic imaging of coronary arteries. In a comparative study 10 postmortem coronary arteriograms were examined with 35-mm cine technique and with flashing tomosynthesis. The degrees of stenosis found with both of these techniques were compared with morphometrically obtained values. A higher correlation coefficient existed for the degrees of stenosis obtained with tomosynthesis and morphometry (r = 0.92, p less than 0.001, SEE = 9%) than for those obtained with cine technique and morphometry (r = 0.82, p less than 0.001, SEE = 16%). The technique has also been successfully carried out in 5 patients with coronary artery disease.
PURPOSE: To investigate the use of magnetic resonance (MR) imaging with dynamic gadopentetate dimeglumine enhancement in hilar cholangiocarcinoma. MATERIALS AND METHODS: Twenty-four patients (14 men, 10 women; aged 27-78 years; mean age, 51 years) with hilar cholangiocarcinoma underwent T2-weighted spin-echo MR imaging in the axial plane and multisection, breath-hold, fast low-angle shot (FLASH) MR imaging in the coronal oblique plane before and at 30, 60, 90, and 120 seconds after bolus injection of gadopentetate dimeglumine. Morphologic features were recorded, and contrast medium enhancement characteristics and contrast-to-noise ratios were calculated for each sequence. RESULTS: All the lesions were hyperintense on T2-weighted spin-echo images and hypointense on FLASH images. On dynamic gadolinium-enhanced images, progressive heterogeneous enhancement was seen in all patients. Intrahepatic ductal dilatation was present in every patient. Intraluminal components were seen in 11 patients, lobar atrophy in 12, and segmental portal venous occlusion or stenosis in 13. Satellite lesions were present in four patients, and hilar lymph nodal enlargement in 11. Contrast-to-noise ratios were statistically significantly higher on T2-weighted spin-echo images than on all other images. CONCLUSION: Hilar cholangiocarcinomas have consistent enhancement and morphologic features that can be demonstrated with dynamic contrast-enhanced MR imaging.
L-type calcium currents were recorded from isolated ventricular myocytes using standard patch-clamp methods. Rapid release of photolabile guanosine 5'-O-(3-thiotriphosphate) (GTP gamma S), tetralithium salt, by flash photolysis of intracellular caged-GTP gamma S increased the magnitude of the L-type calcium current: an effect independent of the ultraviolet flash per se or the production of photolytic by-products. This increase in calcium current was markedly reduced by intracellularly applied guanosine 5-O-(thiodiphosphate), trilithium salt or by an excess of GTP gamma S. It is therefore likely that rapid release of GTP gamma S intracellularly in the absence of an agonist can, via a G protein-mediated mechanism, cause L-type calcium current activation. In the presence of Rp-adenosine 3,5-mono-thionophosphate (Rp-cAMP), photoreleased GTP gamma S results in a transient and much reduced increase in the amplitude of the L-type calcium current. We conclude that activation of Gs coupled to adenylate cyclase and ultimately cAMP-dependent phosphorylation may be primarily responsible for L-type channel activation, although a fast membrane-delimited (direct) pathway, not involving cytoplasmic second messengers, may also contribute to this effect.
It is widely held that the soma and basal dendrites of olfactory bulb mitral cells receive exclusively inhibitory synaptic input from local interneurons. However, the mitral somatodendritic membrane exhibits immunoreactivity for a variety of glutamate receptors, and blocking GABA receptors unmasks mitral cell self-excitation. This excitation is proposed to be mediated either by diffuse spillover of the mitral cells' own released glutamate, or by punctate transmission from glutamate-releasing granule cells. This study examined the pharmacology and kinetics of glutamate sensitivity of mitral cells by flash photolysis of nitroindoline caged glutamates, which facilitate reliable activation of receptors in the synaptic cleft. Wide-field laser uncaging (3.5-ms flash) of approximately 0.5-1 mM glutamate onto the soma activated large currents with fast (3.4-ms rise, 7.5-ms decay) and slow (64-ms rise, >10-s decay) components. In 100 microM APV, slow currents were reduced to 53% of control (257-ms rise, 2-s decay), displayed outward rectification in 1.3 mM Mg2+, and blocked by 15 microM 5,7-dichlorokynurenate. Responses to less, similar 100 microM glutamate were fully antagonized by 100 microM APV, consistent with competitive inhibition at high-affinity NMDA receptors. An APV-resistant NMDA receptor was not observed, refuting the punctate transmission model. Fast currents were blocked by 10 microM NBQX, boosted 3.28-fold by 100 microM cyclothiazide, and resolved into AMPA (40%) and kainate (60%) receptor components by 100 microM SYM2206. The results suggest that self-excitation depends on AMPA, kainite, and conventional NMDA autoreceptors on the mitral cell.
The properties of simple neurons showing selectivity to direction of motion in area 17 of the cat cortex were examined. We analyzed in particular a sample of cells receiving a projection from 0 to 10 degrees in visual angle from the area centralis of the cat retina. Three categories of simple neurons were examined: directionally asymmetric (DA) neurons, directionally selective neurons of the unimodal type (DS1), and bimodal types (DS2). Poststimulus time histograms (PSTH) were obtained to moving white and black bars as well as to static onset sequences and static offset sequences. Our analysis involves a comparison of responses to single static flashes at various receptive-field locations with responses to sequence pairs of static flashes at those same locations. We find that DA neurons are not sensitive to the direction in which a pair of stimuli are presented. Inhibitory and excitatory responses show properties of linear summation whatever the direction of the stimulus sequence. Their behavior is reminiscent of retinal and LGN neurons. The synergy model accounts well for a DA neurons's directional asymmetry. If pairs of stimuli are close enough (usually an interstimulus distance of 20' or less for the central 10 degrees of the cat's visual field), then DS neurons show striking departures from linear summation. Specifically, this departure entails an anisotropic distribution of inhibition. The directional selectivity of DS neurons cannot be explained on the basis of a simple linear combination of their on and off region's responses. Directional selectivity is produced entirely within an on-excitatory discharge region or entirely within an off-excitatory discharge region. The excitatory discharge center of even the simplest unimodal DS neuron can be shown to be decomposable into subunits smaller than that discharge center. The fact that the spread of this anisotropy of inhibition is often much more restricted than the entire extent of the DS neuron's excitatory discharge center argues strongly that underlying subregions or modules are contributing their inputs to DS neurons. A DS neuron does not analyze motion as an isolated unit; to the contrary, it is probably embedded in a pool of mutually "cooperative" DS neurons. The basic module of directional analysis is responsive either to an on-on sequence or an off-off sequence but not to both. It is not selective to an on-off sequence. Therefore, unimodal DS neurons (DS1) are performing an analysis of single moving edges.(ABSTRACT TRUNCATED AT 400 WORDS)
1. If an eccentric, stationary target is flashed while a subject is performing an eye movement in the dark, can this subject make a saccade to the location in space where the target briefly appeared? Different predictions result from alternative hypotheses regarding the manner in which saccade goals are determined. Retinal error being defined as the vector from the eye position at the time of the flash to the position of the target, the retinal-error hypothesis predicts that the saccade vector will be equal to the retinal-error vector. This hypothesis assumes that the oculomotor system ignores the eye displacement between target presentation and saccade. If so, the target will be missed. In contrast, the spatial-error hypothesis predicts that the eye displacement is taken into account by the brain to calculate the target's physical location to which, therefore, a correct saccade could be aimed. 2. At issue is the generality of a fundamental principle of ocular targeting. Previous studies have established that, if the movement is saccadic, eye displacement is used by the oculomotor system to calculate the target's physical location. In the case of pursuit, perceptual experiments on humans suggest that eye displacement is taken into account although its velocity is underestimated. However, in a recent study McKenzie and Lisberger reported that saccade trajectories starting during pursuit conform to the retinal error hypothesis. In other words, velocity underestimation is close to 100%. 3. Although McKenzie and Lisberger's results are very clear, they might have depended on particular experimental conditions. The issue was reinvestigated in a situation facilitating the discrimination of stimuli.(ABSTRACT TRUNCATED AT 250 WORDS)
Octopamine, a major efferent neurotransmitter in the lateral eye of the horseshoe crab (Limulus polyphemus), has previously been shown to modulate photoreceptor responses evoked by long flashes. Quantification of these data indicates that this modulation produced a genuine increase in sensitivity to light which cannot be entirely due to an increase in optical efficiency consequent on an anatomical alteration. Other previous studies demonstrated that extrinsic current can modulate Limulus lateral eye photoreceptor cells by inducing a bistable membrane potential with two distinct states. The present study was therefore undertaken to find out if octopamine could modulate visual responses by inducing prolonged and bistable polarization shifts similar to those demonstrated in several other neural systems. Intracellular microelectrodes were used to execute an electrophysiological study of the receptor potentials evoked in the lateral eye of Limulus when brief (20-ms) flashes were delivered while 50 microM octopamine perfused dark-adapted photoreceptors. The combined chemical and optical stimuli prolonged photoreceptor responses to light to the degree that they often exceeded the duration of the brief stimulus by hundreds of milliseconds. Moreover, these prolonged potentials were clearly bistable because they were categorical--either a prolongation was perceptually clear-cut and present or it was not, with no intermediate patterns being observed. During seawater control perfusions, such prolongations were absent. This appears to be the first demonstration of such categorical and prolonged potentials in a photoreceptor neuron. This finding particularly suggests that efferent-driven neuromodulation can enable the development of a persisting short-term representation of a brief stimulus, with this representation being retained at the most distal possible neural site.
The authors have studied, by means of pattern visual evoked potential (VEP) and flash electroretinogram (ERG) recordings, a group of 15 patients affected by definite multiple sclerosis. All of the subjects examined presented a clinical history indicating involvement of the visual pathways; VEPs were altered in a high percentage of eyes examined (93.3%), while a lower percentage of abnormal ERGs was seen (20% of eyes examined). The only type of ERG alteration found consisted of a pathologic b wave voltage increase, observed mainly with red flash stimuli. This finding could be attributed to an involvement of centrifugal optic nerve fibers having inhibitory functions on retinal cells.
Short-latency flash visual evoked potentials (VEPs) and electroretinograms (ERGs) were recorded in 30 healthy volunteers and 14 patients (7 with retrobulbar neuritis and 7 with retinitis pigmentosa). Simultaneous recordings were performed by corneal, scalp, nasopharyngeal and retrobulbar (5 patients) electrodes. In 18 out of 30 healthy controls a brief sequence of oscillating wavelets was recorded between 15 and 40 ms on the scalp sites behind the vertex. In retrobulbar neuritis (RBN) patients normal responses were recorded by lens, retrobulbar, nasopharyngeal and frontal scalp electrodes. On the contrary none of these patients displayed short-latency activity behind the Cz scalp position. In 5 out of the 7 patients with retinitis pigmentosa, corneal, nasopharyngeal and scalp electrodes failed to detect any reliable waveform time-locked to the flash onset. In the remaining 2, a small lens ERG was recorded, while all other electrodes recorded a sequence of low-volted wavelets initiating 30 ms after the stimulus onset. In these patients an occipital VEP reduced in amplitude and with prolonged latency was also recorded. It is concluded that in presence of a normal corneal ERG because of the presence of volume spread oscillating retinal activity, it is hard to define while part of the scalp recorded, short latency, oscillating potentials is generated in subcortical visual structures.
The purpose of this study was to explore the effects of spatial and temporal properties on the expected responses of visual neurons that have linear receptive fields (RFs), particularly those having a mirror symmetric distribution of spatial subregions. Receptive fields that are symmetric in at least one spatial dimension occur in neurons of the retina, the lateral geniculate nucleus (LGN), and the visual cortex of mammals. Responses to flashing bars, moving bars, and moving edges were studied for different configurations of an analog RF model in which spatial and temporal aspects were varied independently. Responses of the model at intermediate stimulus speeds were found to agree with responses in the literature for X and Y units of the LGN and often for simple units of the visual cortex. In particular, having separated regions of response to light and dark edges, an identifying property of simple cells, was found to be a linear consequence of RF regions responding inversely to stimuli of opposite polarity. Model differences from responses of cortical complex units show that a linear model cannot mimic their responses, and imply that complex units employ major nonlinearities in coding image polarity (light vs dark), which signifies a nonlinearity in coding intensity. Because sudden flux changes inherent in flashing bars test mainly temporal RF properties, and slowly moving edges test mainly spatial properties, these two tests form a useful minimal set with which to describe and classify RFs. The usefulness of this set derives both from its sensitivity to spatial and temporal variables, and from the correlation between the linearity of a cell's processing of stimulus intensity and its RF classification.
Blood volume flow estimation remains an important task for the functional evaluation of internal organs. In vitro and in vivo flow estimation has been carried out using Flash Echo Imaging in harmonic mode after the administration of microbubble-based ultrasound contrast agents. The in vitro flow volume rate correlated with the constant replenishment level but less so with the video intensity decay rate. The in vivo volume flow rates obtained in four dogs agreed well with CVI-Q (time domain correlation) based flow measurement. Our experimental results indicate that the volume flow rate can be accurately estimated in vitro and in vivo using harmonic Flash Echo imaging.
Catalytic reforming is a refining process that converts naphthenes to aromatics by dehydrogenation to make higher octane gasoline blending components. A portion of this wide boiling range hydrocarbon stream can be separated by distillation and used for other purposes. One such application is a mixture of predominantly 9-carbon aromatic molecules (C9 aromatics, primarily isomers of ethyltoluene and trimethylbenzene), which is removed and used as a solvent--High Flash Aromatic Naphtha. A program was initiated to assess the toxicological properties of High Flash Aromatic Naphtha since there may be human exposure through inhalation or external body contact. The current study was conducted to assess the potential for developmental toxicity in the mouse and for reproductive toxicity in the rat. In the developmental toxicity study in CD-1 mice, exposure of dams by inhalation to near lethal levels (1500 ppm) resulted in fetal mortality, reduced weight, delayed ossification, and an increased incidence of cleft palate. At 500 ppm, a level at which maternal weight gain was slightly reduced, fetal weight gain was also reduced, but there was no other evidence of developmental effects. The lowest exposure level (100 ppm) did not cause any maternal or developmental toxicity. There was no consistent evidence of reproductive toxicity in rats, even at exposure levels which resulted in significantly reduced parental weight gain. In addition, when parental exposure was stopped on GD (gestation day) 20, birth weights as well as postnatal survival were generally similar to control values, even in the 1500 ppm exposure group. Postnatal weight gain was also similar to controls early in weaning, but, if maternal exposure was reinitiated, weight gain was reduced in the high exposure group. However, when exposure was continued until delivery, pups in the high exposure group exhibited reduced litter size, birth weight and poor survival. Thus it was likely that the reduction in fetal weight, seen in the developmental toxicity study in mice, was transient and had no postnatal consequences if maternal exposure was terminated at any time prior to delivery.
Flash-evoked visual potentials (VEPs) recorded from the scalp were used in a series of 35 patients with tumors along the visual pathway: 3 orbital tumors, 25 perisellar tumors, 4 intraventricular tumors, and 3 occipital lesions. Preoperatively, various combinations of impaired visual fields and visual acuity were observed in over 90% of the patients. A postoperative decrease in visual function was observed in 3 cases. Of the 25 perisellar lesions, 13 were operated through a standard frontotemporal craniotomy and 12 were operated through a transnasal-transsphenoidal approach. VEPs were highly susceptible to volatile anesthetics, and there was a significant incidence of spontaneous latency increases and amplitude decreases in a large number of patients. There was an unacceptably high number of cases with significant VEP alteration occurring without concomitant visual function change. During trepanation or the transnasal approach, a reversible potential loss was observed in 11 patients, a profoundly altered wave form was seen in 8 cases, and a loss of single peaks was observed in 15 patients. During dissection of the tumor, a reversible potential loss or a potential with unidentifiable peaks was found in 25 cases; however, the VEPs recovered during closure or in the recovery room. There was no correlation between intraoperative VEP changes and the postoperative changes in visual function. In only 1 patient with an insignificant postoperative decrease in visual acuity from 0.4 to 0.3 was there a concomitant intraoperative potential loss. The major conclusion of our findings is that light-emitting diode flash-evoked VEPs demonstrate intraoperative changes that appear too early and too prominently to be caused solely by manipulation of the optic pathways.(ABSTRACT TRUNCATED AT 250 WORDS)
A prospective study using contrast enhanced turbo-FLASH (Fast Low-Angle Shot) magnetic resonance (MR) angiography was performed to assess the arterial anatomy in patients who had advanced atherosclerotic aortoiliac disease. This new imaging sequence was employed in 17 patients and the results were compared with conventional abdominal aortography. MR angiography accurately detected all aortic occlusions (3/3), their sites and their extent. All nine iliac occlusions were correctly identified (sensitivity 100%, specificity of 90%). The sensitivity was 100% for stenosis of 50% or greater in the abdominal aorta, and the iliac and common femoral arteries. The degree of stenosis was overgraded in 20 of 51 lesions (39.2%). Mild stenosis was overgraded as moderate stenosis in 10 and as severe stenosis in three. Moderate stenosis was overgraded as severe stenosis in four. None of the mild or moderate stenoses resulted in areas of signal voids suggestive of occlusions. Three severe stenoses were seen as areas of signal voids (two iliac, one femoral). In the eight patients who had in total 10 aneurysmal dilatations of the aorta or the iliac arteries, MR angiography was superior in demonstrating the true extent of the aneurysms. We conclude that turbo-FLASH MR angiography has the potential to be a useful non-invasive imaging technique for patients with advanced aortoiliac disease.
Correlated experiments on visual reaction time (RT) and visual evoked cortical potentials (VECP's) were performed to assess the effects of illumination level of steady annulus surrounds on the latency of response to centrally presented target flashes (1 and 3 degrees in diameter) over a wide range of retinal illuminances. The latencies of the electrophysiological (VECP) responses are more variable than those of the psychophysical RT responses. For both classes of response, the visual latency for a given target flash luminance is systematically increased (inhibited) by a spatially contiguous annulus with a retinal illuminance that equals or exceeds that of the target. The inhibitory effect of a given annulus increases progressively as the target retinal illuminance is lowered below that of the annulus. The corresponding RT and VECP curves have the same shape, thus suggesting that the motor component of the RT responses is not differentially influenced by variations in target illumination. The inhibitory effects are characteristically greater for the 3 degrees target than for the 1 degree target. Lateral neural inhibition and stray-light models for these data are considered.
The time course of the initial negative wave of the flash electroretinogram of the dark-adapted cat has been found to be critically dependent of contributions from cells of the inner retina, not only for very low-intensity flashes for which the negative scotopic threshold response is dominant but also when the stimulus is sufficiently intense for the rods themselves to contribute directly to the electroretinogram. However, if the inner-retinal responses are blocked pharmacologically or are suppressed by a steady adapting background, the initial negative wave of the remaining electroretinogram (the alpha wave) can be explained as the sum of photoreceptor and bipolar-cell components that can be modeled as described by Lamb and Pugh [J. Physiol. (London) 449, 717 (1992)] and Robson and Frishman [Vis. Neurosci. 12, 837 (1995)], respectively.
The selective suppression of flicker response from LWS cones has been investigated with two approaches. One approach has emphasized the use of light-adaptation conditions, and the other has emphasized the use of dark-adaptation conditions. In both cases, stimuli are arranged to restrict or exceed the ability of adaptation processes to maintain an afferent flicker response, and long-wavelength stimuli are used to overload spectrally opponent processes. By integrating these two approaches, this study shows that diverse manifestations of flicker response suppression can be closely related mechanistically. For instance, the steep flicker TVI slopes that resulted from superimposing temporally modulated (100% contrast) test stimuli on flashed backgrounds corresponded to the disappearance of flicker that resulted from increasing the time-averaged illuminance of temporally modulated stimuli (contrast x < 100%) that were flashed alone in an otherwise dark field. For the stimulus parameters of this study, flicker response suppression was more evident for small (19' diameter) than for large (1 degree diameter) stimuli. However, flicker response suppression was elicited reliably for both sizes by adding a spatially coincident short-wavelength stimulus to the interstimulus interval between presentations of the long-wavelength stimuli. By showing that temporal contrast can be treated as an independent variable for an important set of test/background stimulus combinations, the results of this study make it possible to investigate the means by which changes of contrast gain help to maintain flicker response as assessed in a conventional flicker TVI paradigm. The reduced degree of suppression for relatively large stimuli probably is related to the increased action of spatially extensive contrast gain-control processes. These contrast gain-control processes might not act independently of spectrally opponent processes.