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PubMed2004

Arsenobetaine in Atlantic salmon (Salmo salar L.): influence of seawater adaptation.

Glycine betaine has been suggested to improve the maintenance of ionic and osmotic homeostasis during seawater adaptation in teleost fish. Arsenobetaine may also behave as an osmolyte, due to its structural similarity to glycine betaine. The influence of seawater adaptation on intestinal uptake and muscle accumulation of arsenobetaine in the teleost Atlantic salmon (Salmo salar L.) was investigated. Atlantic salmon (freshwater and seawater adapted) were given a single oral dose of arsenobetaine, which was absorbed over the intestine within 6 h after exposure. Seawater adapted Atlantic salmon had significantly higher levels of accumulated arsenobetaine in blood compared to the freshwater adapted salmon. However, seawater adaptation had no effect on the levels of accumulated arsenobetaine in muscle tissue. Similar retention of the administered dose was found in muscle tissue in both freshwater and seawater adapted salmon, with 49+/-6% and 50+/-10% retention after 144 h, respectively. Results indicate that muscle retention was not influenced by salinity in seawater adapting teleosts.

Adaptation, Physiological↗
PubMed2005

Acid stress adaptation protects Saccharomyces cerevisiae from acetic acid-induced programmed cell death.

In this work evidence is presented that acid stress adaptation protects Saccharomyces cerevisiae from acetic acid-mediated programmed cell death. Exponential-phase yeast cells, non-adapted or adapted to acid stress by 30 min incubation in rich medium set at pH 3.0 with HCl, have been exposed to increasing concentrations of acetic acid and time course changes of cell viability have been assessed. Adapted cells, in contrast to non-adapted cells, when exposed to 80 mM acetic acid for 200 min did not display loss of cell viability associated to morphological alterations typical of apoptosis. Thus, 80 mM acetic acid death-inducing conditions were selected to further characterize the early molecular events leading to such active cell death process. Catalase was specifically activated during acid stress adaptation and protection against acetic acid-induced death was associated with maintenance of its activity during treatment with 80 mM acetic acid. On the other hand, intracellular superoxide dismutase activity was found present at comparable levels both in adapted and in dying yeast cells, excepting in non-adapted cells which displayed a maximum activity value after 15 min acetic acid exposure, corresponding to more than 80% cell viability. This study gives first experimental evidence that H2O2, rather than superoxide, detoxification may have a major role in preventing yeast cell death in response to acetic acid. The results, as a whole, suggest that commitment of S. cerevisiae to a programmed cell death process in response to acetic acid is mediated through a ROS-dependent apoptotic pathway.

Acetic Acid↗
PubMed2004

Spatial discrimination of sound sources in the horizontal plane following an adapter sound.

The effect of a preceding (adapter) sound on the spatial discrimination of two subsequent, successively presented (target) sounds was tested in the horizontal plane. The adapter and the first target were located in front of the subject or 30 degrees to the right of the midline; both sounds were presented either at the same location or at different locations. The second target was located to the right or the left of the first. Sound spectra of the 3-s adapter and the 100-ms targets were either high (4.5-18 kHz) or low (1-4 kHz) in frequency. Fifteen subjects judged the position of the second target relative to the first in a two-alternative forced-choice paradigm. In comparison with a no-adapter control condition, in which no sound preceded, discrimination performance was increased when adapter and first target were presented at the same location and when both sounds consisted of the same frequency spectrum. No improvement occurred when adapter and targets differed in location or frequency. The results are consistent with previous results on post-adaptation discrimination of interaural time differences. Possibly, spatial adaptation of the underlying mechanisms of auditory localization may explain the discrimination aftereffect.

Acoustic Stimulation↗
PubMed2005

Local adaptation and enhanced virulence of Nosema granulosis artificially introduced into novel populations of its crustacean host, Gammarus duebeni.

Local adaptation theory predicts that, on average, most parasite species should be locally adapted to their hosts (more suited to hosts from local than distant populations). Local adaptation has been studied for many horizontally transmitted parasites, however, vertically transmitted parasites have received little attention. Here we present the first study of local adaptation in an animal/parasite system where the parasite is vertically transmitted. We investigate local adaptation and patterns of virulence in a crustacean host infected with the vertically transmitted microsporidian Nosema granulosis. Nosema granulosis is vertically transmitted to successive generations of its crustacean host, Gammarus duebeni and infects up to 46% of adult females in natural populations. We investigate local adaptation using artificial horizontal infection of different host populations in the UK. Parasites were artificially inoculated from a donor population into recipient hosts from the sympatric population and into hosts from three allopatric populations in the UK. The parasite was successfully established in hosts from all populations regardless of location, infecting 45% of the recipients. Nosema granulosis was vertically (transovarially) transmitted to 39% of the offspring of artificially infected females. Parasite burden (intensity of infection) in developing embryos differed significantly between host populations and was an order of magnitude higher in the sympatric population, suggesting some degree of host population specificity with the parasite adapted to its local host population. In contrast with natural infections, artificial infection with the parasite resulted in substantial virulence, with reduced host fecundity (24%) and survival (44%) of infected hosts from all the populations regardless of location. We discuss our findings in relation to theories of local adaptation and parasite-host coevolution.

Adaptation, Physiological↗
PubMed2004

Day to day variability of the dark-adapted pupil diameter.

PURPOSE: To determine the individual variability of the dark-adapted pupil diameter over 2 testing sessions using a standardized dark-adaptation protocol. SETTING: Texas Tech University Health Sciences Center, Lubbock, Texas, USA. METHODS: In this prospective observational cohort study, 40 volunteers with no history of ocular disease, surgery, or injury other than requirement for refractive correction were included. The right eye was tested. A standardized dark-adaptation protocol was used that controlled for accommodation and patient alertness. Infrared, still digital photographs were taken after 5 and 10 minutes of dark adaptation and analyzed independently by 2 investigators using digital-image software. Two test sessions were performed 1 to 7 days apart. Lifestyle factors such as sleep, diet, and exercise were not controlled. RESULTS: The mean subject age was 31.5 years (range 20 to 49 years). There were 20 men; 27 subjects wore correction for myopia, and 13 wore no correction. The mean interval between test sessions was 2 days (range 1 to 7 days). The mean difference and 95% confidence intervals for pupil diameter difference between sessions were as follows: 5-minute readings, +0.032 mm (-0.030 to +0.094); 10-minute readings, -0.006 mm (-0.059 to +0.047); mean of 5- and 10-minute readings, +0.013 mm (-0.038 to +0.064). Using the paired t test, the pupil diameter did not differ significantly between sessions in 5-minute dark adaptation (P =.2980), 10-minute dark adaptation (P =.8263), or the mean (P =.6049). CONCLUSION: Using a consistent dark-adaptation protocol that controlled for alertness, individuals aged 20 to 49 years showed no significant variation in dark-adapted pupil diameter when tested twice in 1 week.

Accommodation, Ocular↗
PubMed2006

Combined pharmacotherapy that increases proliferation and decreases apoptosis optimally enhances intestinal adaptation.

BACKGROUND: Adaptation after massive small bowel resection (SBR) is associated with increased rates of enterocyte proliferation (P) and apoptosis (A). In the present study, we sought to determine the effect of dual therapy designed to increase P and simultaneously reduce A. METHODS: C57Bl/6 mice underwent a 50% small bowel resection (SBR) or sham operation, and then received an inhibitor of apoptosis (pan-caspase inhibitor), a stimulus for proliferation (epidermal growth factor; EGF), a combination, or vehicle control. After 3 days, adaptive morphology (villus height, crypt depth) and rates of enterocyte turnover (proliferation and apoptosis) were measured in the remnant ileum. RESULTS: Adaptation in controls and treated with the inhibitor was similar. EGF-treated mice demonstrated an even greater adaptive response. Combined therapy with the inhibitor and EGF resulted in maximal adaptation as gauged by the greatest increases in villus height and crypt depth and ratio of rates of P to A. CONCLUSION: The capacity for adaptation following massive SBR is maintained via tight regulation of cell production and death. Pharmacologic intervention directed at increasing enterocyte proliferation while simultaneously decreasing apoptosis augments adaptation greater than either intervention alone and may provide a useful strategy to clinically amplify adaptation.

Adaptation, Physiological↗
PubMed2004

Sensorimotor effects on central space representation: prism adaptation influences haptic and visual representations in normal subjects.

Prism adaptation improves visual and haptic manifestations of left neglect, and can induce a small but reliable simulation of left visual neglect in normal individuals. Here, we present two experiments in which the effects of prism adaptation on the representation of space were explored. In Experiment 1, normal subjects were required to locate the centre of a haptically explored circle, before and after adaptation to leftward displacing prisms. In Experiment 2, a visual circle centring task was used. In both tasks, prism adaptation induced a significant rightward shift of performance. In addition, in both experiments, three classical measures of visuo-manual adaptation were taken: the visual shift, the proprioceptive shift and the total shift. The effects found on the haptic and visual tasks did not correlate with any of these measures. This suggests that the effects of prism adaptation on the circle centring tasks did not depend directly on the sensorimotor consequences of the adaptation. These results imply that prism adaptation can affect noetic levels of space representation in normal subjects, supporting the hypothesis that this low-level sensorimotor intervention can exert a bottom-up structuring influence on higher levels of cognitive integration.

Adaptation, Psychological↗
PubMed2006

Synaptic adaptation and odor-background segmentation.

Habituation is a form of non-associative memory that plays an important role in filtering stable or redundant inputs. The present study examines the contribution of habituation and cortical adaptation to odor-background segmentation. Segmentation of target odorants from background odorants is a fundamental computational requirement for the olfactory system. Recent electrophysiological data have shown that odor specific adaptation in piriform cortex neurons, mediated at least partially by synaptic adaptation between the olfactory bulb outputs and piriform cortex pyramidal cells, may provide an ideal mechanism for odor-background segmentation. This rapid synaptic adaptation acts as a filter to enhance cortical responsiveness to changing stimuli, while reducing responsiveness to static, potentially background stimuli. Using previously developed computational models of the olfactory system, we here show how synaptic adaptation at the olfactory bulb input to the piriform cortex, as demonstrated electrophysiologically, creates odor specific adaptation. We show how this known feature of olfactory cortical processing can contribute to adaptation to a background odor and to odor-background segmentation. We then show in a behavioral experiment that the odor-background segmentation is perceptually important and functions at the same time-scale as the synaptic adaptation observed between the olfactory bulb and cortex.

Adaptation, Physiological↗
PubMed2003

Perfect and near-perfect adaptation in a model of bacterial chemotaxis.

The signaling apparatus mediating bacterial chemotaxis can adapt to a wide range of persistent external stimuli. In many cases, the bacterial activity returns to its prestimulus level exactly, and this perfect adaptability is robust against variations in various chemotaxis protein concentrations. We model the bacterial chemotaxis signaling pathway, from ligand binding to CheY phosphorylation. By solving the steady-state equations of the model analytically, we derive a full set of conditions for the system to achieve perfect adaptation. The conditions related to the phosphorylation part of the pathway are discovered for the first time, while other conditions are generalizations of the ones found in previous works. Sensitivity of the perfect adaptation is evaluated by perturbing these conditions. We find that, even in the absence of some of the perfect adaptation conditions, adaptation can be achieved with near-perfect precision as a result of the separation of scales in both chemotaxis protein concentrations and reaction rates, or specific properties of the receptor distribution in different methylation states. Since near-perfect adaptation can be found in much larger regions of the parameter space than that defined by the perfect adaptation conditions, their existence is essential to understand robustness in bacterial chemotaxis.

Adaptation, Physiological↗
PubMedDate not supplied

Characteristics and variability of vertical phoria adaptation in normal adults.

We evaluated the characteristics of phoria adaptation for vertically induced retinal disparity. An adaptive change in the fusion-free ocular alignment, phoria adaptation, was measured with a computer-aided mirror haploscope at 10, 30, and 60 minutes after the start of wearing of a 3-prism-diopter base up prism by 35 normal subjects ranging in age from 21 to 67 years (mean: 37 years). The relationships between phoria adaptation and the subjects' age, the vertical fusional amplitude, the amount of heterophoria, and the starting time of the examination were evaluated. All subjects showed phoria adaptation, with the mean (+/- SD) degree of 0.78 +/- 0.28 degree, 0.96 +/- 0.26 degree and 1.02 +/- 0.30 degrees at 10, 30, and 60 minutes, respectively, after wearing the prism. The repeatability (95% confidence interval) for the measurements was less than +/- 0.24 degree. There was a significant correlation between the vertical fusional amplitude and the gain of phoria adaptation (at 10 and 60 minutes, P < 0.05). The gain of phoria adaptation measured at 60 minutes showed a significant decrease with age (P < 0.01). The results indicate that the time course of phoria adaptation in the vertical direction is similar to that in the horizontal direction and its gain differs considerably among subjects.

Adaptation, Ocular↗
PubMed1997

A direct role for DNA polymerase III in adaptive reversion of a frameshift mutation in Escherichia coli.

The sequences of adaptive reversions of a lac frameshift mutation in Escherichia coli resemble DNA polymerase errors, and the adaptive reversions decrease in strains with an antimutator DNA polymerase III (PolIII) allele. The latter finding could imply that DNA PolIII itself makes adaptive mutations. Alternatively, normal DNA PolIII errors could saturate post-synthesis mismatch repair during adaptive mutation. If so, the antimutator strain would produce fewer adaptive mutations because it possesses greater capacity for mismatch repair which could correct errors made by a polymerase other than DNA PolIII. Mismatch repair capacity is limited specifically during adaptive mutation, necessitating a test of this indirect model. This indirect model is ruled out here by the observation that the antimutator PolIII allele decreases adaptive mutation even in mismatch repair-defective cells. This supports a direct role for DNA PolIII in recombination-dependent adaptive mutation.

Adaptation, Physiological↗
PubMed2002

Ameliorating neglect with prism adaptation: visuo-manual and visuo-verbal measures.

Previous studies have shown that adaptation to rightward displacing prisms improves performance of neglect patients on visuo-manual (VM) tasks such as line cancellation, figure copying, and line bisection [Nature 395 (1998) 166]. The present study further evaluated the effect of prism adaptation (PA) on neglect symptoms by investigating: (a) the range of beneficial effects on common visuo-spatial deficits as well as less frequent phenomena like neglect dyslexia; (b) the duration of improvement following a single exposure to the right optical deviation; (c) the extent to which visuo-spatial performance can be comparatively ameliorated in VM tasks and visuo-verbal (VV) tasks (i.e. involving or not the adapted arm, respectively) and (d) the presence and duration of the manual visuo-motor bias induced by the prismatic adaptation (i.e. the after-effect). We investigated these issues in a group of neglect patients with right hemispheric damage who were also affected by neglect dyslexia. Following a single, brief prismatic adaptation the results showed that (a) several visuo-spatial abilities, including accuracy in reading single words and non-words, considerably improved, (b) the amelioration was long-lasting, continuing for at least 24h, (c) the presence, amount, and duration of neglect amelioration was not limited to VM tasks, but extended to VV tasks and (d) the presence and duration of the after-effect induced by prismatic adaptation remarkably paralleled the presence and duration of the improvement of neglect symptoms. These findings clearly demonstrate that beneficial effects induced by a single PA are very long-lasting and spread over a wide range of visuo-spatial deficits, independent of the type of response required. In addition, our results strongly suggest that the process of adaptation, as revealed by the presence of a visuo-motor after-effect, might be essential for establishing amelioration. In light of its characteristics, the prismatic adaptation technique should be a priority tool for the rehabilitation of the multifaceted hemispatial neglect syndrome.

Adaptation, Psychological↗
PubMed2000

Global motion adaptation.

Image motion is initially detected locally. Local motion signals are then integrated across space in order to specify the global motion of objects or surfaces. It is well known that prolonged exposure to motion causes adaptation at the local motion level. We have investigated whether adaptation also occurs at the global motion level. We have devised a global motion stimulus (a random dot kinematogram) which has equal motion energy in opposite directions but nonetheless gives rise to global motion perception. At the local motion level, adaptation to this stimulus should cause equal adaptation in both directions and should not give rise to an aftereffect. Any aftereffect seen must therefore be attributable to adaptation at the global motion level. We find that following adaptation to this stimulus, judgements of the perceived direction of a test pattern are systematically biased towards the direction opposite to the adapting direction, suggesting that adaptation does occur at a level of visual processing at which global motion is represented.

Adaptation, Physiological↗
PubMed2001

Adaptation to disparity but not to perceived depth.

The purpose of the present study was to investigate whether adaptation can occur to disparity per se. The adapting stimuli were large random-dot patterns of which the two half-images were transformed such that the depth effects induced by the vertical transformations were nulled by horizontal transformations. Thus, the adapting stimuli were perceptually the same, whereas the disparity fields differed from each other. The adapting stimuli were presented for five minutes. During that period, the percept of a fronto-parallel surface did not change. After the adapting period, subjects perceived a thin untransformed strip as either slanted or curved depending on the adapting transformation. The thin strips provided negligible information about the vertical disparity field. In a forced-choice task we measured the amount of horizontal transformation that was required to null the acquired adaptation. We found that the amounts of horizontal transformation required to perceive the test strip fronto-parallel were significantly different from zero. We conclude that the visual system can adapt to disparity signals in the absence of a perceptual drive.

Adaptation, Physiological↗
PubMed2002

Bivectorial transparent stimuli simultaneously adapt mechanisms at different levels of the motion pathway.

The motion aftereffect (MAE) to drifting bivectorial stimuli, such as plaids, is usually univectorial and in a direction opposite to the pattern direction of the plaid. This is true for plaids that are perceived as coherent, but also for other plaids which are seen as transparent for most or all of the adaptation period. The underlying mechanisms of this MAE are still not well understood. In order to assess these mechanisms further, we measured static and dynamic MAEs and their interocular transfer (IOT). Adaptation stimuli were plaids with small (coherent) and large (transparent) angles between the directions of the component gratings and a horizontal grating, which were adjusted in spatial frequency and drift velocity so that the pattern speed and vertical periodicity remained constant. Test stimuli were horizontal static or counterphasing gratings with the same periodicity as the adaptation stimuli. MAE duration was measured for monocular, binocular and IOT conditions. All static MAEs were smallest for the transparent plaid and largest for the grating, while all dynamic MAEs were constant across adaptation stimuli. IOT was twice as big for dynamic MAEs as for static MAEs, and did not vary with the adaptation stimuli. Other adaptation stimuli were plaids that differed in intersection luminance, contrast or spatial frequency, resulting in different amounts of perceived coherence. MAEs and IOT did not vary with perceived coherence. The results suggest that the MAE for bivectorial stimuli consists of low-level adaptation (dependent on local component properties, small IOT), as well as high-level adaptation (dependent on global integrated pattern properties, large IOT), which can be measured independently with static and dynamic test stimuli.

Adaptation, Ocular↗
PubMed2002

Gain adaptation of exogenous shifts of visual attention.

Gain adaptation of saccadic eye movements is the process whereby the size of the saccade is gradually modified if the target is consistently and surreptitiously displaced during the saccade. Because one attends to the saccade target before each saccade, we asked whether covert shifts of exogenous attention might themselves be adaptable. We did this by presenting a peripheral cue and then displacing it by 3 deg after an interval equal to the average time required for attention to shift from a central to a peripheral cue. This interval, as well as the location at which attention landed, was determined by a modification of the line-motion illusion, in which a line appears to shoot from a previously cued location. We found that this adaptation paradigm produced consistent gradual reductions (for back-steps) or increases (for forward-steps) in the magnitude of the shifts of attention. Like saccadic adaptation, adaptation of shifts of attention could be manipulated independently for rightward and leftward shifts. Furthermore, the backward adaptation paradigm also decreased the magnitude of subsequent saccades, even though no saccades had been made during the attentional adaptation. This argues that saccades are targeted to the locus of attention, and when this locus is systematically shifted, so too are subsequent saccades. In conclusion, the adaptability of shifts of attention suggests that attentional shifts, like saccades, are recalibrated using a spatial error signal.

Adaptation, Ocular↗
PubMed2003

Adaptation to vertical disparity induced-depth: implications for disparity processing.

Depth aftereffects produced by prolonged inspection of an object in depth can be mediated by monocular and binocular depth cues. The adapting mechanisms responsible for such effects have not yet been fully determined. Theories of binocular depth aftereffects typically posit a role of an adaptive horizontal disparity sensitive mechanism, implying multiple cue-specific mechanisms for depth aftereffects. Here we examined whether binocular depth aftereffects can be attributed to such a cue-specific mechanism. In Experiment 1 we did so using a technique allowing us to maintain horizontal disparities and vergence constant for our adaptation stimuli, whilst manipulating simulated depth by virtue of a vertical disparity induced-depth effect. We found that depth aftereffects were almost identical to those produced by adaptation to stimuli of equivalent depth produced by conventional horizontal disparity modulations. In Experiment 2, we examined depth aftereffects following adaptation to apparently frontal surfaces produced by different combinations of horizontal and vertical disparity modulations. Aftereffects were close to zero. These results suggest that binocular depth aftereffects are not due to adaptation of a horizontal disparity sensitive mechanism, and we argue that adaptation occurs at the level of a 3D shape sensitive mechanism derived from multiple cues. Experiment 3 was a control to examine whether the two types of adaptation stimuli in Experiment 1 were indeed perceptually the same, since in theory they may differ if vertical disparities influenced metric depth scaling. We found no evidence of this, and concluded that the two classes of stimuli used in Experiment 1, though consisting of very different patterns of disparity, were perceptually equivalent.

Adaptation, Physiological↗
PubMed1997

Specificity of saccadic adaptation in three-dimensional space.

The saccadic system is known to exhibit a considerable degree of short-term plasticity. Earlier studies have shown that saccadic adaptation, rather than being a global process affecting all saccades equally, has a certain degree of spatial resolution. Its localized nature has become apparent from studies in the frontal plane which have shown that short-term saccadic adaptation, induced along a given meridian, transfers to only a limited range of neighbouring directions. Considering that most natural gaze shifts also have a depth component, we investigated whether the directional specificity of the saccadic adaptive system can be generalized to three-dimensional (3-D) space. Binocular eye movements were recorded in seven subjects while they made saccades to visual stimuli in the horizontal plane of regard. Experiments began by recording baseline saccades, all starting from the same fixation point to either a farther target (far saccades) or an equally eccentric nearer target (near saccades). Next, by displacing the target intra-saccadically in opposite directions in alternating far and near trials, we attempted to simultaneously reduce the gain of the far saccades while increasing the gain of the near saccades. These experiments, aimed at eliciting a state of differential gain, were specifically designed to adapt only the saccadic response, since targets were shifted along corresponding iso-vergence circles. To investigate the effect of varying the radial direction difference, similar differential gain adaptation experiments were conducted in the frontal plane for saccades along two different meridians. Our results show that when the saccadic system is pressured, it is capable of adopting different gains simultaneously for equal-direction saccades to different depth planes. Similarly, opposite gain adaptation can also be achieved in the frontal plane, but only if radial saccade directions are sufficiently separated. The fact that short-term saccadic adaptation can be shown to be directionally specific in two perpendicular planes suggests that the adaptation process is restricted to a limited volume of 3-D oculomotor space.

Adaptation, Ocular↗