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PubMed2003

Time-course of S-cone system adaptation to simple and complex fields.

We examine the temporal nature of adaptation at different stages of the S-cone color system. All lights were restricted to the S-cone-only (a constant L and M) cardinal axis in color space passing through mid-white (W). The observer initially adapted to a steady uniform field with a chromaticity on the -S end of the axis or on the +S end of the axis or a complex field composed of chromaticy -S and +S (+/-S adaptation). The observer then readapted to a steady uniform field of chromaticity W for a variable length of time (i.e., 0, 0.1, 0.25, 0.5, 1.0, or 2.0 s). A probe-flash technique was used to measure S-cone discrimination at various points along the S-cone-only cardinal axis. This allowed estimation of the response of the S-cone system over an extended response range. Following exposure to the -S and +S uniform fields, sensitivity was maximal at or near the chromaticity of the initial adaptation field and decreased linearly away from the adapting point. The shift from +S to W occurred more rapidly than the shift from -S to W; both of these shifts can be described by a multiplicative scaling of the S-cone signal. Following +/-S adaptation the threshold curve initially had a shape similar to that measured following -S adaptation, but returned rapidly to the W adaptation state. The shift following +/-S adaptation cannot be described by the multiplicative model, but can be explained by a change in the shape of the non-linearity. The results suggest the existence of fast post-receptoral processes.

Adaptation, Ocular↗
PubMed1996

Adaptation-dependent changes of bipolar cell terminals in fish retina: effects on overall morphology and spinule formation in Ma and Mb cells.

We have investigated the effects of light and dark adaptation on the overall morphology of bipolar cell (BC) terminals in sublaminae a and b of the inner plexiform layer after labelling with Lucifer Yellow (LY) and PKC immunostaining using confocal laser scanning microscopy and serially sectioned material for electron microscopy. Three-dimensional reconstructed terminals showed marked adaptation-dependent changes of their morphology. Terminals of mixed rod-cone BCs in sublamina a (Ma BC) were irregular and scalloped in light adapted, but smooth and regular in dark-adapted specimens. Terminals from mixed rod-cone BCs in sublamina b (Mb BCs) exhibited an opposite behaviour. At the ultrastructural level, bipolar terminals in both sublaminae showed fingerlike extensions (spinules) invaginating presynaptic amacrine cell (AC) processes. Sixty-two percent of the dark-adapted Mb terminals in sublamina b showed spinules, whereas 21% of the light-adapted terminals had spinules. By contrast, 50.6% of the light-adapted Ma terminals in sublamina a formed spinules, compared to 17.8% of the dark-adapted Ma terminals in this sublamina. These observations reflect the functional subdivision of the inner plexiform layer in an inner ON-and an outer OFF-centre lamina. Our findings suggest that the synaptic plasticity of BC axon terminals may be due to differences of BC membrane potential, or the activity of AC input onto bipolar terminals. They may contribute to processes of fine tuning regulating the efficiency of AC-BC interaction under varying adaptation conditions.

Adaptation, Ocular↗
PubMed1998

Visual motion aftereffects: differential adaptation and test stimulation.

The local motion adaptation at the basis of the motion aftereffect (MAE) can be expressed in a variety of ways, depending upon the structure of the test display [Wade et al. (1996). Vision Research, 36, 2167-2175]. Three experiments are reported, which examined the characteristics of the test display and of the local adaptation process. In Experiment 1, MAEs were recorded in the central of three test gratings but their directions depended on the location of the centre relative to the adapting gratings. The effects of adapting motions in different directions were examined in Experiments 2 and 3, in which one or two adapting gratings were presented above or above and below a fixation cross. The upper grating always received the same (leftward) direction of motion during adaptation, and the lower grating was: moving in the opposite direction, stationary, moving in the same direction, or absent. The results indicate that no MAE is visible in the upper grating when a single test grating is observed experiment 2) and only occurs with two test gratings following differential adaptation between the upper and lower gratings (Experiment 3). Thus, the MAE occurs as a consequence of adapting restricted retinal regions to motion but it can only be expressed when differentially adapted regions are also tested.

Adaptation, Ocular↗
PubMed1998

Local velocity representation: evidence from motion adaptation.

Adaptation to a moving visual pattern induces shifts in the perceived motion of subsequently viewed moving patterns. Explanations of such effects are typically based on adaptation-induced sensitivity changes in spatio-temporal frequency tuned mechanisms (STFMs). An alternative hypothesis is that adaptation occurs in mechanisms that independently encode direction and speed (DSMs). Yet a third possibility is that adaptation occurs in mechanisms that encode 2D pattern velocity (VMs). We performed a series of psychophysical experiments to examine predictions made by each of the three hypotheses. The results indicate that: (1) adaptation-induced shifts are relatively independent of spatial pattern of both adapting and test stimuli; (2) the shift in perceived direction of motion of a plaid stimulus after adaptation to a grating indicates a shift in the motion of the plaid pattern, and not a shift in the motion of the plaid components; and (3) the 2D pattern of shift in perceived velocity radiates away from the adaptation velocity, and is inseparable in speed and direction of motion. Taken together, these results are most consistent with the VM adaptation hypothesis.

Adaptation, Ocular↗
PubMed1999

Time course of motion adaptation: motion-onset visual evoked potentials and subjective estimates.

The aim of this study was to quantitatively describe the dynamics of adaptation to visual motion with electrophysiological and psychophysical methods in man. We recorded visual evoked potentials (VEPs) to motion onset of random dot patterns from occipital and occipito-temporal electrodes during a succession of adaptation-recovery sequences. In these sequences the test stimulus was used to set the adaptation level: seven trials with 70% motion duty cycle (adaptation) followed by seven trials of 7% motion duty cycle (recovery). In a similar paradigm we determined the length of the perceptual motion after-effect to obtain a psychophysical measure of the time course of motion adaptation. Our results show a highly significant reduction of the N2 amplitude in the maximally compared to the minimally adapted condition (P < 0.001). Electrophysiological and psychophysical results both indicate that adaptation to visual motion is faster than recovery: The data were fit with an exponential model yielding adaptation and recovery time constants, respectively, of 2.5 and 10.2 s for the N2 amplitude (occipito temporal derivation) and of 7.7 and 16.7 s for the perceptual motion after-effect. Implications for the design of motion stimuli are discussed, e.g. a motion stimulus moving 10% of the time may lead to about 30% motion adaptation.

Adaptation, Ocular↗
PubMed1998

Adaptation in a rotating artificial gravity environment.

The centripetal force generated by a rotating space vehicle is a potential source of artificial gravity. Minimizing the cost of such a vehicle dictates using the smallest radius and highest rotation rate possible, but head movements made at high rotation rates generate disorienting, nauseogenic cross-coupled semicircular canal stimulation. Early studies suggested 3 or 4 rpm as the highest rate at which humans could adapt to this vestibular stimulus. These studies neglected the concomitant Coriolis force actions on the head/neck system. We assessed non-vestibular Coriolis effects by measuring arm and leg movements made in the center of a rotating room turning at 10 rpm and found that movement endpoints and trajectories are initially deviated; however, subjects readily adapt with 10-20 additional movements, even without seeing their errors. Equilibrium point theories of motor control errantly predict that Coriolis forces will not cause movement endpoint errors so that subjects will not have to adapt their reaching movements during rotation. Adaptation of movement trajectory acquired during Coriolis force perturbations of one arm transfers to the unexposed arm but there is no intermanual transfer of endpoint adaptation indicating that neuromotor representations of movement endpoint and trajectory are separable and can adapt independently, also contradictory to equilibrium point theories. Touching a surface at the end of reaching movements is required for complete endpoint adaptation in darkness but trajectory adapts completely with or without terminal contact. We have also made the first kinematic measurements of unconstrained head movements during rotation, these movements show rapid adaptation to Coriolis force perturbations. Our results point to methods for achieving full compensation for rotation up to 10 rpm.

Adaptation, Physiological↗
PubMed1999

Multiple immediate-early gene expression during physiological and endocrine adaptation to repeated stress.

This study had three objectives: (i) to determine whether there were individual differences in the activation and adaptation of a range of immediate-early genes to repeated restraint stress, (ii) to monitor physiological responses (endocrine, cardiovascular and core temperature) and their adaptation with repeated presentations of the stressor, and (iii) to determine whether any of these indices were altered by dehydroepiandrosterone, an anti-glucocorticoid steroid known to be reduced in humans by stress. Four groups of male rats were implanted subcutaneously with either dehydroepiandrosterone or control (paraffin) pellets. They were then subjected to either a single or 14 days of restraint (60 min/day) or transferred to the testing room (unstressed). Repeatedly stressed animals and their controls were also implanted with intra-abdominal telemetric transmitters to record heart rate and core temperature. Protein products for c-fos,fos-b, c-jun and jun-b were displayed by immunocytochemistry. Areas examined included the ventrolateral septum, hypothalamic paraventricular nucleus, amygdala, locus coeruleus and nucleus of the solitary tract. Acute restraint increased Fos immunoreactivity in all of the areas examined, with the exception of the medial amygdala. The pattern of induction for Fos-B and Jun-B was similar, while c-Jun was only increased in the septum (though constitutive levels were high in most structures compared to the other proteins examined). After 14 days of restraint, immediate-early gene immunostaining was reduced in all of the areas examined, though the extent of adaptation depended on the area and immediate-early gene. In the forebrain, Fos expression adapted in the paraventricular nucleus, amygdala and septum, whereas Fos-B and c-Jun adapted incompletely in the septum. In contrast, Jun-B behaved like Fos. In the brainstem, Fos, Fos-B and Jun-B expression adapted in the nucleus of the solitary tract (but not the locus coeruleus). Corticosterone levels were still raised above baseline, but the response was blunted compared to acute stress. There was marked stress-induced hypothermia which did not adapt during the restraint session, but this returned to baseline during restraint after about five days. In contrast, stress-induced tachycardia did not change during repeated restraint. Dehydroepiandrosterone implants had no clear-cut effects on any immunostaining following acute stress, though there was a trend towards lessened adaptation of the Fos response in the septum after steroid treatment. Dehydroepiandrosterone also did not affect the cardiovascular or endocrine responses to repeated restraint. These experiments show that adaptation of the expression of multiple immediate-early genes occurs during repeated restraint, but in a site-specific pattern in the brains of male rats.

Adaptation, Physiological↗
PubMed2000

Evidence for adaptive response and implication in pulse-simulated low-dose-rate radiotherapy.

PURPOSE: Pulsed-dose-rate (PDR) brachytherapy as a substitute for continuous low-dose-rate (LDR) brachytherapy has a number of clinical advantages. However, early results show that some cells can exhibit an adaptive response to radiation and in PDR where many pulses are given such an adaptive response may play an important role in the outcome. METHODS AND MATERIALS: Nine human cell lines (two normal fibroblast and seven tumor) were evaluated for an adaptive response. Cells were given either a single adapting dose before a challenge dose or given PDR sequences for which the average dose rate matched the LDR dose rate. Response was assessed using the colony survival assay. RESULTS: Five of the nine cell lines showed an adapting response to single small doses of radiation. Three of these cell lines were further investigated for adapting response to PDR and two of the three lines (one ovarian carcinoma and one glioma) showed an adaptive response which was dependent on pulse size and interval. CONCLUSION: The data show that an adaptive response can occur in human cells and that it can vary among cell lines. In addition, PDR sequences also produced an adaptive response which could have an affect on PDR therapy if such a response is found in tissues.

Adaptation, Physiological↗
PubMed1997

Monkey superior colliculus activity during short-term saccadic adaptation.

This article concerns the neural mechanisms that underlie short-term saccadic adaptation in the rhesus monkey. By means of a consistent intrasaccadic target displacement, the relation between visual input and motor output was gradually changed in three monkeys, such that they made hypometric saccades. During this process, the activity of saccade-related burst neurons in the intermediate and deep layers of the Superior Colliculus (SC) was recorded in two of the monkeys. Our findings show that, like in humans, only saccades evoked within a restricted field around the adaptation target were adapted. However, unlike in humans, the kinematic properties of adapted saccades also changed systematically during the adaptation process. Typically, adapted saccades were slower and had a longer duration than would be expected on the basis of the main sequence for nonadapted visually guided movements. During adaptation, saccade-related activity of units in the SC remained appropriate for the saccade that was required to foveate the initial target, rather than for the saccade that was actually made. This means that adaptation caused a dissociation between SC activity and the ensuing saccade. Thus, the activity of the colliculus was better described in "required eye displacement coordinates" than in "actual eye displacement coordinates." Our data provide further evidence for the hypothesis that short-term saccadic adaptation acts at a level downstream from the SC, presumably at a stage that determines the kinematics of saccadic eye movements.

Adaptation, Physiological↗
PubMed2002

Selective and delay adaptation of human saccades.

The consistently triggered step back of a target during primary saccades of a human subject induced a gradual change in gain, the ratio of the saccade amplitude to the target eccentricity. After a few hundred trials, subjects were able to foveate the displaced target in a single saccade. Presentation of a displaced target showed that human memory guided saccades have gain adaptation just like the well-established adaptation of visually guided saccades. Examining the transfer of adaptation between the memory guided saccade and two other types of visually guided saccades showed that each saccade transferred a 10-25% adapted gain change to the other saccades. However, any pair of the three saccades acquired different gains by adaptation in the same horizontal direction simultaneously, hence each saccade had adaptive capability independent of the others. Adaptation took place even when the appearance of a displaced target was delayed by 400-600 ms from the end of a primary saccade. These findings have important implications about the adaptation, particularly the location and temporal property of the adaptive mechanism in saccade generation.

Adaptation, Physiological↗
PubMed1997

Computer prediction of adaptive bone remodelling around noncemented femoral prostheses: the relationship between damage-based and strain-based algorithms.

Several mathematical models to predict tissue adaptation have been derived since Julius Wolff proposed a function-form relationship for bone. These can be formulated as computational procedures (algorithms) to predict bone adaptation around implants. The objective of this paper was to further develop the damage-adaptive algorithm, to test its validity, and to determine the relationship between it and algorithms based on strain energy. This was achieved using finite element models of the proximal femur, one for the intact case and another for the case where a noncemented hip prosthesis is implanted. The finite models were generated using CT scan data. Initial bone resorption patterns around a femoral prosthesis following total hip arthroplasty were computed for both damage-adaptive and strain-adaptive adaptation rules. It is found that the damage-adaptive algorithm can successfully predict the bone's adaptive behaviour in response to altered mechanical loading provided that account is taken of the nonlinear nature of damage accumulation. Predictions are made using a strain energy stimulus for comparison with the damage stimulus, and a theoretical relationship between the two is proposed. It is shown that an advantage of the damage approach over the strain-based approach is that the nonlinearity required to replicate clinically observed resorption patterns can be derived theoretically, whereas for strain-adaptive remodelling, empirical relationships are assumed.

Adaptation, Physiological↗
PubMed2006

Saccadic adaptation in Chiari type II malformation.

BACKGROUND: Saccadic adaptation corrects errors in saccadic amplitude. Experimentally-induced saccadic adaptation provides a method for studying motor learning. The cerebellum is a major participant in saccadic adaptation. Chiari type II malformation (CII) is a developmental deformity of the cerebellum and brainstem that is associated with spina bifida. We investigated the effects of CII on saccadic adaptation. METHOD: We measured eye movements using an infrared eye tracker in 21 subjects with CII (CII group) and 39 typically developing children (control group), aged 8-19 years. Saccadic adaptation was induced experimentally using targets that stepped horizontally 120 to the right and then stepped backward 3 degrees during saccades. RESULTS: Saccadic adaptation was achieved at the end of the adaptation phase in participants in each group. Saccadic amplitude gain decreased by 6.9% in the CII group and 9.3% in the control group. The groups did not differ significantly (p = 0.27). Amplitude gain reduction was significantly less in the CII participants who had multiple shunt revisions. Regression analyses revealed no effects of spinal lesion level, presence of nystagmus, or cerebellar vermis dysmorphology on saccadic adaptation. CONCLUSION: The neural circuits involved in saccadic adaptation appear to be functionally intact in CII.

Adaptation, Physiological↗
PubMed2000

Studies of the phenomenon of host adaptation in Salmonella.

To study the phenomenon of host adaptation in Salmonella, a mathematical model has been developed which permits a definition and experimental investigation of the specific interaction between the adapted serovar and the adequate host. After experimental infection using a mixture of equal parts of two Salmonella strains, A and B, the bacterial concentrations CA and CB were determined in the organs of the animals infected. If an animal of species a and an animal of species b are infected with the same mixture of strain A adapted to a and strain B adapted to b, an expression: log10Qab = log10CaA + log10CbB - log10CaB - log10CbA may be calculated which describes the influence of the specific serovar-host interaction on the dynamics of the bacterial count. The variable Qab was determined using four Salmonella dublin, four Salmonella choleraesuis and five Salmonella gallinarum/pullorum strains in a total of 63 pairs of different hosts (calf and pig, calf and chicken, or pig and chicken). On this basis, the following statements can be made. The epidemiologically defined host adaptation of Salmonellas is accompanied by a specific agent-host interaction between the adapted serovar and adequate host. It promotes adherence and spreading of the agent in the adequate host. The effect was particularly expressed on day 3 post-infection and could be detected both in the lumen of the anterior sections of the intestine and in the intestinal lymph nodes and the liver. In part, the host-independent strain characteristics had a greater influence than the specific serovar-host interaction on the dynamics of the bacterial count. Strains of non-adapted serovars may thus result in a more intense colonization and invasion of the host than simultaneously administered bacteria of a serovar which is adapted to the respective host. The effects of a specific serovar-host interaction on colonization of and spreading in the host should be considered only as a component which contributes to the phenomenon of host adaptation.

Adaptation, Physiological↗
PubMed1992

The different types of general cold adaptation in man.

Different types of general cold adaptation have been described over the last 50 years. Metabolic adaptation (Alacaluf Indians, Arctic Indians Eskimos), insulative adaptation (coastal Aborigines of tropical northern Australia), hypothermic adaptation (bushmen of the Kalahari desert, Peruvian Indians) and insulative hypothermic adaptation (Central Australian Aborigines, nomadic Lapps, Korean and Japanese diving women). These different types of cold adaptation are related to the intensity of the cold stress and to individual factors such as diet, the level of physical fitness and body fat content. Thus, in natural environments, man develops a strategy of adaptation to cold, which takes into account environmental and individual factors. This strategy is susceptible to be modified when these conditions change. Caloric intake deficit could have been responsible for the hypothermic adaptation observed after J.-L. Etienne's journey to the North Pole. Physiological responses were adapted to maintain an acceptable level of energetic reserves with a moderate hypothermia, which was not life threatening for the climatic conditions encountered by the polar explorer.

Acclimatization↗
PubMed1982

Adaptation to optically reduced size.

Previous investigators have reported some difficulty in obtaining evidence for adaptation to optically reduced size. A study is reported in which a ballistic target-pointing task was used to examine such adaptation. In the first experiment size was reduced either by means of negative spherical lenses, or cylindrical lenses which reduced image size in only one dimension. Both lens types produced a negative aftereffect of adaptation, which increased as a function of lens strength. There was also a tendency for cylindrical lenses to give larger aftereffects. In a second experiment, in which a modified adaptation procedure was used, adaptation to cylindrical distortion was found to be significantly greater than adaptation to equivalent spherical distortion. These data are interpreted with respect to the relative amounts of distance distortion induced by viewing through the different lens types. The third experiment employed a cylindrical lens and a mental rotation procedure to determine whether adaptation in the first two experiments may have been visual or visuomotor in nature. Results indicated that adaptation was not purely visual. It is concluded that it is possible to demonstrate adaptation to size distortion by using an appropriate procedure.

Adaptation, Psychological↗
PubMed2006

Goalpha regulates olfactory adaptation by antagonizing Gqalpha-DAG signaling in Caenorhabditis elegans.

The heterotrimeric G protein G(o) is abundantly expressed in the mammalian nervous system and modulates neural activities in response to various ligands. However, G(o)'s functions in living animals are less well understood. Here, we demonstrate that GOA-1 G(o)alpha has a fundamental role in olfactory adaptation in Caenorhabditis elegans. Impairment of GOA-1 G(o)alpha function and excessive activation of EGL-30 G(q)alpha cause a defect in adaptation to AWC-sensed odorants. These pathways antagonistically modulate olfactory adaptation in AWC chemosensory neurons. Wild-type animals treated with phorbol esters and double-mutant animals of diacylglycerol (DAG) kinases, dgk-3; dgk-1, also have a defect in adaptation, suggesting that elevated DAG signals disrupt normal adaptation. Constitutively active GOA-1 can suppress the adaptation defect of dgk-3; dgk-1 double mutants, whereas it fails to suppress the adaptation defect of animals with constitutively active EGL-30, implying that GOA-1 acts upstream of EGL-30 in olfactory adaptation. Our results suggest that down-regulation of EGL-30-DAG signaling by GOA-1 underlies olfactory adaptation and plasticity of chemotaxis.

Adaptation, Physiological↗
PubMed2003

Influences of dietary adaptation and source of resistant starch on short-chain fatty acids in the hindgut of rats.

The effect of adaptation time on the concentration and pattern of short-chain fatty acids (SCFA) formed in the hindgut of rats given resistant starch (RS) in the form of raw potato starch (RPS) or high-amylose maize starch (HAS) was evaluated. Each starchy material was tested in diets containing 100 g indigestible carbohydrates/kg DM, and fed for 13, 28 and 42 d. At the end of each period, the content of SCFA was determined in caecum, distal colon and faeces. The caecal concentration of total and individual SCFA increased for both diets with increasing adaptation time. The concentration of butyric acid was higher in the group fed RPS than in that fed HAS at all adaptation times. The caecal proportion of butyric acid was low both in rats fed RPS and HAS (6 and 4 %, respectively) following 13 d of adaptation. However, after 28 d of adaptation, the proportion of butyric acid had increased to 19 % in rats given RPS. A longer adaptation period (42 d) did not increase the proportion of butyric acid further. With HAS, there was also a significant (P<0.01) increase in the proportion of butyric acid with longer adaptation time. However, the increase was much slower and the proportion of butyric acid reached 6 and 8 % after 28 and 42 d respectively. It is concluded that the pattern of SCFA formed from RS in rats is dependent on adaptation time. It cannot be excluded that the different patterns of SCFA reported in the literature for RS may be due to the time of adaptation.

Adaptation, Physiological↗
PubMed2006

Changes in implicit time of the multifocal electroretinogram response following contrast adaptation.

PURPOSE: Contrast adaptation, produced by prolonged viewing of high contrast gratings, has been suggested to occur at both retinal and cortical locations within the visual pathway. We sought to investigate the characteristics of retinal contrast adaptation using the multifocal electroretinogram (mfERG). METHODS: Twenty subjects, with a mean age of 27.8 +/- 5.3 years, underwent mfERG testing using VERIS I. The mfERG was measured after 10 minutes of adaptation to 94% contrast, 5 cyc/deg, sinusoidal, vertical gratings and to an equi-luminance blank control. The mfERG stimulus array consisted of 61-scaled hexagons and flickered according to a pseudorandom binary m-sequence (213-1). Changes in amplitude and implicit time of the first-order kernel were analyzed to determine the effect of contrast adaptation on retinal responses. RESULTS: Adaptation to the vertical grating pattern produced a 2.5 ms increase in implicit time, and the response delay was greatest in the more peripheral parts of the retina (7.6 degrees to 30 degrees ). Contrast adaptation did not produce statistically significant changes to the amplitude of the mfERG waveform. CONCLUSIONS: Contrast adaptation produced by prolonged viewing of high contrast gratings had a significant effect on retinal responses. It has been suggested that contrast adaptation may play a role in the development of nearwork induced myopia; further work investigating retinal contrast adaptation in myopic individuals may be of interest.

Adaptation, Ocular↗