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PubMed1993

Control of the complexity of associative memory dynamics by neuronal adaptation.

An abstract neural network model of the Hopfield type is extended to incorporate neuronal adaptation by defining the state of a neuron in terms of two variables, activity and excitability. The model is formulated to represent the regulation of the firing rate of action potentials in a biological system via the neuron cell membrane afterhyperpolarization by the effect of intracellular calcium ion concentration on the conductance of calcium sensitive potassium channels. It is shown that the complexity, and thus the exploratory degree, of associative memory dynamics are controlled by neuronal adaptability. At low adaptability, the dynamics have fixed point attractors corresponding to direct memory retrieval. In a subsequent region of adaptability values, a simple limit cycle persists with frequency increasing with adaptability. The range of frequencies agrees with that observed for theta rhythms of activity in the brain. A higher degree of freedom of the associative process corresponding to more complex dynamics, either limit cycles of varying complexity and period or chaotic behaviour, results at higher adaptability. In the brain, the neuronal adaptability is regulated by neuromodulators which suppress adaptation and increase absolute firing rates of action potentials. An associative process can be started at low concentration of neuromodulators as an exploratory search of state space during which firing rates are low. As the concentration of neuromodulators increases, the state space search becomes simpler cyclic and more restricted, and firing rates increase. Eventually, a particular stored state is retrieved and its activity is high. This correspondence between the complexity of associative memory dynamics and the concentration of neuromodulators is consistent with the observation for Alzheimer's disease of selective degeneracy of neurons releasing the neuromodulator acetylcholine. In an artificial neural network, inclusion of adaptation among neuronal properties allows control of the degree of freedom of associative processes and thus extends the range of possible applications.

Adaptation, Physiological↗
PubMed2001

Model of geometrical and smooth muscle tone adaptation of carotid artery subject to step change in pressure.

Recent experimental studies have shown significant alterations of the vascular smooth muscle (VSM) tone when an artery is subjected to an elevation in pressure. Therefore, the VSM participates in the adaptation process not only by means of its synthetic activity (fibronectins and collagen) or proliferative activity (hypertrophy and hyperplasia) but also by adjusting its contractile properties and its tone level. In previous theoretical models describing the time evolution of the arterial wall adaptation in response to induced hypertension, the contribution of VSM tone has been neglected. In this study, we propose a new biomechanical model for the wall adaptation to induced hypertension, including changes in VSM tone. On the basis of Hill's model, total circumferential stress is separated into its passive and active components, the active part being the stress developed by the VSM. Adaptation rate equations describe the geometrical adaptation (wall thickening) and the adaptation of active stress (VSM tone). The evolution curves that are derived from the theoretical model fit well the experimental data describing the adaptation of the rat common carotid subjected to a step increase in pressure. This leads to the identification of the model parameters and time constants by characterizing the rapidity of the adaptation processes. The agreement between the results of this simple theoretical model and the experimental data suggests that the theoretical approach used here may appropriately account for the biomechanics underlying the arterial wall adaptation.

Adaptation, Physiological↗
PubMed1999

Magnitude of functional adaptation after intestinal resection.

Intestinal adaptation after resection has been much studied, but rarely examined in an integrative context. Hence we assessed the effects of resection and subsequent adaptation on the quantitative relationship between dietary glucose load and gut capacity to transport glucose. The ratio of capacity to load is termed the "safety factor." Our objectives were to determine 1) the time course of intestinal adaptation after resection, 2) whether adaptation is quantitatively complete, 3) whether survival requires maintaining a safety factor of at least 1.0 for glucose transport, 4) the effect of altered energy demands on adaptation, and 5) the relationship between the amount of tissue removed and the magnitude of functional adaptation. We performed 80% resection of the small intestine on Sprague-Dawley rats and measured small intestinal glucose uptake capacity, dietary glucose load, and gut gross morphology at 1, 5, and 10 wk postsurgery. Nearly all aspects of adaptation were complete by 1 wk postsurgery. After resection, remnant small intestine mass increased by over fivefold within 1 wk, to reach 50-70% of its preresection value. However, mass-specific glucose uptake activity was reduced, so that intestinal regeneration restored uptake capacity to only 33% of control values. Increased energetic demands had only modest effects on intestinal adaptation. Although the safety factor for small intestinal glucose uptake remained <1.0 (i.e., capacity < load) after adaptation to resection, nearly all rats survived. Hindgut fermentation of nonabsorbed nutrients appeared to contribute to that survival, despite inadequate small intestinal capacity. After less massive resection surgeries (25, 50, and 75% resections), the percent increase in glucose uptake capacity increased with the amount of tissue removed.

Adaptation, Physiological↗
PubMed1988

Vertical vestibuloocular reflex in cat: asymmetry and adaptation.

1. We studied eye velocity during the first 2 s of the vertical vestibuloocular reflex (VOR) elicited from cats placed on their sides (90 degrees roll position) and rotated about an earth vertical axis. Vestibular stimuli were presented in the dark and consisted of brief trapezoidal velocity profiles. Eye movements were recorded with a magnetic search coil, and eye velocity was analyzed with high temporal resolution. 2. The first 2 s of upward or downward eye velocity after the onset of head rotation was characterized and compared. Adaptive changes in VOR gain (eye/head velocity) were then induced, and upward and downward eye velocity responses were again compared. 3. The early time course of the vertical VOR was complex. After a latency of approximately 15 ms, eye velocity increased rapidly until it was equal in magnitude and opposite in direction to head velocity. The peak eye velocity decayed within less than 1 s to a plateau of slow-phase eye velocity (SPEV) equal to approximately -0.6 times the head velocity. Peak upward and downward eye velocity was symmetric. The transition from peak to plateau was more rapid for the downward VOR (slow phases downward) than for the upward VOR (slow phases upward). The plateau attained by upward SPEV was approximately 15% higher than the plateau attained by downward SPEV. 4. VOR gain adaptation was symmetric. The percentage change in adapted upward eye velocity equalled the percentage change in adapted downward eye velocity. Both peak and plateau SPEV adapted, but peak eye velocity adapted less than plateau eye velocity. VOR latency was unchanged by adaptation. 5. The trajectory of the VOR response to steps of head velocity could be divided into an invariant and a variant interval. The invariant interval consisted of the initial approximately 15 ms of the eye movement. Neither direction of head movement (upward vs. downward) nor adaptation of the VOR gain effected the eye movement trajectory during the invariant interval. The variant interval began approximately 30 ms after the onset of head movement and approximately 15 ms after the onset of eye movement. In unadapted animals, downward eye speed exceeded upward eye speed during the variant interval. In adapted animals, eye speed during the variant interval, but not during the invariant interval, diverged from eye speed in the unadapted state. We suggest that the initial invariant interval (approximately 15 ms) of the eye movement response trajectory may represent the direct response of the classically described three-neuron arc.(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Physiological↗
PubMed1996

Response sensitivity and voltage gain of the rod- and cone-horizontal cell synapses in dark- and light-adapted tiger salamander retina.

1. Rods, cones, and horizontal cells (HCs) were recorded in superfused, flat-mounted isolated retinas of the larval tiger salamander, Ambystoma tigrinum, under dark- and light-adapted conditions. 2. Under dark-adapted conditions, HC responses to dim 500-nm light stimuli were mediated only by rods. In the linear voltage range (near the dark potentials), the average response to a light step of 0.5 s (500 nm, 0.438 photons per micron2 per s) was 0.41 +/- 0.06 (SD) mV for rods and 1.86 +/- 0.52 mV for HCs. The step sensitivity of rods was approximately 0.94 mV per photon micron2 s, or 0.032 mV per activated rhodopsin molecule (Rh*) rod second, and the step sensitivity of HCs was approximately 4.25 +/- 1.19 mV per photon micron2 s or 0.14 +/- 0.04 mV per Rh* rod second. The chord voltage gain of the rod-HC synapse had an average value of 4.54 and a range from 2.68 to 7.32. 3. By the use of the spectral subtraction method, we found that the average cone-mediated HC response to a 750-nm light step that elicited an average cone response of 0.73 +/- 0.20 mV was 1.15 +/- 0.31 mV. The step sensitivity of cones under dark-adapted conditions was 0.0012 mV per photon micron2 s, and that of the cone-mediated-HC response was 0.0019 mV per photon micron2 s. The chord voltage gains of the cone-HC synapses under dark-adapted conditions had an average value of 1.58 and a range from 0.82 to 2.05. 4. Under light-adapted conditions (with a 500-nm/-2.40 background light, which desensitized rod responses but did not substantially reduce the cone responses), the cones had an average response to a light step of 0.5 s (500 nm/-3.3) of 0.78 +/- 0.09 mV, and this response did not vary with time. The HC response to the same light step had an average value of 3.95 +/- 3.41 mV 3 min after the background light onset, and it increased with time until reaching a steady-state value of 5.95 +/- 3.63 mV approximately 15 min after the background light onset. The average chord voltage gain of the cone-HC synapse under such light-adapted conditions was 5.06 at 3 min after background light onset and 7.63 at 15 min after background light onset. These values are approximately 3-5 times higher than the chord voltage gain of the cone-HC synapse under dark-adapted conditions. 5. The background-induced increase of the chord voltage gain of the cone-HC synapse suggests that similarly to the rod-HC synapse, the voltage gain of the cone-HC synapse in the tiger salamander retina can also be modulated by light. Additionally, our results suggest that certain time-dependent process(es) in the synaptic cleft or postsynaptic membrane may be responsible for such modulation. 6. In addition to determining the average values of response sensitivity and chord voltage gains of the rod- and cone-HC synapses, we studied the variation of these parameters among different HCs. HCs with higher rod-HC synaptic gain had lower cone-HC synaptic gain, and HCs with lower rod-HC synaptic gain exhibited higher cone-HC synaptic gain under both dark- and light-adapted conditions. This suggests that the rod-HC and cone-HC synaptic gains in HCs are complementary to each other, and voltage responses of all HCs under dark- or light-adapted conditions are of comparable amplitudes.

Adaptation, Physiological↗
PubMed1997

Effects of adaptation on neural coding by primary sensory interneurons in the cricket cercal system.

Methods of stochastic systems analysis were applied to examine the effect of adaptation on frequency encoding by two functionally identical primary interneurons of the cricket cercal system. Stimulus reconstructions were obtained from a linear filtering transformation of spike trains elicited in response to bursts of broadband white noise air current stimuli (5-400 Hz). Each linear reconstruction was compared with the actual stimulus in the frequency domain to obtain a measure of waveform coding accuracy as a function of frequency. The term adaptation in this paper refers to the decrease in firing rate of a cell after the onset or increase in power of a white noise stimulus. The increase in firing rate after stimulus offset or decrease in stimulus power is assumed to be a complementary aspect of the same phenomenon. As the spike rate decreased during the course of adaptation, the total amount of information carried about the velocity waveform of the stimulus also decreased. The quality of coding of frequencies between 70 and 400 Hz decreased dramatically. The quality of coding of frequencies between 5 and 70 Hz decreased only slightly or even increased in some cases. The disproportionate loss of information about the higher frequencies could be attributed in part to the more rapid loss of spikes correlated with high-frequency stimulus components than of spikes correlated with low-frequency components. An increase in the responsiveness of a cell to frequencies > 70 Hz was correlated with a decrease in the ability of that cell to encode frequencies in the 5-70 Hz range. This nonlinear property could explain the improvement seen in some cases in the coding accuracy of frequencies between 5 and 70 Hz during the course of adaptation. Waveform coding properties also were characterized for fully adapted neurons at several stimulus intensities. The changes in coding observed through the course of adaptation were similar in nature to those found across stimulus powers. These changes could be accounted for largely by a change in neural sensitivity. The effect of adaptation on the coding of stimulus power was examined by measuring the response curves to steps in stimulus power before and after exposure to an adapting stimulus. Adaptation caused a loss of information about the mean stimulus power but did not cause any improvement in the coding of changes in stimulus power. The unadapted response of the cells did not show any saturation even at the highest powers used in these experiments.

Acoustic Stimulation↗
PubMed2000

Effect of adaptation to telescopic spectacles on the initial human horizontal vestibuloocular reflex.

Gain of the vestibuloocular reflex (VOR) not only varies with target distance and rotational axis, but can be chronically modified in response to prolonged wearing of head-mounted magnifiers. This study examined the effect of adaptation to telescopic spectacles on the variation of the VOR with changes in target distance and yaw rotational axis for head velocity transients having peak accelerations of 2,800 and 1,000 degrees /s(2). Eye and head movements were recorded with search coils in 10 subjects who underwent whole body rotations around vertical axes that were 10 cm anterior to the eyes, centered between the eyes, between the otoliths, or 20 cm posterior to the eyes. Immediately before each rotation, subjects viewed a target 15 or 500 cm distant. Lighting was extinguished immediately before and was restored after completion of each rotation. After initial rotations, subjects wore 1.9x magnification binocular telescopic spectacles during their daily activities for at least 6 h. Test spectacles were removed and measurement rotations were repeated. Of the eight subjects tolerant of adaptation to the telescopes, six demonstrated VOR gain enhancement after adaptation, while gain in two subjects was not increased. For all subjects, the earliest VOR began 7-10 ms after onset of head rotation regardless of axis eccentricity or target distance. Regardless of adaptation, VOR gain for the proximate target exceeded that for the distant target beginning at 20 ms after onset of head rotation. Adaptation increased VOR gain as measured 90-100 ms after head rotation onset by an average of 0.12 +/- 0.02 (SE) for the higher head acceleration and 0.19 +/- 0.02 for the lower head acceleration. After adaptation, four subjects exhibited significant increases in the canal VOR gain only, whereas two subjects exhibited significant increases in both angular and linear VOR gains. The latencies of linear and early angular target distance effects on VOR gain were unaffected by adaptation. The earliest significant change in angular VOR gain in response to adaptation occurred 50 and 68 ms after onset of the 2,800 and 1,000 degrees /s(2) peak head accelerations, respectively. The latency of the adaptive increase in linear VOR gain was approximately 50 ms for the peak head acceleration of 2,800 degrees /s(2), and 100 ms for the peak head acceleration of 1,000 degrees /s(2). Thus VOR gain changes and latency were consistent with modification in the angular VOR in most subjects, and additionally in the linear VOR in a minority of subjects.

Adaptation, Ocular↗
PubMed2000

Dendritic calcium accumulation associated with direction-selective adaptation in visual motion-sensitive neurons in vivo.

Motion adaptation in directionally selective tangential cells (TC) of the fly visual system has previously been explained as a presynaptic mechanism. Based on the observation that adaptation is in part direction selective, which is not accounted for by the former models of motion adaptation, we investigated whether physiological changes located in the TC dendrite can contribute to motion adaptation. Visual motion in the neuron's preferred direction (PD) induced stronger adaptation than motion in the opposite direction and was followed by an afterhyperpolarization (AHP). The AHP subsides in the same time as adaptation recovers. By combining in vivo calcium fluorescence imaging with intracellular recording, we show that dendritic calcium accumulation following motion in the PD is correlated with the AHP. These results are consistent with a calcium-dependent physiological change in TCs underlying adaptation during continuous stimulation with PD motion, expressing itself as an AHP after the stimulus stops. However, direction selectivity of adaptation is probably not solely related to a calcium-dependent mechanism because direction-selective effects can also be observed for fast moving stimuli, which do not induce sizeable calcium accumulation. In addition, a comparison of two classes of TCs revealed differences in the relationship of calcium accumulation and AHP when the stimulus velocity was varied. Thus the potential role of calcium in motion adaptation depends on stimulation parameters and cell class.

Adaptation, Physiological↗
PubMed1985

The effect of spatial adaptation on perceived contrast.

Perceived contrast was assessed by contrast-matching between adjacent sinusoidal gratings of the same spatial frequency (3 cycles/degree), before and after adaptation to gratings of various contrasts. On logarithmic axes, the effect of adaptation was large for test contrasts below the adapting contrast, but absent for test contrasts higher than the adapting contrast. This result rules out a simple gain-reduction hypothesis, in which adaptation would attenuate all test contrasts by the same proportion. Instead, results for all combinations of adapting and test contrast levels (including threshold elevation) conformed fairly closely to a simple subtractive rule: any test contrast presented after adaptation behaved as if one-third of the adapting contrast were subtracted from it. Though not exact, this may be a useful descriptive rule. Deviations from the simple rule may be explained by increased variance in the visual response at high adapting contrasts, combined with nonlinearity at low test contrasts. A subtractive effect at the psychophysical level does not necessarily conflict with evidence for contrast gain reduction at the single-cell level.

Adaptation, Ocular↗
PubMedDate not supplied

Properties of acoustic reflex adaptation.

The dynamic behavior of the acoustic reflex to continuous sinusoidal stimuli was investigated. The major purpose was to determine the temporal characteristics of reflex adaptation as frequency (0.5, 1.0, 2.0, 3.0, 4.0 kHz) and suprathreshold level (6, +12, +18 dB re reflex threshold) were systematically varied. Repeated measurements were made with an impedance bridge on six normal listeners. Both relative and absolute impedance changes were analyzed. The results revealed large intersubject variability. Four general conclusions were reached regarding the effect of stimulus frequency and suprathreshold level on adaptation: 1) as the stimulus frequency increases, the rate of adaptation increases; 2) the adaptation curves appear to form distinct groups, at the low frequencies adaptation rates are significantly slower than those at 2.0 kHz and above; 3) the onset of adaptation occurs at an earlier time for the higher frequencies; and 4) the rate of adaptation was found to be independent of suprathreshold level. The changes in adaptation with frequency of the stimulus may be expressed by an equation involving inter-related time constants for the growth and adaptation portions of the reflex curve in accordance with a descriptive model suggested by Tietze.

Acoustic Stimulation↗
PubMed2005

Testing for adaptive evolution of the female reproductive protein ZPC in mammals, birds and fishes reveals problems with the M7-M8 likelihood ratio test.

BACKGROUND: Adaptive evolution appears to be a common feature of reproductive proteins across a very wide range of organisms. A promising way of addressing the evolutionary forces responsible for this general phenomenon is to test for adaptive evolution in the same gene but among groups of species, which differ in their reproductive biology. One can then test evolutionary hypotheses by asking whether the variation in adaptive evolution is consistent with the variation in reproductive biology. We have attempted to apply this approach to the study of a female reproductive protein, zona pellucida C (ZPC), which has been previously shown by the use of likelihood ratio tests (LRTs) to be under positive selection in mammals. RESULTS: We tested for evidence of adaptive evolution of ZPC in 15 mammalian species, in 11 avian species and in six fish species using three different LRTs (M1a-M2a, M7-M8, and M8a-M8). The only significant findings of adaptive evolution came from the M7-M8 test in mammals and fishes. Since LRTs of adaptive evolution may yield false positives in some situations, we examined the properties of the LRTs by several different simulation methods. When we simulated data to test the robustness of the LRTs, we found that the pattern of evolution in ZPC generates an excess of false positives for the M7-M8 LRT but not for the M1a-M2a or M8a-M8 LRTs. This bias is strong enough to have generated the significant M7-M8 results for mammals and fishes. CONCLUSION: We conclude that there is no strong evidence for adaptive evolution of ZPC in any of the vertebrate groups we studied, and that the M7-M8 LRT can be biased towards false inference of adaptive evolution by certain patterns of non-adaptive evolution.

Adaptation, Biological↗
PubMed1989

The role of sensory adaptation in the retina.

Adaptation, a change in response to a sustained stimulus, is a widespread property of sensory systems, occurring at many stages, from the most peripheral energy-gathering structures to neural networks. Adaptation is also implemented at many levels of biological organization, from the molecule to the organ. Despite adaptation's diversity, it is fruitful to extract some unifying principles by considering well-characterized components of the insect visual system. A major function of adaptation is to increase the amount of sensory information an organism uses. The amount of information available to an organism is ultimately defined by its environment and its size. The amount of information collected depends upon the ways in which an organism samples and transduces signals. The amount of information that is used is further limited by internal losses during transmission and processing. Adaptation can increase information capture and reduce internal losses by minimizing the effects of physical and biophysical constraints. Optical adaptation mechanisms in compound eyes illustrate a common trade-off between energy (quantum catch) and acuity (sensitivity to changes in the distribution of energy). This trade-off can be carefully regulated to maximize the information gathered (i.e. the number of pictures an eye can reconstruct). Similar trade-offs can be performed neurally by area summation mechanisms. Light adaptation in photoreceptors introduces the roles played by cellular constraints in limiting the available information. Adaptation mechanisms prevent saturation and, by trading gain for temporal acuity, increase the rate of information uptake. By minimizing the constraint of nonlinear summation (imposed by membrane conductance mechanisms) a cell's sensitivity follows the Weber-Fechner law. Thus, a computationally advantageous transformation is generated in response to a cellular constraint. The synaptic transfer of signals from photoreceptors to second-order neurones emphasizes that the cellular constraints of nonlinearity, noise and dynamic range limit the transmission of information from cell to cell. Synaptic amplification is increased to reduce the effects of noise but this resurrects the constraint of dynamic range. Adaptation mechanisms, both confined to single synapses and distributed in networks, remove spatially and temporally redundant signal components to help accommodate more information within a single cell. The net effect is a computationally advantageous removal of the background signal. Again, the cellular constraints on information transfer have dictated a computationally advantageous operation.

Adaptation, Physiological↗
PubMed1980

Motion and vision. III. Stabilized pattern adaptation.

It has been suggested that local variations of retinal sensitivity may be responsible for elevating the threshold in pattern-adaptation experiments of the Blakemore-Campbell type. Subjects are unable to scan high-contrast gratings uniformly enough to eliminate this possibility. To control this effect, we performed grating-adaptation experiments under stabilized-image conditions, while both adapting and test targets were moved at retinal velocities determined by the experimenter. By means of an afterimage technique, we also measured the strength of the retinal sensitivity mask that forms under these conditions. Varying the spatial frequency and velocity of the adapting stimulus, we inferred the spatial and temporal properties of the principal mechanism that contributes to the afterimage. We found that the Blakemore-Campbell effect persists at adapting velocities that are fast enough to rule out local variations of retinal sensitivity. More surprisingly, even the clearly visible afterimages that occur at a retinal velocity of 0.1 deg/s seem to have no effect on pattern adaptation. (Sensitivity masking can raise the adapted threshold, but only at adapting velocities slower than normal eye movements). By manipulating the image velocity, we were able to shift the spatial frequencies of some threshold-elevation curves, but these shifts were not great enough to suggest that velocity tuning plays important role in pattern adaptation.

Adaptation, Ocular↗
PubMed2003

Time course of adaptation to stimuli presented along cardinal lines in color space.

Visual sensitivity is a process that allows the visual system to maintain optimal response over a wide range of ambient light levels and chromaticities. Several studies have used variants of the probe-flash paradigm to show that the time course of adaptation to abrupt changes in ambient luminance depends on both receptoral and postreceptoral mechanisms. Though a few studies have explored how these processes govern adaptation to color changes, most of this effort has targeted the L-M-cone pathway. The purpose of our work was to use the probe-flash paradigm to more fully explore light adaptation in both the L-M- and the S-cone pathways. We measured sensitivity to chromatic probes presented after the onset of a 2-s chromatic flash. Test and flash stimuli were spatially coextensive 2 degrees fields presented in Maxwellian view. Flash stimuli were presented as excursions from white and could extended in one of two directions along an equiluminant L-M-cone or S-cone line. Probes were presented as excursions from the adapting flash chromaticity and could extend either toward the spectrum locus or toward white. For both color lines, the data show a fast and slow adaptation component, although this was less evident in the S-cone data. The fast and slow components were modeled as first- and second-site adaptive processes, respectively. We find that the time course of adaptation is different for the two cardinal pathways. In addition, the time course for S-cone stimulation is polarity dependent. Our results characterize the rapid time course of adaptation in the chromatic pathways and reveal that the mechanics of adaptation within the S-cone pathway are distinct from those in the L-M-cone pathways.

Adaptation, Ocular↗
PubMed1991

Effects of chromatic adaptation on opponent interactions in monkey increment-threshold spectral-sensitivity functions.

The effects of chromatic adaptation on the opponent interactions of cone mechanisms were investigated by using increment-threshold spectral-sensitivity (ITSS) functions and threshold-versus-radiance (TVR) curves in rhesus monkey subjects. The TVR curves showed shape- and field-sensitivity invariance for both 580- and 500-nm adapting backgrounds and indicated that three cone mechanisms were mediating detection over moderate adapting-field intensity levels. Differential adaptation between the long-wavelength-sensitive (L) and the middle-wavelength-sensitive (M) opponent (L - M) and nonopponent (L + M) channels and the short-wavelength-sensitive (S) channel caused changes in the shape of the ITSS function as the adapting-field intensity was increased without changes in the level of cone interaction. Chromatic adaptation also resulted in significant changes in the shape of the ITSS functions, but it still exhibited characteristic L-M opponent interactions. Converting ITSS data to cone-contrast coordinates for R-G adapting fields indicated that the relative contribution of the L and M cones at the second site was approximately equal (detection contour slope approximately 1). Consequently, most of the changes in the shape of ITSS functions under chromatic adaptation are explained by the von Kries adaptation principle. ITSS functions on a green background also exhibited opponent interactions between S cones and longer-wavelength cones. The cone-contrast coordinates, when expressed for S cones, showed that the inhibitory interactions occur because the S-cone signal subtracts from both M and L cones.

Adaptation, Ocular↗
PubMed1990

The effect of an adaptation period to soybean oil additions in the diets of young pigs.

Utilization of soybean oil (SBO) in swine starter diets and the effect of an adaptation period to SBO on performance was studied in two 4-wk experiments with pigs initially 4 to 5 wk of age. One trial was extended an additional 4 wk and apparent DE was measured during the 4th wk postweaning. Corn-soybean meal-based diets were used in which SBO was substituted for cornstarch at 2, 4 and 6% of the diet in Exp. 1 and at 3 and 6% of the diet in Exp. 2. In Exp. 2, SBO was added either initially (adaptation) or after 2 wk (no adaptation). In Exp. 1 daily gain and efficiency of feed utilization were improved (P less than .05) by adding SBO during wk 3 and 4, but not earlier. Feed intake was not affected by treatment. In Exp. 2, for the initial 4-wk postweaning period, there was no effect of SBO addition on growth rate; feed intake was depressed (P less than .05) when SBO was added at wk 3, and efficiency of feed utilization was improved (P less than .05) for pigs fed SBO without an adaptation period. The primary improvements in performance occurred in the 3rd and 4th wk postweaning, with a tendency for pigs to perform better without an adaptation period. During wk 4, pigs adapted to SBO consumed more (P less than .05) feed but tended to be less efficient (P less than .10) than nonadapted pigs. With or without adaptation, apparent DE was unaffected by SBO additions. Regardless of adaptation period, SBO additions depressed feed intake (P less than .05) and improved efficiency of feed utilization (P less than .01) for the 5- to 8-wk growing phase. In conclusion, adding SBO the first 2 wk postweaning did not improve performance; an adaptation period was not necessary for a performance response from added SBO.

Adaptation, Physiological↗
PubMed2002

Effects of restricted versus conventional dietary adaptation on feedlot performance, carcass characteristics, site and extent of digestion, digesta kinetics, and ruminal metabolism.

Three experiments were conducted to determine effects of restricting intake of the final finishing diet as a means of dietary adaptation compared with diets increasing in grain over a period of 20 to 22 d on overall cattle performance, carcass characteristics, digestibility, digesta kinetics, and ruminal metabolism. In Exp. 1, 84 Angus x Hereford yearling steers (initial BW = 418 +/- 29.0 kg) were fed for 70 d. Restricting intake during adaptation had no effect (P > 0.10) on overall ADG:DMI, but decreased (P < 0.05) DMI compared with ad libitum access to adaptation diets, which resulted from differences during the initial 28 d of the experiment. In Exp. 2, 150 mixed crossbred steer calves (initial BW = 289 +/- 22.9 kg) were fed for an average of 173 d. Restricting intake decreased (P < 0.01) overall daily gain (1.51 vs 1.65 kg/d) and DMI (8.68 vs 9.15 kg/d) compared with ad libitum fed steers; however, ADG:DMI was not influenced (P > 0.10) by adaptation method. Experiment three used eight ruminally and duodenally fistulated steers (initial BW = 336 +/- 20 kg) in a completely random design. Total tract digestibility, digesta kinetics and ruminal metabolism were determined. Restricting intake reduced (P < 0.10) daily DMI variation from d 1 through 7, 8 through 14, and 22 through 28 compared with ad libitum feeding of three adaptation diets. Restricted steers had reduced (adaptation method x period interaction, P < 0.05) intakes and fecal excretions of ADF and greater OM digestibilities on d 4 through 7, 11 through 14, and 18 through 21. Digesta kinetics and ruminal metabolism were generally not affected (P > 0.10) by adaptation method. Our results suggest that restricted-feeding of the final diet as a means of dietary adaptation can be used in finishing cattle with few problems from acidosis or related intake variation. In light-weight steers (Exp. 2), disruptions in intake during the adaptation period might have resulted in restriction for an extended period, which decreased (P < 0.01) hot carcass weight compared with calves fed ad libitum. Effects of limit feeding during the initial 28 d of the feeding period on site and extent of digestion, digesta kinetics, and ruminal metabolism were minimal, supporting few differences in performance across the finishing period for yearling cattle.

Adaptation, Physiological↗
PubMed1996

Gastric adaptation to aspirin and stress enhances gastric mucosal resistance against the damage by strong irritants.

BACKGROUND: Gastric mucosal adaptation to injury induced by repeated application of aspirin (ASA) or stress is a well-documented phenomenon, but it is known whether such adaptation affects the mucosal tolerance to other strong irritants. METHODS: In this study gastric adaptation was induced by repeated daily administration of acidified ASA for 4 consecutive days (Series A) or by 3.5H of water immersion and restraint stress (WRS) applied every other day for up to 8 days (series B). When the adaptation to ASA or WRS was fully developed, rats of series A and B were challenged with strong irritants such as 100% ethanol, 200 mM acidified taurocholate (TC), or 25% NaCl for 1 h or with WRS for 3.5 h. RESULTS: ASA or WRS applied once produced numerous gastric lesions and deep histologic necrosis accompanied by a decrease in gastric blood flow. With repeated application of ASA or stress the mucosal adaptation to ASA and WRS developed; the area of gastric lesions was reduced by 86% and 56%, respectively, and this was accompanied by a marked decrease of superficial and deep necrosis, and increase in gastric blood flow (GBF) and the enhancement of mucosal regeneration. An increase in mucosal and luminal contents of epidermal growth factor (EGF) and in mucosal expression of EGF receptors was also observed in the mucosa adapted to ASA or stress. In rats adapted to ASA or stress and then challenged with 100% ethanol, 200 mm TC, 25% NaCl, stress or ASA, the areas of macroscopic gastric lesions and deep histologic necrosis were remarkable reduced as compared with those in non-adapted vehicle-treated rats. This was also accompanied by a significant decrease in (GBF), a marked increase of mucosal and luminal contents of EGF and expression of its receptors, and enhanced mucosal cell proliferation. CONCLUSIONS: Gastric adaptation to ASA or stress enhances mucosal resistance to the injury induced by strong irritants, and this appears to be mediated by mucosal regeneration, probably resulting from increased luminal and mucosal contents of EGF and excessive expression of its receptors.

Adaptation, Physiological↗