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PubMed1989

Comparison of accommodative adaptation using laser and infra-red optometers.

Previous investigations have reported differences in the rate of decay of accommodative adaptation depending on the form of optometer used to assess dark-focus (DF). This study has used both laser and infra-red optometers to measure pre- and post-task values of DF in 10 subjects. DF was assessed before and immediately after an 8 min near-vision task performed at the subjective near-point of accommodation. Examination of the data from the two optometers revealed significant differences in both magnitude and distribution of pre-task DF. Additionally variations in the post- to pre-task shift in DF were observed between the two methods of assessment. Using the laser optometer, six subjects exhibited positive adaptation following the near-task which was not apparent with the infra-red optometer. The data suggest that both instruments may not be sampling open-loop accommodation; the laser optometer is particularly vulnerable to extraneous influences.

Accommodation, Ocular↗
PubMed1993

Accommodative adaptation and age of onset of myopia.

Tonic accommodation in an empty field and accommodative adaptation, defined as accommodation shift after 2 min viewing of a 4 D near task, were measured using an infrared optometer. Subjects were classified into three types: emmetropes (n = 18), early onset myopes (n = 18) and late onset myopes (n = 15). The relationship between accommodative adaptation and the onset age of myopia were compared. There was no statistical difference in the pre-task tonic accommodation among the three subject groups. However, the accommodative adaptation differed in the three groups during the 5 min post-task period. The average accommodative adaptation of emmetropia, early onset myopia and late onset myopia were 0.66, 0.27 and 1.19 D, respectively. Accommodative adaptation in the late onset myopia group was significantly higher than in the emmetropia group. Furthermore, the accommodative adaptation in the early onset myopia group was significantly lower than in the emmetropia group. Two possible aetiologies of myopia are discussed: one for the group which shows low accommodative adaptation that has no relationship with the age of onset and another for the group which shows high accommodative adaptation that has a relationship to an onset age of 15 years or later. The aetiology is also considered with regard to a potentiating chemical effect on the synapses of the ciliary muscle.

Accommodation, Ocular↗
PubMed2005

The effect of a beta-adrenoceptor antagonist on accommodative adaptation in Hong Kong children.

PURPOSE: Increased susceptibility to nearwork-induced accommodative adaptation has been suggested as a risk factor for myopia development. We investigated whether accommodative adaptation may explain in part the high prevalence of myopia in Hong Kong children and examined the effect of beta-antagonism with topical timolol maleate on accommodative adaptation. METHODS: Thirty children (10 emmetropes and 20 myopes) aged between 8 and 12 years were recruited. Tonic accommodation was measured before and after 5 min of video game-playing using an open-field Shin-Nippon autorefractor. Measurements were repeated 30 min after timolol instillation. RESULTS: Children with progressing myopia demonstrated accommodative adaptation following the near task, whereas stable myopes showed counter-adaptive, hyperopic accommodative changes. Timolol increased the magnitude of accommodative adaptation in the stable myopes but had little effect on responses of the progressing myopes or emmetropes. CONCLUSIONS: Neuropharmacological modulation of the accommodative system may have a possible etiological role in the progression of myopia.

Accommodation, Ocular↗
PubMed1997

Linear transduction of natural stimuli by dark-adapted and light-adapted rods of the salamander, Ambystoma tigrinum.

1. We examined signal, noise and response properties of salamander rod photoreceptors by measuring: (a) the circulating current of rods which were adapted to darkness and to a wide range of backgrounds; (b) contrasts of natural environments; (c) the effect of adaptation on the linear response range of rods; and (d) the behaviour of rods responding to dynamically modulated stimuli having a range of contrasts found in nature. 2. In the dark, the circulating current contained two noise components analogous to those described in toad. A discrete noise component consisted of events occurring at a rate of 1 event per 32 s (21 degrees C) and had a variance of 0.036 pA2. A continuous noise component contributed 0.022 pA2 to the dark current, roughly equal to the discrete noise variance. 3. Exposure to a wide range of steady backgrounds (suppressing up to 80% of the circulating current), elicited a sustained fluctuating photocurrent having a power spectrum which resembled those of single photon responses and was consistent with the linear summation of single photon events; this indicates that the primary source of noise in the current is caused by the light. 4. Eighty-nine per cent of the contrasts (C) measured in natural environments had magnitude of C < 50%, where C = magnitude of I - Imean/magnitude of Imean. The linear response range elicited by brief flashes expanded with brighter backgrounds, well-encompassing flash contrasts of 100%. 5. Dynamically modulated stimuli and incremental flashes having contrasts similar to those in natural scenes elicited small currents which deviated by a few picoamps about the mean and the transfer functions computed from each type of stimulus-response pair closely corresponded to one another. These results indicate that in natural environments, rods behave as linear small-signal transducers of light.

Adaptation, Ocular↗
PubMed1993

Influence of proximal, accommodative and disparity stimuli upon the vergence system.

The most important cues to the normal vergence response are retinal disparity, accommodative effort and perceived distance (proximal cue). In the past, proximal cues have been thought to contribute little to the total vergence response but more recent studies have suggested that they play an important role. The relative contributions of the proximal, accommodative and disparity cues to the vergence response were assessed by measuring the effect upon the vergence system when each of these cues were altered. The effect upon the vergence system was measured by the change in 'phoria, the change of fixation disparity and the amount of prism adaptation after 210 s of binocular viewing. The results indicate that the greatest effect of cue disharmony occurred when the proximal and disparity cues were altered. A finding which signifies the importance of the proximal cue to the overall vergence response.

Accommodation, Ocular↗
PubMedDate not supplied

Phase-shifted direction adaptation of the vestibulo-ocular reflex in cat.

The ability of the vestibulo-ocular reflex (VOR) to alter the phase of the motor output relative to the sensory input is examined. Alert cats were trained for 2 h with 0.25 Hz sinusoidal horizontal vestibular and vertical optokinetic rotational stimuli. In each experiment the optokinetic training stimulus was phase shifted by 0 degree, +45 degrees, -45 degrees, or 90 degrees from the vestibular stimulus. Vertical and horizontal eye movements were measured during horizontal rotations in darkness before and after the training procedure. Phase-advance experiments (+45 degrees) produced an adaptive vertical VOR with a mean phase of +28 degrees. After phase-delay experiments (-45 degrees), the adapted VOR had a mean phase of -19 degrees. The peak adaptive change in VOR gain was at or near the 0.25 Hz training frequency in each experimental group, but the gain depended in a complex manner on the testing frequency and the degree of phase shift of the training stimulus. Training with a 45 degrees phase-delayed optokinetic stimulus produced an adaptive vertical VOR with a gain that was relatively higher at frequencies below the training stimulus than at those that were above. Training with a 45 degrees phase-advanced optokinetic stimulus produced an adaptive vertical VOR with a gain that was higher at frequencies above the training frequency than at those that were below. During training with a phase-shifted optokinetic stimulus, adjustment of the relative efficacies of two neural pathways, a velocity pathway and an integrating pathway, could account for gain dependence on testing frequency and phase shift. This was corroborated by a model of the VOR that incorporates parallel velocity and integrating pathways. Data from 45 degrees phase advances were fit by increasing the gain of the velocity versus integrating pathway, whereas 45 degrees phase delay data were fit by decreasing the gain of the direct versus integrating pathway. The models altered the time constants of either the common oculomotor integrator or the velocity storage mechanism.

Adaptation, Ocular↗
PubMed2001

Adaptation in vertebrate photoreceptors.

When light is absorbed within the outer segment of a vertebrate photoreceptor, the conformation of the photopigment rhodopsin is altered to produce an activated photoproduct called metarhodopsin II or Rh(*). Rh(*) initiates a transduction cascade similar to that for metabotropic synaptic receptors and many hormones; the Rh(*) activates a heterotrimeric G protein, which in turn stimulates an effector enzyme, a cyclic nucleotide phosphodiesterase. The phosphodiesterase then hydrolyzes cGMP, and the decrease in the concentration of free cGMP reduces the probability of opening of channels in the outer segment plasma membrane, producing the electrical response of the cell. Photoreceptor transduction can be modulated by changes in the mean light level. This process, called light adaptation (or background adaptation), maintains the working range of the transduction cascade within a physiologically useful region of light intensities. There is increasing evidence that the second messenger responsible for the modulation of the transduction cascade during background adaptation is primarily, if not exclusively, Ca(2+), whose intracellular free concentration is decreased by illumination. The change in free Ca(2+) is believed to have a variety of effects on the transduction mechanism, including modulation of the rate of the guanylyl cyclase and rhodopsin kinase, alteration of the gain of the transduction cascade, and regulation of the affinity of the outer segment channels for cGMP. The sensitivity of the photoreceptor is also reduced by previous exposure to light bright enough to bleach a substantial fraction of the photopigment in the outer segment. This form of desensitization, called bleaching adaptation (the recovery from which is known as dark adaptation), seems largely to be due to an activation of the transduction cascade by some form of bleached pigment. The bleached pigment appears to activate the G protein transducin directly, although with a gain less than Rh(*). The resulting decrease in intracellular Ca(2+) then modulates the transduction cascade, by a mechanism very similar to the one responsible for altering sensitivity during background adaptation.

Adaptation, Ocular↗
PubMed1980

Accommodation, convergence, and distance perception in low illumination.

The role of oculomotor adjustments for distance perception in dim light was investigated while preserving the natural interactions between accommodation and convergence. The results show that perceived distance in the dark is biased toward an intermediate value that is correlated with the vergence adjustment assumed in darkness but unrelated to the dark focus of accommodation. A subsequent experimient showed that short-term adaptation to base-out prisms and negative lenses of corresponding strength affects perceived distance and dark convergence but has no influence on the dark focus of accommodation. These findings were interpreted as indicating that convergence is a more important distance cue than accommodation under low illumination and that the physiological resting states of convergence and accommodation are relatively independent.

Accommodation, Ocular↗
PubMed1999

Adaptation model of nearwork-induced transient myopia.

A nearwork model was developed to determine whether variation in accommodative adaptation gain, KA, can account for the differences in the dynamic decay timecourse following near work in hyperopes (HYP), emmetropes (EMM), early-onset myopes (EOM), and late-onset myopes (LOM). The model incorporated a proximal component into a previously-developed adaptation model of accommodation and vergence. It was used to simulate the nearwork-induced transient myopia (NITM) response following 10 min of congruent binocular near viewing (5 D, 5 MA). The accommodative adaptation gain, KA, value was varied from 1.0 to 6.0 in increments of 0.5. For the hyperopes, an additional constraint was imposed wherein the accommodative response was biased on the under-accommodated side of the deadspace operator (i.e., depth-of-focus). In addition, the effect of prolonged nearwork was simulated by alternating between 1 hr of congruent near viewing (3 D, 3 MA) and 5 min of congruent far viewing (0.25 D, 0.25 MA) over a 160 hr period representing one work-month with 40 hours of nearwork per week. The steady-state rms value of the accommodative error was measured as a function of KA. It was found that the NITM timecourses for HYP, EMM, EOM, and LOM could be simulated accurately using KA values of 2.0, 2.5, 4.0 and 5.5, respectively. The long-term final steady-state rms of the accommodative error was found to increase from 0.182 D to 0.188 D as KA increased from 1 to 6. This indicated a small and progressive increase in residual accommodative error for higher KA values, which was associated with EOM and LOM. Thus, NITM for the different refractive groups could be quantified by the accommodative adaptation gain element, with KA for the HYP, EMM, and EOM and LOM groups having lower, intermediate, and higher values, respectively. The larger rms for higher KA values suggests that a myopic individual may have a predisposition to exhibit a slightly larger long-term accommodative error, which may stimulate axial elongation and in turn promote the progression of axial myopia.

Accommodation, Ocular↗
PubMed1992

Symptoms related to abnormal tonic state: experimental results and computer simulations.

There have been numerous attempts to relate tonic accommodation and tonic vergence and their adaptive capabilities to a variety of parameters in vision science and clinical optometry. In this paper, investigations attempting to correlate the tonic state with nearwork symptoms will be reviewed. Results suggest that tonic vergence is more closely linked to near symptoms than is tonic accommodation. The results will be discussed in terms of a steady-state model of accommodation and vergence.

Accommodation, Ocular↗
PubMed1999

Photoreceptor function of retinal transplants implicated by light-dark shift of S-antigen and rod transducin.

The aim was to demonstrate functional properties of transplanted histologically normal photoreceptors. Subretinal intact-sheet transplants of fetal E17-E20 rat retinas to light-damaged albino rat eyes were fixed in light or dark, 2 to 42 weeks after transplantation, and stained immunohistochemically for certain phototransduction proteins. In light adapted transplants, transducin was predominantly found in inner segments of parallel-organized photoreceptors. Transducin shifted to the outer segments with dark-adaptation. S-antigen distribution was opposite to transducin. Rhodopsin distribution did not change. The shift of signal transduction proteins correlated to the light conditions indicates that normal phototransduction processes were established in photoreceptors of transplanted retinal sheets.

Adaptation, Ocular↗