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PubMed1982

Mechanisms of light adaptation in rat retina.

Green, Dowling, Siegel and Ripps (1975) J. gen. Physiol. 65, 483-502 found that both receptors and post-receptoral elements regulate the process of light adaptation in skate retina. As a test of the generality of this conclusion, we repeated their experiments on the retina of the intact albino rat. Increment threshold and intensity-response functions of aspartate-isolated receptor potentials, ERG b-waves and single retinal ganglion cell axons were measured, and all were found to be similar to those described by Green et al. (1975). In particular, the adaptive properties of the b-wave and ganglion cells were similar to each other, but different from those of the receptor potential. We conclude that the retinal mechanisms of light adaptation are similar in rat and skate.

Adaptation, Ocular↗
PubMed1984

Evidence for both photopic and scotopic characteristics in the c-wave of chicken and frog ERG.

The electroretinographic c-wave was studied in two species with duplex retinas, the frog (rod-dominant) and the chicken (highly cone-dominant). In both species a cone driven c-wave was recorded in addition to the classical rod-driven c-wave. An attempt was made to specify the differential characteristics with respect to time-course, time integration, adaptational changes and spectral sensitivity of cone-driven vs rod-driven c-waves. These data confirm the generality of the c-wave generation by both rod and cone systems.

Adaptation, Ocular↗
PubMed1986

The relation between sensitivity changes and response time scale in the barnacle photoreceptor.

Responses to brief light flashes were recorded intracellularly from the photoreceptors of the barnacle in order to study the relation between changes in sensitivity and latency. Conditioning lights either increased the response to a test flash (facilitation) or reduced it (desensitization). In both cases there was a shortening of the response latency. Similar observations were made when background illumination was used instead of conditioning lights. These effects were not qualitatively altered when the extracellular Ca2+ concentration was lowered. The results suggest that facilitation is not the result of a reduction of intracellular Ca2+ concentration; i.e. it is not the reverse of desensitization. Since during facilitation there is an increase in photoresponse associated with latency shortening it can be suggested that the underlying mechanism is an enhancement of the effective light intensity. The experiments do not provide quantitative evidence for this idea.

Adaptation, Ocular↗
PubMed1987

Light and aging effects on vitamin E in the retina and retinal pigment epithelium.

Experiments were performed to determine the effects of senescence and light adaptation on vitamin E levels in the neural retina and RPE-choroid-sclera of pigmented rats. Aging resulted in significant increases in alpha-tocopherol levels in both tissues, the effect being most pronounced in the RPE-choroid-sclera. The state of light adaptation had no influence on alpha-tocopherol levels in the neural retina at any of the ages examined, whereas in the RPE-choroid-sclera, alpha-tocopherol levels were substantially higher in light-adapted than in dark-adapted animals at all three ages (12, 22, and 32 months) at which they were measured. The effect of light adaptation on RPE-choroid-scleral alpha-tocopherol levels was most pronounced in the oldest age group.

Adaptation, Ocular↗
PubMed1990

The oscillatory potentials in response to stimuli of photopic intensities delivered in dark-adaptation: an explanation for the conditioning flash effect.

Previous studies reported that the oscillatory potentials (OPs) evoked to the first flash of a series were always smaller than those produced by the later flashes. This conditioning flash effect (CFE) was suggested to arise from rod inhibition of cone-mediated OPs. We investigated this CFE with the use of two stimulus intensities: 10 cd sec m-2 and 1 cd sec m-2. While the highest intensity did yield the previously reported CFE, the dimmest intensity did not. Our results further indicated that with the brightest stimulus, there is a significant increase in the interpeak interval of the OPs, while dimmest stimuli failed to reveal a similar marked increase. We also noted a significant correlation between the frequency domain of the OPs (as estimated with the interpeak interval) and the amplitude of the OPs (individual or collective: SOPs). Our results would also suggest that the observed CFE could result from a cone inhibition of rod-mediated OPs.

Adaptation, Ocular↗
PubMed1991

Studies on rod horizontal cell S-potential in dependence of the dark/light adapted state: a comparative study in Cyprinus carpio and Scyliorhinus canicula retinas.

Changes in light sensitivity, response time-course and electrical coupling of rod driven horizontal cells (RHC) were examined in the dark and light adapted states by intracellular recording. Comparative analyses were made of two fishes from different photic environments. RHC of Cyprinus carpio and external horizontal cells (EHC) of Scyliorhinus canicula retinas showed similar changes of their electrical responses to light stimuli when the dark-adapted retina was light-adapted: a decrease in sensitivity, an acceleration in the response time-course and an increase in the coupling strength.

Adaptation, Ocular↗
PubMed1992

Developmental lead exposure selectively alters the scotopic ERG component of dark and light adaptation and increases rod calcium content.

Electrophysiological studies have established that lead exposure produces selective rod deficits. The present electroretinographic (ERG) and correlated calcium experiments examined whether low-level or moderate-level developmental lead exposure (peak blood lead of 19 and 59 micrograms/dl, respectively) altered dark adaptation and/or light adaptation. Developmental lead exposure produced long-term dose-response (1) decreases in the slope of the increment threshold function only at scotopic adapting backgrounds, (2) decreases only in the sensitivity of the rod phase of dark adaptation and (3) increases in the calcium content of rod outer segments which may partially mediate the ERG results. The relevance and applicability of these data to lead-exposed children have yet to be established.

Adaptation, Ocular↗
PubMed1992

Quantal noise and decision rules in dynamic models of light adaptation.

To evaluate some of the consequences of including probabilistic processes (e.g. quantal noise) in a computable model of light-adaptation dynamics, we considered the behavior of a general class of models. These models contain four stages: (1) early noise; (2) a deterministic filtering and gain-changing stage; (3) late noise; (4) a decision rule that is either an ideal (signal-known-exactly) detector or a peak-trough detector. With the ideal detector and without late noise, the observer's sensitivity as a function of mean luminance and temporal frequency is not affected by the filtering and gain-changing stage. Consequently, if the early noise is entirely quantal fluctuations, sensitivity will always be a square-root function of mean luminance and a uniform (flat) function of temporal frequency. This latter prediction is contradicted by all known data; either the ideal-detector is the wrong decision rule or sensitivity is almost always limited by sources of noise other than quantal fluctuations. With the peak-trough detector, however, with or without late noise, the observer's sensitivity as a function of temporal frequency does reflect the sensitivity of the low-level filtering and gain-changing stage. Late noise is needed, however, if the observer's sensitivity as a function of mean luminance is to go through both a square-root and a Weber region. Comparing these conclusions to similar work on the spatial frequency dimension highlights differences between the spatial and temporal frequency domains. Finally, on the basis of these analyses and evidence from the literature, we question whether quantal fluctuations limit visual sensitivity under any condition.

Adaptation, Ocular↗
PubMed1995

Evidence for two sites of adaptation affecting the dark-adapted ERG of cats and primates.

The present study compared the effects of full-field steady adapting backgrounds on the sensitivity of the scotopic threshold response (STR) of the dark-adapted ERG and scotopic PII (b-wave and d.c.-component) to Ganzfeld flashes in cats (n = 4), macaque monkeys (n = 2), and one human subject. In cats, the sensitivity of the STR was reduced by a factor of 2 by backgrounds that were 500 times weaker than backgrounds reducing PII; and for the primates, the STR was reduced by backgrounds almost 100 times weaker than those reducing PII. Since the STR is generated more proximally in the retina than PII, these results provide evidence for proximal and more distal retinal sites of postreceptoral light adaptation. A practical implication is that dim scattered room light can remove the STR from the ERG while hardly affecting PII.

Adaptation, Ocular↗
PubMed1995

Differential effects of low versus high doses of apomorphine on retinal dopamine metabolism in light- and dark-adapted rabbits.

Previous electrophysiologic results from this laboratory indicate that apomorphine exerts a differential dose-related effect on rabbit electroretinograms, with low doses increasing the b-wave and higher doses decreasing this parameter. Results were interpreted as reflecting apomorphine's agonistic properties at two different receptors: 1.0 mg/kg acting at the postsynaptic site, and the lower dose, 0.01 mg/kg, preferentially stimulating inhibitory autoreceptors. The purpose of this experiment was to investigate further this hypothesis by determining retinal levels of dopamine, dihydroxyphenylacetic acid, and homovanillic acid in retinas of light- or dark-adapted rabbits treated with saline, 1.0, 0.1, or 0.01 mg/kg apomorphine intravenously. Results indicate that in dark-adapted rabbits only the highest dose tested, 1.0 mg/kg, decreased dopamine concentrations. In animals exposed to light, the lowest dose tested, 0.01 mg/kg, significantly reduced dopamine and metabolite levels, whereas the highest dose unexpectedly increased retinal dopamine turnover. Results are discussed in terms of receptor sites and the influence of lighting conditions.

3,4-Dihydroxyphenylacetic Acid↗
PubMed2006

Non-visual biological effect of lighting and the practical meaning for lighting for work.

The effects of good lighting extend much further than we used to think. Recent medical and biological research has consistently shown that light entering the human eyes has, apart from a visual effect, also an important non-visual biological effect on the human body. As a consequence, good lighting has a positive influence on health, well-being, alertness, and even on sleep quality. Our better understanding of the diversity in lighting effects teaches us that new rules governing the design of good and healthy lighting installations are required. Thanks to the recent discovery of a novel photoreceptor in the eye and its probable distribution within the eye we can now begin to define these new rules. These will guide us to dynamic lighting installations: that is to say dynamic in lighting level and dynamic in tint of whiteness of the lighting colour.

Adaptation, Ocular↗
PubMed2006

Effect of light exposure on the accumulation and depletion of retinyl ester in the chicken retina.

A previous study has shown that in the cone-rich chicken retina, 11-cis retinyl ester increases with light exposure and decreases in subsequent dark adaptation. The purpose of this research is to study how light exposure (intensity and duration) determine the rate of accumulation and utilization as well as the size of this 11-cis retinyl ester pool in the chicken retina. Chickens were dark-adapted overnight before exposure to different light intensities and durations. Animals were sampled at regular time intervals. 11-cis retinal and 11-cis retinyl ester were extracted from the retina and analyzed by HPLC. An increase in light intensity from 1,000 and 2,000 Lux (for a 20 min exposure) increased the amount of 11-cis retinyl ester from 0.38 to 0.75 nmol/mg. An increase in the duration of light exposure from 10 to 20 min (at 2,000 Lux) also increased the amount of 11-cis retinyl ester in the chicken retina (from 0.37 to 0.75 nmol/mg). This 11-cis retinyl ester pool in the chicken retina was rapidly reduced to baseline level ( approximately 0.20 nmol/mg) upon dark adaptation. The rate of accumulation of 11-cis retinyl ester was dependent on light intensity and duration of exposure and the maximum rate was approximately 0.03 nmol/mg/min. In comparison, dark adaptation was associated with a significantly higher rate of 11-cis retinyl ester depletion (approximately 0.05), indicating that light exposure and dark adaptation were associated with different biochemical steps of retinoid storage and utilization. Results from this study are the first to show that the size of the 11-cis retinyl ester pool, as well as the rate of its accumulation and depletion in the cone-rich chicken retina, are determined by the intensity and duration of light exposure. These data support the suggestion that a light-driven cone cycle exists in the chicken retina.

Adaptation, Ocular↗