scholarly journals Visual pigment and photoreceptor sensitivity in the isolated skate retina.

1978 ◽  
Vol 71 (4) ◽  
pp. 369-396 ◽  
Author(s):  
D R Pepperberg ◽  
P K Brown ◽  
M Lurie ◽  
J E Dowling
Keyword(s):  
Dark Adaptation ◽  
Visual Pigment ◽  
Response Curve ◽  
Time Course ◽  
Light Adaptation ◽  
Receptor Sensitivity ◽  
Strong Light ◽  
Receptor Response ◽  
Intensity Response ◽  
Isolated Retina

Photoreceptor potentials were recorded extracellularly from the aspartate-treated, isolated retina of the skate (Raja oscellata and R. erinacea), and the effects of externally applied retinal were studied both electrophysiologically and spectrophotometrically. In the absence of applied retinal, strong light adaptation leads to an irreversible depletion of rhodopsin and a sustained elevation of receptor threshold. For example, after the bleaching of 60% of the rhodopsin initially present in dark-adapted receptors, the threshold of the receptor response stabilizes at a level about 3 log units above the dark-adapted value. The application of 11-cis retinal to strongly light-adapted photoreceptors induces both a rapid, substantial lowering of receptor threshold and a shift of the entire intensity-response curve toward greater sensitivity. Exogenous 11-cis retinal also promotes the formation of rhodopsin in bleached photoreceptors with a time-course similar to that of the sensitization measured electrophysiologically. All-trans and 13-cis retinal, when applied to strongly light-adapted receptors, fail to promote either an increase in receptor sensitivity or the formation of significant amounts of light-sensitive pigment within the receptors. However, 9-cis retinal isin. These findings provide strong evidence that the regeneration of visual pigment in the photoreceptors directly regulates the process of photochemical dark adaptation.

The Effect of Changed Extracellular Calcium and Sodium Concentration on the Electroretinogram of the Crayfish Retina

1980 ◽  
Vol 35 (3-4) ◽  
pp. 308-318 ◽  
Author(s):  
H. Stieve ◽  
I. Claßen-Linke
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Calcium Concentration ◽  
Light Adaptation ◽  
Sodium Concentration ◽  
Strong Increase ◽  
Calcium Stores ◽  
Half Time ◽  
Astacus Leptodactylus ◽  
External Calcium

Abstract The electroretinogram (ERG) of the isolated retina of the crayfish Astacus leptodactylus evoked by strong 10 ms light flashes at constant 5 min intervals was measured while the retina was continuously superfused with various salines which differed in Ca2+ -and Na+ -concentrations. The osmotic pressure of test- and reference-saline was adjusted to be identical by adding sucrose. Results: 1. Upon raising the calcium-concentration of the superfusate in the range of 20-150 mmol/l (constant Na+ -concentration: 208 mmol/l) the peak amplitude hmax and the half time of decay t2 of the ERG both decrease gradually up to about 50% in respect to the corresponding value in reference saline. 2. The recovery of the ERG due to dark adaptation following the “weakly light adapted state” is greatly diminished in high external [Ca2+]ex. 3. Lowering the external calcium-concentration (10 →1 mmol/l) causes a small increase in hmax and a strong increase of the half time of decay t2 (about 180%). Upon lowering the calcium concentration of the superfusate to about 1 nmol/l by 1 mmol/l of the calcium buffer EDTA, a slowly augmenting diminution of the ERG height hm SLX occurs. How­ever, a strong retardation of the falling phase of the ERG characterized by an increase in t2 occurs quickly. Even after 90 min stay in the low calcium saline the retina is still not inexcitable; hmax is 5 - 10% of the reference value. The diminution of hmax occurs about six-fold faster when the buffer concentration is raised to 10 mmol/l EDTA. 4. Additional lowering of the Na+ -concentration (208 →20.8 mmol/l) in a superfusate with a calcium concentration raised to 150 mmol/l causes a strong reduction of the ERG amplitude hmax to about 10%. 5. In a superfusate containing 1 nmol/l calcium such lowering of the sodium concentration (208 → 20.8 mmol/l) causes a diminution of the ERG height to about 40% and the shape of the ERG to become polyphasic; at least two maxima with different time to peak values are observed. Interpretation: 1. The similarity of effects, namely raising external calcium concentration and light adaptation on the one hand and lowering external calcium and dark adaptation on the other hand may indicate that the external calcium is acting on the adaptation mechanism of the photoreceptor cells, presumably by influencing the intracellular [Ca2+]. 2. The great tolerance of the retina against Ca2+ -deficiency in the superfusate might be effected by calcium stores in the retina which need high Ca2+ -buffer concentrations in the superfusate to become exhausted. 3. In contrast to the Limulus ventral nerve photoreceptor there does not seem to be an antagonis­ tic effect of sodium and calcium in the crayfish retina on the control of the light channels. 4. The crayfish receptor potential seems to be composed of at least two different processes. Lowering calcium-and lowering external sodium-concentration both diminish the height and change the time course of the two components to a different degree. This could be caused by in­ fluencing the state of adaptation and thereby making the two maxima separately visible.

Changes of Acuity during Light and Dark Adaptation in the Dragonfly Compound Eye

1990 ◽  
Vol 45 (1-2) ◽  
pp. 137-142 ◽  
Author(s):  
Eric J. Warrant ◽  
Robert B. Pinter
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Light Adaptation ◽  
Compound Eye ◽  
Sensitivity Function ◽  
The State ◽  
Intracellular Recordings ◽  
Acceptance Angle ◽  
Angular Sensitivity ◽  
Rapid Reduction

Abstract Intracellular recordings of angular sensitivity from the photoreceptors of Aeschnid dragonflies (Hemianax papuensis and Aeschna brevistyla) are used to determine the magnitude and time course of acuity changes following alterations of the state of light or dark adaptation. Acuity is defined on the basis of the acceptance angle, Δρ (the half-width of the angular-sensitivity function). The maximally light-adapted value of Δρ is half the dark-adapted value, indicating greater acuity during light adaptation. Following a change from light to dark adaptation, Δρ increases slowly, requiring at least 3 min to reach its dark-adapted value. In contrast, the reverse change (dark to light) induces a rapid reduction of Δρ , and at maximal adapting luminances, this reduction takes place in less than 10 sec.

scholarly journals Time-course of adaptations for electroretinography and pupillography

2021 ◽  
Vol 9 (4) ◽  
Author(s):  
Ken Asakawa
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Light Adaptation ◽  
Light Condition ◽  
Pupillary Response ◽  
Implicit Time ◽  
Scotopic Vision ◽  
Adaptation Time ◽  
Practical Applications ◽  
Rod Response

Cones are primarily involved in photopic vision and light adaptation. Rods are responsible for scotopic vision and dark adaptation. The typical time-courses of light and dark adaptations have been known for century. However, information regarding the minimal adaptation time for electroretinography (ERG) and pupillography would be helpful for practical applications and clinical efficiency. Therefore, we investigated the relationship between adaptation time and the parameters of ERG and pupillography. Forty-six eyes of 23 healthy women (mean age, 21.7 years) were enrolled. ERG and pupillography were tested for right and left eyes, respectively. ERG with a skin electrode was used to determine amplitude (µV) and implicit time (msec) by the records of rod-, flash-, cone-, and flicker-responses with white light (0.01–30 cd·s/m2). Infrared pupillography was used to record the pupillary response to 1-sec stimulation of red light (100 cd/m2). Cone- and flicker- (rod-, flash-, and pupil) responses were recorded after light (dark) adaptation at 1, 5, 10, 15, and 20 min. Amplitude was significantly different between 1 min and ≥5 or ≥10 min after adaptation in b-wave of cone- or rod-response, respectively. Implicit time differed significantly between 1 min and ≥5 min after adaptation with b-wave of cone- and rod-response. There were significant differences between 1 min and ≥10 or ≥5 min after dark adaptation in parameter of minimum pupil diameter or constriction rate, respectively. Consequently, light-adapted ERGs can be recorded, even in 5 min of light adaptation time without special light condition, whereas dark-adapted ERGs and pupillary response results can be obtained in 10 min or longer of dark adaptation time in complete darkness.

scholarly journals Light and dark adaptation in Phycomyces phototropism.

1984 ◽  
Vol 84 (1) ◽  
pp. 101-118 ◽  
Author(s):  
P Galland ◽  
V E Russo
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Growth Response ◽  
Light Adaptation ◽  
Abnormal Behavior ◽  
Adaptation Level ◽  
Intensity Level ◽  
Wild Type ◽  
Adaptation Mechanism ◽  
Intensity Range

Light and dark adaptation of the phototropism of Phycomyces sporangiophores were analyzed in the intensity range of 10(-7)-6 W X m-2. The experiments were designed to test the validity of the Delbrück-Reichardt model of adaptation (Delbrück, M., and W. Reichardt, 1956, Cellular Mechanisms in Differentiation and Growth, 3-44), and the kinetics were measured by the phototropic delay method. We found that their model describes adequately only changes of the adaptation level after small, relatively short intensity changes. For dark adaptation, we found a biphasic decay with two time constants of b1 = 1-2 min and b2 = 6.5-10 min. The model fails for light adaptation, in which the level of adaptation can overshoot the actual intensity level before it relaxes to the new intensity. The light adaptation kinetics depend critically on the height of the applied pulse as well as the intensity range. Both these features are incompatible with the Delbrück-Reichardt model and indicate that light and dark adaptation are regulated by different mechanisms. The comparison of the dark adaptation kinetics with the time course of the dark growth response shows that Phycomyces has two adaptation mechanisms: an input adaptation, which operates for the range adjustment, and an output adaptation, which directly modulates the growth response. The analysis of four different types of behavioral mutants permitted a partial genetic dissection of the adaptation mechanism. The hypertropic strain L82 and mutants with defects in the madA gene have qualitatively the same adaptation behavior as the wild type; however, the adaptation constants are altered in these strains. Mutation of the madB gene leads to loss of the fast component of the dark adaptation kinetics and to overshooting of the light adaptation under conditions where the wild type does not overshoot. Another mutant with a defect in the madC gene shows abnormal behavior after steps up in light intensity. Since the madB and madC mutants have been associated with the receptor pigment, we infer that at least part of the adaptation process is mediated by the receptor pigment.

scholarly journals THE REGENERATION OF VISUAL PURPLE IN THE LIVING ANIMAL

1942 ◽  
Vol 26 (1) ◽  
pp. 27-47 ◽  
Author(s):  
James C. Peskin
Keyword(s):  
Vitamin A ◽  
Dark Adaptation ◽  
Light Adaptation ◽  
Living Animal ◽  
First Order ◽  
Visual Threshold ◽  
Isolated Retina ◽  
Lower Temperature ◽  
Initial Delay ◽  
Sigmoid Shape

1. The accumulation of visual purple in the retina after bleaching by light has been studied in the intact eye of the frog. The data show that duration and intensity of light adaptation, which influence the course of human dark adaptation as measured in terms of visual threshold, have a similar influence on the course of visual purple regeneration. 2. At 25°C. frogs which have been light adapted to 1700 millilamberts and then placed in the dark, show an increase in visual purple concentration which begins immediately and continues for 70 minutes until a maximum concentration is attained. The increase, although beginning at once, is slow at first, then proceeds rapidly, and finally slows up towards the end. Frogs which have been adapted to 9500 millilamberts show essentially the same phenomenon except that the initial slow period is strongly delayed so that almost no visual purple is formed in the first 10 minutes. 3. At 15°C. the initial delay in visual purple regeneration occurs following light adaptation to both 1700 and 9500 millilamberts. The delay is about 10 minutes and is slightly longer following the higher light adaptation. 4. The entire course of visual purple accumulation in the dark takes longer at the lower temperature than at the higher. The temperature coefficient for 10°C. is about 1.8. 5. In contrast to the behavior of the isolated retina which has small amounts of vitamin A and large amounts of retinene immediately after exposure to light, the intact eye has large amounts of vitamin A and little retinene after exposure to light for 10 minutes. In the intact eye during dark adaptation, the amount of vitamin A decreases markedly while retinene decreases only slightly in amount. If retinene is formed in the intact eye, the change from retinene to vitamin A must therefore occur rapidly in contrast to the slow change in the isolated retina. 6. The course of visual purple regeneration may be described by the equation for a first order autocatalyzed reaction. This supposes that the regeneration of visual purple is catalyzed by visual purple itself and accounts for the sigmoid shape of the data.

Movement of retinal along cone and rod photoreceptors

1994 ◽  
Vol 11 (2) ◽  
pp. 389-399 ◽  
Author(s):  
Jing Jin ◽  
Gregor J. Jones ◽  
M. Carter Cornwall
Keyword(s):  
Cell Body ◽  
Dark Adaptation ◽  
Visual Pigment ◽  
Outer Segment ◽  
Light Adaptation ◽  
Rod Photoreceptors ◽  
Rod Outer Segment ◽  
Rods And Cones ◽  
Outer Segments ◽  
Rod Cell

AbstractSingle isolated photoreceptors can be taken through a visual cycle of light adaptation by bleaching visual pigment, followed by dark adaptation when supplied with 11–cis retinal. Light adaptation after bleaching is manifested by faster response kinetics and a permanent reduction in sensitivity to light flashes, presumed to be due to the presence of bleached visual pigment. The recovery of flash sensitivity during dark adaptation is assumed to be due to regeneration of visual pigment to pre-bleach levels. In previous work, the outer segments of bleached, light-adapted cells were exposed to 11–cis retinal. In the present work, the cell bodies of bleached photoreceptors were exposed. We report a marked difference between rods and cones. Bleached cones recover sensitivity when their cell bodies are exposed to 11–cis retinal. Bleached rods do not. These results imply that retinal can move freely along the cone photoreceptor, but retinal either is not taken up by the rod cell body or retinal cannot move from the rod cell body to the rod outer segment. The free transfer of retinal along cone but not along rod photoreceptors could explain why, during dark adaptation in the retina, cones have access to a store of 11–cis retinal which is not available to rods. Additional experiments investigated the movement of retinal along bleached rod outer segments. The results indicate that retinal can move along the rod outer segment, but that this movement is slow, occurring at about the same rate as the regeneration of visual pigment.

scholarly journals The Duplex Nature of the Retina of the Nocturnal Gecko as Reflected in the Electroretinogram

1961 ◽  
Vol 44 (6) ◽  
pp. 1143-1158 ◽  
Author(s):  
Eberhard Dodt ◽  
Karl Heinz Jessen
Keyword(s):  
Electrical Activity ◽  
Dark Adaptation ◽  
Light Adaptation ◽  
Slow Phase ◽  
Strong Light ◽  
Increment Threshold ◽  
Hemidactylus Turcicus ◽  
Low Levels ◽  
Different Levels ◽  
Effect Of Light

The effect of light and dark adaptation on the electrical activity in two species of nocturnal gecko, Hemidactylus turcicus and Tarentola mauritanica was studied. The electroretinogram of both species changes from the scotopic type in the dark-adapted state to the photopic type after strong light adaptation. For the scotopic response fusion frequencies up to 18 flashes per sec. are obtained in both species. For the photopic response fusion frequencies up to 50 flashes per sec. are seen in Tarentola, and up to 25 flashes per sec. in Hemidactylus. Proceeding from dark to light adaptation the increment threshold (dI) is measured at different levels of adaptive illumination (I). At low levels of illumination the dI/I ratio is found to be small and at high levels of illumination to be large. No difference in the dI/I ratio is obtained for test lights of 462 and 605 mµ. During dark adaptation the change of threshold after exposure to moderate and weak lights (up to 103 times dark threshold) is rather fast. After light adaptation to strong light (106 times dark threshold) duplex dark adaptation curves are seen with a break separating a fast and a slow phase of dark adaptation. The significance of these results from a retina which possesses sense cells of only one type is discussed.

scholarly journals The Function of Photomechanical Movements in the Retina of the Rainbow Trout (Salmo Gairdneri)

1982 ◽  
Vol 96 (1) ◽  
pp. 389-403 ◽  
Author(s):  
R. H. DOUGLAS
Keyword(s):  
Rainbow Trout ◽  
Dark Adaptation ◽  
Visual Pigment ◽  
Time Course ◽  
Temporal Correlation ◽  
Salmo Gairdneri ◽  
Direct Sunlight ◽  
Pigment Concentrations ◽  
Wave Sensitivity ◽  
Effect Of Light

1. The function of photomechanical movements in the retina of rainbow trout (Salmo gairdneri) was investigated by determining both the effect of light on the level of extractable visual pigment, and the electroretinographic b-wave sensitivity, during various stages of photomechanical light and dark adaptation. 2. Dark-adapted fish, light-adapted fish, and dark-adapted fish exposed to ten minutes direct sunlight had on average visual pigment concentrations of 100, 82 and 36% respectively. 3. The intensity of illumination required to bleach a specified amount of visual pigment in the light-adapted retina was found to be 1.29 log units higher than that needed to bleach the same amount of visual pigment in a dark-adapted eye. 4. The level of extractable visual pigment was observed to be relatively constant over natural twilight periods. 5. A close temporal correlation was observed between the time course of electroretinographic adaptation, measured by the b-wave sensitivity, and photomechanical changes. 6. All these observations tend to support the hypothesis that photomechanical movements serve, at least in part, to protect the rod visual pigment from overstimulation in the light-adapted retina.

The Sensitivity of the Ventral Nerve Photoreceptor of Limulus Recovers after Light Adaptation in Two Phases of Dark Adaptation

1986 ◽  
Vol 41 (5-6) ◽  
pp. 657-667 ◽  
Author(s):  
I. Claßen-Linke ◽  
H. Stieve
Keyword(s):  
Dark Adaptation ◽  
Time Course ◽  
Light Adaptation ◽  
Light Flash ◽  
Light Response ◽  
Receptor Potential ◽  
Second Phase ◽  
Two Phases ◽  
Ventral Nerve Photoreceptor ◽  
External Calcium

The time course of the recovery of the sensitivity of the Limulus ventral nerve photoreceptor was measured during dark adaptation following light adaptation by a bright 1 or 5 s illumination. The stimulus intensity ICR of a 300 μs light flash evoking a response of criterion amplitude (receptor potential or receptor current under voltage clamp conditions) was used as measure of sensitivity.The time course of dark adaptation shows two phases with time constants in the range of 5-9 s and 300-500 s (15 °C). Only the first of the two phases is significantly changed when the extracel- lular Ca2+-concentration is varied.The power function ICR = a·Io-tDA-b gives a good data fit for each of the two phases of dark adaptation. In the first phase the factor ax and the exponent bx are decreased when the external calcium is lowered from 10 mmol/1 to 250 μmol/1. Conversely a1 and b1 are increased when the Ca2+-concentration is raised to 40 mmol/1. For the second phase neither a2 nor b2 is changed significantly upon the changes in calcium concentration in the same experiments.The two phases of dark adaptation reflect the behaviour of the two components C1 and C2 of the electrical light response (receptor potential or receptor current). Under the conditions described here C, determines the size of the light response during the first phase of dark adaptation whereas C2 mainly influences the size of the response during the second phase.Interpretation: The fast first phase of dark adaptation is determined by the change in intracellu- lar Ca2+-concentration. The slower second phase of dark adaptation is not primarily calcium- controlled.

scholarly journals Intracellular recordings from gecko photoreceptors during light and dark adaptation.

1975 ◽  
Vol 66 (5) ◽  
pp. 617-648 ◽  
Author(s):  
J Kleinschmidt ◽  
J E Dowling
Keyword(s):  
Membrane Potential ◽  
Dark Adaptation ◽  
Horizontal Cell ◽  
Intracellular Recordings ◽  
Receptor Sensitivity ◽  
Intensity Curve ◽  
Voltage Range ◽  
Voltage Change ◽  
Sensitivity Change ◽  
Compression Treatment

Intracellular recordings were obtained from rods in the Gekko gekko retina and the adaptation characteristics of their responses studied during light and dark adaptation. Steady background illumination induced graded and sustained hyperpolarizing potentials and compressed the incremental voltage range of the receptor. Steady backgrounds also shifted the receptor's voltage-intensity curve along the intensity axis, and bright backgrounds lowered the saturation potential of the receptor. Increment thresholds of single receptors followed Weber's law over a range of about 3.5 log units and then saturated. Most of the receptor sensitivity change in light derived from the shift of the voltage-intensity curve, only little from the voltage compression. Treatment of the eyecup with sodium aspartate at concentrations sufficient to eliminate the beta-wave of the electroretinogram (ERG) abolished initial transients in the receptor response, possibly indicating the removal of horizontal cell feedback. Aspartate treatment, however, did not significantly alter the adaptation characteristics of receptor responses, indicating that they derive from processes intrinsic to the receptors. Dark adaptation after a strongly adapting stimulus was similarly associated with temporary elevation of membrane potential, initial lowering of the saturation potential, and shift of the voltage-intensity curve. Under all conditions of adaptation studied, small amplitude responses were linear with light intensity. Further, there was no unique relation between sensitivity and membrane potential suggesting that receptor sensitivity is controlled at least in part by a step of visual transduction preceding the generation of membrane voltage change.

Sign in / Sign up

Export Citation Format

Share Document