Sensitivity facilitation in the insect eye

Summary ERG amplitude facilitation, observed in the eye ofAtta sexdens after light adaptation, was studied as a function of duration and intensity of adaptation, of dark interval between adapting and test stimuli, and of level of steady background illumination. Results show that sensitivity facilitation in this eye cannot be regarded as a minor effect since it covers a 2 log unit range, the same as that obtained for conditions that produce sensitivity reduction. Maximum facilitation occurs with short and intense light adaptation. The time span of the effect is close to 2 min, and its maximum amplitude may be attained up to 20 s after light adaptation. Increase in background illumination gradually erases facilitation. However, the facilitated response is less sensitive to background illumination than the dark adapted response. Long durations of light adaptation cause ERG decrease, or inhibition. A comparison of these two end results of light adaptation suggests that they arise from different processes, perhaps with distinct origins.Supported by a grant from Fundação de Amparo à Pesquisa do Estado de São Paulo, to the senior author (Contract n 71/1141)With a Fellowship from Fundação de Amparo à Pesquisa do Estado de São Paulo (N 74/388)We wish to express our appreciation to Henrique Fix for his editorial assistance, and to Celia Jablonka for laboratory help.     

On the role of horizontal cells in the mechanism of retinal adaptation

We recorded by intracellular means responses of horizontal cells of the turtle retina to light increase and decrease of different values against the starting adapting level. In measuring these responses, curves reflecting the dependence of membrane potential deflection on light intensity (amplitude characteristics — ACh) were plotted. It is demonstrated that the ACh of transitional processes (on- and off-peaks) is considerably steeper than ACh of the plateau of the potential, but embraces a much smaller range of light intensities (slightly more than 1 log. un.). During a change in intensity of the adapting background (up to 3 log. un.), the ACh of transitional processes shifts along the scale of light intensities in such a way that its steep part remains in the zone of adapting light. We followed the dynamics in time of ACh shift after the transition from one adapting brightness to another. The ACh of total impulse response was plotted for ganglionic cells of the turtle at different intensities of adapting light. Comparison of these curves with the ACh of horizontal cells shows that its peripheral components are responsible for adaptive shifts of ACh of the visual system and that horizontal cells play an important role in the mechanism of adaptation. It is hypothesized that adaptive ACh shifts are the consequence of positive feedback between the horizontal cells and receptors.Institute of Problems of Information Transmission, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 1, No. 2, pp. 210–218, September–October, 1969.     

Light-induced reduction in excitation efficiency in the trp mutant of Drosophila

In the transient receptor potential (trp) mutant of Drosophila, the receptor potential appears almost normal in response to a flash but quickly decays to baseline during prolonged illumination. Photometric and early receptor potential measurements of the pigment suggest that the pigment is normal and that the decay of the trp response during illumination does not arise from a reduction in the available photopigment molecules. However, there is reduction in pigment concentration with age. Light adaptation cannot account for the decay of the trp response during illumination: in normal Drosophila a dim background light shortens the latency and rise time of the response and also shifts the intensity response function (V-log I curve) to higher levels of light intensity with relatively little reduction in the maximal amplitude (Vmax) of response. In the trp mutant, a dim background light or short, strong adapting light paradoxically lengthens the latency and rise time of the response and substantially reduces Vmax without a pronounced shift of the V-log I curve along the I axis. The effect of adapting light on the latency and V-log I curve seen in trp are associated with a reduction in effective stimulus intensity (reduction in excitation efficiency) rather than with light adaptation. Removing extracellular Ca+2 reduces light adaptation in normal Drosophila, as evidenced by the appearance of "square" responses to strong illumination. In the trp mutant, removing extracellular Ca+2 does not prevent the decay of the response during illumination.     

Intracellular recordings from gecko photoreceptors during light and dark adaptation

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.     

SENSORY ADAPTATION AND THE STATIONARY STATE

1. Experiments are described which measure the sensitivity of animals exposed to continued illumination to which they have become adapted. It is shown that the amount of outside light energy necessary to stimulate an adapted animal increases with the intensity of the adapting illumination. 2. The data are analyzed quantitatively in terms of the reversible reaction S ⇌ P + A shown previously to account for the photic sensitivity of these animals. This analysis demonstrates that, though the amount of incident energy necessary for a minimal response varies with the adapting intensity, the actual amount of photochemical decomposition required to set off the sensory mechanism is a constant quantity. 3. The ability of these animals to come into sensory equilibrium with any sustained illumination is accounted for quantitatively by the presence of a stationary state in the reversible photochemical reaction S ⇌ P + A during which the concentrations of the three components are constant. 4. It is shown that the concentrations of these substances at the stationary state are automatically controlled by the outside intensity. Therefore, given the sensory mechanism as a basis, the adaptation of the animals to light and the consequent changes in sensitivity, are determined entirely by the light to which the animals are exposed. 5. Because of the properties of the stationary state, and of the constancy of photochemical decomposition for a minimal effect, it is suggested that the sensory system is not only the traditional receptor system, but is also a protecting layer which stabilizes and buffers the relation between the nervous system and the environment.     

Receptive fields of visual cortical neurons during changes in parameters of photic stimulation in cats

Spatial excitability contours in receptive fields of visual cortical neurons during changes in the physical and physiological parameters of photic stimulation were investigated in acute experiments on immobilized cats under conditions of dark, mesopic, and low photopic adaptation. With the change from dark to low mesopic adaptation the shape and size of the receptive fields detected by testing with flashes of constant intensity are unchanged, but with the transition to low photopic adaptation the receptive field becomes long and very narrow in 72% of cases, and the acuity of its orientational and directional tuning becomes much sharper. Against an unchanged background illumination, loss of brightness of the test light slit leads to narrowing of the measurable receptive field. Excitability contours of the receptive field estimated on the basis of absolute threshold of the cell response and level of intensity necessary to obtain the same number of spikes in the response become much narrower as the threshold criterion rises and during dark adaptation. Reactivity contours of the receptive field in response to stimulation of physiologically equal intensities (equal to the increase in threshold) under conditions of photopic adaptation also are much narrower than reactivity contours under conditions of dark adaptation. Evaluation of receptive fields with allowance for the possible contribution of effects of light scatter on the screen and in the ocular media showed that in most cases their size cannot be explained by these phenomena.Institute of Higher Nervous Activity and Neurophysiology, Academy of Sciences of the USSR, Moscow. Translated from Neirofiziologiya, Vol. 12, No. 2, pp. 115–123, March–April, 1980.     

S-Potentials in the Skate Retina : Intracellular recordings during light and dark adaptation

The S-potentials recorded intracellularly from the all-rod retina of the skate probably arise from the large horizontal cells situated directly below the layer of receptors. These cells hyperpolarize in response to light, irrespective of stimulus wavelength, and the responses in photopic as well as scotopic conditions were found to be subserved by a single photopigment with λ_max = 500 nm. The process of adaptation was studied by recording simultaneously the threshold responses and membrane potentials of S-units during both light and dark adaptation. The findings indicate that the sensitivity of S-units, whether measured upon steady background fields or in the course of dark adaptation, exhibits changes similar to those demonstrated previously for the ERG b-wave and ganglion cell discharge. However, the membrane potential level of the S-unit and its sensitivity to photic stimulation varied independently for all the adapting conditions tested. It appears, therefore, that visual adaptation in the skate retina occurs before the S-unit is reached, i.e., at the receptors themselves.     

鲤科鱼视网膜光感受器电位的明适应特性

本实验室以前曾报道,视网膜电图 b 波的敏感度在明适应过程中的变化因背景光强而异:在较弱背景光时随时间逐渐降低,当背景光强达到一定水平后,则在明适应过程中出现一定程度的回复。本工作应用分离、灌流的鲤科鱼视网膜,详细地考察了用谷氨酸分离的感受器电位(PⅡ)的明适应特性。在较弱背景光下,PⅡ敏感度除初始时降低外,不随时间作进一步变化。当背景光强达到一定水平后,与 b 波相似,PⅡ敏感度也随时间而回复。对 PⅡ光谱敏感性和不同波长辨增阈的测定表明,PⅡ的这两型变化交替的光强恰为视杆系统与视锥系统活动交替的光强;当背景光完全压抑视杆系统的活动后(仅接收视杆输入的水平细胞的胞内记录的反应完全被压抑),PⅡ即呈现回复型变化。这些结果提示,b 波的回复型变化部分地反映了视锥细胞的明适应特性。     

A novel Ca2+-feedback mechanism extends the operating range of mammalian rods to brighter light

Sensory cells adjust their sensitivity to incoming signals, such as odor or light, in response to changes in background stimulation, thereby extending the range over which they operate. For instance, rod photoreceptors are extremely sensitive in darkness, so that they are able to detect individual photons, but remain responsive to visual stimuli under conditions of bright ambient light, which would be expected to saturate their response given the high gain of the rod transduction cascade in darkness. These photoreceptors regulate their sensitivity to light rapidly and reversibly in response to changes in ambient illumination, thereby avoiding saturation. Calcium ions (Ca²⁺) play a major role in mediating the rapid, subsecond adaptation to light, and the Ca²⁺-binding proteins GCAP1 and GCAP2 (or guanylyl cyclase–activating proteins [GCAPs]) have been identified as important mediators of the photoreceptor response to changes in intracellular Ca²⁺. However, mouse rods lacking both GCAP1 and GCAP2 (GCAP^−/−) still show substantial light adaptation. Here, we determined the Ca²⁺ dependency of this residual light adaptation and, by combining pharmacological, genetic, and electrophysiological tools, showed that an unknown Ca²⁺-dependent mechanism contributes to light adaptation in GCAP^−/− mouse rods. We found that mimicking the light-induced decrease in intracellular [Ca²⁺] accelerated recovery of the response to visual stimuli and caused a fourfold decrease of sensitivity in GCAP^−/− rods. About half of this Ca²⁺-dependent regulation of sensitivity could be attributed to the recoverin-mediated pathway, whereas half of it was caused by the unknown mechanism. Furthermore, our data demonstrate that the feedback mechanisms regulating the sensitivity of mammalian rods on the second and subsecond time scales are all Ca²⁺ dependent and that, unlike salamander rods, Ca²⁺-independent background-induced acceleration of flash response kinetics is rather weak in mouse rods.     

Dynamics of chromatic adaptation in cones of freshwater turtle

The closer the wavelength of a steady background of monochromatic light is to the peak sensitivity of a cone that is being illuminated, the stronger is the desensitization of that cone; this is chromatic adaptation. A model of the freshwater turtle retina with the neural components of chromatic adaptation via negative feedback circuits is used to simulate and study various aspects of chromatic adaptation. An internal negative feedback circuit resides solely within the cone pedicle and thereby, its adaptive effects are relatively specific, so that univariance is maintained. The cone-L-horizontal cell circuit is an external negative feedback circuit and its adaptive effects are less specific since all 3 chromatic cone types are involved, so that univariance is violated. Chromatic adaptation is the result of the decrease in the cone gain due to the dependency of the gains of the negative feedback circuits on the mean illuminance level. The results of the model are consistent with von Kries law, but the changes in gains of the cones due to chromatic adaptation are dependent on wavelength, intensity of the adapting light and size.     

Adaptation in the Ventral Eye of Limulus is Functionally Independent of the Photochemical Cycle, Membrane Potential, and Membrane Resistance

The early receptor potential (ERP), membrane potential, membrane resistance, and sensitivity were measured during light and/or dark adaptation in the ventral eye of Limulus. After a bright flash, the ERP amplitude recovered with a time constant of 100 ms, whereas the sensitivity recovered with an initial time constant of 20 s. When a strong adapting light was turned off, the recovery of membrane potential and of membrane resistance had time-courses similar to each other, and both recovered more rapidly than the sensitivity. The receptor depolarization was compared during dark adaptation after strong illumination and during light adaptation with weaker illumination; at equal sensitivities the cell was more depolarized during light adaptation than during dark adaptation. Finally, the waveforms of responses to flashes were compared during dark adaptation after strong illumination and during light adaptation with weaker illumination. At equal sensitivities (equal amplitude responses for identical flashes), the responses during light adaptation had faster time-courses than the responses during dark adaptation. Thus neither the photochemical cycle nor the membrane potential nor the membrane resistance is related to sensitivity changes during dark adaptation in the photoreceptors of the ventral eye. By elimination, these results imply that there are (unknown) intermediate process(es) responsible for adaptation interposed between the photochemical cycle and the electrical properties of the photoreceptor.     

Physiological roles of Na+/Ca2+ exchange in Limulus ventral photoreceptors

In previous work we have presented evidence for electrogenic Na+/Ca2+ exchange in Limulus ventral photoreceptors (1989. J. Gen. Physiol. 93:473-492). This article assesses the contributions to photoreceptor physiology from Na+/Ca2+ exchange. Four separate physiological processes were considered: maintenance of resting sensitivity, light-induced excitation, light adaptation, and dark adaptation. (a) Resting sensitivity: reduction of [Na+]o caused a [Ca2+]o-dependent reduction in light sensitivity and a speeding of the time courses of the responses to individual test flashes; this effect was dependent on the final value to which [Na+]o was reduced. The desensitization caused by Na+ reduction was dependent on the initial sensitivity of the photoreceptor; in fully dark-adapted conditions no desensitization was observed; in light-adapted conditions, extensive desensitization was observed. (b) Excitation: Na+ reduction in fully dark-adapted conditions caused a Ca2+o-dependent depolarizing phase in the receptor potential that persisted beyond the stimulus duration and was evoked by a bright adapting flash. (c) Light adaptation: the degree of desensitization induced by a bright adapting flash was Na+o dependent, being larger with lower [Na+]o. Na+ reduction enhanced light adaptation only at intensities brighter than 4 x 10(-6) W/cm2. In addition to being Na+o dependent, light adaptation was Ca2+o dependent, being greater at higher [Ca2+]o. (d) Dark adaptation: the recovery of light sensitivity after adapting illumination was Na+o dependent. Dark adaptation after bright illumination in voltage-clamped and in unclamped conditions was faster in normal-Na+ saline than in reduced Na+ saline. The final sensitivity to which photoreceptors recovered was lower in reduced-Na+ saline when bright adapting illumination was used. The results suggest the involvement of Na+/Ca2+ exchange in each of these physiological processes. Na+/Ca2+ exchange may contribute to these processes by counteracting normal elevations in [Ca2+]i.     

Sinusoidal and delta function responses of visual cells of the Limulus eye

Dynamic responses of visual cells of the Limulus eye to stimuli of sinusoids and narrow pulses of light superimposed on a nonzero mean level have been obtained. Amplitudes and phase angles of averaged sinusoidal generator potential are plotted with respect to frequency of intensity modulation for different mean levels of light adaptation. At frequencies above 10 CPS, generator potential amplitudes decrease sharply and phase lag angle increases. At frequencies below 1 CPS, amplitude decreases. A maximum of amplitude in the region of 1 to 2 CPS is apparent with increased mean intensity. The generator potential responses are compared with those of differential equation models. Variation of gain with mean intensity for incremental stimuli is consistent with logarithmic sensitivity of the photoreceptor. Frequency response of the photoreceptor derived from narrow pulses of light predicts the frequency response obtained with sinusoidal stimuli, and the photoreceptor is linear for small signals in the light-adapted state.     

THE VISIBILITY OF SINGLE LINES AT VARIOUS ILLUMINATIONS AND THE RETINAL BASIS OF VISUAL RESOLUTION

The visual resolution of a single opaque line against an evenly illuminated background has been studied over a large range of background brightness. It was found that the visual angle occupied by the thickness of the line when it is just resolved varies from about 10 minutes at the lowest illuminations to 0.5 second at the highest illuminations, a range of 1200 to 1. The relation between background brightness and just resolvable visual angle shows two sections similar to those found in other visual functions; the data at low light intensities represent rod vision while those at the higher intensities represent cone vision. With violet light instead of white the two sections become even more clearly defined and separated. The retinal image produced by the finest perceptible line at the highest brightness is not a sharp narrow shadow, but a thin broad shadow whose density distribution is described in terms of diffraction optics. The line of foveal cones occupying the center of this shadow suffers a decrease in the light intensity by very nearly 1 per cent in comparison either with the general retinal illumination or with that on the row of cones to either side of the central row. Since this percentage difference is near the limit of intensity discrimination by the retina, its retinal recognition is probably the limiting factor in the visual resolution of the line. The resolution of a line at any light intensity may also be limited by the just recognizable intensity difference, because this percentage difference varies with the prevailing light intensity. As evidence for this it is found that the just resolvable visual angle varies with the light intensity in the same way that the power of intensity discrimination of the eye varies with light intensity. It is possible that visual resolution of test objects like hooks and broken circles is determined by the recognition of intensity differences in their diffracted images, since the way in which their resolution varies with the light intensity is similar to the relation between intensity discrimination and light intensity.     

DARK ADAPTATION IN DINEUTES

The level of dark adaptation of the whirligig beetle can be measured in terms of the threshold intensity calling forth a response. The course of dark adaptation was determined at levels of light adaptation of 6.5, 91.6, and 6100 foot-candles. All data can be fitted by the same curve. This indicates that dark adaptation follows parts of the same course irrespective of the level of light adaptation. The intensity of the adapting light determines the level at which dark adaptation will begin. The relation between log aI ₀ (instantaneous threshold) and log of adapting light intensity is linear over the range studied.     

The relevance of the brightness to visual acuity,predation, and activity of visually hunting ground-beetles (Coleoptera,Carabidae)

Summary Carabid species of the visually hunting type living in dim habitats have larger frontal ommatidia and gain their optimal visual performance with lower light intensity than species inhabiting bright places.The latter phenomenon is based upon the mechanisms of light adaptation, which reduce the acceptance angles of the ommatidia thus increasing their visual acuity. In more sensitive ommatidia adaptation occurs with lower light intensity.The differences between the species concerning the intensity dependence of their visual performance are regarded as an effect of natural selection. Thereafter an apposition eye more sensitive to light should be advantageous in a dim environment.This hypothesis has been investigated and verified by observation of the predation behaviour of Notiophilus biguttatus confronted with Collembola: From 1 to 500 lux the hunting success of the beetles increased proportionally to the light intensity.Measurements of the activity at dawn and at dusk under natural conditions showed that the beginning and the conclusion of activity are correlated with a critical level of illumination. Notiophilus biguttatus starts being active if the illumination is sufficient for successful hunting.Supported by the Deutsche ForschungsgemeinschaftSupported by the Österreichischer Forschungsrat     

Properties of the on-transient of the intracellular response in the barnacle photoreceptor

We have studied the on-transient of the receptor potential of the barnacle photoreceptor. Its amplitude has previously been shown to depend on light intensity and state of light-dark adaptation. We have examined its dependence on 1) the presence of a prolonged depolarizing afterpotential (PDA), 2) a background light, 3) added alcohol, or 4) decreased K⁺ concentration in the bath. We find that the relative on-transient amplitude tends to increase initially with increasing depolarization arising from 1)–4) and then to decrease again at higher depolarization. This behavior is qualitatively explainable by the cell's currentvoltage characteristics and by the adapting effect of the stimulus on the conductances arising from the PDA, the background light and the alcohol.Based on material presented at the European Neurosciences Meeting, Florence, September 1978     

Role of intracellular calcium and sodium in light adaptation in the retina of the honey bee drone (Apis mellifera, L)

In the honey bee drone, the decrease in sensitivity to light of a retinula cell exposed to background illumination was found to be accurately reflected by the difference in amplitude between the initial transient depolarization and the lowest steady depolarization evoked by the background light. It is shown that both the decrease in sensitivity to light and the accompanying drop in potential from the transient to the plateau can be prevented by injecting EGTA intracellularly. A decrease in duration and amplitude of responses to short test flashes such as observed immediately after illumination was found to occur too when Ca or Na, but not K, Li, or Mg injected into dark-adapted retinula cells. Injection of EGTA into a retinula cell maintained a steady state of light adaptation, was found to cause an increase in amplitude and duration of the response to a short test flash, thus producing the effects of dark adaptation. It is suggested that, in the retina of the honey bee drone, an increase in intracellular calcium concentration plays a central role in light adaptation and that an increase in intracellular sodium concentration, resulting from the influx of sodium ions during the responses to light, could lead to this increase in intracellular free calcium.     

Adaptation in Cones: A General Model

Three features appear to characterize steady-state light adaptation in vertebrate cone photoreceptors: (a) the shape of the “log intensity-response” curve at different levels of adaptation is the same, the only change with adaptation is in the position of the point on the curve about which the cones operate; (b) at high adapting intensities the operating point becomes fixed in position; (c) this fixed position is at the steepest point of the log intensity-response curve. These three features can be described by a mathematical model.     

The effect of light adaptation on the dynamic properties of phototransduction in the fly,Phormia regina

The static and dynamic characteristics of phototransduction were studied in photoreceptors of the compound eye of the fly Phormia regina (Calliphoridae) using a green light emitting diode driven by a controlled current source. The LED provides sufficiently intense light to investigate the behaviour of the receptors over about half of the dark adapted range of the response versus log intensity curve. The effects of constant adapting light intensities upon the step response and upon the frequency response and coherence functions were examined. Using both methods the effect of light adaptation upon receptor sensitivity can be closely approximated by a similar linear dependence of log sensitivity upon log adapting intensity. However, there was no reliably detectable effect of light adaptation upon the time constant of the response over the range of adapting intensities used.Abbreviation LED Light Emitting Diode