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PubMed1984

Functional abnormalities in vincristine-induced night blindness.

Various noninvasive test procedures were used to evaluate retinal function in a patient who had become night blind following vincristine chemotherapy. The results obtained were strikingly similar to those reported previously in subjects with recessively inherited stationary night blindness; the dark-adaptation curve was monophasic (ie, no evidence of a scotopic branch), rhodopsin kinetics were entirely normal, and spectral threshold data revealed the presence of residual rod-mediated vision. Also like the heritable condition, the b-wave of the ERG was depressed grossly despite normal a-wave potentials. These findings, and the fact that vincristine is known to disrupt the structural integrity of neuronal microtubules, suggest that the drug-induced defect involves the process of synaptic transmission between the photoreceptors and their second-order neurons.

Adaptation, Ocular↗
PubMed1980

The effect of prolonged light and dark adaptation on lens regeneration in the adult newt Triturus viridescens.

Light intensity has been shown to affect lens regeneration in adult newts. Experiments were designed to study the effects of different light controlled environments on lens regeneration in the newt T, viridescens. Animals were preadapted to three light conditions: control, light from below and dark for ninety (90) days prior to lentectomy. The newts remained in the controlled environments post-lentectomy to test the effects of light preadaptation on lens regeneration. The results indicate that controlled light sources from below cannot stimulate the ventral iris to regenerate a new lens or inhibit the dorsal iris from normal lens regeneration. Lens regeneration in preadapted dark animals is similar in rate and amount to the control group indicating a totally dark environment does not always inhibit lens regeneration.

Adaptation, Ocular↗
PubMed1995

Automated perimetry with bright and dark stimuli.

Conventional perimeters use bright stimuli. In this study, dark stimuli were also used. Dark stimuli are employed for testing due to their lack of effects of local scatter and are utilized with the purpose of preferentially stimulating the off-system, but their presentation with optical methods is difficult. This problem is solved by the use of a computer monitor. The objective of this study was to compare directly measurements obtained with bright and dark stimuli. Therefore, the central 30 degrees of the visual field of ten subjects with no ophthalmologic pathology was examined with bright and dark stimuli (size 10- and 30-min-of-arc). Threshold estimation was performed with the 4/2 method. Concerning the 10-min-of-arc dark stimulus, no measurement outside the central 15 degrees could be performed because of insufficient dynamic range (sometimes even the darkest stimulus was not seen). Comparing the results obtained using bright and dark stimuli of the same size, we could not find a significant difference in sensitivity for this age group.

Adaptation, Ocular↗
PubMed1994

Visual readaptation after flash exposure under scotopic conditions. A study using optokinetic nystagmus as an indicator of visual perception.

The purpose of the present study was to establish a method for objective measurements of visual readaptation after flash exposures and to define a model for measurements. Influences of target direction, luminance and velocity on optokinetic nystagmus (OKN) were investigated under scotopic conditions. Visual readaptation was measured using OKN as an indicator of visual perception after exposure to a flash. The interval between the triggering of the flash and the reoccurrence of OKN was defined as the visual readaptation time (RAT). A Goldmann perimeter hemisphere was used for flash stimulation. A horizontally moving vertical grating projected inside the hemisphere was used as the OKN stimulus. Eye movements were recorded by DC electrooculography (EOG). The dependence of RAT on the dose of the flash, the wavelength of the flash and the luminance of the OKN target were investigated. The precision of the measurement method was studied. This includes the analysis of the variance due to the experimental occasions, the repeated exposures, the sexes of the subjects, the methods for recognition of OKN and the ways of visual adaptation before measurements. The contributions of retinal receptor and the neural activity to RAT were investigated by electroretinography (ERG). The influences of target direction and luminance on binocular motion perception and OKN as well as monocular OKN were examined at various target velocities. The dependence of the frequency and amplitude of eye jerks during monocular OKN on target luminance and velocity were also examined. It was found that RAT increases with increasing doses of the flash or decreasing luminance of the grating. RAT is most extended after flashes near 520 nm. RAT does not differ between experimental occasions, between a manual and a semi-automatic method for recognition of OKN, between the sexes and between goggle adaptation and ordinary dark adaptation. There is a reduction of RAT due to repeated flash exposures. The data collected indicate that a well-defined model is crucial for measurements of RAT. The measurement of ERG showed that RAT is mediated by both retinal receptor and the neural activities. The receptor component depends on the wavelength of the flash while the neural component is wavelength-independent. Moreover, it was found that motion perception and OKN gain does not differ between right and left target directions. For a given target velocity, motion perception and OKN gain under both binocular and monocular viewing conditions increase with increasing luminance of the target with an exponential decay. The maximum OKN gain decreases as target velocity increases.(ABSTRACT TRUNCATED AT 400 WORDS)

Adaptation, Ocular↗
PubMed1998

Effect of eye closures and openings on photostasis in albino rats.

PURPOSE: To determine the effects of eye closure and opening on photostasis, the regulation of light absorption by retinal rods in the albino rat. METHODS: The approach was to measure the effect of eye closure and opening on rhodopsin bleaching in situ and to use those results to simulate what happens to rhodopsin when a living rat opens or closes its eyes during daylight exposure. Completely dark-adapted, dead albino rats, each with one eye closed or open, were exposed to a standard lighting situation. The rhodopsin bleaching rate in closed versus open eyes was measured. Rhodopsin bleached at a more reduced rate in closed eyes than in open eyes. This measured reduction of rate in closed eyes was applied to a simulation of rhodopsin bleaching in open and closed eyes. The simulation used idealized conditions to verify the simulation itself, and then it was applied to previously published photostasis results. RESULTS: Rhodopsin in closed eyes bleaches at half the rate found in open eyes. The absorption spectrum of rat red blood cells was compared with the rate rhodopsin absorption spectrum, and the comparison showed that blood does not absorb the main-band wavelengths of rhodopsin. Simulating rhodopsin bleaching with eyes closed (half intensity) and open (full intensity) during daylight hours showed a slight effect on the total number of photons absorbed in an entire day. The simulation set limits to the maximal effect of eyes open all day versus eyes closed all day. At a habitat intensity of 200 lux, for example this maximal effect (eyes always open versus always closed) was calculated to be +/- 9%. At the lowest intensity, 3 lux, this maximal effect was +/- 28%, but it is only 1% at the highest intensity, 400 lux. CONCLUSIONS: Eye closures and openings have a slight effect on photostasis in albino rats. There are two reasons for this: The eyelids reduce the effective bleaching intensity by half. Moreover, during the "dim-out" of closure, rhodopsin continues to regenerate and approaches a new, higher value. This accumulation of rhodopsin enhances the rate of photon absorption because the rate is proportional to the product (rhodopsin x intensity). Thus, the increased rhodopsin concentration in the rods partially compensates for the reduced intensity of lid closure, and the photon absorption rates, with eyes closed, do not decrease by the full factor of 2 implied by the intensity reduction. In addition, when the eyes are subsequently opened after such a dim-out, the retina is suddenly exposed again to the full intensity of the environment. At this time, photon absorption rate, rhodopsin x intensity, is transiently higher than just before eye opening. Thus, the compensatory interplay between bleaching and regeneration in closed and open eyes results in the near compensation of light absorption and maintenance of the stasis close to 10(16) photons per eye per day.

Absorption↗