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Biomedical subjects

D van Norren

Publications and source records attributed to D van Norren.

80 records · Page 5Linked to original sources

Two-band model of heterochromatic flicker.

We have attempted to reconcile the results of several recent chromatic flicker studies. By adjusting the relative amplitudes of red and green sine-wave stimuli that were flickering in opposite phase, we obtained conditions varying from purely chromatic (red-green) stimulation, through each "silent-cone" condition, to purely luminous (homochromatic) stimulation. We also tested the effects of adapting backgrounds in each condition. Our results can be explained in terms of a low-frequency band that represents the opponent-color response, and a high-frequency band that represents the achromatic response. These two bands respond in various proportions, depending on the red-green stimulus ratio. Chromatic adaptation generally affects the low- and high-frequency bands differently and hence changes the shape of the flicker sensitivity curve. However, if the temporally varying waveform and the adapting background are both chosen to stimulate the same cone type, then the opponent-color and achromatic bands are both attenuated by the same amount. In this case, the shapes of the silent-red and silent-green flicker curves are preserved under chromatic adaptation. We conclude that none of these flicker curves are controlled by the temporal characteristics of independent cone types.

Color Perception↗

Influence of anesthetics, ethyl alcohol, and Freon on dark adaptation of monkey cone ERG.

Cone dark adaptation curves were measured in a rhesus monkey using the electroretinogram (ERG) response to a 40 Hz flickering stimulus. The influence of anesthetics on the time course of dark adaptation was studied. All volatile anesthetics tested (methoxyflurane, halothane, enflurane, ether, chloroform) retarded dark adaptation but to different degrees; urethane, ethyl alcohol, and Freon 11 also retarded dark adaptation. No effect was found for barbiturates and ketamine. It seems unlikely that metabolites play a role in the observed phenomena. A literature survey reveals that several studies on dark adaptation or visual pigment regeneration might have suffered from influences of the anesthetic used. The cause of the phenomenon might lie either in anesthetics-induced membrane changes or in hindrance of the isomeration of 11-trans retinal to 11-cis retinal.

Anesthetics↗

Cone dark adaptation: the influence of halothane anesthesia.

Cone dark adaptation (da) (measured with an electroretinogram [ERG] method) is found to be severely retarded when the subject (human and macaque monkey) is under halothane anesthesia. The degree of retardation depends both on the halothane level and on the bleach history. The effect of bleach history shows a great similarity with psychophysical findings concerning foveal da. Interpretation of halothane effects, therefore, is possible in terms of an existing model on cone pigment kinetics.

Anesthesia, Inhalation↗

Flicker responses in monkey lateral geniculate nucleus and human perception of flicker.

An analysis was made of the impulse discharge patterns-evoked by sinusoidal luminance modulation-of single cells in the lateral geniculate nucleus of the macaque monkey. The goal was to determine whether a correspondence could be observed between flicker detection by human subjects in psychophysical experiments and electrophysiological measurements of discharge patterns of single cells of the lateral geniculate nucleus. We found that the average discharge patterns of single cells exhibited the following behavior when mean retinal illumination was changed: In the low-frequency region (less than about 10 Hz) the response strength (impulses/sec) is independent of the mean luminance, in accordance with Weber's law; in the high-frequency region (above about 10 Hz) the response depends on the absolute modulation amplitude, in accordance with the Ferry-Porter law. Therefore the main features of human critical flicker frequency data are already present in the cellular (lateral geniculate nucleus) response of the macaque monkey. However, the steepness of high frequency fall-off in the response characteristics of these cells is much less than the corresponding fall-off in the human critical-flicker-frequency curves.

Animals↗