PubMed · 7331247
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S M Dawis. 1981. The compression model: a re-examination.. https://doi.org/10.1016/0042-6989(81)90223-6
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The refractive state of hatchling chicks rapidly compensates to applied optical defocus through alteration in eye growth. The mechanism is capable of sensing whether the plane of focus lies in front of or behind the photoreceptors, however, its nature and site of action within the retina are unknown. We attempted to create an imbalance in the adaptation of the retinal ON and OFF mechanisms previously implicated in refractive control through pharmacological interventions, by rearing chicks from 4 to 9 days of age with a monocular +10 D, 0 D or -10 D lens, in an environment illuminated by a moving or stationary plaid of luminance gradients. When the plaid moved in one direction a local Fast-ON sawtooth luminance modulation was produced, while plaid motion in the other direction resulted in a Fast-OFF sawtooth modulation. Significantly reduced refractive compensation accompanied +10 D lens/Fast-OFF and -10 D lens/Fast-ON rearing, but not for the other conditions. Thus the refractive compensation mechanism depends on the nature of the temporal contrast of the environment, suggesting a relationship between the sign of defocus and the state of adaptation of the retinal ON and OFF subsystems.
We sought to determine the extent to which red-green, colour-opponent mechanisms in the human visual system play a role in the perception of drifting luminance-modulated targets. Contrast sensitivity for the directional discrimination of drifting luminance-modulated (yellow-black) test sinusoids was measured following adaptation to isoluminant red-green sinusoids drifting in either the same or opposite direction. When the test and adapt stimuli drifted in the same direction, large sensitivity losses were evident at all test temporal frequencies employed (1-16 Hz). The magnitude of the loss was independent of temporal frequency. When adapt and test stimuli drifted in opposing directions, large sensitivity losses were evident at lower temporal frequencies (1-4 Hz) and declined with increasing temporal frequency. Control studies showed that this temporal-frequency-dependent effect could not reflect the activity of achromatic units. Our results provide evidence that chromatic mechanisms contribute to the perception of luminance-modulated motion targets drifting at speeds of up to at least 32 degrees s(-1). We argue that such mechanisms most probably lie within a parvocellular-dominated cortical visual pathway, sensitive to both chromatic and luminance modulation, but only weakly selective for the direction of stimulus motion.
The signaling pathways that couple light photoreception to entrainment of the circadian clock have yet to be deciphered. Two prominent groups of candidates for the circadian photoreceptors are opsins (e.g., melanopsin) and blue-light photoreceptors (e.g., cryptochromes). We have previously showed that the zebrafish is an ideal model organism in which to study circadian regulation and light response in peripheral tissues. Here, we used the light-responsive zebrafish cell line Z3 to dissect the response of the clock gene zPer2 to light. We show that the MAPK (mitogen-activated protein kinase) pathway is essential for this response, although other signaling pathways may also play a role. Moreover, action spectrum analyses of zPer2 transcriptional response to monochromatic light demonstrate the involvement of a blue-light photoreceptor. The Cry1b and Cry3 cryptochromes constitute attractive candidates as photoreceptors in this setting. Our results establish a link between blue-light photoreceptors, probably cryptochromes, and the MAPK pathway to elicit light-induced transcriptional activation of clock genes.