1985
DOI: 10.1085/jgp.86.5.671
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Circadian regulation of retinomotor movements. I. Interaction of melatonin and dopamine in the control of cone length.

Abstract: In lower vertebrates, cone retinomotor movements occur in response to changes in lighting conditions and to an endogenous circadian clock. In the light, cone myoids contract, while in the dark, they elongate . In order to test the hypothesis that melatonin and dopamine may be involved in the regulation of cone movement, we have used an in vitro eyecup preparation from Xenopus laevis that sustains light-and dark-adaptive cone retinomotor movement . Melatonin mimics darkness by causing cone elongation . Dark-and… Show more

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Cited by 263 publications
(163 citation statements)
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“…The circadian oscillators in photoreceptors are endogenous and able to function independently in the absence of other retinal inputs (Cahill and Besharse 1993;Thomas et al 1993;Ko et al 2001). Photoreceptor circadian oscillators regulate retinomotor movement (Pierce and Besharse 1985;Burnside 2001), outer segment disc shedding and membrane renewal (LaVail 1980;Besharse and Dunis 1983), morphological changes at synaptic ribbons (Adly et al 1999), gene expression (Korenbrot and Fernald 1989;Pierce et al 1993;Haque et al 2002), and the gating behavior of ion channels (Ko et al 2001) among other photoreceptor activities. Importantly, photoreceptors are more sensitive to intense light damage at night than during the day, even in animals that have been maintained in constant darkness (DD) for several days after circadian lightdark (LD) cycle entrainment (Vaughan et al 2002).…”
mentioning
confidence: 99%
“…The circadian oscillators in photoreceptors are endogenous and able to function independently in the absence of other retinal inputs (Cahill and Besharse 1993;Thomas et al 1993;Ko et al 2001). Photoreceptor circadian oscillators regulate retinomotor movement (Pierce and Besharse 1985;Burnside 2001), outer segment disc shedding and membrane renewal (LaVail 1980;Besharse and Dunis 1983), morphological changes at synaptic ribbons (Adly et al 1999), gene expression (Korenbrot and Fernald 1989;Pierce et al 1993;Haque et al 2002), and the gating behavior of ion channels (Ko et al 2001) among other photoreceptor activities. Importantly, photoreceptors are more sensitive to intense light damage at night than during the day, even in animals that have been maintained in constant darkness (DD) for several days after circadian lightdark (LD) cycle entrainment (Vaughan et al 2002).…”
mentioning
confidence: 99%
“…A variety of visual behaviors, such as photoreceptor cell disk shedding (Young, 1967;LaVail, 1976;Besharse et al, 1988;Bassi and Powers, 1990), rod and cone myoid movement (Pierce and Besharse, 1985;Dearry and Burnside, 1986), retinal pigment epithelium granule migration (Bruenner and Burnside, 1986), opsin expression (Korenbrot and Fernald, 1989;Pierce et al, 1993), and retinal sensitivity (Barlow, 1983;Powers, 1986, 1987), display robust day-night rhythms. In frogs, for example, the expression of rod opsin mRNA fluctuates between the day and night; it is high in the day and low at night.…”
mentioning
confidence: 99%
“…Melatonin is synthesized in and released from photoreceptor cells (e.g., Redburn and Mitchell, 1989;Iuvone et al, 1990;Cahill and Besharse, 1992;Zawilska and Iuvone, 1992;Thomas et al, 1993;Wiechmann and Craft, 1993), and dopamine is synthesized in amacrine and interplexiform cells (reviewed in Ehinger, 1977;Iuvone, 1986). In retina, melatonin activates rod photoreceptor disk shedding (Besharse and Dunis, 1983;Besharse et al, 1984) and promotes dark-adaptive retinomotor movements (Cheze and Ali, 1976;Pang and Yew, 1979;Pierce and Besharse, 1985). In contrast, dopamine inhibits rod photoreceptor disk shedding (Pierce and Besharse, 1986;Besharse et al, 1988) and promotes light-adaptive retinomotor movements (Pierce and Besharse, 198.5;Dearry and Burnside, 1986).…”
mentioning
confidence: 99%