Our long-term goals are 1) to understand the mechanism that generates circadian rhythmicity in the retina and 2) to elucidate the role played by rhythmic synthesis of melatonin in retinal function. We will begin by defining optimal culture conditions for studying circadian rhythms of melatonin synthesis in in vitro preparations of isolated neural retinas from rats and mice. We will then measure the activity of the enzymes involved in melatonin synthesis and the breakdown products produced by its catabolism in order to define the proximate source of the circadian rhythmicity. We will determine whether dopamine is also produced rhythmically by cultured retinas. Using mice and rats with genetic defects that affect specific cell types in the retina we will ask which cell types are essential for synthesis and degradation of melatonin (and dopamine) and which are essential for circadian oscillation. We will define the response of the retinal circadian oscillators to light pulses and explore the light input pathway using pharmacological agents that block or mimic the resetting effects of light. Finally we will ask whether melatonin is causally involved in synchronized rhythmic outer segment disc shedding by comparing disc shedding in C3H mice, whose retinas synthesize melatonin rhythmically, with disc shedding in C57 mice whose retinas, like their pineal glands, make no melatonin at all. What we learn about rhythmicity in mammalian retinas in culture is likely to be applicable to pathologies of retinal function in humans, particularly since so many aspects of retinal physiology have been shown to be rhythmic.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
5R01MH056647-05
Application #
6343731
Study Section
Visual Sciences C Study Section (VISC)
Program Officer
Winsky, Lois M
Project Start
1997-01-01
Project End
2001-12-31
Budget Start
2001-01-01
Budget End
2001-12-31
Support Year
5
Fiscal Year
2001
Total Cost
$258,687
Indirect Cost
Name
University of Virginia
Department
Biology
Type
Schools of Arts and Sciences
DUNS #
001910777
City
Charlottesville
State
VA
Country
United States
Zip Code
22904
Sellix, Michael T; Murphy, Zachary C; Menaker, Michael (2013) Excess androgen during puberty disrupts circadian organization in female rats. Endocrinology 154:1636-47
Murphy, Zachary C; Pezuk, Pinar; Menaker, Michael et al. (2013) Effects of ovarian hormones on internal circadian organization in rats. Biol Reprod 89:35
Sellix, Michael T; Evans, Jennifer A; Leise, Tanya L et al. (2012) Aging differentially affects the re-entrainment response of central and peripheral circadian oscillators. J Neurosci 32:16193-202
Sellix, Michael T; Menaker, Michael (2010) Circadian clocks in the ovary. Trends Endocrinol Metab 21:628-36
Sellix, Michael T; Currie, Jake; Menaker, Michael et al. (2010) Fluorescence/luminescence circadian imaging of complex tissues at single-cell resolution. J Biol Rhythms 25:228-32
Sellix, Michael T; Yoshikawa, Tomoko; Menaker, Michael (2010) A circadian egg timer gates ovulation. Curr Biol 20:R266-7
Yoshikawa, Tomoko; Sellix, Michael; Pezuk, Pinar et al. (2009) Timing of the ovarian circadian clock is regulated by gonadotropins. Endocrinology 150:4338-47
Yamazaki, Shin; Yoshikawa, Tomoko; Biscoe, Elizabeth W et al. (2009) Ontogeny of circadian organization in the rat. J Biol Rhythms 24:55-63
Vujovic, Nina; Davidson, Alec J; Menaker, Michael (2008) Sympathetic input modulates, but does not determine, phase of peripheral circadian oscillators. Am J Physiol Regul Integr Comp Physiol 295:R355-60
Kwak, Yongho; Lundkvist, Gabriella B; Brask, Johan et al. (2008) Interferon-gamma alters electrical activity and clock gene expression in suprachiasmatic nucleus neurons. J Biol Rhythms 23:150-9

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