The suprachiasmatic nucleus (SCN) of the mammalian hypothalamus is part of a system that controls the near 24-hour (circadian) rhythms in many physiological processes and behaviors. This timing system generates circadian behaviors, synchronizes them to local time, sets an appropriate phase relationship between each behavior and daily environmental cycles, and sculpts the duration and amplitude of each behavior in response to particular environmental conditions (e.g., seasonal photoperiod). Although it is highly likely that individual SCN neurons generate circadian periodicities, it is uncertain whether these complex circadian behaviors arise at the level of single cells, through cellular interactions within the SCN tissue, or through interactions with other neural and/or non-neural systems. Furthermore, the pathways and mechanisms by which the SCN conveys timing information to other brain regions remain largely unexplored. The proposed experiments will examine the circadian properties and mechanisms of intercellular communication of neurons in vivo, and in cultured tissues and dispersals. Changes in the duration of the photoperiod or period of the light:dark cycle result in classically described changes in the time of activity onset, the duration of activity, or the expressed period of activity rhythms.
Specific aim 1 will determine the level of cellular organization and mechanisms responsible for maintaining an appropriate phase relationship between the behavior and local time, the kinetics of resynchronization (e.g., phase shifting transients), and the control of circadian waveform by entraining stimulus parameters.
Specific aim 2 will address the neural origins of plasticity in circadian behavior. We will determine whether changes in period and waveform are generated at the level of single SCN neurons, within the SCN or at other levels of neural organization. Finally, specific aim 3 will determine the locus of age-related deterioration of some of the behaviors examined in specific aims 1 and 2. These experiments will be aided greatly by the recent development of new technologies that enable recording of cellular rhythmicity for weeks in vitro. We will measure molecular rhythmicity by monitoring per1:luciferase activity in transgenic cells and electrical activity from individual neurons using multielectrode arrays. These procedures allow us to record from neurons taken from animals at least 9 months of age. Taken together, these studies will provide insights into how different levels of neural organization contribute to the generation and control of mammalian circadian behaviors.

Agency
National Institute of Health (NIH)
Institute
National Institute of Mental Health (NIMH)
Type
Research Project (R01)
Project #
1R01MH062517-01
Application #
6230954
Study Section
Special Emphasis Panel (ZRG1-IFCN-3 (01))
Project Start
2000-12-22
Project End
2003-11-30
Budget Start
2000-12-22
Budget End
2001-11-30
Support Year
1
Fiscal Year
2001
Total Cost
$288,992
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; 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
Nakamura, Takahiro J; Nakamura, Wataru; Yamazaki, Shin et al. (2011) Age-related decline in circadian output. J Neurosci 31:10201-5
Lundkvist, Gabriella B S; Sellix, Michael T; Nygård, Mikael et al. (2010) Clock gene expression during chronic inflammation induced by infection with Trypanosoma brucei brucei in rats. J Biol Rhythms 25:92-102
Nakamura, Takahiro J; Sellix, Michael T; Kudo, Takashi et al. (2010) Influence of the estrous cycle on clock gene expression in reproductive tissues: effects of fluctuating ovarian steroid hormone levels. Steroids 75:203-12
Nakamura, Takahiro J; Sellix, Michael T; Menaker, Michael et al. (2008) Estrogen directly modulates circadian rhythms of PER2 expression in the uterus. Am J Physiol Endocrinol Metab 295:E1025-31
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
Davidson, Alec J; Yamazaki, Shin; Arble, Deanna M et al. (2008) Resetting of central and peripheral circadian oscillators in aged rats. Neurobiol Aging 29:471-7
Davidson, A J; Sellix, M T; Daniel, J et al. (2006) Chronic jet-lag increases mortality in aged mice. Curr Biol 16:R914-6
Davidson, Alec J; Straume, Martin; Block, Gene D et al. (2006) Daily timed meals dissociate circadian rhythms in hepatoma and healthy host liver. Int J Cancer 118:1623-7
Davidson, A J; London, B; Block, G D et al. (2005) Cardiovascular tissues contain independent circadian clocks. Clin Exp Hypertens 27:307-11

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