Circadian rhythms order vital functions from the molecular to behavioral level. They are controlled by a biological clock that generates a near 24-h time base, into which afferent neuronal signals relaying information about environmental time and organismic state are integrated, and from which circadian rhythms are orchestrated. Our long-rang objective is to understand the cellular and molecular mechanisms that regulate the biological clock in suprachiasmatic nucleus (SCN) of the mammalian brain. Our extensive studies of the SCN brain slice preparation from rat have demonstrated that this circadian clock undergoes spontaneous circadian oscillation in SCN neuronal activity and concomitant modulation of sensitivities to phase-resetting stimuli. By monitoring the activity rhythm of the ensemble of SCN neurons, we have shown that the SCN clock regulates its own sensitivity to afferent signals in a circadian pattern that correlates with discrete periods in the environmental cycle of day and night. These changes persists in vitro, and thus are generated entirely within the SCN. Thus, the clock itself restricts activation of specific intracellular signaling pathways to specific time domains within the 24-h cycle. We propose to focus upon daytime mechanisms of SCN regulation. Photic and arousal stimuli have been proposed to initiate daytime clock resetting. The present proposal develops naturally from our finding that the SCN rhythm can be reset in the brain slice in the day, but not night, by treatments affecting cAMP pathways.
Our specific aims i nclude: 1) To identify the neurotransmitter(s) that activate cAMP; 2) To evaluate the behavioral context in which this pathway is activated; and 3) To characterize the relationship between cAMP stimulation and transcriptional activation. The results of these experiments will provide insights into integration of signals at this brain site, as well as to understanding of the cellular and molecular mechanisms by which these signals interact with the timekeeping mechanism. This research has basic relevance for understanding integrative brain function, for developing strategies for drug chronotherapeutics and for ameliorating internal desynchronization manifested as disordered hormonal and sleep patterns, depression and physiological decline with aging.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS022155-12
Application #
2460507
Study Section
Neurology B Subcommittee 2 (NEUB)
Program Officer
Baughman, Robert W
Project Start
1986-09-15
Project End
2000-07-31
Budget Start
1997-08-01
Budget End
1998-07-31
Support Year
12
Fiscal Year
1997
Total Cost
Indirect Cost
Name
University of Illinois Urbana-Champaign
Department
Biochemistry
Type
Schools of Arts and Sciences
DUNS #
041544081
City
Champaign
State
IL
Country
United States
Zip Code
61820
Gillette, Martha U; Abbott, Sabra M (2009) BIOLOGICAL TIMEKEEPING. Sleep Med Clin 4:99-110
Beaulé, Christian; Mitchell, Jennifer W; Lindberg, Peder T et al. (2009) Temporally restricted role of retinal PACAP: integration of the phase-advancing light signal to the SCN. J Biol Rhythms 24:126-34
Tischkau, Shelley A; Gillette, Martha U (2005) Oligodeoxynucleotide methods for analyzing the circadian clock in the suprachiasmatic nucleus. Methods Enzymol 393:593-610
Buchanan, Gordon F; Gillette, Martha U (2005) New light on an old paradox: site-dependent effects of carbachol on circadian rhythms. Exp Neurol 193:489-96
Gerdin, Matthew J; Masana, Monica I; Rivera-Bermudez, Moises A et al. (2004) Melatonin desensitizes endogenous MT2 melatonin receptors in the rat suprachiasmatic nucleus: relevance for defining the periods of sensitivity of the mammalian circadian clock to melatonin. FASEB J 18:1646-56
Tischkau, Shelley A; Mitchell, Jennifer W; Pace, Laura A et al. (2004) Protein kinase G type II is required for night-to-day progression of the mammalian circadian clock. Neuron 43:539-49
Burgoon, P W; Lindberg, P T; Gillette, M U (2004) Different patterns of circadian oscillation in the suprachiasmatic nucleus of hamster, mouse, and rat. J Comp Physiol A Neuroethol Sens Neural Behav Physiol 190:167-71
Tischkau, Shelley A; Weber, E Todd; Abbott, Sabra M et al. (2003) Circadian clock-controlled regulation of cGMP-protein kinase G in the nocturnal domain. J Neurosci 23:7543-50
Barnes, Jessica W; Tischkau, Shelley A; Barnes, Jeffrey A et al. (2003) Requirement of mammalian Timeless for circadian rhythmicity. Science 302:439-42
Tischkau, Shelley A; Mitchell, Jennifer W; Tyan, Sheue-Houy et al. (2003) Ca2+/cAMP response element-binding protein (CREB)-dependent activation of Per1 is required for light-induced signaling in the suprachiasmatic nucleus circadian clock. J Biol Chem 278:718-23

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