The suprachiasmatic nuclei (SCN) of the hypothalamus are endogenous oscillators that serve a well-defined, critical role in the generation and entrainment of the daily (circadian) oscillations of physiology, metabolism and behavior of mammals. Our broad research objective is to understand the molecular, cellular and neurophysiological mechanisms by which the SCN keep 24-hr time. The model species studied is the rat. The SCN pacemaker survives intact in the hypothalamic brain slice where it is accessible to experiments aimed at dissecting cellular mechanisms. Our methodological approach combines brain slice culture with neurophysiological techniques that measure the circadian rhythm of the ensemble neuronal activity and whole cell recordings in the slice as well as biochemical analyses that measure cyclic nucleotide levels, enzyme activities and proteins phosphorylated, and immunocytochemical/in situ hybridization techniques that identify and localize molecules of interest. The present proposal develops naturally from our finding that the SCN rhythm can be reset in the brain slice by treatments affecting cAMP-,cGMP- or pertussis toxin-sensitive pathways. Further, even under the constant conditions in the slice chamber, the pacemaker substrates are changing so that the rhythm is reset by cAMP in subjective day, by cGMP during subjective night and by melatonin during the day/night transition.
Our specific aims i nclude: A) to more fully explore the role of cAMP/protein kinase A in SCN function (by examining the activity, concentration and phosphorylation state of protein kinase A (PKA), localizing the sites of cAMP and PKA effects, and the involvement of transcription/translation in cAMP stimulation); B) to more fully explore the role of cGMP/protein kinase G at night (by determining the activity, concentration and phosphorylation state of protein kinase G (PKG), localizing cGMP and PKG effect; C) to examine the regulation of cyclic nucleotide phosphodiesterase (by determining the level and regulation of cAMP and cGMP phosphodiesterase activities) and D) to understand the relationship of other second messenger/kinase systems in generating circadian time (by exploring the interactive role of protein kinases in time-keeping). Because the SCN integrates most circadian behaviors and metabolic changes, this study has basic relevance of understanding many brain and metabolic dysfunctions, including sleep disorders and certain forms of mental illness.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS022155-10
Application #
2264404
Study Section
Neurology B Subcommittee 2 (NEUB)
Project Start
1986-09-15
Project End
1996-08-31
Budget Start
1995-09-01
Budget End
1996-08-31
Support Year
10
Fiscal Year
1995
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
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
Tischkau, Shelley A; Gillette, Martha U (2005) Oligodeoxynucleotide methods for analyzing the circadian clock in the suprachiasmatic nucleus. Methods Enzymol 393:593-610
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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