Assessment of the properties of the circadian pacemaker and its functioning in organisms is often dependent on analysis of the various output rhythms generated by a central oscillator. Often, sophisticated time series analysis (TSA) is required to identify the rhythmic components (i.e., intrinsic period and endogenous phase) in the data collected. Each estimate obtained through TSA must be tested for validity so that even subtle discriminations are made with statistical confidence that is standard across all projects. Formulation of mathematical models to describe the physiological systems can assist in providing both testable predictions for experimentation and interspecies comparisons. Use of a common language for presentation of data allow for common modeling procedures and also facilitates the exchange of result between projects. Several lines of evidence indicate that across mammalian species aging causes the pacemaker to speed up, possibly by a reduction in the cell count of the SCN. Aging might then be expected to weaken pacemaker influence, but the evidence here is less robust, partly because rhythm strength is more difficult to quantify than rhythm period. It is in devising methods for assessing pacemaker strength that models will be especially valuable. The basic concept will be to measure the pacemaker against other physiological processes with which it interacts. These other process must themselves be model some will be clearly rhythmic while others may be essentially random. Quantification of the various influences which the pacemaker can exert will provide a direct measure of its physiological significance. Services from the Analytic core will be available on-site for each project investigator through a common programming language, and exchange of data between laboratories will be facilitated by data management assistance. The Analytic Core will establish standards for graphic presentations to enable investigators to readily understand results for comparison across projects. Analysis requiring statistical formulation, TSA or mathematical modeling modified for specialized objectives will also be provided by the Analytical Core.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Program Projects (P01)
Project #
5P01AG009975-03
Application #
3768457
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1993
Total Cost
Indirect Cost
Name
Brigham and Women's Hospital
Department
Type
DUNS #
071723621
City
Boston
State
MA
Country
United States
Zip Code
02115
Leise, Tanya L; Goldberg, Ariella; Michael, John et al. (2018) Recurring circadian disruption alters circadian clock sensitivity to resetting. Eur J Neurosci :
Zitting, Kirsi-Marja; Münch, Mirjam Y; Cain, Sean W et al. (2018) Young adults are more vulnerable to chronic sleep deficiency and recurrent circadian disruption than older adults. Sci Rep 8:11052
McHill, Andrew W; Hull, Joseph T; McMullan, Ciaran J et al. (2018) Chronic Insufficient Sleep Has a Limited Impact on Circadian Rhythmicity of Subjective Hunger and Awakening Fasted Metabolic Hormones. Front Endocrinol (Lausanne) 9:319
Li, Peng; Yu, Lei; Lim, Andrew S P et al. (2018) Fractal regulation and incident Alzheimer's disease in elderly individuals. Alzheimers Dement 14:1114-1125
Todd, William D; Fenselau, Henning; Wang, Joshua L et al. (2018) A hypothalamic circuit for the circadian control of aggression. Nat Neurosci 21:717-724
Naganuma, Fumito; Bandaru, Sathyajit S; Absi, Gianna et al. (2018) Melanin-concentrating hormone neurons contribute to dysregulation of rapid eye movement sleep in narcolepsy. Neurobiol Dis 120:12-20
Asgari-Targhi, Ameneh; Klerman, Elizabeth B (2018) Mathematical modeling of circadian rhythms. Wiley Interdiscip Rev Syst Biol Med :e1439
Kroeger, Daniel; Absi, Gianna; Gagliardi, Celia et al. (2018) Galanin neurons in the ventrolateral preoptic area promote sleep and heat loss in mice. Nat Commun 9:4129
Gottlieb, Daniel J; Ellenbogen, Jeffrey M; Bianchi, Matt T et al. (2018) Sleep deficiency and motor vehicle crash risk in the general population: a prospective cohort study. BMC Med 16:44
Biello, Stephany M; Bonsall, David R; Atkinson, Lynsey A et al. (2018) Alterations in glutamatergic signaling contribute to the decline of circadian photoentrainment in aged mice. Neurobiol Aging 66:75-84

Showing the most recent 10 out of 208 publications