The goal of this proposal is to foster my development into an independent investigator and educator focused on elucidating the mechanisms by which disruption of daily rhythms contributes to obesity. Studies in rodents and humans have demonstrated that the timing of food intake is altered in obese individuals, but little is known about how this phenotype contributes to the pathophysiology of obesity. To investigate the tuning of rhythmic metabolic processes and how they are altered in diet-induced obesity, I developed an acute model to monitor eating behavior and tissue rhythms in mice fed high-fat diet for one week. My preliminary studies demonstrate that the daily rhythm of eating behavior is immediately altered and the timing of the circadian clock in the liver is robustly advanced during consumption of high-fat diet rich in saturated fat. The proposed studies aim to elucidate the mechanism whereby consumption of high-fat diet alters eating behavior and liver physiology. In this proposal, real-time imaging of eating behavior and monitoring of liver bioluminescence rhythms will be utilized to test the hypothesis that consumption of a diet rich in saturated fat (bt not monounsaturated fat) alters daily rhythms of feeding behavior and liver physiology through a toll-like receptor 4-mediated mechanism. To achieve the goals of this proposal, I will combine my experience in circadian biology with new techniques assaying metabolic physiology. I will draw from the strengths of my co-mentors and mentoring committee and from my prior training to cultivate an independent and novel line of research. Key elements of my career development plan include didactic coursework in metabolic physiology, immersion in an intellectual environment rich in the study of metabolism and circadian biology, and acquisition of career development skills through formal seminars, workshops, and interactions with junior and senior scientists. By bringing together a talented mentoring team, a synergistic research environment with state-of-the-art equipment and facilities, and training in career success, this career development award will allow me to achieve my long-term career goal of becoming a successful independent scientist whose research broadly impacts human health.

Public Health Relevance

Roughly two-thirds of U.S. adults aged 20 and over are overweight or obese, and the prevalence has increased sharply for both adults and children since the mid-1970's. It has recently been recognized that consumption of high-fat diet not only causes obesity, but also alters the timing of food intake. The proposed studies aim to elucidate the mechanism whereby consumption of high-fat diet alters daily rhythms of eating behavior and physiology.

Agency
National Institute of Health (NIH)
Institute
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
Type
Research Scientist Development Award - Research & Training (K01)
Project #
5K01DK098321-02
Application #
8731231
Study Section
Digestive Diseases and Nutrition C Subcommittee (DDK)
Program Officer
Hyde, James F
Project Start
2013-09-06
Project End
2016-06-30
Budget Start
2014-07-01
Budget End
2015-06-30
Support Year
2
Fiscal Year
2014
Total Cost
Indirect Cost
Name
Vanderbilt University Medical Center
Department
Internal Medicine/Medicine
Type
Schools of Medicine
DUNS #
City
Nashville
State
TN
Country
United States
Zip Code
37212
Pendergast, Julie S; Wendroth, Robert H; Stenner, Rio C et al. (2017) mPeriod2 Brdm1 and other single Period mutant mice have normal food anticipatory activity. Sci Rep 7:15510
Palmisano, Brian T; Stafford, John M; Pendergast, Julie S (2017) High-Fat Feeding Does Not Disrupt Daily Rhythms in Female Mice because of Protection by Ovarian Hormones. Front Endocrinol (Lausanne) 8:44
Branecky, Katrina L; Niswender, Kevin D; Pendergast, Julie S (2015) Disruption of Daily Rhythms by High-Fat Diet Is Reversible. PLoS One 10:e0137970