Targeting of the circadian clock via CK1δ/ε to improve glucose homeostasis in obesity

• Published in: Scientific reports Vol. 6; no. 1; p. 29983
• Main Authors: Cunningham, Peter S., Ahern, Siobhán A., Smith, Laura C., da Silva Santos, Carla S., Wager, Travis T., Bechtold, David A.
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 21.07.2016; Nature Publishing Group
• Subjects: 59/5; 631/378/1385/1330; 631/443/319/1557; 631/443/319/1642/393; 64/60; 96/106; Adipose Tissue, White - metabolism; Adipose Tissue, White - pathology; Animals; Behavior, Animal; Casein Kinase Idelta - metabolism; Casein Kinase Iepsilon - metabolism; Circadian Clocks - genetics; Circadian Rhythm; CLOCK Proteins - genetics; CLOCK Proteins - metabolism; Diet, High-Fat; Gene Expression Regulation; Glucose - metabolism; Gonads - metabolism; Homeostasis; Humanities and Social Sciences; Hypothalamus - metabolism; Inflammation - pathology; Male; Mice, Inbred C57BL; Mice, Obese; multidisciplinary; Obesity - metabolism; Organ Specificity - genetics; PPAR alpha - metabolism; Science
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/srep29983

Growing evidence indicates that disruption of our internal timing system contributes to the incidence and severity of metabolic diseases, including obesity and type 2 diabetes. This is perhaps not surprising since components of the circadian clockwork are tightly coupled to metabolic processes across the body. In the current study, we assessed the impact of obesity on the circadian system in mice at a behavioural and molecular level and determined whether pharmacological targeting of casein kinase 1δ and ε (CK1δ/ε), key regulators of the circadian clock, can confer metabolic benefit. We demonstrate that although behavioural rhythmicity was maintained in diet-induced obesity (DIO), gene expression profiling revealed tissue-specific alteration to the phase and amplitude of the molecular clockwork. Clock function was most significantly attenuated in visceral white adipose tissue (WAT) of DIO mice and was coincident with elevated tissue inflammation and dysregulation of clock-coupled metabolic regulators PPARα/γ. Further, we show that daily administration of a CK1δ/ε inhibitor (PF-5006739) improved glucose tolerance in both DIO and genetic ( ob/ob ) models of obesity. These data further implicate circadian clock disruption in obesity and associated metabolic disturbance and suggest that targeting of the clock represents a therapeutic avenue for the treatment of metabolic disorders.