Meal frequency and timing in health and disease DOI Open Access
Mark P. Mattson, David B. Allison, Luigi Fontana

и другие.

Proceedings of the National Academy of Sciences, Год журнала: 2014, Номер 111(47), С. 16647 - 16653

Опубликована: Ноя. 17, 2014

Although major research efforts have focused on how specific components of foodstuffs affect health, relatively little is known about a more fundamental aspect diet, the frequency and circadian timing meals, potential benefits intermittent periods with no or very low energy intakes. The most common eating pattern in modern societies, three meals plus snacks every day, abnormal from an evolutionary perspective. Emerging findings studies animal models human subjects suggest that restriction as 16 h can improve health indicators counteract disease processes. mechanisms involve metabolic shift to fat metabolism ketone production, stimulation adaptive cellular stress responses prevent repair molecular damage. As data optimal crystalizes, it will be critical develop strategies incorporate those patterns into care policy practice, lifestyles population.

Язык: Английский

The AMPK signalling pathway coordinates cell growth, autophagy and metabolism DOI
Maria M. Mihaylova, Reuben J. Shaw

Nature Cell Biology, Год журнала: 2011, Номер 13(9), С. 1016 - 1023

Опубликована: Сен. 1, 2011

Язык: Английский

Процитировано

2641

Central and Peripheral Circadian Clocks in Mammals DOI
Jennifer A. Mohawk, Carla B. Green, Joseph S. Takahashi

и другие.

Annual Review of Neuroscience, Год журнала: 2012, Номер 35(1), С. 445 - 462

Опубликована: Май 20, 2012

The circadian system of mammals is composed a hierarchy oscillators that function at the cellular, tissue, and systems levels. A common molecular mechanism underlies cell-autonomous oscillator throughout body, yet this clock adapted to different functional contexts. In central suprachiasmatic nucleus (SCN) hypothalamus, coupled population neuronal acts as master pacemaker for organism drive rhythms in activity rest, feeding, body temperature, hormones. Coupling within SCN network confers robustness pacemaker, which turn provides stability overall temporal architecture organism. Throughout majority cells clocks are intimately enmeshed metabolic pathways. Thus, an emerging view adaptive significance their fundamental role orchestrating metabolism.

Язык: Английский

Процитировано

1999

Time-Restricted Feeding without Reducing Caloric Intake Prevents Metabolic Diseases in Mice Fed a High-Fat Diet DOI Creative Commons
Megumi Hatori, Christopher Vollmers, Amir Zarrinpar

и другие.

Cell Metabolism, Год журнала: 2012, Номер 15(6), С. 848 - 860

Опубликована: Май 17, 2012

Язык: Английский

Процитировано

1753

Pathophysiology and treatment of type 2 diabetes: perspectives on the past, present, and future DOI
Steven E. Kahn, Mark E. Cooper, Stefano Del Prato

и другие.

The Lancet, Год журнала: 2013, Номер 383(9922), С. 1068 - 1083

Опубликована: Дек. 3, 2013

Язык: Английский

Процитировано

1548

Transcriptional Architecture and Chromatin Landscape of the Core Circadian Clock in Mammals DOI

Nobuya Koike,

Seung Hee Yoo,

Hung-Chung Huang

и другие.

Science, Год журнала: 2012, Номер 338(6105), С. 349 - 354

Опубликована: Сен. 1, 2012

Transcription Around the Clock The biological clock that controls daily rhythms in mammalian physiology and behavior is thought to be regulated large part by transcriptional events (see Perspective Doherty Kay ). Koike et al. (p. 349 ; published online 30 August) produced a comprehensive analysis of these across entire mouse liver genome over 24-hour period. Only ∼22% cycling messenger RNA transcripts were driven de novo transcription, suggesting posttranscriptional also play an important regulatory role clock. Biological timing organisms can respond rhythmic cues from environment. Morf 379 , 23 explored how one such cue, cycles ambient temperature, influence circadian cells. Cold-inducible RNA–binding protein (CIRP) accumulates when body temperature low. A systematic search for binding partners CIRP identified encoding core components Loss decreased amplitude gene expression cells lacking adapted more quickly cycles.

Язык: Английский

Процитировано

1354

The two‐process model of sleep regulation: a reappraisal DOI Open Access
Alexander A. Borbély,

Serge Daan,

Anna Wirz‐Justice

и другие.

Journal of Sleep Research, Год журнала: 2016, Номер 25(2), С. 131 - 143

Опубликована: Янв. 14, 2016

In the last three decades two-process model of sleep regulation has served as a major conceptual framework in research. It been applied widely studies on fatigue and performance to dissect individual differences regulation. The posits that homeostatic process (Process S) interacts with controlled by circadian pacemaker C), time-courses derived from physiological behavioural variables. simulates successfully timing intensity diverse experimental protocols. Electrophysiological recordings suprachiasmatic nuclei (SCN) suggest S C interact continuously. Oscillators outside SCN are linked energy metabolism evident SCN-lesioned arrhythmic animals subjected restricted feeding or methamphetamine administration, well human subjects during internal desynchronization. intact these peripheral oscillators may dissociate central rhythm. A sleep/fast wake/feed phase segregate antagonistic anabolic catabolic metabolic processes tissues. deficiency Process was proposed account for both depressive disturbances antidepressant effect deprivation. supported development novel non-pharmacological treatment paradigms psychiatry, based manipulating phase, light exposure. conclusion, remains conceptually useful promoting integration rhythm Sleep appears have not only short-term, use-dependent function; it also serves enforce rest fasting, thereby supporting optimization at appropriate 24-h cycle.

Язык: Английский

Процитировано

1347

Social Jetlag and Obesity DOI Creative Commons
Till Roenneberg, Karla V. Allebrandt, Martha Merrow

и другие.

Current Biology, Год журнала: 2012, Номер 22(10), С. 939 - 943

Опубликована: Май 1, 2012

Язык: Английский

Процитировано

1239

Links between metabolism and cancer DOI Open Access
Chi V. Dang

Genes & Development, Год журнала: 2012, Номер 26(9), С. 877 - 890

Опубликована: Май 1, 2012

Metabolism generates oxygen radicals, which contribute to oncogenic mutations. Activated oncogenes and loss of tumor suppressors in turn alter metabolism induce aerobic glycolysis. Aerobic glycolysis or the Warburg effect links high rate glucose fermentation cancer. Together with glutamine, via provides carbon skeletons, NADPH, ATP build new cancer cells, persist hypoxia that rewires metabolic pathways for cell growth survival. Excessive caloric intake is associated an increased risk cancers, while restriction protective, perhaps through clearance mitochondria mitophagy, thereby reducing oxidative stress. Hence, between are multifaceted, spanning from low incidence large mammals specific rates altered resulting mutated enzymes genes.

Язык: Английский

Процитировано

957

Adverse Metabolic Consequences in Humans of Prolonged Sleep Restriction Combined with Circadian Disruption DOI
Orfeu M. Buxton, Sean W. Cain,

Shawn O’Connor

и другие.

Science Translational Medicine, Год журнала: 2012, Номер 4(129)

Опубликована: Апрель 11, 2012

Epidemiological studies link short sleep duration and circadian disruption with higher risk of metabolic syndrome diabetes. We tested the hypotheses that prolonged restriction concurrent disruption, as can occur in people performing shift work, impairs glucose regulation metabolism. Healthy adults spent >5 weeks under controlled laboratory conditions which they experienced an initial baseline segment optimal sleep, 3 (5.6 hours per 24 hours) combined (recurring 28-hour "days"), followed by 9 days recovery re-entrainment. Exposure to measurements taken at same phase, decreased participants' resting rate increased plasma concentrations after a meal, effect resulting from inadequate pancreatic insulin secretion. These parameters normalized during stable Thus, humans, alters metabolism could increase obesity

Язык: Английский

Процитировано

871

Bile Acid Signaling in Metabolic Disease and Drug Therapy DOI
Tiangang Li, John Y.L. Chiang

Pharmacological Reviews, Год журнала: 2014, Номер 66(4), С. 948 - 983

Опубликована: Июль 29, 2014

Bile acids are the end products of cholesterol catabolism. Hepatic bile acid synthesis accounts for a major fraction daily turnover in humans. Biliary secretion generates flow and facilitates hepatobiliary lipids, lipophilic metabolites, xenobiotics. In intestine, essential absorption, transport, metabolism dietary fats lipid-soluble vitamins. Extensive research last 2 decades has unveiled new functions as signaling molecules metabolic integrators. The acid-activated nuclear receptors farnesoid X receptor, pregnane constitutive androstane vitamin D G protein-coupled receptor play critical roles regulation lipid, glucose, energy metabolism, inflammation, drug detoxification. exhibits strong diurnal rhythm, which is entrained by fasting refeeding well nutrient status plays an important role maintaining homeostasis. Recent revealed interaction liver gut microbiota metabolism. Circadian disturbance altered contribute to pathogenesis diseases, inflammatory bowel nonalcoholic fatty disease, diabetes, obesity. their derivatives potential therapeutic agents treating diseases liver.

Язык: Английский

Процитировано

797