| Literature DB >> 29107505 |
Nuria Martinez-Lopez1, Elena Tarabra2, Miriam Toledo1, Marina Garcia-Macia1, Srabani Sahu1, Luisa Coletto2, Ana Batista-Gonzalez1, Nir Barzilai3, Jeffrey E Pessin3, Gary J Schwartz4, Sander Kersten5, Rajat Singh6.
Abstract
Autophagy failure is associated with metabolic insufficiency. Although caloric restriction (CR) extends healthspan, its adherence in humans is poor. We established an isocaloric twice-a-day (ITAD) feeding model wherein ITAD-fed mice consume the same food amount as ad libitum controls but at two short windows early and late in the diurnal cycle. We hypothesized that ITAD feeding will provide two intervals of intermeal fasting per circadian period and induce autophagy. We show that ITAD feeding modifies circadian autophagy and glucose/lipid metabolism that correlate with feeding-driven changes in circulating insulin. ITAD feeding decreases adiposity and, unlike CR, enhances muscle mass. ITAD feeding drives energy expenditure, lowers lipid levels, suppresses gluconeogenesis, and prevents age/obesity-associated metabolic defects. Using liver-, adipose-, myogenic-, and proopiomelanocortin neuron-specific autophagy-null mice, we mapped the contribution of tissue-specific autophagy to system-wide benefits of ITAD feeding. Our studies suggest that consuming two meals a day without CR could prevent the metabolic syndrome.Entities:
Keywords: POMC; aging; autophagy; caloric restriction; circadian; fatty liver; gluconeogenesis; metabolic syndrome; myogenic progenitors; twice-a-day feeding
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Year: 2017 PMID: 29107505 PMCID: PMC5718973 DOI: 10.1016/j.cmet.2017.09.020
Source DB: PubMed Journal: Cell Metab ISSN: 1550-4131 Impact factor: 27.287