@article{6314fd30dbad4548bd5836c88d3b1613,
title = "System-wide Benefits of Intermeal Fasting by Autophagy",
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. Our studies suggest that consuming two meals a day with complete food restriction in between the meals is sufficient to lower blood glucose and lipid levels. This simple dietary approach activates a cell “cleansing system” called autophagy in liver, fat, brain, and muscle that helps prevent obesity and diabetes.",
keywords = "POMC, aging, autophagy, caloric restriction, circadian, fatty liver, gluconeogenesis, metabolic syndrome, myogenic progenitors, twice-a-day feeding",
author = "Nuria Martinez-Lopez and Elena Tarabra and Miriam Toledo and Marina Garcia-Macia and Srabani Sahu and Luisa Coletto and Ana Batista-Gonzalez and Nir Barzilai and Pessin, {Jeffrey E.} and Schwartz, {Gary J.} and Sander Kersten and Rajat Singh",
note = "Funding Information: We thank Drs. M. Komatsu and K. Tanaka (Tokyo Metropolitan Institute of Medical Science, Japan) for Atg7flox/flox mice, Dr. J. Elmquist (UT Southwestern Medical Center, USA) for POMC-ERT2-Cre mice, and Dr. F. Villarroya (University of Barcelona) for helpful suggestions. This work was supported by R01 AG043517 (to R.S.), P30 DK020541 (Einstein Diabetes Research Center), and P01 AG031782 (to R.S.). A.B.-G. is supported by NIH NIA T32 AG023475. M.T. is supported by American Diabetes Association grant 1-17-PMF-011. I thank N.M.-L., E.T., S.S., M.T., A.B.-G., and M.G.-M, who participated in ITAD feeding of our colonies twice each day for the last 6 years come rain or snow. Funding Information: We thank Drs. M. Komatsu and K. Tanaka (Tokyo Metropolitan Institute of Medical Science, Japan) for Atg7 flox/flox mice, Dr. J. Elmquist (UT Southwestern Medical Center, USA) for POMC-ERT2-Cre mice, and Dr. F. Villarroya (University of Barcelona) for helpful suggestions. This work was supported by R01 AG043517 (to R.S.), P30 DK020541 ( Einstein Diabetes Research Center ), and P01 AG031782 (to R.S.). A.B.-G. is supported by NIH NIA T32 AG023475 . M.T. is supported by American Diabetes Association grant 1-17-PMF-011 . I thank N.M.-L., E.T., S.S., M.T., A.B.-G., and M.G.-M, who participated in ITAD feeding of our colonies twice each day for the last 6 years come rain or snow. Publisher Copyright: {\textcopyright} 2017 Elsevier Inc.",
year = "2017",
month = dec,
day = "5",
doi = "10.1016/j.cmet.2017.09.020",
language = "English (US)",
volume = "26",
pages = "856--871.e5",
journal = "Cell Metabolism",
issn = "1550-4131",
publisher = "Cell Press",
number = "6",
}