Time-restricted eating

Time-restricted eating is a form of daily fasting wherein the time of the day during which a person eats is limited, or compressed. People who practice time-restricted eating typically eat during an 8- to 12-hour daytime window and fast during the remaining 12 to 16 hours. Unlike intermittent fasting, which involves caloric restriction, time-restricted eating permits a person to eat as much as they want during the eating window. Time-restricted eating aligns the eating and fasting cycles to the body’s innate 24-hour circadian system.[1] Within the scientific literature, time-restricted eating primarily refers to human trials, while time-restricted feeding primarily refers to animal studies; however, both terms are occasionally used interchangeably.

The circadian system is composed of multiple cellular clocks found in all cells throughout the body. These clocks orchestrate the regulation of gene expression that coordinates metabolic programs needed to support bodily functions. Of the entire human genome, approximately 15 percent of the genes display daily oscillations, or fluctuations, in their activity. Many of these genes participate in carbohydrate, lipid, and cholesterol metabolism.[2] In both animal studies and human trials, time-restricted feeding and eating have elicited beneficial health effects, including weight loss, reduced fat mass, improved heart function, and enhanced aerobic capacity, without altering diet quality or quantity.[3]

The circadian component of time-restricted eating

In mammals, the circadian system is organized in a hierarchical manner, with the suprachiasmatic nucleus, or SCN, a tiny region of the brain located within the hypothalamus, acting as the master “clock.” The SCN, in turn, coordinates the body’s peripheral clocks, such as those found in the liver, pancreas, muscles, and fatty tissue.[4] Consequently, the master clock drives rhythms of rest and activity that determine eating-fasting cycles.[5] Together, the SCN and peripheral clocks comprise the core clock components. The rhythms of the core clocks are dynamic over the lifespan and change markedly with age, becoming increasingly deranged. These derangements are associated with aging and disease.

Light is the primary signal that entrains the master clock to set the body’s 24-hour circadian cycle, synchronizing the SCN to external light-dark cycles. Other external cues, such as body temperature, oxygen delivery to tissues, and food intake also have the capacity to permanently alter the circadian system. These cues are commonly referred to as zeitgeber (a combination of two German terms, meaning “time giver”) signals. The zeitgeber signals elicit alterations in the SCN and peripheral clocks’ activities, which can subsequently alter the expression of genes involved in metabolism. 

Food intake is the dominant zeitgeber signal in the peripheral clocks.[6] Circulating nutrients from the diet, such as glucose, amino acids, and fatty acids, and their relative quantities possess zeitgeber capacity[7] [8] [9] and can desynchronize the peripheral clocks from the SCN. For example, specific nutritional challenges in mice, such as high dietary fat intake, elicit systemic changes in circadian regulation even after just three days of the challenge.[10] [11]

Timing of food intake also determines the body’s physiological response to food, especially the peripheral circadian rhythms, as seen with time-dependent alterations in glucose metabolism. For example, a trial that monitored the glycemic response to the same meal at different times of the day demonstrated that the postprandial (after a meal) glucose increase was lowest in the morning and highest in the evening.[12] Given the zeitgeber signaling capacity of food, time-restricted eating has emerged as a key intervention to maintain synchronized circadian rhythms between the master and peripheral clocks as a means to improve health. 

Time-restricted eating and metabolic health

The circadian system is profoundly intertwined with an organism’s metabolism to optimize performance over a 24-hour cycle. Disruption of the circadian system, whether by shift work, overeating, or aging, likely contributes to the derangement of metabolic and neurological systems. 

Human trials are now demonstrating the potential of time-restricted eating as a novel means to prevent or reverse metabolic diseases. In a study in which obese people followed an 8-hour time-restricted eating regimen for 12 weeks, participants experienced a 3 percent weight loss, compared to the control group, whose weight remained stable.[13]Furthermore, men at risk for type 2 diabetes who adhered to either a 9-hour “early” time-restricted eating window (8 a.m. to 5 p.m.) or a “delayed” window (12 p.m. to 9 p.m.) experienced a 36 percent reduction in their glycemic response to a meal as well as reduced fasting triglycerides. These findings suggest that there is likely some flexibility in determining the window during which a person eats when practicing time-restricted eating.[14]

Studies also show that time-restricted eating improves circulating insulin and blood pressure independent of weight loss. For example, in a small study involving eight overweight men with prediabetes who were randomized to early time-restricted eating (a 6-hour eating period, with dinner before 3 p.m.) or a control schedule (a 12-hour eating period) for five weeks, the morning systolic and diastolic blood pressure readings of the participants in the 6-hour time-restricted eating window decreased by 11mm and 10mm, respectively, which is comparable to the improvements commonly observed with anti-hypertensive medications such as angiotensin-converting enzyme, or ACE, inhibitors. In addition, the fasting insulin levels of participants in the 6-hour window decreased by 3.4mU/L, and plasma levels of 8-isoprostane, a marker for lipid oxidative stress, decreased by 14 percent.[15]

Recent animal studies have revealed that time-restricted eating can improve metabolic health. Mice that were fed a variety of obesogenic diets while following an 8- to 10-hour time-restricted weekday eating regimen experienced an attenuation of metabolic syndrome through improvements in glucose tolerance and insulin resistance, protection against hypercholesterolemia, and reductions in whole-body fat accumulation. These effects were maintained even when the time-restricted feeding was temporarily disrupted by unrestricted eating on the weekends.[16] Furthermore, time-restricted feeding of rodents has been shown to reverse the progression of type 2 diabetes and obesity.[17]

Time-restricted eating and muscle mass and exercise performance

In addition to the metabolic improvements observed in obese and overweight individuals, time-restricted eating has demonstrated beneficial effects in healthy adults. In conjunction with resistance training, an 8-hour time-restricted eating window in healthy males resulted in a decrease in blood glucose, blood insulin, and fat mass, while maintaining muscle mass.[18] Furthermore, resistance-trained females who followed an 8-hour time-restricted eating window and fasted for 16 hours per day did not experience skeletal muscle atrophy. Rather, they experienced muscle hypertrophy and performance similar to women in a control diet group who ate all their food within a 13-hour per day period. Notably, the two groups’ dietary intake were similar in energy and protein content.[19]

Time-restricted feeding also appears to enhance the aerobic capacity of mice. Mice that ate during a 9-hour time-restricted feeding window ran approximately one hour longer than mice of similar weight that had unrestricted access to food.[20]

Time-restricted eating and longevity

There is some animal evidence that time-restricted feeding also elicits long term health benefits, as evidenced by increased lifespan. Mice that were fed one meal per day lived approximately 11 to 14 percent longer when fed the same caloric content as mice that ate freely, suggesting that time-restricted feeding not only improves metabolic health but may be a contributor to longevity even in the absence of caloric restriction.[21]

Coffee and time-restricted eating

As described above, nutrients such as glucose, amino acids, and fatty acids possess zeitgeber capacity and can activate peripheral clocks such as those in the liver.[7] [8] [9] It is unclear whether caffeine, such as that found in black coffee, can act as a zeitgeber to activate peripheral clocks. Since time-restricted eating has a circadian component to it, and caffeine disrupts circadian rhythms through its stimulating effects, some argue that it could affect peripheral clocks. For example, caffeine consumption at night induced a 40-minute shift in the body’s internal clock, about half the shift that occurred after three hours of night-time bright light exposure.[22] Additionally, caffeine is taken up in the gut and metabolized in the liver, activating metabolic processes in those tissues and potentially starting the circadian clocks.[23]

However, some time-restricted eating studies demonstrating health benefits have included black coffee in their protocols. For example, when women who were in remission for breast cancer practiced a time-restricted eating protocol that included an 11-hour window of eating and a 13-hour period of fasting in which black coffee consumption was permitted, the women experienced a 36 percent reduction in breast cancer recurrence.[24] In a pilot study in which people with diabetes practiced time-restricted eating within a 4- to 8-hour window but were allowed to drink coffee and tea during the fasting period, the participants showed improvements in glucose regulation and weight loss. Notably, they also had an 18 percent reduction in caloric intake, a potential confounder for their findings.[25] Lastly, polyphenols in caffeinated or decaffeinated coffee induce autophagy in the liver, muscle, and heart in mice four hours after consumption.[26]

Genetic mechanisms

The circadian system in most cells relies primarily on two feedback loops in which the translation of core clock genes is regulated by their own protein products. These interlocking feedback loops generate rhythmic transcription cycles to control sleep-wake and eating-fasting cycles by driving the expression of thousands of target genes.

Many of these genes that follow rhythmic patterns are involved in metabolism and can directly interact with the core clock genes to coordinate metabolic programs. For example, the peroxisome proliferator-activated receptors family (PPARs) follow circadian oscillations, and their various isoforms can regulate adipocyte differentiation and fatty acid synthesis (PPAR𝛾), modulate the fatty acid oxidation and amino acid catabolism in the liver (PPARα), and regulate the inflammatory process as well as increase muscle fatty acid oxidation (PPARẟ). The two isoforms PPARα and PPAR𝛾 have been shown to interact with other clock genes, leading to time-dependent alterations of lipid metabolism.[9] Genes involved in glucose uptake and metabolism, such as the hepatic glucose transporter and the enzyme glucokinase, also show daily rhythms, which likely coincide with alterations in glucose and insulin sensitivity at various times of the day.[27]

Further linking the circadian clock and metabolism, animal studies, clinical studies, and observational studies have demonstrated that frequent disruptions in light-dark and eating-fasting cycles can lead to circadian dysregulation and metabolic dysfunction. Mice whose core clock genes have been knocked out develop metabolic syndrome and become obese, indicating a link between circadian regulation and metabolism.[28] [29] [30] [31] [32]. Furthermore, shift workers and healthy people who intentionally disrupt their circadian rhythms exhibit signs of metabolic dysfunction and higher incidence of several chronic diseases, including cancer.[33] [34] Genome-wide association studies, or GWAS, have also uncovered human gene polymorphisms in the principal circadian clock gene, CLOCK, that are associated with overweight or obesity.[35][36] [37]

Disruptions in the body’s innate 24-hour clocks due to irregular light-dark cycles and unrestricted eating have been implicated in the pathogenesis of several metabolic and neurological diseases, as well as cancer. Time-restricted eating, however, is emerging as a potential strategy for avoiding major dietary changes while improving overall metabolic health. Further research likely will elucidate many of the mechanisms that elicit these beneficial effects while also uncovering the therapeutic potential of time-restricted eating to prevent or improve the prognosis of age-related diseases.

Learn more about time-restricted eating in this episode with Dr. Satchin Panda

Hide References

  1.  ^  DOI: 0.3390/ijms20081911
  2.  ^  Duffield, G. E. DNA microarray analyses of circadian timing: the genomic basis of biological time J. Neuroendocrinol. 15, no. 10 (October 2003): 991–1002. 
  3.  ^  Longo, Valter D., and Satchidananda Panda. Fasting, Circadian Rhythms, and Time-Restricted Feeding in Healthy Lifespan Cell Metabolism 23, no. 6 (June 2016): 1048–59. doi:10.1016/j.cmet.2016.06.001. 
  4.  ^  Mohawk, Jennifer A., Carla B. Green, and Joseph S. Takahashi. Central and Peripheral Circadian Clocks in Mammals Annual Review of Neuroscience 35, no. 1 (July 2012): 445–62. doi:10.1146/annurev-neuro-060909-153128. 
  5.  ^  Vieira, Elaine, Thomas P. Burris, and Ivan Quesada. Clock genes, pancreatic function, and diabetes Trends in Molecular Medicine 20, no. 12 (December 2014): 685–93. doi:10.1016/j.molmed.2014.10.007. 
  6.  ^  Damiola, F. Restricted feeding uncouples circadian oscillators in peripheral tissues from the central pacemaker in the suprachiasmatic nucleus Genes & Development 14, no. 23 (December 2000): 2950–61. doi:10.1101/gad.183500. 
  7. a b  Hirota, Tsuyoshi, Toshiyuki Okano, Koichi Kokame, Hiroko Shirotani-Ikejima, Toshiyuki Miyata, and Yoshitaka Fukada. Glucose Down-regulatesPer1andPer2mRNA Levels and Induces Circadian Gene Expression in Cultured Rat-1 Fibroblasts Journal of Biological Chemistry 277, no. 46 (September 2002): 44244–51. doi:10.1074/jbc.m206233200. 
  8. a b  Oike, Hideaki, Kanji Nagai, Tatsunobu Fukushima, Norio Ishida, and Masuko Kobori. Feeding Cues and Injected Nutrients Induce Acute Expression of Multiple Clock Genes in the Mouse Liver PLoS ONE Edited by Shin Yamazaki. 6, no. 8 (August 2011): e23709. doi:10.1371/journal.pone.0023709. 
  9. a b c  Grimaldi, Benedetto, Marina Maria Bellet, Sayako Katada, Giuseppe Astarita, Jun Hirayama, Rajesh H. Amin, James G. Granneman, Daniele Piomelli, Todd Leff, and Paolo Sassone-Corsi. PER2 Controls Lipid Metabolism by Direct Regulation of PPAR Cell Metabolism 12, no. 5 (November 2010): 509–20. doi:10.1016/j.cmet.2010.10.005. 
  10.  ^  Eckel-Mahan, Kristin L., Vishal R. Patel, Sara de Mateo, Ricardo Orozco-Solis, Nicholas J. Ceglia, Saurabh Sahar, Sherry A. Dilag-Penilla, Kenneth A. Dyar, Pierre Baldi, and Paolo Sassone-Corsi. Reprogramming of the Circadian Clock by Nutritional Challenge Cell 155, no. 7 (December 2013): 1464–78. doi:10.1016/j.cell.2013.11.034. 
  11.  ^  Kohsaka, Akira, Aaron D. Laposky, Kathryn Moynihan Ramsey, Carmela Estrada, Corinne Joshu, Yumiko Kobayashi, Fred W. Turek, and Joseph Bass. High-Fat Diet Disrupts Behavioral and Molecular Circadian Rhythms in Mice Cell Metabolism 6, no. 5 (November 2007): 414–21. doi:10.1016/j.cmet.2007.09.006. 
  12.  ^  Cauter, Eve Van, Kenneth S. Polonsky, and Andre’ J. Scheen. Roles of Circadian Rhythmicity and Sleep in Human Glucose Regulation Endocrine Reviews 18, no. 5 (October 1997): 716–38. doi:10.1210/edrv.18.5.0317. 
  13.  ^  Gabel, Kelsey, Kristin K. Hoddy, Nicole Haggerty, Jeehee Song, Cynthia M. Kroeger, John F. Trepanowski, Satchidananda Panda, and Krista A. Varady. Effects of 8-hour time restricted feeding on body weight and metabolic disease risk factors in obese adults: A pilot study Nutrition and Healthy Aging 4, no. 4 (June 2018): 345–53. doi:10.3233/NHA-170036. 
  14.  ^  Hutchison, Amy T., Prashant Regmi, Emily N.C. Manoogian, Jason G. Fleischer, Gary A. Wittert, Satchidananda Panda, and Leonie K. Heilbronn. Time-Restricted Feeding Improves Glucose Tolerance in Men at Risk for Type 2 Diabetes: A Randomized Crossover Trial Obesity , April 2019. doi:10.1002/oby.22449. 
  15.  ^  Sutton, Elizabeth F., Robbie Beyl, Kate S. Early, William T. Cefalu, Eric Ravussin, and Courtney M. Peterson. Early Time-Restricted Feeding Improves Insulin Sensitivity, Blood Pressure, and Oxidative Stress Even without Weight Loss in Men with Prediabetes Cell Metabolism 27, no. 6 (June 2018): 1212–21.e3. doi:10.1016/j.cmet.2018.04.010. 
  16.  ^  Chaix, Amandine, Terry Lin, Hiep D. Le, Max W. Chang, and Satchidananda Panda. Time-Restricted Feeding Prevents Obesity and Metabolic Syndrome in Mice Lacking a Circadian Clock Cell Metabolism 29, no. 2 (February 2019): 303–19.e4. doi:10.1016/j.cmet.2018.08.004. 
  17.  ^  Sherman, Hadas, Yoni Genzer, Rotem Cohen, Nava Chapnik, Zecharia Madar, and Oren Froy. Timed high-fat diet resets circadian metabolism and prevents obesity The FASEB Journal 26, no. 8 (August 2012): 3493–3502. doi:10.1096/fj.12-208868. 
  18.  ^  Moro, Tatiana, Grant Tinsley, Antonino Bianco, Giuseppe Marcolin, Quirico Francesco Pacelli, Giuseppe Battaglia, Antonio Palma, Paulo Gentil, Marco Neri, and Antonio Paoli. Effects of eight weeks of time-restricted feeding (16/8) on basal metabolism, maximal strength, body composition, inflammation, and cardiovascular risk factors in resistance-trained males Journal of Translational Medicine 14, no. 1 (October 2016). doi:10.1186/s12967-016-1044-0. 
  19.  ^  Tinsley, Grant M, M Lane Moore, Austin J Graybeal, Antonio Paoli, Youngdeok Kim, Joaquin U Gonzales, John R Harry, Trisha A VanDusseldorp, Devin N Kennedy, and Megan R Cruz. Time-restricted feeding plus resistance training in active females: a randomized trial The American Journal of Clinical Nutrition , July 2019. doi:10.1093/ajcn/nqz126. 
  20.  ^  Chaix, Amandine, Amir Zarrinpar, Phuong Miu, and Satchidananda Panda. Time-Restricted Feeding Is a Preventative and Therapeutic Intervention against Diverse Nutritional Challenges Cell Metabolism 20, no. 6 (December 2014): 991–1005. doi:10.1016/j.cmet.2014.11.001. 
  21.  ^  Mitchell, Sarah J., Michel Bernier, Julie A. Mattison, Miguel A. Aon, Tamzin A. Kaiser, R. Michael Anson, Yuji Ikeno, Rozalyn M. Anderson, Donald K. Ingram, and Rafael de Cabo. Daily Fasting Improves Health and Survival in Male Mice Independent of Diet Composition and Calories Cell Metabolism 29, no. 1 (January 2019): 221–28.e3. doi:10.1016/j.cmet.2018.08.011. 
  22.  ^  Burke, Tina M., Rachel R. Markwald, Andrew W. McHill, Evan D. Chinoy, Jesse A. Snider, Sara C. Bessman, Christopher M. Jung, John S. O’Neill, and Kenneth P. Wright. Effects of caffeine on the human circadian clock in vivo and in vitro Science Translational Medicine 7, no. 305 (September 2015): 305ra146–305ra146. doi:10.1126/scitranslmed.aac5125. 
  23.  ^  Paula Lima, Juliana de, and Adriana Farah. CHAPTER 15. Caffeine Metabolism and Health Effects Coffee In , 340–63. Royal Society of Chemistry, 2019. doi:10.1039/9781788015028-00340. 
  24.  ^  Marinac, Catherine R., Sandahl H. Nelson, Caitlin I. Breen, Sheri J. Hartman, Loki Natarajan, John P. Pierce, Shirley W. Flatt, Dorothy D. Sears, and Ruth E. Patterson. Prolonged Nightly Fasting and Breast Cancer Prognosis JAMA Oncology 2, no. 8 (August 2016): 1049. doi:10.1001/jamaoncol.2016.0164. 
  25.  ^  Arnason, Terra G, Matthew W Bowen, and Kerry D Mansell. Effects of intermittent fasting on health markers in those with type 2 diabetes: A pilot study World Journal of Diabetes 8, no. 4 (2017): 154. doi:10.4239/wjd.v8.i4.154. 
  26.  ^  Pietrocola, Federico, Shoaib Ahmad Malik, Guillermo Mariño, Erika Vacchelli, Laura Senovilla, kariman chaba, Mireia Niso-Santano, Maria Chiara Maiuri, Frank Madeo, and Guido Kroemer. Coffee induces autophagy in vivo Cell Cycle 13, no. 12 (April 2014): 1987–94. doi:10.4161/cc.28929. 
  27.  ^  Frese, T., I. Bazwinsky, E. Mühlbauer, and E. Peschke. Circadian and Age-dependent Expression Patterns of GLUT2 and Glucokinase in the Pancreatic -Cell of Diabetic and Nondiabetic Rats Hormone and Metabolic Research 39, no. 8 (August 2007): 567–74. doi:10.1055/s-2007-984471. 
  28.  ^  Turek, F. W. Obesity and Metabolic Syndrome in Circadian Clock Mutant Mice Science 308, no. 5724 (May 2005): 1043–45. doi:10.1126/science.1108750. 
  29.  ^  Marcheva, Biliana, Kathryn Moynihan Ramsey, Ethan D. Buhr, Yumiko Kobayashi, Hong Su, Caroline H. Ko, Ganka Ivanova, et al. Disruption of the clock components CLOCK and BMAL1 leads to hypoinsulinaemia and diabetes Nature 466, no. 7306 (June 2010): 627–31. doi:10.1038/nature09253. 
  30.  ^  Dyar, Kenneth A., Stefano Ciciliot, Lauren E. Wright, Rasmus S. Biensø, Guidantonio M. Tagliazucchi, Vishal R. Patel, Mattia Forcato, et al. Muscle insulin sensitivity and glucose metabolism are controlled by the intrinsic muscle clock Molecular Metabolism 3, no. 1 (February 2014): 29–41. doi:10.1016/j.molmet.2013.10.005. 
  31.  ^  Lamia, Katja A., Stephanie J. Papp, Ruth T. Yu, Grant D. Barish, N. Henriette Uhlenhaut, Johan W. Jonker, Michael Downes, and Ronald M. Evans. Cryptochromes mediate rhythmic repression of the glucocorticoid receptor Nature 480, no. 7378 (December 2011): 552–56. doi:10.1038/nature10700. 
  32.  ^  Lamia, K. A., K.-F. Storch, and C. J. Weitz. Physiological significance of a peripheral tissue circadian clock Proceedings of the National Academy of Sciences 105, no. 39 (September 2008): 15172–77. doi:10.1073/pnas.0806717105. 
  33.  ^  McHill, Andrew W., Edward L. Melanson, Janine Higgins, Elizabeth Connick, Thomas M. Moehlman, Ellen R. Stothard, and Kenneth P. Wright. Impact of circadian misalignment on energy metabolism during simulated nightshift work Proceedings of the National Academy of Sciences 111, no. 48 (November 2014): 17302–7. doi:10.1073/pnas.1412021111. 
  34.  ^  Yuan, Xia, Chenjing Zhu, Manni Wang, Fei Mo, Wei Du, and Xuelei Ma. Night Shift Work Increases the Risks of Multiple Primary Cancers in Women: A Systematic Review and Meta-analysis of 61 Articles Cancer Epidemiology Biomarkers & Prevention 27, no. 1 (January 2018): 25–40. doi:10.1158/1055-9965.epi-17-0221. 
  35.  ^  Sookoian, Silvia, Carolina Gemma, Tomas Fernández Gianotti, Adriana Burgueño, Gustavo Castaño, and Carlos Jose Pirola. Genetic variants of Clock transcription factor are associated with individual susceptibility to obesity The American Journal of Clinical Nutrition 87, no. 6 (June 2008): 1606–15. doi:10.1093/ajcn/87.6.1606. 
  36.  ^  Garaulet, Marta, Yu-Chi Lee, Jian Shen, Laurence D Parnell, Donna K Arnett, Michael Y Tsai, Chao-Qiang Lai, and Jose M Ordovas. CLOCK genetic variation and metabolic syndrome risk: modulation by monounsaturated fatty acids The American Journal of Clinical Nutrition 90, no. 6 (October 2009): 1466–75. doi:10.3945/ajcn.2009.27536. 
  37.  ^  Sookoian, Silvia, Tomas Fernandez Gianotti, Adriana Burgueño, and Carlos Jose Pirola. GENE-GENE INTERACTION BETWEEN SEROTONIN TRANSPORTER (SLC6A4) ANDCLOCKMODULATES THE RISK OF METABOLIC SYNDROME IN ROTATING SHIFTWORKERS Chronobiology International 27, no. 6 (July 2010): 1202–18. doi:10.3109/07420528.2010.496913.