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Syncing Exercise With Meals and Circadian Clocks

Heden, Timothy D.1; Kanaley, Jill A.2

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Exercise and Sport Sciences Reviews: January 2019 - Volume 47 - Issue 1 - p 22-28
doi: 10.1249/JES.0000000000000172
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Key Points

  • Energy metabolism and insulin sensitivity are influenced by central (i.e., brain) and peripheral (i.e., skeletal muscle, liver, adipose tissue) circadian rhythms.
  • Diurnal variations in energy metabolism and insulin secretion are found in healthy nondiabetic individuals with greater insulin sensitivity and glucose or lipid tolerance in the morning, which all gradually worsen in the afternoon and evening.
  • Individuals with type 2 diabetes (T2D) have an inverted circadian rhythm in insulin sensitivity that is improved in the evening and thereafter begins to worsen overnight and into the morning ultimately resulting in abnormally elevated morning glycemia and lipemia (i.e., dawn phenomenon).
  • Exercise after meals, compared with exercise before meals, reduces postprandial glycemia and lipemia more in individuals with T2D.
  • Exercise in the evening, compared with exercise in the morning, has a more beneficial impact on glycemia and lipemia in individuals with T2D.

INTRODUCTION

Individuals with type 2 diabetes (T2D) are characterized by impaired fasting glucose and lipid levels, postprandial hyperglycemia and hypertriglyceridemia, and other complications that lead to cardiovascular diseases. Hyperglycemia and hypertriglyceridemia in T2D cause cardiovascular disease by promoting endothelial dysfunction through several known mechanisms including increased oxidative stress (1), advanced glycosylation end products (2), endothelial progenitor cell senescence (3), and inflammation (3). After meals, glucose and lipid concentrations can fluctuate dramatically depending on the meal composition and the metabolic health status of an individual. Minimizing these excursions is necessary to prevent diabetes and atherosclerosis-associated disorders in healthy individuals and to provide protection against diabetes progression and the development of its associated cardiovascular complications. Exercise is critical in controlling postprandial levels because of its ability to alter energy metabolism and insulin sensitivity. Thus, the interplay between exercise and meals can be manipulated to maintain metabolic control.

Glucose and lipid metabolism also are impacted by circadian rhythms. The circadian system comprises a central brain pacemaker (suprachiasmatic nucleus) along with cell-autonomous circadian rhythms in liver, muscle, and adipose tissue that work in synergy to modulate a range of metabolic processes including insulin sensitivity and energy metabolism (4). Metabolically healthy individuals have the most optimal liver and peripheral insulin sensitivity and glycemic control in the morning, which gradually worsens through the remainder of the day (5,6). Intriguingly, individuals with diabetes have an inverted circadian rhythm with insulin sensitivity and glycemia relatively better in the evening but worsening during the overnight and early morning period resulting in morning hyperglycemia and hyperlipidemia (i.e., dawn phenomenon) (7–9). Thus, disruption in the chronobiology in T2D is a major underlying factor contributing to hyperglycemia and hypertriglyceridemia.

Improvements in peripheral insulin sensitivity and realignment of the circadian cycle can be achieved by sleep, diet, and physical activity/exercise, which is a fundamental component of improving hyperglycemia and hypertriglyceridemia in T2D. The exercise recommendations set by the American College of Sports Medicine recommend the prescription of exercise with considerations of frequency, duration, type, and mode of exercise but do not consider exercise timing, which may be a critical component particularly in those affected by chronic disease. We now know that metabolism clearly shows circadian rhythms both at a central level and a peripheral level; thus, we speculate that there may be a temporal optimization of exercise to modulate endogenous glucose production, β-cell function, and tissue insulin sensitivity. Potentially prescribing exercise based on time of day may attenuate postprandial glycemia and lipemia, which in turn may modulate the dawn phenomena by lowering morning fasting glucose and triglyceride levels. This review explores the novel hypothesis that evening postprandial exercise is the optimal time to exercise to improve glycemia and lipemia in T2D. We also discuss potential mechanisms for the superior benefits of exercise after an evening dinner in this population.

EXERCISE TIMING AND POSTPRANDIAL METABOLISM

Pre Versus Postprandial Exercise and Glycemia

Postprandial glycemia is a major risk factor for heart disease in T2D. Most (10–18), but not all (19), studies show that exercising after meals has a greater benefit on postprandial glycemia compared with premeal exercise in individuals with T2D. Early work in T2D by Larsen et al. (12,13) showed that both moderate- (45 min at 53% V˙O2max) and high-intensity interval cycling exercise (four bouts, each bout consisting of 3 min at 56% V˙O2max, 4 min at 98%, and 6 min of rest) beginning 45 min after breakfast reduced postprandial glucose levels after breakfast but had no impact on glycemia after a subsequent lunch meal. Improvements in postprandial glucose responses were due to an increased rate of glucose disappearance (i.e., enhanced muscle glucose uptake). Subsequent studies in T2D revealed that moderate-intensity cycling exercise (1 h at 60% V˙O2max) in the fasted (preprandial) state has little impact on glucose levels during exercise, whereas postprandial exercise (0–8 h postprandial) reduces glucose levels during exercise between 28% and 43%, with the largest reductions occurring when exercise was performed within 5 h after eating (14,15,18). Colberg et al. (11) showed that 20 min of self-paced treadmill walking 15 to 20 min after eating a dinner meal reduced postprandial blood glucose levels in individuals with T2D, whereas the same bout of exercise performed immediately before dinner had no impact on postprandial blood glucose levels.

Likewise, work from our lab (10) in individuals with T2D has shown that ~45 min of resistance training (3 sets of 10 repetitions using 10 repetition maximum weight, 8 different exercises) either before (finished ~30 min before dinner) or beginning 45 min after eating dinner lowers postprandial glucose levels, but that postdinner exercise tended to reduce postprandial glycemia to a greater extent. Recent work (20) also has shown that 60 min of moderate-intensity (12 on Borg 6–20 scale) treadmill walking after breakfast, but not before breakfast, attenuated glycemia over the next 22 h in hyperglycemic individuals. In contrast to these studies, one study has shown that moderate- (55% V˙O2max) or high-intensity cycling exercise (15 bouts of 4 min at 40% V˙O2max, 1 min at 100% V˙O2max) performed before breakfast had a greater benefit on most aspects of glycemia compared with exercise after breakfast, although both exercise times improved glycemia to some extent in individuals with T2D (19). Taken together, most studies indicate that postprandial exercise, compared with premeal exercise, has a greater benefit on postprandial glycemia in individuals with T2D.

The mechanism for the superior benefit of postmeal exercise on postprandial glycemia may be multifactorial. Skeletal muscle accounts for 50%–75% of insulin-stimulated glucose uptake (21,22), and although insulin stimulates GLUT 4 translocation and glucose uptake through an insulin receptor/insulin receptor substrate/phosphatidylinositol-3-kinase/Akt axis (23), skeletal muscle contraction increases GLUT 4 translocation and glucose uptake via activation of a sucrose nonfermenting adenosine monophosphate kinase (AMPK)–related kinase/AMPK/TBC1D1/TBC1D4 signaling node (24,25). When combined, both insulin and muscle contractions stimulate glucose uptake to a greater extent than either stimulus alone (26). Thus, the greater benefit of postprandial exercise on glycemia is due to the synergy between insulin and muscular contraction to increase glucose uptake (Fig. 1). In addition to its direct effects on skeletal muscle, insulin also reduces hepatic glucose output. Therefore, the elevation in postprandial insulin levels and subsequent reduction in hepatic glucose output immediately before exercise in the postprandial state also may contribute to the reduction in glucose excursions. Further combining this mechanism with what is known about the circadian shifts in glucose metabolism supports our novel hypothesis that there may be temporal optimization of exercise. It is important to note that this hypothesis is based on the acute effects of exercise, but longer-term exercise training of varying modes, volumes, and intensities that results in differential adaptations in skeletal muscle and liver metabolism may have different effects. In addition, modified β-cell function could potentially alter this mechanism.

Figure 1
Figure 1:
The muscle, liver, and adipose tissue metabolic responses to moderate exercise in individuals with type 2 diabetes (T2D) in the fasted state versus exercise in the postprandial state.

Pre Versus Postprandial Exercise and Lipemia

In addition to hyperglycemia, hypertriglyceridemia also is a major risk factor for heart disease in individuals with T2D (27). Compared with glycemia, fewer studies have examined the impact of pre versus postprandial exercise on lipemia in individuals with T2D, but the available research suggests postprandial exercise is more beneficial. For instance, Gill et al. (28) reported that 90 min of moderate intensity (50% V˙O2max) treadmill walking the day before a high-fat meal (~16–18 h before) did not impact postprandial triglyceride responses in individuals with T2D, whereas Tobin et al. (29) reported that 60 min of moderate intensity (57% V˙O2max) cycling exercise beginning 90 min after a high-fat meal reduced postprandial triglyceride concentrations in individuals with T2D. Interestingly, Dalgaard et al. (30) found that 40 min of cycling exercise (40% V˙O2max) either the day before a high-fat test meal or 3.5 h after a high-fat test meal did not alter postprandial triglyceride levels significantly in individuals with T2D. It should be noted that subjects in this study consumed a considerable amount of alcohol (40 g), which may counteract the impact of exercise on triglyceride levels. In addition, discrepancies in the findings between studies may be due to the timing of exercise relative to the meal. Tobin et al. (29) found that exercise 90 min after the meal reduced postprandial triglyceride levels, whereas Dalgaard et al. (30) found exercise 3.5 h after eating did not impact postprandial triglyceride levels in T2D. Data from our lab show that resistance exercise 45 min after a dinner meal (3 sets of 10 repetitions using 10 repetition maximum weight, 8 different exercises), but not before a dinner meal (ending ~30 min before the meal), reduced postprandial triglyceride responses in T2D, which was due to a reduction in very low-density lipoprotein (VLDL) triglyceride levels (10). Thus, evidence is accumulating that postprandial exercise should be performed close to the meal to reduce subsequent postprandial triglyceride responses, but the exact timing for exercise has not been elucidated.

The two predominant forms of triglyceride-rich lipoproteins in the blood are chylomicrons and VLDL lipoproteins. Chylomicrons and VLDL particles are cleared via the same lipolytic pathway by lipoprotein lipase, although lipoprotein lipase has a much greater affinity for chylomicron than VLDL (31). Because during acute insulin infusion (32) or exercise (33) VLDL secretion is reduced, we hypothesize that the superior benefit of postprandial exercise on reducing postprandial VLDL concentrations is due to the synergy of insulin and exercise to reduce hepatic VLDL secretion. Moreover, insulin increases lipoprotein lipase activity in adipose tissue, whereas exercise increases the activity of lipoprotein lipase in the skeletal muscle (34), possibly contributing to reductions in VLDL with postprandial exercise. Taken together, we speculate that acute postprandial exercise reduces triglyceride excursions more effectively than preprandial exercise in T2D because of the synergy of elevated insulin levels and exercise to reduce hepatic VLDL secretion and enhance catabolism of VLDL by lipoprotein lipase. More research needs to be conducted, particularly with long-term exercise training, in this area on individuals with metabolic disruptions.

CIRCADIAN MODULATION OF METABOLISM: ROLE OF EXERCISE

Endogenous central and peripheral circadian rhythms regulate endocrinology and metabolism in alignment with the sleep/wake cycle across a typical 24-h day (4). Most studies that have advocated either preprandial or postprandial exercise in controlling postprandial glycemia or lipemia in T2D primarily have focused on early morning hours (breakfast meal) when the meal is preceded by an overnight fast. Only a few studies have examined these changes at meals other than breakfast or across an entire day of eating, and these studies do not consider the diurnal variation in glucose and lipid tolerance or insulin sensitivity when being reported.

In healthy nondiabetic individuals, diurnal variations in glucose tolerance have been reported, which usually show a peak in the morning (6,35–39) with impairments in glucose tolerance in the afternoon and evening; these time-of-day effects are independent of the fasting duration (40). These variations are attributed to the insulin secretory response and β-cell responsiveness that are higher in the morning than at the other times of day, as well as alterations in hepatic insulin extraction, which is lower in the morning than evening indicating diurnal differences in insulin clearance (5,6,41,42). For example, Van Cauter et al. (6) demonstrated that in the evening, there is a failure of insulin secretion to increase in proportion to changes in postprandial glucose responses as is seen with meals earlier in the day, implying that there may be a circadian variation in the responsiveness of β-cells to glucose or circadian changes in insulin sensitivity in healthy, nondiabetic individuals. Lee reported that in normal-weight nondiabetic individuals, glucose tolerance diminished by ~40% from morning to evening and insulin sensitivity was impaired ~ 35%, whereas in obese individuals, glucose tolerance was not reduced (41). Likewise, Saad et al. (5) further confirmed these findings in healthy volunteers with normal fasting glucose levels. These subjects ingested identical mixed meals at 0700, 1300, and 1900 h with similar physical activity. The postprandial glucose excursion was lower at 0700 h than 1300 and 1900 h, whereas β-cell responsivity to glucose and the disposition index was higher. Using a triple-tracer technique they showed that meal glucose rate of appearance did not differ between meals, but they observed the presence of a diurnal pattern of glucose tolerance with a lower postprandial glucose excursion at breakfast than at lunch and dinner. Reduced β-cell responsiveness and insulin action with increased hepatic insulin extraction after lunch and dinner than breakfast led to the appearance of the diurnal pattern. In addition, preprandial glucagon concentrations were significantly lower at 0700 h than 1300 and 1900 h, whereas the postprandial glucagon excursion was significantly higher at 0700 h than at 1300 and 1900 h. More recently, Leung et al. (43) showed that the postprandial glucose integrated area under the curve (iAUC) was higher in the evening (2000 h) compared with the morning (0800 h), and that after a low glycemic index meal trial, postprandial glucose and insulin iAUC at evening (2000 h) and midnight (0000 h) were higher than the morning but not significantly different between evening and midnight. Thus, meal intake at night, even when composed of low glycemic ingredients, contributes to higher glucose excursions and concomitantly greater insulin levels, compared with an equivalent meal in the morning. Thus, exercise in the evening may be more beneficial to improve insulin sensitivity and glucose or lipid tolerance at a time of day when they are typically worst.

In T2D, disrupted chronobiology is suggested to be a major factor contributing to hyperglycemia and hypertriglyceridemia. For instance, disruptions in circadian rhythmicity through genetic modifications of the molecular clock enzymes CLOCK and BMAL1 in pancreatic islets promote the development of diabetes in animal models (44). In healthy humans, using a 9-h phase advance to mistime sleep and simulate night shift work worsens glycemia and lipemia (45,46). In obese individuals, diurnal variations have been reported to be attenuated, phase delayed, or absent (36,41), whereas in individuals with T2D, the diurnal rhythm may be absent or phase delayed by several hours. Boden et al. (7) used a 24-h hyperglycemic clamping procedure and found that the glucose infusion rate (i.e., insulin sensitivity), but not the glucose disappearance rate, changed rhythmically over 24 h and these changes were accounted for by circadian changes in hepatic glucose production. Thus, they observed an inverted circadian rhythm where insulin sensitivity was highest at night (1900 h) and then gradually worsened during the overnight period and was worst in the morning (0800 h). Furthermore, individuals with T2D exhibit clear rhythms in hepatic glycogen storage (47). These circadian changes in hepatic glucose production in individuals with T2D likely contribute to the early morning rise in glucose and triglycerides, which is known as the dawn phenomenon (7).

Subsequent work showed that the increase in nocturnal endogenous glucose production was mediated by an increase in liver gluconeogenesis and β-cell glucose insensitivity during the night (i.e., lack of insulin secretion despite rise in glucose levels) (8). Melatonin levels during the night were related closely to endogenous glucose production, and compared with healthy controls, peaked much later in the night in T2D. Furthermore, the dinner meal is typically the biggest meal of the day for many individuals and previous work has shown that a moderate to large size dinner meal (>30% total daily caloric intake) causes a greater early morning rise in blood glucose (48). Given the known role of exercise to improve insulin sensitivity and glycemia or lipemia, we propose that exercising after dinner (the biggest meal of the day in Western societies) may be the most optimal time of day to exercise to not only improve glycemia and lipemia after dinner but during the overnight period and into the next day (Fig. 2).

Figure 2
Figure 2:
The circadian changes in the hormonal and metabolic responses to meals and exercise in an individual with type 2 diabetes (T2D) throughout a 24-h period. Changes in these profiles are illustrated for a day with no exercise or a day with evening exercise.

Time of Day of Exercise

The impact of exercise at various times of the day has been well studied in healthy individuals with the outcomes being athletic performance (49). Recently, it was shown that 24 wk of combined strength and endurance training in the evening lead to greater gains in muscle mass compared with exercise in the morning in young healthy men (50). It would be predicted that these greater gains in muscle mass with evening exercise potentially lead to greater improvements in glycemia given that muscle mass is the largest sink for glucose disposal. However, to our knowledge, the impact of exercise at specific times of the day on glycemia and lipemia has not been investigated directly in individuals with or without T2D.

During the overnight period in individuals with T2D, a dysynchrony between endogenous hepatic insulin sensitivity, circulating hormones, and metabolites occurs resulting in a rise in endogenous glucose output ultimately causing fasting hyperglycemia in the morning. Thus, performing exercise or physical activity in the evening, when postprandial glycemia is the worst and hepatic insulin sensitivity begins to worsen due to circadian rhythms, may provide the most benefit not only to improve postprandial glycemia after dinner but also to enhance insulin sensitivity into the nocturnal period and lower fasting morning blood glucose levels in individuals with T2D. Indirect evidence from different studies support our hypothesis that exercise in the evening may be the most effective time to exercise for individuals with T2D. For instance, exercising after lunch had a minimal impact on glycemia over the following 24 hours (17), whereas work from our lab (10) and Colberg et al. (51) has shown that exercise in the evening reduces glycemia during exercise and the overnight period, when glycemic control is the poorest. Another study (16) found that simply providing advice to walk for 10 min after meals was more effective at improving glycemia, especially when walking was performed after the dinner meal, compared with advice to exercise without specifying timing. Although these studies do not directly compare the effects of exercise at various times of the day on glycemia or lipemia in individuals with T2D, when observed together they provide some evidence that exercise after dinner may be the most optimal time to exercise for individuals with T2D to improve glycemia and lipemia.

Given that glycemic excursions are large after every meal in individuals with T2D, another strategy may be to perform exercise/physical activity after each main meal throughout the day. Indeed, several investigations have found that breaking up prolonged sitting with bouts of standing/physical activity improves postprandial glycemia and lipemia, and some show that this strategy is more effective than morning exercise alone. For example, work from our group has shown that in obese, insulin-resistant individuals short, frequent periods of exercise throughout the day and evening attenuate glycemia to a greater degree than an equal amount of exercise performed continuously in the morning (52). Duvivier et al. (53) showed that breaking up prolonged sitting with standing and light-intensity walking throughout the day and evening improved glycemic control and insulin sensitivity more effectively than a single exercise session performed ~2 h after breakfast, suggesting that exercise in the morning and evening is more effective than morning exercise alone. Likewise, Dempsey et al. (54) showed that interrupting prolonged sitting with short bouts of walking or simple resistance activities every 30 min throughout a 7-h period improved glycemic control during the day and overnight period, whereas Grace et al. (55) showed that breaking up prolonged sitting over a 7-h postmeal period with light walking or resistance exercise reduced many different triglyceride species. These studies further support our hypothesis that adding exercise to the evening period is most effective at improving glycemia and lipemia in T2D.

The mechanism by which evening exercise is superior to exercise at other times of the day may be due to alterations in melatonin signaling. Individuals at risk of T2D have increased expression of melatonin receptors in the pancreas, and in cell culture experiments, melatonin has been shown to inhibit β-cell glucose-stimulated insulin secretion (56), which may contribute to the dawn phenomenon. Buxton et al. (57) demonstrated that exercise in the evening phase advanced the onset of the melatonin peak in healthy nondiabetic individuals, compared with morning, afternoon, and nighttime exercise, whereas nighttime exercise (after midnight) robustly increased melatonin concentrations. In contrast, Monteleone et al. (58) reported that exercise at night (~11 pm) blunts the nocturnal increase in plasma melatonin levels in healthy individuals (58). It is not known how exercise at night impacts melatonin levels in individuals with T2D, but we speculate that evening exercise but not nighttime exercise potentially may relieve melatonin-induced inhibition in β-cell glucose-stimulated insulin secretion. This would allow more insulin to be secreted when nocturnal endogenous glucose production and plasma glucose levels rise during the night and ultimately prevent the dawn phenomenon. Furthermore, exercise could reduce melatonin receptor expression in the pancreas in individuals with T2D, which also would improve nocturnal β-cell glucose-stimulated insulin secretion and lower fasting plasma glucose levels the following morning. Moreover, exercise before fasting overnight will improve hepatic insulin sensitivity, which will attenuate the early morning rise in endogenous glucose production and triglyceride secretion and prevent the dawn phenomenon in T2D.

CONSIDERATIONS

Complicating the interpretation and implementation of many of the above studies is the variability in human physiology such that disease progression as well as individual behaviors can dampen or accentuate many of the responses reported in these studies. This results in the observations within data sets of responders and nonresponders to studied interventions. To date, the research on the time of day of exercise is limited and the effects of evening exercise and postprandial activity need to be studied considerably more in individuals with T2D. The work that has been done has focused on acute bouts of exercise at different times of day when the longer-term effects may be very different and due to different mechanisms. Exercise after long periods of fasting are taking place when lipolysis is high, gluconeogenesis could be elevated resulting in increased endogenous glucose production, which might further worsen postprandial glycemia and lipemia.

Research examining the first and second meal on glucose levels shows that in healthy individuals, the glucose levels at breakfast often are higher than at lunch when given the same meal composition. It is speculated that endogenous glucose production is high at breakfast and eating a meal acts as a primer to the tissues either altering their sensitivity to insulin or altering the pancreatic response to the glucose signal. This would be particularly critical in an insulin insensitive, T2D individual with metabolic inflexibility. Superimposing exercise on these metabolic conditions results in dramatic shifts in metabolism that can vary with different types of exercise (aerobic vs resistance), duration and intensity of exercise, and acute versus chronic effects of exercise. Although not as practical, exercise can be split into multiple bouts during the day (including fasting and postprandial state exercise) and result in different responses in glucose and lipid excursions.

Lastly, animal data have supported the idea for temporal coordination of metabolism in the context of health and disease (59) as disruption of metabolism and circadian clock function is observed with behavior misalignment, or high-fat diet. Sleep restriction also has been linked with perturbations in the circadian and metabolic system.

SUMMARY AND FUTURE DIRECTIONS

The impact of dose, frequency, and intensity of exercise on cardiovascular fitness, metabolism, and strength has been well characterized and is included in most exercise prescriptions. Although we know that circadian rhythms are controlled centrally with peripheral tissues imposing their own rhythms, there is a paucity of exercise research in humans directly comparing exercise at various times relative to meal ingestion or time of day and its impact on glycemia and lipemia in T2D. Herein, we provide evidence that acute postprandial exercise, compared with premeal exercise, has a greater benefit on postprandial glucose and triglyceride levels in individuals with T2D, as well as demonstrate that evening exercise appears to be more beneficial to improve these important clinical outcomes.

The link between chronobiology, exercise, and energy metabolism in the setting of T2D is not well understood and represents an emerging and ripe area for future study. Future research should address the acute and long-term impact of aerobic, resistance, or combined exercise training regimens at various times relative to a meal, at separate times of the day, and at various times relative to medication use, and varying modes, volumes, and intensities of exercise on metabolic health and lifespan in individuals with T2D. As for pharmacological prescriptions, we should start to think about temporal optimization of exercise in relation to meals as well as with time-of-day effects particularly in individuals in various disease states. The inclusion of consideration of exercise timing allows more diversity in our exercise prescription instead of a one-size-fits-all prescription.

Acknowledgments

The authors were funded by the following grants while writing this article: NIH DK109556 (T.D.H.), DK110338 (T.D.H.), and DK101513 (J.A.K.).

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Keywords:

exercise timing; glucose excursions; triglyceride; postprandial; type 2 diabetes; metabolism

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