Claire Laurens
Isabelle de Glisezinski
Dominique Larrouy
Isabelle Harant1,2
Cedric Moro- 1INSERM, UMR 1048, Institute of Metabolic and Cardiovascular Diseases, Obesity Research Laboratory, Toulouse, France
- 2Paul Sabatier University, Toulouse, France
- 3Department of Physiological Functional Explorations, Rangueil University Hospital, Toulouse, France
Exercise is a powerful and effective preventive measure against chronic diseases by increasing energy expenditure and substrate mobilization. Long-duration acute exercise favors lipid mobilization from adipose tissue, i.e., lipolysis, as well as lipid oxidation by skeletal muscles, while chronic endurance exercise improves body composition, facilitates diet-induced weight loss and long-term weight maintenance. Several hormones and factors have been shown to stimulate lipolysis in vitro in isolated adipocytes. Our current knowledge supports the view that catecholamines, atrial natriuretic peptide and insulin are the main physiological stimuli of exercise-induced lipolysis in humans. Emerging evidences indicate that contracting skeletal muscle can release substances capable of remote signaling to organs during exercise. This fascinating crosstalk between skeletal muscle and adipose tissue during exercise is currently challenging our classical view of the physiological control of lipolysis, and provides a conceptual framework to better understand the pleotropic benefits of exercise at the whole-body level.
Introduction
Physical exercise is one of the most effective lifestyle interventions to fight against many chronic diseases and in particular obesity and type 2 diabetes. Health benefits of exercise are achieved through an improvement of energy metabolism and glucose homeostasis. These benefits are sustained over the long term through an improvement of body composition induced by muscle hypertrophy and fat mass loss (Ross and Bradshaw, 2009; Peterson et al., 2011; Stoner et al., 2016; Evans et al., 2019; Hsu et al., 2019; Viana et al., 2019). Importantly, even if exercise training interventions usually have a very modest impact on body weight, a consistent observation is a reduction of waist circumference and visceral white adipose tissue (WAT) mass, and is therefore an efficient strategy to reduce cardiometabolic risk in obese individuals (Wewege et al., 2017).
During an exercise bout, skeletal muscle relies on both fatty acids (FA) and glucose as fuels to sustain muscle fiber contraction. When exercise is performed at high intensity and for a short duration, muscle cells primarily rely on glucose and muscle glycogen as fuels, which is mainly released from muscle and liver glycogen stores. However, if the exercise is performed at a moderate intensity and for a longer duration, FA will become the main source of energy to sustain muscle contraction. Indeed, FA oxidation in muscle is dependent of FA supply from different sources: FA released through lipolysis of triacylglycerols (TG) stored within WAT, from circulating very low-density lipoproteins-TG (VLDL-TG), from intramyocellular triacylglycerols (IMTG) and potentially TG stored within inter/intra-muscular adipose tissue (IMAT). The contribution of VLDL-TG to whole-body lipid oxidation varies from 5 to 10% at rest and seems to be marginal during exercise (Wolfe et al., 1985; Kiens and Lithell, 1989). Fatty acids-derived from IMTG and peripheral WAT are thus by far the major sources of lipid fuels during exercise (Horowitz, 2003). Their relative contribution to exercise energy expenditure is influenced by a number of factors such as exercise intensity, duration, and training status (Horowitz and Klein, 2000). Low to moderate intensity exercise, ranging from 25 to 65% of maximal oxygen consumption (VO2max), is associated with a 5 to 10-fold increase in whole-body lipid oxidation compared to rest (Romijn et al., 1993). A large part of the increase in FA availability is supplied by WAT lipolysis, which increases by 2–4 times (Romijn et al., 1993; Klein et al., 1994; Krauzova et al., 2018). In this review, we will discuss the effects of acute and chronic exercise on abdominal WAT lipolysis in lean and obese individuals.
Effect of Acute Exercise on Adipose Tissue Lipolysis
Main FA Sources
Numerous studies have demonstrated a tight link between lipolysis and FA oxidation during exercise. Indeed, a positive correlation has been observed between lipolytic rate measured in vitro in isolated adipocytes and whole-body resting FA oxidation in healthy individuals (Imbeault et al., 2000). In addition, a strong positive relationship has been described between subcutaneous abdominal WAT lipolysis and whole-body FA oxidation measured during an exercise bout in endurance-trained subjects (Moro et al., 2014). Furthermore, the adipose triglyceride lipase (ATGL) activity is increased during exercise in WAT from lean and obese individuals (Petridou et al., 2017).
The abdominal WAT is made of two main fat compartments, subcutaneous WAT (SCAT) on one side, and visceral WAT on the other side. Exercise mostly activates lipolysis in SCAT, as only 5–10% of circulating long-chain FA are released from visceral adipose tissue in lean subjects (Horowitz, 2003; Nielsen et al., 2004). Abdominal SCAT lipolytic response is dependent on both exercise intensity and duration (Horowitz, 2003). In addition, it has been suggested that subcutaneous abdominal lipolysis is greater than gluteo-femoral lipolysis both in men and women, and that men have a relative “resistance” to norepinephrine-mediated lipolysis due to higher adipocyte content of alpha2-adrenergic receptors that inhibits lipolysis (Leibel and Hirsch, 1987; Jensen and Johnson, 1996; Moro et al., 2007). However, in these studies, the relative lipolytic rate measured in vitro on isolated adipocytes, in situ through microdialysis, and in vivo using A–V differences appeared similar between men and women, thus indicating that the greater lipid mobilization observed during exercise in women is mostly accounted for by a higher subcutaneous fat mass compared to men.
Main Lipolytic Hormones and Factors
The activation of SCAT lipolysis during exercise can be attributed to an increase in plasma catecholamines concentration, which stimulates beta-adrenergic receptors on the adipocyte plasma membrane leading to the intracellular activation of the hormone-sensitive lipase (HSL; Horowitz, 2003). However, we have previously shown that local infusion of the beta-blocking agent propranolol in the SCAT only partially inhibits exercise-induced lipolysis (Moro et al., 2004; Verboven et al., 2018). The 60–70% residual lipolysis was found to correlate with plasma atrial natriuretic peptide (ANP) concentration (Moro et al., 2004, 2008). The role of ANP in exercise-induced lipolysis was then further confirmed during repeated bouts of endurance exercise in lean healthy and obese individuals (Moro et al., 2006; Koppo et al., 2010). Thus, besides the well-known role of catecholamines on exercise-induced WAT lipolysis, the increase of plasma ANP, along with the decrease of plasma insulin (Moro et al., 2007), in relation to exercise intensity actively contribute to enhance adipocyte lipolysis during exercise. Interestingly, when exercise is performed the day after an exercise-bout when muscle glycogen stores are still low, lipolysis is increased compared with the same exercise performed after a resting day, in elite cyclists (Moro et al., 2014). Strikingly, this observation could not be explained by the aforementioned classical lipolytic agents, therefore suggesting that other factors may participate in the activation of WAT lipolysis during exercise (Moro et al., 2014). Recent evidence indicate that proteins secreted by muscle fibers during contraction, the so-called myokines, could activate WAT lipolysis in humans. Indeed, interleukin-6 (IL-6) was the first myokine to be discovered and IL-6 plasma levels were increased in response to an acute exercise bout (Pedersen et al., 2001; Reihmane and Dela, 2014). A recent clinical study has demonstrated that IL-6 is required to reduce visceral adipose tissue mass in response to exercise training (Wedell-Neergaard et al., 2019). However, the role of IL-6 in the activation of WAT lipolysis is still a matter of debate, as IL-6 acute treatment does not activate adipocyte lipolysis in vitro (Trujillo et al., 2004). In addition, an acute elevation of IL-6 in vivo was described to increase whole-body lipolysis due to a rise in muscle FA release, while WAT lipolysis remained unchanged (Wolsk et al., 2010). Irisin is another myokine that has been described to increase WAT lipolysis through an indirect mechanism involving WAT browning (Bostrom et al., 2012). However, altthough some experiments performed in rodents suggest that exercise-released myokines may activate WAT browning (Stanford et al., 2015), the relevance of such mechanism in humans remains controversial (Norheim et al., 2014; Lehnig and Stanford, 2018).
More recently, we identified a novel myokine secreted by contracting human primary skeletal muscle cells, called growth and differentiation factor 15 (GDF15), which enhances adipocyte lipolysis in vitro (Laurens et al., 2020). Furthermore, GDF15 was also secreted following both high-intensity or moderate-intensity exercise in humans in vivo, and recombinant GDF15 protein was able to activate lipolysis in subcutaneous WAT explants (Laurens et al., 2020).
White adipose tissue has also been described to produce soluble factors that may act in a paracrine/autocrine fashion to sustain lipolysis during exercise such as interleukin-15 (IL-15). It has been demonstrated that IL-15 can be produced by SCAT during a one h-cycling exercise, which is known to increase WAT lipolysis. In addition, resting IL-15 secretion correlates with SCAT lipolysis, and an infusion of IL-15 through microdialysis activates SCAT lipolysis in lean subjects while it suppresses lipolysis in obese subjects (Pierce et al., 2015). However, no correlations were observed between IL-15 secretion and lipolysis during exercise. Thus, whether IL-15 contributes to exercise-induced lipolysis is still debated and warrants further investigations.
Exercise Intensity
The relative contribution of FA utilization during an exercise bout depends on its intensity. White adipose tissue lipolysis increases from low to moderate intensities and decreases at high intensity (Romijn et al., 1993). Indeed, when exercise is performed at high intensity, glucose is the major energy substrate to rapidly fuel the contracting muscle. However, as exercise intensity decreases, a switch occurs and lipids become the major energy substrate (i.e., crossover concept) (Brooks and Mercier, 1994). The concept of “Fatmax” has then been taken up by Jeukendreup and colleagues to describe the exercise intensity, expressed as a percent of VO2max, eliciting the maximal reliance on fat as fuel oxidized in skeletal muscle (Jeukendrup and Wallis, 2005). At this intensity, half of the FA oxidized by muscle fibers are supplied by WAT lipolysis, the remaining part being intracellularly provided by IMTG pools. Fatmax value differs for each individual and mostly depends on body weight, diet, sex, and training status (Jeukendrup and Wallis, 2005). For instance, the Fatmax has been measured at 48% of VO2max in a large cohort of lean sedentary individuals, while it was around 65% in endurance trained subjects (Achten et al., 2002; Jeukendrup and Wallis, 2005). Interestingly, Fatmax was found to be lower in men than in women (45% vs 52% of VO2max, respectively) (Jeukendrup and Wallis, 2005). As stated earlier, the greater lipid oxidation at a given exercise intensity in women is accounted for by a higher lipid mobilization at a same relative exercise intensity due to a higher subcutaneous fat mass. Furthermore, Fatmax is lower in obese than in lean individuals (Perez-Martin et al., 2001). However, even if Fatmax has been widely used in exercise-based weight-loss programs, this concept has also raised some criticisms. First, Fatmax is highly dependent on diet and nutritional state, as the body relies more on carbohydrates (CHO) as fuel when they are highly available such as in postprandial conditions. Second, FA oxidation rate is similar in a large range of exercise intensities, usually from about 45 to 75% of maximal aerobic capacity, and thus does not differ much from the peak value (i.e., Fatmax value). Third, the amount of FA burned throughout 24 h not only depends on FA oxidized during exercise but also during the post-exercise recovery period, especially when exercise is performed at high intensity. Finally, Fatmax is a rate of FA oxidation, but the total amount of FA utilized is dependent on energy expenditure and high intensity exercise elicits the largest energy expenditure. Thus, training at Fatmax intensity may not confer further weight-loss benefit than other training interventions performed at higher exercise intensities.
Exercise Duration
The contribution of FA to fuel the contracting muscle also depends on exercise duration. Studies from different groups have shown that FA oxidation gradually increases during a prolonged exercise bout while CHO oxidation decreases (Ravussin et al., 1986; Klein et al., 1994). This goes along with an increase of lipolysis with exercise duration (de Glisezinski et al., 2003; Lafontan et al., 2008). Interestingly, it has been shown that the activity of muscle HSL decreases during a prolonged exercise bout (Watt et al., 2003). This is a consequence of the increased uptake of circulating FA by muscle fibers, which in turn decreases lipolysis and oxidation of IMTG stores. The increase of WAT lipolysis is mostly due to the increase of plasma levels of pro-lipolytic hormones during prolonged exercise. Indeed, catecholamines secretion increases as a function of exercise duration. This increase is more pronounced for epinephrine than for norepinephrine, probably due to a slightly lower glycemia (de Glisezinski et al., 2003) and to the fact that norepinephrine secretion is mostly impacted by exercise intensity (Leuenberger et al., 1993). In line with this observation, we have previously demonstrated that epinephrine is the main beta-adrenergic agent contributing to exercise-induced lipolysis in SCAT (de Glisezinski et al., 2009). We have shown that this increase of adipocyte lipolysis is not only dependent on the beta-adrenergic stimulation by catecholamines but also on the reduction of plasma insulin level and the increase of plasma ANP (Arner et al., 1990; Moro et al., 2004). For instance, ANP plasma level was found to be particularly high after running a marathon, and could participate in the activation of WAT lipolysis to compensate the acute elevation of energy demand during long-distance running (Niessner et al., 2003).
Finally, the whole energy expenditure elicited by exercise has also to be taken into account when considering the contribution of FA burned in response to exercise, as a high percentage does not always reflect a large amount of FA burned if the energy expenditure elicited by the exercise bout is low. Exercise energy expenditure is linked to both exercise intensity and duration.
Impact of Osbesity
Importantly, we and others have observed that exercise-induced SCAT lipolysis is lower in obese subjects than in non-obese subjects (Stich et al., 2000; Mittendorfer et al., 2004; Ross and Bradshaw, 2009). This was attributed to a higher sensitivity of anti-lipolytic alpha2-adrenergic receptors and a lower sensitivity of pro-lipolytic beta-adrenergic receptors in obese subjects (Stich et al., 2000). However, due to the higher fat mass in obese versus non-obese individuals, plasma FA concentration was higher in obese individuals both at rest and during exercise (Stich et al., 2000). In addition, the expression of the ANP clearance receptor NPRC is higher in adipocytes from obese subjects than in lean healthy individuals, and could participate in a lower lipolysis activation in response to ANP secretion during exercise (Dessi-Fulgheri et al., 2003; Kovacova et al., 2016; Ryden et al., 2016). Thus, while basal lipolytic rate is higher in obese vs non-obese subjects, exercise-induced lipolysis is reduced in obese subjects. This adaptive response in obesity could be seen as a protective mechanism to avoid excessive release of FA into the bloodstream during an exercise bout.
Increased Lipolysis During Post-Exercise Recovery
The relationship between exercise intensity and FA oxidation, and therefore FA release from WAT lipolysis, is not as straightforward as initially thought. The role of FA as nutrients during post-exercise recovery has been described in a recent review by Bente Kiens’ group (Lundsgaard et al., 2020). Briefly, even if high-intensity exercise (i.e., performed at an intensity over 75% of the subject’s maximal aerobic power) elicits a low FA oxidation rate during the exercise bout, the post-exercise FA utilization is higher than after a low intensity exercise bout (Pillard et al., 2010). This greater FA oxidation after a high-intensity exercise bout is mainly reflected by a decrease of the respiratory quotient (Marion-Latard et al., 2003) and appears independent of energy expenditure during 6 h post-exercise. This is a consequence of the preferential use of CHO to replenish muscle glycogen stores which have been depleted during the high-intensity exercise bout, which favors FA as major fuels during 24–48 h after the exercise bout (Tremblay et al., 1994; Kiens and Richter, 1998). We have previously shown in isolated adipocytes that, after a long-duration exercise bout, the WAT displays an increased responsiveness to beta-adrenergic lipolytic agents, which may participate to the increased FA availability during the recovery period (Harant et al., 2002). Strikingly, this increase in post-exercise FA consumption is more pronounced in men than in women (Henderson et al., 2007). In addition, using stable isotope-labeled palmitate infusion, Magkos et al. (2009) have observed that the exercise-induced increase of FA utilization during the post-exercise recovery period is greater in subjects with a low resting plasma FA availability and is greater after an exercise resulting in high energy demand. Interestingly, it has been demonstrated that post-exercise lipolysis is stimulated in the SCAT by an increase of plasma growth hormone level, which is secreted by somatotropic cells during the exercise bout (Enevoldsen et al., 2007). A recent study performed in mice also evoked a role of IL-6, a myokine secreted by skeletal muscle fibers during exercise, in the regulation of WAT lipid metabolism during the exercise recovery (Knudsen et al., 2017).
In summary, it appears critical to consider the post-exercise recovery period to fully assess the impact of different exercise modalities on FA utilization and thus body weight loss.
Effect of Exercise Training on Adipose Tissue Lipolysis
Exercise training improves FA mobilization during an exercise bout. Indeed, it has been shown that FA appearance rate (Ra) in the blood is higher in endurance trained subjects compared to sedentary controls (Coggan et al., 2000). Exercise training affects both the sensitivity of WAT to catecholamines, but also their secretion during exercise, which is reduced in response to a given absolute workload after training (Kjaer et al., 1987; Riviere et al., 1989; Arner, 1995). Transversal studies performed on SCAT adipocytes have suggested that beta-adrenergic sensitivity is higher in trained subjects than in sedentary controls (Crampes et al., 1986; Crampes et al., 1989; Riviere et al., 1989). In addition, longitudinal studies have demonstrated that endurance training improves the beta-adrenergic lipolytic response of isolated adipocytes in obese subjects (De Glisezinski et al., 1998a; Moro et al., 2009).
Furthermore, exercise training improves ANP responsiveness in obese subjects, but it is yet unclear whether this is due to an increase of ANP plasma concentration or to an increase of ANP receptors on the adipocyte cell surface (Moro et al., 2005). Indeed, we were able to show through in situ microdialysis experiments in SCAT of young overweight men, that 4 months of aerobic training improve both beta-adrenergic and ANP lipolytic responses (Stich et al., 1999; Moro et al., 2005). Finally, insulin concentration decreases with training status but the impact on WAT lipolysis is partly counterbalanced by an improvement of WAT insulin sensitivity with exercise training (Polak et al., 2005; Riis et al., 2019). Strikingly, even if exercise-induced lipolysis is higher in trained subjects, plasma FA concentration is lower both at rest and during exercise (Crampes et al., 2003; de Glisezinski et al., 2003). This could be explained by an increase of FA utilization by skeletal muscle in trained subjects. Indeed, the amount of both resting and exercise-induced FA oxidation is higher after a training program, resulting in an increased oxygen consumption (de Glisezinski et al., 2003). The improvement of exercise-induced lipolysis observed in endurance-trained obese subjects also seems to be partially due to a reduction of the anti-lipolytic effect of alpha2-adrenergic receptors in the SCAT, which may be a consequence of a lower epinephrine plasma levels, the main alpha2-adrenergic ligand. Indeed, the anti-lipolytic activity of alpha2-adrenergic receptors was reduced after endurance training in lean and obese subjects (De Glisezinski et al., 2001; Richterova et al., 2004). Interestingly, similar adaptations of WAT lipolytic response have been found after a resistance training program in obese individuals (Polak et al., 2005).
Finally, it has been observed that the exercise intensity which elicits the higher lipolytic rate is increased with exercise training (Perez-Martin et al., 2001; Achten et al., 2002). Thus, while the maximal FA utilization is reached at intensities of 30% of maximal aerobic power in sedentary subjects, it is achieved around 65% in trained individuals. This means that the total amount of FA mobilized during an exercise bout is higher in trained subjects because both energy expenditure and the percentage of FA used are increased. In addition, high intensity training elicits a gain of muscle mass which impacts basal metabolic rate and thus may increase energy expenditure and consequently impact FA oxidation during resting periods and body weight loss (Heydari et al., 2012; Osawa et al., 2014; Schubert et al., 2017; Batrakoulis et al., 2018).
Altogether, these data suggest that an exercise training program combining high-intensity and moderate intensity exercise bouts could optimize daily FA utilization and optimize body weight loss in overweight or obese individuals.
Impact of Diet and Time of the Day on Exercise-Induced Lipolysis
Carbohydrates availability influences exercise-induced lipolysis. Indeed, glucose ingestion during an exercise bout reduces SCAT lipolysis and partially inhibits FA oxidation (De Glisezinski et al., 1998b). Exercising in the fasting state has been shown to increase FA oxidation and whole-body lipolysis in healthy subjects (Vicente-Salar et al., 2015; Andersson Hall et al., 2016; Hansen et al., 2017). This appears to be a compelling approach to achieve maximal fat utilization during exercise. Interestingly, a recent study has shown that exercising after a high-protein breakfast has similar effects on lipolysis than exercising in the fasting state (Saghebjoo et al., 2020). Furthermore, volunteers fed for 5 days with a high-fat diet display a higher WAT lipolytic rate during exercise than people fed with a CHO-rich diet, which can be explained by a higher catecholamine response and lower insulinemia (Suljkovicova et al., 2002).
Numerous review articles have described the impact of time of the day on exercise efficiency, but very few focused on lipid metabolism and WAT lipolysis (Chtourou and Souissi, 2012; Seo et al., 2013; Dollet and Zierath, 2019; Parr et al., 2020). A few studies have shown that exercise performed during the evening elicits a higher reliance on lipids compared to exercise performed during the morning (Aoyama and Shibata, 2020). In addition, a crossover study performed in young men has demonstrated that an endurance exercise bout performed during the evening enhances plasma epinephrine, IL-6 and plasma FA levels compared to the same exercise performed during the morning, thus suggesting that evening exercise is the most effective to achieve high rates of WAT lipolysis (Kim et al., 2015). However, data are still scarce and future studies should be performed to fully address this question.
Calorie Restriction and Exercise Induced Weight Loss
Many studies have shown that calorie restriction is more efficient at reducing body weight than exercise training, and that combining exercise training with a caloric restriction intervention confers a slight additional benefit to achieve weight loss compared to calorie restriction alone (Miller et al., 1997; Swift et al., 2018). However, exercise has an important role in body weight maintenance after weight loss (Swift et al., 2018). Indeed, calorie restriction-induced weight loss increases WAT sensitivity to lipolytic stimuli produced during exercise (Mauriege et al., 1999). Furthermore, exercise protects against loss of lean body mass during calorie restriction, and avoids a drop of resting metabolic rate (Chomentowski et al., 2009).
Therefore, even if combining exercise to a calorie restriction intervention does not achieve further weight loss than calorie restriction alone, exercise potentiates visceral fat mass loss and a sustained improvement of body composition (You et al., 2006), and prevents from the well-described “yo-yo” effect of dieting.
Current Gaps in Research
There are many additional questions that remains to be answered to fully understand the impact of exercise on WAT lipolysis and body composition. Indeed, future studies should aim at identifying unknown lipolytic factors secreted during exercise, such as myokines and potentially micro-RNAs released in extracellular vesicles in response to muscle contraction (Whitham et al., 2018). Understanding the complex inter-organ crosstalk during exercise will pave the way to new areas of research and could lead to the discovery of new molecular players with a potential therapeutic role.
Finally, research efforts should also focus on refining exercise training modalities to achieve a maximal and sustained improvement in body composition, especially in overweight or obese individuals. Assessing the combination of time-restricted eating patterns with exercise training sessions performed during the fasting state could be an attractive approach to potentiate fat mass loss.
Conclusion
Collectively, there is little debate that exercise training facilitates abdominal weight loss in overweight and obese individuals. Chronic exercise has largely demonstrated its ability to facilitate weight loss during calorie restriction and maintenance of long-term weight loss. A number of studies suggest that combining moderate and high intensity exercise can provide additional benefits on weight loss, at least in part, by favoring higher rates of energy expenditure during exercise and greater FA oxidation rates during post-exercise recovery. Although canonical lipolytic systems and hormones have been studied in detail during the past 30 years, more recent studies uncovered a muscle-adipose tissue crosstalk mediated by myokines regulating WAT lipolysis. However, much remains to be discovered. With the discovery that contracting muscles can produce myokines capable of remotely targeting organs, including WAT, our current knowledge will likely be challenged in the next few years.
Author Contributions
CL and CM wrote and revised the manuscript. IG, IH, and DL edited and revised the manuscript. All authors contributed to the article and approved the submitted version.
Conflict of Interest
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Acknowledgments
We are very grateful to Dr. François Crampes for his contribution to the aforementioned studies, for outstanding discussion and critical reading of the manuscript.
References
Achten, J., Gleeson, M., and Jeukendrup, A. E. (2002). Determination of the exercise intensity that elicits maximal fat oxidation. Med. Sci. Sports Exerc. 34, 92–97. doi: 10.1097/00005768-200201000-00015
Andersson Hall, U., Edin, F., Pedersen, A., and Madsen, K. (2016). Whole-body fat oxidation increases more by prior exercise than overnight fasting in elite endurance athletes. Appl. Physiol. Nutr. Metab. 41, 430–437. doi: 10.1139/apnm-2015-0452
Aoyama, S., and Shibata, S. (2020). Time-of-day-dependent physiological responses to meal and exercise. Front. Nutr. 7:18. doi: 10.3389/fnut.2020.00018
Arner, P. (1995). Impact of exercise on adipose tissue metabolism in humans. Int. J. Obes Relat. Metab. Disord. 19(Suppl. 4), S18–S21.
Arner, P., Kriegholm, E., Engfeldt, P., and Bolinder, J. (1990). Adrenergic regulation of lipolysis in situ at rest and during exercise. J. Clin. Invest. 85, 893–898. doi: 10.1172/jci114516
Batrakoulis, A., Jamurtas, A. Z., Georgakouli, K., Draganidis, D., Deli, C. K., Papanikolaou, K., et al. (2018). High intensity, circuit-type integrated neuromuscular training alters energy balance and reduces body mass and fat in obese women: a 10-month training-detraining randomized controlled trial. PLoS One 13:e0202390. doi: 10.1371/journal.pone.0202390
Bostrom, P., Wu, J., Jedrychowski, M. P., Korde, A., Ye, L., Lo, J. C., et al. (2012). A PGC1-alpha-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature 481, 463–468.
Brooks, G. A., and Mercier, J. (1994). Balance of carbohydrate and lipid utilization during exercise: the “crossover” concept. J. Appl. Physiol. 76, 2253–2261. doi: 10.1152/jappl.1994.76.6.2253
Chomentowski, P., Dube, J. J., Amati, F., Stefanovic-Racic, M., Zhu, S., Toledo, F. G., et al. (2009). Moderate exercise attenuates the loss of skeletal muscle mass that occurs with intentional caloric restriction-induced weight loss in older, overweight to obese adults. J. Gerontol A Biol. Sci. Med. Sci. 64, 575–580. doi: 10.1093/gerona/glp007
Chtourou, H., and Souissi, N. (2012). The effect of training at a specific time of day: a review. J. Strength Cond. Res. 26, 1984–2005. doi: 10.1519/jsc.0b013e31825770a7
Coggan, A. R., Raguso, C. A., Gastaldelli, A., Sidossis, L. S., and Yeckel, C. W. (2000). Fat metabolism during high-intensity exercise in endurance-trained and untrained men. Metabolism 49, 122–128. doi: 10.1016/s0026-0495(00)90963-6
Crampes, F., Beauville, M., Riviere, D., and Garrigues, M. (1986). Effect of physical training in humans on the response of isolated fat cells to epinephrine. J. Appl. Physiol. 61, 25–29. doi: 10.1152/jappl.1986.61.1.25
Crampes, F., Marion-Latard, F., Zakaroff-Girard, A., De Glisezinski, I., Harant, I., Thalamas, C., et al. (2003). Effects of a longitudinal training program on responses to exercise in overweight men. Obes Res. 11, 247–256. doi: 10.1038/oby.2003.38
Crampes, F., Riviere, D., Beauville, M., Marceron, M., and Garrigues, M. (1989). Lipolytic response of adipocytes to epinephrine in sedentary and exercise-trained subjects: sex-related differences. Eur. J. Appl. Physiol. Occup. Physiol. 59, 249–255. doi: 10.1007/bf02388324
De Glisezinski, I., Crampes, F., Harant, I., Berlan, M., Hejnova, J., Langin, D., et al. (1998a). Endurance training changes in lipolytic responsiveness of obese adipose tissue. Am. J. Physiol. 275, E951–E956.
De Glisezinski, I., Harant, I., Crampes, F., Trudeau, F., Felez, A., Cottet-Emard, J. M., et al. (1998b). Effect of carbohydrate ingestion on adipose tissue lipolysis during long-lasting exercise in trained men. J. Appl. Physiol. 84, 1627–1632. doi: 10.1152/jappl.1998.84.5.1627
de Glisezinski, I., Larrouy, D., Bajzova, M., Koppo, K., Polak, J., Berlan, M., et al. (2009). Adrenaline but not noradrenaline is a determinant of exercise-induced lipid mobilization in human subcutaneous adipose tissue. J. Physiol. 587(Pt 13), 3393–3404. doi: 10.1113/jphysiol.2009.168906
De Glisezinski, I., Marion-Latard, F., Crampes, F., Berlan, M., Hejnova, J., Cottet-Emard, J. M., et al. (2001). Lack of alpha(2)-adrenergic antilipolytic effect during exercise in subcutaneous adipose tissue of trained men. J. Appl. Physiol. 91, 1760–1765. doi: 10.1152/jappl.2001.91.4.1760
de Glisezinski, I., Moro, C., Pillard, F., Marion-Latard, F., Harant, I., Meste, M., et al. (2003). Aerobic training improves exercise-induced lipolysis in SCAT and lipid utilization in overweight men. Am. J. Physiol. Endocrinol. Metab. 285, E984–E990.
Dessi-Fulgheri, P., Sarzani, R., and Rappelli, A. (2003). Role of the natriuretic peptide system in lipogenesis/lipolysis. Nutr. Metab. Cardiovasc. Dis. 13, 244–249. doi: 10.1016/s0939-4753(03)80018-2
Dollet, L., and Zierath, J. R. (2019). Interplay between diet, exercise and the molecular circadian clock in orchestrating metabolic adaptations of adipose tissue. J. Physiol. 597, 1439–1450. doi: 10.1113/jp276488
Enevoldsen, L. H., Polak, J., Simonsen, L., Hammer, T., Macdonald, I., Crampes, F., et al. (2007). Post-exercise abdominal, subcutaneous adipose tissue lipolysis in fasting subjects is inhibited by infusion of the somatostatin analogue octreotide. Clin. Physiol. Funct. Imaging 27, 320–326. doi: 10.1111/j.1475-097x.2007.00754.x
Evans, P. L., McMillin, S. L., Weyrauch, L. A., and Witczak, C. A. (2019). Regulation of skeletal muscle glucose transport and glucose metabolism by exercise training. Nutrients 11:2432. doi: 10.3390/nu11102432
Hansen, D., De Strijcker, D., and Calders, P. (2017). Impact of endurance exercise training in the fasted state on muscle biochemistry and metabolism in healthy subjects: can these effects be of particular clinical benefit to type 2 diabetes mellitus and insulin-resistant patients? Sports Med. 47, 415–428. doi: 10.1007/s40279-016-0594-x
Harant, I., Marion-Latard, F., Crampes, F., de Glisezinski, I., Berlan, M., Stich, V., et al. (2002). Effect of a long-duration physical exercise on fat cell lipolytic responsiveness to adrenergic agents and insulin in obese men. Int. J. Obes Relat. Metab. Disord. 26, 1373–1378. doi: 10.1038/sj.ijo.0802072
Henderson, G. C., Fattor, J. A., Horning, M. A., Faghihnia, N., Johnson, M. L., Mau, T. L., et al. (2007). Lipolysis and fatty acid metabolism in men and women during the postexercise recovery period. J. Physiol. 584(Pt 3), 963–981. doi: 10.1113/jphysiol.2007.137331
Heydari, M., Freund, J., and Boutcher, S. H. (2012). The effect of high-intensity intermittent exercise on body composition of overweight young males. J. Obes 2012:480467.
Horowitz, J. F. (2003). Fatty acid mobilization from adipose tissue during exercise. Trends Endocrinol. Metab. 14, 386–392. doi: 10.1016/s1043-2760(03)00143-7
Horowitz, J. F., and Klein, S. (2000). Lipid metabolism during endurance exercise. Am. J. Clin. Nutr. 72(2 Suppl.), 558S–563S.
Hsu, K. J., Liao, C. D., Tsai, M. W., and Chen, C. N. (2019). Effects of exercise and nutritional intervention on body composition, metabolic health, and physical performance in adults with sarcopenic obesity: a meta-analysis. Nutrients 11:2163. doi: 10.3390/nu11092163
Imbeault, P., Tremblay, A., Despres, J., and Mauriege, P. (2000). beta-adrenoceptor-stimulated lipolysis of subcutaneous abdominal adipocytes as a determinant of fat oxidation in obese men. Eur. J. Clin. Invest. 30, 290–296. doi: 10.1046/j.1365-2362.2000.00634.x
Jensen, M. D., and Johnson, C. M. (1996). Contribution of leg and splanchnic free fatty acid (FFA) kinetics to postabsorptive FFA flux in men and women. Metabolism 45, 662–666. doi: 10.1016/s0026-0495(96)90040-2
Jeukendrup, A. E., and Wallis, G. A. (2005). Measurement of substrate oxidation during exercise by means of gas exchange measurements. Int. J. Sports Med. 26(Suppl. 1), S28–S37.
Kiens, B., and Lithell, H. (1989). Lipoprotein metabolism influenced by training-induced changes in human skeletal muscle. J. Clin. Invest. 83, 558–564. doi: 10.1172/jci113918
Kiens, B., and Richter, E. A. (1998). Utilization of skeletal muscle triacylglycerol during postexercise recovery in humans. Am. J. Physiol. 275, E332–E337.
Kim, H. K., Konishi, M., Takahashi, M., Tabata, H., Endo, N., Numao, S., et al. (2015). Effects of acute endurance exercise performed in the morning and evening on inflammatory cytokine and metabolic hormone responses. PLoS One 10:e0137567. doi: 10.1371/journal.pone.0137567
Kjaer, M., Secher, N. H., and Galbo, H. (1987). Physical stress and catecholamine release. Baillieres Clin. Endocrinol. Metab. 1, 279–298. doi: 10.1016/s0950-351x(87)80064-2
Klein, S., Coyle, E. F., and Wolfe, R. R. (1994). Fat metabolism during low-intensity exercise in endurance-trained and untrained men. Am. J. Physiol. 267(6 Pt 1), E934–E940.
Knudsen, J. G., Gudiksen, A., Bertholdt, L., Overby, P., Villesen, I., Schwartz, C. L., et al. (2017). Skeletal muscle IL-6 regulates muscle substrate utilization and adipose tissue metabolism during recovery from an acute bout of exercise. PLoS One 12:e0189301. doi: 10.1371/journal.pone.0189301
Koppo, K., Larrouy, D., Marques, M. A., Berlan, M., Bajzova, M., Polak, J., et al. (2010). Lipid mobilization in subcutaneous adipose tissue during exercise in lean and obese humans. Roles of insulin and natriuretic peptides. Am. J. Physiol. Endocrinol. Metab. 299, E258–E265.
Kovacova, Z., Tharp, W. G., Liu, D., Wei, W., Xie, H., Collins, S., et al. (2016). Adipose tissue natriuretic peptide receptor expression is related to insulin sensitivity in obesity and diabetes. Obesity 24, 820–828. doi: 10.1002/oby.21418
Krauzova, E., Tuma, P., de Glisezinski, I., Stich, V., and Siklova, M. (2018). Metformin does not inhibit exercise-induced lipolysis in adipose tissue in young healthy lean men. Front. Physiol. 9:604. doi: 10.3389/fphys.2018.00604
Lafontan, M., Moro, C., Berlan, M., Crampes, F., Sengenes, C., and Galitzky, J. (2008). Control of lipolysis by natriuretic peptides and cyclic GMP. Trends Endocrinol. Metab. 19, 130–137. doi: 10.1016/j.tem.2007.11.006
Laurens, C., Parmar, A., Murphy, E., Carper, D., Lair, B., Maes, P., et al. (2020). Growth and differentiation factor 15 is secreted by skeletal muscle during exercise and promotes lipolysis in humans. JCI Insight 5:e131870.
Lehnig, A. C., and Stanford, K. I. (2018). Exercise-induced adaptations to white and brown adipose tissue. J. Exp. Biol. 221(Pt Suppl. 1):jeb161570. doi: 10.1242/jeb.161570
Leibel, R. L., and Hirsch, J. (1987). Site- and sex-related differences in adrenoreceptor status of human adipose tissue. J. Clin. Endocrinol. Metab. 64, 1205–1210. doi: 10.1210/jcem-64-6-1205
Leuenberger, U., Sinoway, L., Gubin, S., Gaul, L., Davis, D., and Zelis, R. (1993). Effects of exercise intensity and duration on norepinephrine spillover and clearance in humans. J. Appl. Physiol. 75, 668–674. doi: 10.1152/jappl.1993.75.2.668
Lundsgaard, A. M., Fritzen, A. M., and Kiens, B. (2020). The importance of fatty acids as nutrients during post-exercise recovery. Nutrients 12:280. doi: 10.3390/nu12020280
Magkos, F., Mohammed, B. S., Patterson, B. W., and Mittendorfer, B. (2009). Free fatty acid kinetics in the late phase of postexercise recovery: importance of resting fatty acid metabolism and exercise-induced energy deficit. Metabolism 58, 1248–1255. doi: 10.1016/j.metabol.2009.03.023
Marion-Latard, F., Crampes, F., Zakaroff-Girard, A., De Glisezinski, I., Harant, I., Stich, V., et al. (2003). Post-exercise increase of lipid oxidation after a moderate exercise bout in untrained healthy obese men. Horm. Metab. Res. 35, 97–103. doi: 10.1055/s-2003-39051
Mauriege, P., Imbeault, P., Langin, D., Lacaille, M., Almeras, N., Tremblay, A., et al. (1999). Regional and gender variations in adipose tissue lipolysis in response to weight loss. J. Lipid Res. 40, 1559–1571.
Miller, W. C., Koceja, D. M., and Hamilton, E. J. (1997). A meta-analysis of the past 25 years of weight loss research using diet, exercise or diet plus exercise intervention. Int. J. Obes Relat. Metab. Disord. 21, 941–947. doi: 10.1038/sj.ijo.0800499
Mittendorfer, B., Fields, D. A., and Klein, S. (2004). Excess body fat in men decreases plasma fatty acid availability and oxidation during endurance exercise. Am. J. Physiol. Endocrinol. Metab. 286, E354–E362.
Moro, C., Crampes, F., Sengenes, C., De Glisezinski, I., Galitzky, J., Thalamas, C., et al. (2004). Atrial natriuretic peptide contributes to physiological control of lipid mobilization in humans. FASEB J. 18, 908–910. doi: 10.1096/fj.03-1086fje
Moro, C., Harant, I., Badin, P. M., Patarca, F. X., Guilland, J. C., Bourlier, V., et al. (2014). Influence of lipolysis and fatty acid availability on fuel selection during exercise. J. Physiol. Biochem. 70, 583–591.
Moro, C., Pasarica, M., Elkind-Hirsch, K., and Redman, L. M. (2009). Aerobic exercise training improves atrial natriuretic peptide and catecholamine-mediated lipolysis in obese women with polycystic ovary syndrome. J. Clin. Endocrinol. Metab. 94, 2579–2586. doi: 10.1210/jc.2009-0051
Moro, C., Pillard, F., de Glisezinski, I., Crampes, F., Thalamas, C., Harant, I., et al. (2007). Sex differences in lipolysis-regulating mechanisms in overweight subjects: effect of exercise intensity. Obesity 15, 2245–2255. doi: 10.1038/oby.2007.267
Moro, C., Pillard, F., De Glisezinski, I., Harant, I., Riviere, D., Stich, V., et al. (2005). Training enhances ANP lipid-mobilizing action in adipose tissue of overweight men. Med. Sci. Sports Exerc. 37, 1126–1132. doi: 10.1249/01.mss.0000170124.51659.52
Moro, C., Pillard, F., de Glisezinski, I., Klimcakova, E., Crampes, F., Thalamas, C., et al. (2008). Exercise-induced lipid mobilization in subcutaneous adipose tissue is mainly related to natriuretic peptides in overweight men. Am. J. Physiol. Endocrinol. Metab. 295, E505–E513.
Moro, C., Polak, J., Hejnova, J., Klimcakova, E., Crampes, F., Stich, V., et al. (2006). Atrial natriuretic peptide stimulates lipid mobilization during repeated bouts of endurance exercise. Am. J. Physiol. Endocrinol. Metab. 290, E864–E869.
Nielsen, S., Guo, Z., Johnson, C. M., Hensrud, D. D., and Jensen, M. D. (2004). Splanchnic lipolysis in human obesity. J. Clin. Invest. 113, 1582–1588. doi: 10.1172/jci21047
Niessner, A., Ziegler, S., Slany, J., Billensteiner, E., Woloszczuk, W., and Geyer, G. (2003). Increases in plasma levels of atrial and brain natriuretic peptides after running a marathon: are their effects partly counterbalanced by adrenocortical steroids? Eur. J. Endocrinol. 149, 555–559. doi: 10.1530/eje.0.1490555
Norheim, F., Langleite, T. M., Hjorth, M., Holen, T., Kielland, A., Stadheim, H. K., et al. (2014). The effects of acute and chronic exercise on PGC-1alpha, irisin and browning of subcutaneous adipose tissue in humans. FEBS J. 281, 739–749. doi: 10.1111/febs.12619
Osawa, Y., Azuma, K., Tabata, S., Katsukawa, F., Ishida, H., Oguma, Y., et al. (2014). Effects of 16-week high-intensity interval training using upper and lower body ergometers on aerobic fitness and morphological changes in healthy men: a preliminary study. Open Access J. Sports Med. 5, 257–265. doi: 10.2147/oajsm.s68932
Parr, E. B., Heilbronn, L. K., and Hawley, J. A. (2020). A time to eat and a time to exercise. Exerc. Sport Sci. Rev. 48, 4–10. doi: 10.1249/jes.0000000000000207
Pedersen, B. K., Steensberg, A., and Schjerling, P. (2001). Exercise and interleukin-6. Curr. Opin. Hematol. 8, 137–141.
Perez-Martin, A., Dumortier, M., Raynaud, E., Brun, J. F., Fedou, C., Bringer, J., et al. (2001). Balance of substrate oxidation during submaximal exercise in lean and obese people. Diabetes Metab. 27(4 Pt 1), 466–474.
Peterson, M. D., Sen, A., and Gordon, P. M. (2011). Influence of resistance exercise on lean body mass in aging adults: a meta-analysis. Med. Sci. Sports Exerc. 43, 249–258. doi: 10.1249/mss.0b013e3181eb6265
Petridou, A., Chatzinikolaou, A., Avloniti, A., Jamurtas, A., Loules, G., Papassotiriou, I., et al. (2017). Increased triacylglycerol lipase activity in adipose tissue of lean and obese men during endurance exercise. J. Clin. Endocrinol. Metab. 102, 3945–3952. doi: 10.1210/jc.2017-00168
Pierce, J. R., Maples, J. M., and Hickner, R. C. (2015). IL-15 concentrations in skeletal muscle and subcutaneous adipose tissue in lean and obese humans: local effects of IL-15 on adipose tissue lipolysis. Am. J. Physiol. Endocrinol. Metab. 308, E1131–E1139.
Pillard, F., Van Wymelbeke, V., Garrigue, E., Moro, C., Crampes, F., Guilland, J. C., et al. (2010). Lipid oxidation in overweight men after exercise and food intake. Metabolism 59, 267–274. doi: 10.1016/j.metabol.2009.07.023
Polak, J., Moro, C., Klimcakova, E., Hejnova, J., Majercik, M., Viguerie, N., et al. (2005). Dynamic strength training improves insulin sensitivity and functional balance between adrenergic alpha 2A and beta pathways in subcutaneous adipose tissue of obese subjects. Diabetologia 48, 2631–2640. doi: 10.1007/s00125-005-0003-8
Ravussin, E., Bogardus, C., Scheidegger, K., LaGrange, B., Horton, E. D., and Horton, E. S. (1986). Effect of elevated FFA on carbohydrate and lipid oxidation during prolonged exercise in humans. J. Appl. Physiol. 60, 893–900. doi: 10.1152/jappl.1986.60.3.893
Reihmane, D., and Dela, F. (2014). Interleukin-6: possible biological roles during exercise. Eur. J. Sport Sci. 14, 242–250. doi: 10.1080/17461391.2013.776640
Richterova, B., Stich, V., Moro, C., Polak, J., Klimcakova, E., Majercik, M., et al. (2004). Effect of endurance training on adrenergic control of lipolysis in adipose tissue of obese women. J. Clin. Endocrinol. Metab. 89, 1325–1331. doi: 10.1210/jc.2003-031001
Riis, S., Christensen, B., Nellemann, B., Moller, A. B., Husted, A. S., Pedersen, S. B., et al. (2019). Molecular adaptations in human subcutaneous adipose tissue after ten weeks of endurance exercise training in healthy males. J. Appl Physiol. 126, 569–577. doi: 10.1152/japplphysiol.00989.2018
Riviere, D., Crampes, F., Beauville, M., and Garrigues, M. (1989). Lipolytic response of fat cells to catecholamines in sedentary and exercise-trained women. J. Appl. Physiol. 66, 330–335. doi: 10.1152/jappl.1989.66.1.330
Romijn, J. A., Coyle, E. F., Sidossis, L. S., Gastaldelli, A., Horowitz, J. F., Endert, E., et al. (1993). Regulation of endogenous fat and carbohydrate metabolism in relation to exercise intensity and duration. Am. J. Physiol. 265(3 Pt 1), E380–E391.
Ross, R., and Bradshaw, A. J. (2009). The future of obesity reduction: beyond weight loss. Nat. Rev. Endocrinol. 5, 319–325. doi: 10.1038/nrendo.2009.78
Ryden, M., Backdahl, J., Petrus, P., Thorell, A., Gao, H., Coue, M., et al. (2016). Impaired atrial natriuretic peptide-mediated lipolysis in obesity. Int. J. Obes 40, 714–720. doi: 10.1038/ijo.2015.222
Saghebjoo, M., Kargar-Akbariyeh, N., Mohammadnia-Ahmadi, M., and Saffari, I. (2020). How to exercise to increase lipolysis and insulin sensitivity: fasting or following a single high-protein breakfast. J. Sports Med. Phys. Fitness 60, 625–633.
Schubert, M. M., Clarke, H. E., Seay, R. F., and Spain, K. K. (2017). Impact of 4 weeks of interval training on resting metabolic rate, fitness, and health-related outcomes. Appl. Physiol. Nutr. Metab. 42, 1073–1081. doi: 10.1139/apnm-2017-0268
Seo, D. Y., Lee, S., Kim, N., Ko, K. S., Rhee, B. D., Park, B. J., et al. (2013). Morning and evening exercise. Integr. Med. Res. 2, 139–144.
Stanford, K. I., Middelbeek, R. J., and Goodyear, L. J. (2015). Exercise effects on white adipose tissue: beiging and metabolic adaptations. Diabetes 64, 2361–2368. doi: 10.2337/db15-0227
Stich, V., De Glisezinski, I., Crampes, F., Hejnova, J., Cottet-Emard, J. M., Galitzky, J., et al. (2000). Activation of alpha(2)-adrenergic receptors impairs exercise-induced lipolysis in SCAT of obese subjects. Am. J. Physiol. Regul. Integr. Comp. Physiol. 279, R499–R504.
Stich, V., de Glisezinski, I., Galitzky, J., Hejnova, J., Crampes, F., Riviere, D., et al. (1999). Endurance training increases the beta-adrenergic lipolytic response in subcutaneous adipose tissue in obese subjects. Int. J. Obes Relat. Metab. Disord. 23, 374–381. doi: 10.1038/sj.ijo.0800829
Stoner, L., Rowlands, D., Morrison, A., Credeur, D., Hamlin, M., Gaffney, K., et al. (2016). Efficacy of exercise intervention for weight loss in overweight and obese adolescents: meta-analysis and implications. Sports Med. 46, 1737–1751. doi: 10.1007/s40279-016-0537-6
Suljkovicova, H., Marion-Latard, F., Hejnova, J., Majercik, M., Crampes, F., De Glisezinski, I., et al. (2002). Effect of macronutrient composition of the diet on the regulation of lipolysis in adipose tissue at rest and during exercise: microdialysis study. Metabolism 51, 1291–1297. doi: 10.1053/meta.2002.35190
Swift, D. L., McGee, J. E., Earnest, C. P., Carlisle, E., Nygard, M., and Johannsen, N. M. (2018). The effects of exercise and physical activity on weight loss and maintenance. Prog. Cardiovasc. Dis. 61, 206–213.
Tremblay, A., Simoneau, J. A., and Bouchard, C. (1994). Impact of exercise intensity on body fatness and skeletal muscle metabolism. Metabolism 43, 814–818. doi: 10.1016/0026-0495(94)90259-3
Trujillo, M. E., Sullivan, S., Harten, I., Schneider, S. H., Greenberg, A. S., and Fried, S. K. (2004). Interleukin-6 regulates human adipose tissue lipid metabolism and leptin production in vitro. J. Clin. Endocrinol. Metab. 89, 5577–5582. doi: 10.1210/jc.2004-0603
Verboven, K., Stinkens, R., Hansen, D., Wens, I., Frederix, I., Eijnde, B. O., et al. (2018). Adrenergically and non-adrenergically mediated human adipose tissue lipolysis during acute exercise and exercise training. Clin. Sci. 132, 1685–1698. doi: 10.1042/cs20180453
Viana, R. B., Naves, J. P. A., Coswig, V. S., de Lira, C. A. B., Steele, J., Fisher, J. P., et al. (2019). Is interval training the magic bullet for fat loss? A systematic review and meta-analysis comparing moderate-intensity continuous training with high-intensity interval training (HIIT). Br. J. Sports Med. 53, 655–664. doi: 10.1136/bjsports-2018-099928
Vicente-Salar, N., Urdampilleta Otegui, A., and Roche Collado, E. (2015). Endurance training in fasting conditions: biological adaptations and body weight management. Nutr. Hosp. 32, 2409–2420.
Watt, M. J., Heigenhauser, G. J., O’Neill, M., and Spriet, L. L. (2003). Hormone-sensitive lipase activity and fatty acyl-CoA content in human skeletal muscle during prolonged exercise. J. Appl. Physiol. 95, 314–321. doi: 10.1152/japplphysiol.01181.2002
Wedell-Neergaard, A. S., Lang Lehrskov, L., Christensen, R. H., Legaard, G. E., Dorph, E., Larsen, M. K., et al. (2019). Exercise-induced changes in visceral adipose tissue mass are regulated by IL-6 signaling: a randomized controlled trial. Cell Metab. 29, 844.e3–855.e3.
Wewege, M., van den Berg, R., Ward, R. E., and Keech, A. (2017). The effects of high-intensity interval training vs. moderate-intensity continuous training on body composition in overweight and obese adults: a systematic review and meta-analysis. Obes Rev. 18, 635–646. doi: 10.1111/obr.12532
Whitham, M., Parker, B. L., Friedrichsen, M., Hingst, J. R., Hjorth, M., Hughes, W. E., et al. (2018). Extracellular vesicles provide a means for tissue crosstalk during exercise. Cell Metab. 27, 237.e4–251.e4.
Wolfe, R. R., Shaw, J. H., and Durkot, M. J. (1985). Effect of sepsis on VLDL kinetics: responses in basal state and during glucose infusion. Am. J. Physiol. 248(6 Pt 1), E732–E740.
Wolsk, E., Mygind, H., Grondahl, T. S., Pedersen, B. K., and van Hall, G. (2010). IL-6 selectively stimulates fat metabolism in human skeletal muscle. Am. J. Physiol. Endocrinol. Metab. 299, E832–E840.
Keywords: adipose tissue, lipolysis, fatty acids, exercise, weight loss
Citation: Laurens C, de Glisezinski I, Larrouy D, Harant I and Moro C (2020) Influence of Acute and Chronic Exercise on Abdominal Fat Lipolysis: An Update. Front. Physiol. 11:575363. doi: 10.3389/fphys.2020.575363
Received: 23 June 2020; Accepted: 18 November 2020;
Published: 07 December 2020.
Edited by:
Jørgen Jensen, Norwegian School of Sport Sciences, NorwayReviewed by:
Céline Aguer, Institut du Savoir Montfort (ISM), CanadaHenning Bay Nielsen, Zealand University Hospital, University of Copenhagen, Denmark
Copyright © 2020 Laurens, de Glisezinski, Larrouy, Harant and Moro. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Cedric Moro, Q2VkcmljLk1vcm9AaW5zZXJtLmZy