Physical exercise has long been recognized as an effective and economic strategy to promote brain health in humans. The cellular and structural changes in the brains of exercised animals, including enhancements of neurogenesis and synaptogenesis, dendritic remodeling, and synaptic plasticity, have been considered as the key biological alterations accounting for exercise-elicited benefits to brain health. However, what transduces body movements into the above-mentioned changes remains largely unknown. Emerging theories indicate that physical activity triggers the release of various factors into the circulation from skeletal muscle (neurotrophins, myokines, and cytokines) and/or adipose tissue (adipokines). In this chapter, we review several of these molecules that are potentially implicated in this process, including neurotrophic factors (BDNF, IGF-1, and VEGF), adipokines (adiponectin and irisin), and myokines/cytokines (IL-15). The relationship, either causal or concomitant, between levels of these molecules (particularly in the blood) and brain function after exercise may help to identify biomarkers that can serve as objective indicators to evaluate exercise therapy on diseased or ageing brain. In addition, unmasking biomarkers may be instrumental in elucidating the mechanisms mediating exercise-induced brain health, thereby contributing to novel drug discovery for treatments to maintain brain health.
- brain health
- hippocampal plasticity
- physical exercise
With an ageing population worldwide, there is an increasing interest in interventions that allow for healthy ageing. Currently, physical exercise is the best known intervention that can effectively maintain or even enhance brain health. Physical exercise is beneficial to brain health and cognitive function, especially in elderly people . Clinical studies have demonstrated that more physical activity is associated with a lower risk of ageing-related neurodegenerative disorders, such as Alzheimer’s disease (AD)  and Parkinson’s disease (PD) . Owing to the heterogeneity of exercise
Effects of physical exercise on the brain are most apparent in the hippocampus, a brain region involved in learning and memory. Animal studies have indicated that physical exercise robustly improves hippocampal structural and functional plasticity by enhancing the generation of adult-born neurons (adult neurogenesis) in the hippocampal dentate gyrus (DG) [4, 5], increasing dendritic complexity and spine density [6-8], as well as promoting synaptic plasticity . It is thought that important mediators for these exercise-triggered beneficial effects include neurotrophic factor produced in the brain such as brain-derived neurotrophic factor (BDNF) , as well as factors secreted by peripheral organs, such as insulin-like growth factor 1 (IGF-1)  and vascular endothelial growth factor (VEGF) . In addition to these well-known factors, emerging evidence has suggested that many other peripheral molecules known to be induced by physical exercise may also affect brain health, particularly those secreted by skeletal muscle and/or adipose tissues, termed myokines (e.g., irisin), cytokines (e.g., interleukin-5 (IL-15)), and adipokines (e.g., adiponectin)(Figure 1).
Biomarkers are measurable indicators of normal biological and pathogenic states, as well as pharmacological responses to treatment intervention . They can be used for clinical assessment of treatment effect or disease state. The biomarker should be present at baseline and its levels should be changed in response to treatment or disease state such that its levels can be used to predict the ultimate response. The ideal biomarkers should be easy to measure and quantify, and most importantly, they should closely correlate with the parameters being measured. Unfortunately, there are no conclusions on any one of the biomarkers that can fulfill the characteristics so far. Multiple biomarkers are likely needed for measurements in clinical studies, since using multiple biomarkers may be able to increase sensitivity, specificity, and predictive abilities for clinical diagnosis . With the necessity to develop a biomarker panel to better evaluate exercise-induced cognitive enhancement, in this chapter, we first summarize the influences of physical exercise training on brain health, involving both animals and humans, and discuss the possible underlying mechanisms. Next, we summarize the effect of physical exercise on regulating potential peripheral biomarker candidates. Finally, we address the relationship between exercise-biomarkers and hippocampal plasticity with available literatures.
2. Beneficial effect of physical exercise on learning and memory in animals and humans
Extensive evidence from animal studies has reliably shown that the enhancement of adult-born neurons in the hippocampus, termed as hippocampal neurogenesis, may underlie the exercise-induced improvements on cognitive function. Seminal studies by van Praag and collaborators (1999) have shown that exercise in the form of wheel running not only increased hippocampal neurogenesis [4, 5], but also improved performance in the Morris water maze, and selectively increased the long-term potentiation (LTP) in the mouse DG . These initial studies showed that not only does physical activity upregulate hippocampal neurogenesis, but it can also improve the capacity for hippocampal neurons to undergo synaptic plasticity and facilitate hippocampal-dependent learning and memory behavior in the same animals. Three months of physical exercise in humans was correlated with the increased blood volume in the DG, as measured by functional magnetic resonance imaging (fMRI) and improved cognitive function . Exercise is indeed known to increase the cerebral blood flow , blood-brain-barrier permeability , and angiogenesis [17-20]. Given the relationship between angiogenesis and neurogenesis [21, 22], cognition improvement  following exercise can be interpreted as a result of increased hippocampal angiogenesis and therefore neurogenesis.
The beneficial effects of physical exercise on cognitive function imply that it may be used as a treatment to prevent of cognitive decline in age-related neurodegenerative diseases. Exercise has been shown to prevent a number of factors that decline with age, such as the decreases in hippocampal cell proliferation, neurogenesis , LTP, and neurotrophin levels . Moreover, in aged mice, physical exercise can enhance hippocampal-dependent learning . The benefits of exercise are not limited to midlife or aged adulthood, as rats submitted to a physical exercise regime during early postnatal development retained increases in hippocampal neurogenesis and improvement in spatial memory into their adult loves , highlighting the long-lasting benefits of physical exercise on brain plasticity throughout the lifespan .
Physical exercise has emerged in recent years as one of the most effective, affordable, and simple strategies for healthy aging, and therefore has the potential as a preventative treatment for cognitive decline associated with neurodegenerative diseases . A meta-analysis has shown that 1–12 months of exercise in healthy adults is associated with significant behavioral benefits including ameliorated memory, processing speed, and attention . Moreover, a regular exercise regime during not only adulthood , but also midlife  reduce the risk of developing dementia and preserve cognition later in life, which suggests that physical exercise may play a role in preventing age-related cognitive decline. In fact, a recent observational study has found a reduction in the risk of developing AD and other forms of dementia in individuals that exercise regularly, as opposed to those that did not engage in physical activity . Physical exercise is beneficial to cognition across the life span, with its most significant effect on cognitive tasks involving the prefrontal cortex and the hippocampus .
3. Mechanism of physical exercise-induced hippocampal plasticity
Animal studies have suggested that physical exercise increases structural (e.g., neurogenesis and dendritic remodeling) and functional plasticity (e.g., synaptic plasticity) in the hippocampus (Figure 2).
Running distance is used as the physical assessment of voluntary running in animal studies, where a positive correlation between running distance and levels of neurogenesis in the hippocampus have been reliably shown in the literature using mice [34-36]. However, running distance is not the only variable that can affect the exercise-induced increases in hippocampal neurogenesis. Additional factors such as the genetic background [34, 37], age of the animals [38, 39], whether the running is forced or voluntary [4, 40-42], whether the animals are housed alone or in a group , and the duration of the running regime  can all affect neurogenesis following exercise. While there is some variability among studies of exercise, increases in neurogenesis are consistently reported in the literature [4, 25, 45, 46]. Long-term wheel running (2–4 months) with female C57 mice significantly increases the process of neuronal survival and neurogenesis concomitant with enhanced synaptic plasticity and improved performance in the Morris water maze . Others have found that there appear to be discrete stages at which voluntary running affects cell proliferation and differentiation. Namely, voluntary running in adult male C56B/L mice results in an increase in proliferating cells that peaks at 3 days following short-term running, which returns to basal levels following running for 32  or 35 days . Meanwhile, significant increases in neuronal differentiation are only observed following 10 days of voluntary running . These data indicate that voluntary-running-induced increases in cell proliferation occurs during the earliest stages of running while a longer period of running promotes neuronal differentiation of adult-born cells.
3.2. Synaptic plasticity
Synaptic plasticity refers to changes in the way in which neurons communicate as a result of prior experience. Two forms of synaptic plasticity have been shown in the hippocampus, the LTP, where synaptic responses to a particular input are increased following a conditioning episode for memory formation, and the long-term depression (LTD), where synaptic responses to an input are decreased following a conditioning episode, which is recently implicated in memory clearance. The effects of exercise on
3.3. Dendritic remodeling and synaptogenesis
In addition to increasing neurogenesis in the DG, voluntary wheel running can promote increased dendritic complexity or spine density in hippocampal subregions including the DG, CA1, CA3, and entorhinal cortex (EC) subregions . Retroviral labeling of newborn neurons in the DG showed that voluntary running accelerates spine maturation with increased proportions of mushroom spines , which suggests that running may enhance the functional integration of newborn neurons into existing neuronal circuits. Moreover, voluntary wheel running increases both spine density and dendritic length of dentate granule cells . Particularly, running increases the proportion of cells with higher dendritic complexity . Two months of voluntary running also increase spine density in the CA1 subregion and layer III of the EC . However, a longer period of running may be needed to trigger structural changes in the CA3 region because running for 2 weeks increases spine density in the DG and CA1 regions, but not in the CA3 region . Increases of dendritic branching and spine density of CA3 pyramidal neurons are only observed after running for 4 weeks .
4. Potential biomarkers of physical exercise-promoted brain health
4.1. Neurotrophic factors
220.127.116.11. Animal studies
BDNF levels can be increased by exercise [56, 57], with the increase occurring as early as 2–7 days of running , and it remains elevated for the whole duration of running , even extending to an additional 2 weeks following the end of the running period . Increases in BDNF are important not only for the promotion of neurogenesis but also the enhancement of functional plasticity in the forms of LTP and behavioral learning and memory performance [5, 59, 60]. A direct link between BDNF and neurogenesis has been revealed by acutely knocking down BDNF in the DG by the lentivirus-mediated RNA interference, which resulted in a remarkable reduction in adult neurogenesis . Additionally, 1 month following 2 weeks of BDNF overexpression significantly increases neuronal differentiation .
18.104.22.168. Human studies
Erickson and colleagues reported that physical exercise as an intervention for the aging population not only attenuated the age-related loss of hippocampal volume but also increased the serum levels of BDNF in these individuals . Increases in hippocampal BDNF levels are thought to contribute to the upregulation of hippocampal neurogenesis seen with antidepressant treatment . In fact, clinical studies have reported decreased serum BDNF levels in depressive patients, which were improved following treatment with antidepressants . Given the well-established link between neurotrophins and adult hippocampal neurogenesis, it is reasonable to speculate that peripheral levels of these factors may be used as biomarkers of hippocampal neurogenesis. While the exact relationship between peripheral levels of neurotrophic factors and hippocampal neurogenesis has not reliably been established, progress has been made in this respect. Rasmussen and colleagues provided the first evidence that BDNF in the brain is a major contributor to the increase in plasma BDNF in response to exercise . More recently, Yau and colleagues (2012) investigated the interaction of hippocampal neurogenesis, plasma neurotrophin levels, and cognitive performance in a rat stress model. They found that acute stress enhanced spatial learning as well as both hippocampal and plasma BDNF levels, but these findings were independent of hippocampal neurogenesis . When chronic stress was administered, it significantly decreased hippocampal BDNF levels, hippocampal neurogenesis, and impaired spatial learning without affecting plasma BDNF levels . While 28 days of voluntary running increased hippocampal neurogenesis and spatial learning, plasma BDNF levels were not significantly altered by exercise in rats . While there is still possibility to use peripheral levels of neurotrophins as biomarkers correlating to changes in hippocampal neurogenesis, the interaction between these two factors remains to be understood and is far from a simple, linear relationship. It is possible that in order to fully depict changes in hippocampal neurogenesis at the periphery, we must examine multiple neurotrophins simultaneously, as peripheral BDNF changes may only be evident once substantial changes in BDNF levels have first occurred in the brain. This dissociation between central and peripheral BDNF levels shown in animals has also been reported in human subjects. Following 3 months of endurance training in healthy individuals, blood samples from the internal jugular vein but not the peripheral vessels showed increased BDNF levels . Understandably, the responses of plasma or serum levels of BDNF varied considerably between studies; however, many reported a transient increase in plasma/serum levels of BDNF following exercise . Lee and colleagues (2014) recently showed that adolescent athletes have lower resting serum levels of both BDNF and VEGF, and also showed improved brain function in the medial-temporal and frontal areas specifically compared to age-matched controls .
22.214.171.124. Animal studies
IGF-1 is another important growth factor that is shown to increase as a result of exercise . This growth factor is taken up by the hippocampus from the bloodstream; however, if this process is blocked by subcutaneous infusions of IGF-1 antiserum, the exercise-mediated increase in neurogenesis is inhibited . When IGF-1 is injected systemically in sedentary rats, it can mimic the effects of exercise and lead to enhancements in neurogenesis . When IGF-1 is taken up by neurons, it can lead to increased firing and sensitivity of the neuron, which may stimulate BDNF and c-fos expression , which can, in turn, increase neurogenesis in the surrounding area.
126.96.36.199. Human studies
IGF-1 is a neurotrophic factor that is primarily secreted from the liver  that can readily be transported across the blood-brain and blood-cerebrospinal fluid barriers . In the brain, IGF-1 plays a critical role in the creation of new neurons and synapses where transgenic overexpression of IGF-1 promotes neurogenesis and synaptogenesis in the hippocampus during postnatal development . Both 6 and 20 days after exogenous IGF-1 is administered, there is an increase in the number of hippocampal cell proliferation . Clinical studies have established a positive correlation between serum IGF-1 levels and cognitive function [76-78]. Additionally, following two 60-minute cycling sessions, middle-aged men show increased peripheral IGF-1 levels , which has also been replicated in road cyclists . While there is evidence to suggest that there is a link among peripheral IGF-1, exercise and cognitive function, a direct relationship among peripheral IGF-1, brain IGF-1, hippocampal neurogenesis, and hippocampus-specific function has yet to be established. In contrast to studies of acute exercise, sustained physical exercise has been shown to either have no effect  or reduce peripheral IGF-1 levels in healthy subjects , regardless of previous experience as athletes  or exercise intensity . As with BDNF, the relationship between IGF-1 in the body and brain in response to exercise is ambiguous.
188.8.131.52. Animal studies
Angiogenesis and vascular function are enhanced in response to exercise in many brain areas, which may improve normal neural function, and also potentially offer protection during insult . Magnetic resonance imaging of both mice and humans has suggested a correlation between exercise, DG blood flow, and neurogenesis; however, histological examination of the vasculature did not show exercise-induced changes in mice . Increased blood flow can also increase the exposure to growth factors [56, 85] that can influence neurogenesis, such as VEGF. This neurotrophin, which is known for its role in stimulating angiogenesis, is increased following exercise  and may play a role in enhancing neurogenesis [21, 86]. Interestingly, new neurons in the DG tend to cluster around the local microvasculature [11, 87], and if VEGF is blocked, the exercise-induced increase in neurogenesis is abolished .
184.108.40.206. Human studies
VEGF is a 45-kDa heparin-binding homodimeric glycoprotein that is secreted by skeletal muscles and can be released into the vascular system . Levels of VEGF have been shown to increase in skeletal muscle following acute physical exercise [89, 90]. VEGF mRNA expression in human muscle is elevated after 30 minutes of exercise . Plasma VEGF levels are decreased in the femoral vein following 3 hours of two-legged kicking exercise meanwhile skeletal muscle VEGF mRNA expression was increased . Similarly, arterial VEGF plasma levels are decreased following 10 days of exercise . Kraus and colleagues have reported increased plasma VEGF levels following 2 hours of exercise in well-trained endurance athletes, but not sedentary controls at any time points . The first link between exercise-induced functional improvements in the temporal cortex and changes of BDNF, IGF-1, and VEGF has recently been reported in healthy elderly subjects . Following a 7-week regime of aerobic exercise, there was increased connectivity between the bilateral parahippocampi and the bilateral temporal gyri, which was associated with increased peripheral levels of BDNF, IGF-1, and VEGF. In teens that exercise regularly, Lee and colleagues showed improved frontal and temporal lobe cognitive function when compared to age-matched teens that did not exercise . In contrast to what was seen in the study of elderly subjects, in the teen study there was a negative correlation between peripheral levels of BDNF and VEGF with temporal and frontal lobe functions. These studies raise critical questions regarding the type and duration of exercise as well as the age and previous exercise experience of the subjects.
5. Changes of other potential peripheral factors in response to physical exercise
Skeletal muscle and adipose tissues have recently been identified as major secretory organs in the maintenance of metabolic functions of the body. Myokines are identified as peptides and cytokines that are released by muscle fibers and can act in a paracrine or endocrine manner . Adipokines are identified as hormones that are involved in metabolic functions and mediate the crosstalk between adipose tissues and the brain . In response to physical exercise, these factors may have a crosstalk to regulate the secretion of myokines and adipokines, and work in concert to regulate many biological activities such as immune responses, neuroplasticity, and neurogenesis. Although linkage between hippocampal neurogenesis and levels of myokines or adipokines are still unclear, emerging animal studies have given us hints regarding their potential role in mediating the effect of exercise on regulating hippocampal plasticity.
5.1.1. Animal studies
Adiponectin, which is a protein secreted by adipose tissue, is well-known for its effects on metabolism and the cardiovascular system including antidiabetic, antiinflammatory, and antiatherosclerosis functions [96, 97]. Recent work has uncovered a role for adiponectin, as a peripheral factor mediating exercise-induced hippocampal cell proliferation . Adiponectin has previously been shown to stimulate proliferation but not differentiation of adult hippocampal progenitor cells
5.1.2. Human studies
Levels of plasma adiponectin are positively correlated with physical activity . However, effects of acute or chronic exercise training on modulating adiponectin levels are inconsistent and require further study. Circulating concentrations of adiponectin in normal individuals range from 5 to 20 μg/ml . In clinical studies of acute exercise training, the reported levels of adiponectin have been varied, where some groups report increases [104, 105], decreases , or no changes [107-109]. The effect of exercise on adiponectin seems to be intensity dependent, because the acute effect of exercise in the form of volume-extended rowing training significantly increases adiponectin levels in elite athletes immediately and 30 minutes postexercise, but leads to decreased adiponectin levels in less elite athletes . Both aerobic and resistance training with moderate to high intensity have been reported to significantly increase adiponectin levels , suggesting that the intensity of physical exercise is important to modulate adiponectin levels. Since adequate duration and intensity of physical training may be needed to augment circulating adiponectin levels, more detailed examinations of how adiponectin levels are manipulated by different forms and durations of exercise are necessary to provide insight regarding the role of adiponectin as a useful biomarker for evaluating the beneficial effects of physical exercise on the brains.
5.2.1. Animal studies
In 2012, irisin was discovered as a novel exercise hormone for mediating the beneficial effects of exercise on metabolism . Irisin is encoded by the
5.2.2. Human studies
Circulating irisin and its levels in adipose tissue are significantly associated with Fndc5 gene expression in adipose tissue. The Fndc5 gene is more strongly expressed in muscle than in adipose tissue by a 200-fold increase. Of note, obese patients and those with type 2 diabetes have lower circulating levels of irisin and
5.3. Myokines/cytokine-interleukin 15 (IL-15)
5.3.1. Animal studies
IL-15 is a proinflammatory cytokine which can be secreted by muscle cells. IL-15 is stable in the circulation and can reach the parenchyma through the blood-brain barrier . Beck and colleagues observed increases in hippocampal IL-15 expression and concurrent neurogenesis in IL-2-null mice . Direct administration of IL-15 modulated neuronal differentiation of rat neural stem cells
5.3.2. Human studies
How IL-15 level is modulated by physical exercise is still unclear. An acute endurance exercise failed to elevate muscle IL-15 levels , whereas acute resistance exercise was reported to increase IL-15 mRNA expression without affecting its protein content in muscle . Interestingly, a prolonged 12-week endurance exercise only raised the muscle IL-15 protein content without any changes at its mRNA levels . This suggests divergent regulatory mechanisms mediating IL-15 production during muscle contraction. Plasma IL-15 concentrations were elevated by acute resistance exercise . However, chronic resistance exercise seemed to have no such effect . Therefore, more studies with the unified training paradigm are needed to identify the dynamic changes of IL-15.
In summary, the changes of central and/or peripheral neurotrophins, adipokines, myokines, or cytokines in response to physical training are still inconclusive so far. In human subjects, it is important to consider that age, health status, and previous exercise experience as well as general fitness can all play a role. Exercise with insufficient duration or intensity or form may not necessarily affect the expression of the above-mentioned factors. Therefore, answering the questions that by which type of and to what extent the exercise should be performed in the specific population are of particular significance. Further research is required to validate the use of exercise-modulated peripheral factors as the potential biomarkers for monitoring brain health following exercise intervention. Future direction should be focused on characterizing changes of aforementioned potential biomarkers and cognitive performance in different targeted groups. Identifying different biomarker panels may be necessary to examine the beneficial effect of exercise on targeted populations, since this will provide a more complete assessment with a better characterization on the effect of exercise on brain health.
The work is supported by Hong Kong Health and Medical Research Fund and by funds of Leading Talents of Guangdong (2013), and National Natural Science Foundation of China (#81501171).
Bherer L. Cognitive plasticity in older adults: effects of cognitive training and physical exercise. Ann N Y Acad Sci. 2015;1337:1–6.
Buchman AS, Boyle PA, Yu L, Shah RC, Wilson RS, Bennett DA. Total daily physical activity and the risk of AD and cognitive decline in older adults. Neurology. 2012;78(17):1323–1329.
Chen H, Zhang SM, Schwarzschild MA, Hernan MA, Ascherio A. Physical activity and the risk of Parkinson disease. Neurology. 2005;64(4):664–669.
van Praag H, Kempermann G, Gage FH. Running increases cell proliferation and neurogenesis in the adult mouse dentate gyrus. Nat Neurosci. 1999;2(3):266–270.
van Praag H, Christie BR, Sejnowski TJ, Gage FH. Running enhances neurogenesis, learning, and long-term potentiation in mice. Proc Natl Acad Sci U S A. 1999;96(23):13427–13431.
Yau SY, Lau BW, Tong JB, Wong R, Ching YP, Qiu G, et al. Hippocampal neurogenesis and dendritic plasticity support running-improved spatial learning and depression-like behaviour in stressed rats. PLoS One. 2011;6(9):e24263.
Eadie BD, Redila VA, Christie BR. Voluntary exercise alters the cytoarchitecture of the adult dentate gyrus by increasing cellular proliferation, dendritic complexity, and spine density. J Comp Neurol. 2005;486(1):39–47.
Stranahan AM, Khalil D, Gould E. Running induces widespread structural alterations in the hippocampus and entorhinal cortex. Hippocampus. 2007;17(11):1017–1022.
Berchtold NC, Chinn G, Chou M, Kesslak JP, Cotman CW. Exercise primes a molecular memory for brain-derived neurotrophic factor protein induction in the rat hippocampus. Neuroscience. 2005;133(3):853–861.
Trejo JL, Carro E, Torres-Aleman I. Circulating insulin-like growth factor I mediates exercise-induced increases in the number of new neurons in the adult hippocampus. J Neurosci. 2001;21(5):1628–1634.
Fabel K, Fabel K, Tam B, Kaufer D, Baiker A, Simmons N, et al. VEGF is necessary for exercise-induced adult hippocampal neurogenesis. Eur J Neurosci. 2003;18(10):2803–2812.
Naylor S. Biomarkers: current perspectives and future prospects. Expert Rev Mol Diagn. 2003;3(5):525–529.
Schmidt HD, Shelton RC, Duman RS. Functional biomarkers of depression: diagnosis, treatment, and pathophysiology. Neuropsychopharmacology. 2011;36(12):2375–2394.
Pereira AC, Huddleston DE, Brickman AM, Sosunov AA, Hen R, McKhann GM, et al. An in vivo correlate of exercise-induced neurogenesis in the adult dentate gyrus. Proc Natl Acad Sci U S A. 2007;104(13):5638–5643.
Yancey SL, Overton JM. Cardiovascular responses to voluntary and treadmill exercise in rats. J App Physiol. 1993;75(3):1334–1340.
Sharma HS, Cervos-Navarro J, Dey PK. Increased blood-brain barrier permeability following acute short-term swimming exercise in conscious normotensive young rats. Neurosci Res. 1991;10(3):211–221.
Black JE, Isaacs KR, Anderson BJ, Alcantara AA, Greenough WT. Learning causes synaptogenesis, whereas motor activity causes angiogenesis, in cerebellar cortex of adult rats. Proc Natl Acad Sci U S A. 1990;87(14):5568–5572.
Isaacs KR, Anderson BJ, Alcantara AA, Black JE, Greenough WT. Exercise and the brain: angiogenesis in the adult rat cerebellum after vigorous physical activity and motor skill learning. J Cerebral Blood Flow Metabol. 1992;12(1):110–119.
Kleim JA, Cooper NR, VandenBerg PM. Exercise induces angiogenesis but does not alter movement representations within rat motor cortex. Brain Research. 2002;934(1):1–6.
Swain RA, Harris AB, Wiener EC, Dutka MV, Morris HD, Theien BE, et al. Prolonged exercise induces angiogenesis and increases cerebral blood volume in primary motor cortex of the rat. Neuroscience. 2003;117(4):1037–1046.
Jin K, Zhu Y, Sun Y, Mao XO, Xie L, Greenberg DA. Vascular endothelial growth factor (VEGF) stimulates neurogenesis in vitro and in vivo. Proc Natl Acad Sci U S A. 2002;99(18):11946–11950.
Louissaint A, Jr., Rao S, Leventhal C, Goldman SA. Coordinated interaction of neurogenesis and angiogenesis in the adult songbird brain. Neuron. 2002;34(6):945–960.
Kronenberg G, Bick-Sander A, Bunk E, Wolf C, Ehninger D, Kempermann G. Physical exercise prevents age-related decline in precursor cell activity in the mouse dentate gyrus. Neurobiol Aging. 2006;27(10):1505–1513.
O'Callaghan RM, Griffin EW, Kelly AM. Long-term treadmill exposure protects against age-related neurodegenerative change in the rat hippocampus. Hippocampus. 2009;19(10):1019–1029.
van Praag H, Shubert T, Zhao C, Gage FH. Exercise enhances learning and hippocampal neurogenesis in aged mice. J Neurosci. 2005;25(38):8680–8685.
Gomes da Silva S, Unsain N, Masco DH, Toscano-Silva M, de Amorim HA, Silva Araujo BH, et al. Early exercise promotes positive hippocampal plasticity and improves spatial memory in the adult life of rats. Hippocampus. 2012;22(2):347–358.
Leuner B, Gould E, Shors TJ. Is there a link between adult neurogenesis and learning? Hippocampus. 2006;16(3):216–224.
Ahlskog JE, Geda YE, Graff-Radford NR, Petersen RC. Physical exercise as a preventive or disease-modifying treatment of dementia and brain aging. Mayo Clinic Proc. 2011;86(9):876–884.
Smith PJ, Blumenthal JA, Hoffman BM, Cooper H, Strauman TA, Welsh-Bohmer K, et al. Aerobic exercise and neurocognitive performance: a meta-analytic review of randomized controlled trials. Psychosom Med. 2010;72(3):239–252.
Ratey JJ, Loehr JE. The positive impact of physical activity on cognition during adulthood: a review of underlying mechanisms, evidence and recommendations. Rev Neurosci. 2011;22(2):171–185.
Hamer M, Chida Y. Physical activity and risk of neurodegenerative disease: a systematic review of prospective evidence. Psychol Med. 2009;39(1):3–11.
Lautenschlager NT, Cox K, Cyarto EV. The influence of exercise on brain aging and dementia. Biochim Biophys Acta. 2012;1822(3):474–481.
Prakash RS, Voss MW, Erickson KI, Kramer AF. Physical activity and cognitive vitality. Annu Rev Psychol. 2015;66:769–797.
Clark PJ, Kohman RA, Miller DS, Bhattacharya TK, Brzezinska WJ, Rhodes JS. Genetic influences on exercise-induced adult hippocampal neurogenesis across 12 divergent mouse strains. Genes Brain Behav. 2011;10(3):345–353.
Holmes MM, Galea LA, Mistlberger RE, Kempermann G. Adult hippocampal neurogenesis and voluntary running activity: circadian and dose-dependent effects. J Neurosci Res. 2004;76(2):216–222.
Rhodes JS, van Praag H, Jeffrey S, Girard I, Mitchell GS, Garland T, Jr., et al. Exercise increases hippocampal neurogenesis to high levels but does not improve spatial learning in mice bred for increased voluntary wheel running. Behav Neurosci. 2003;117(5):1006–1016.
Merritt JR, Rhodes JS. Mouse genetic differences in voluntary wheel running, adult hippocampal neurogenesis and learning on the multi-strain-adapted plus water maze. Behav Brain Res. 2015;280:62–71.
Kim YP, Kim H, Shin MS, Chang HK, Jang MH, Shin MC, et al. Age-dependence of the effect of treadmill exercise on cell proliferation in the dentate gyrus of rats. Neurosci Lett. 2004;355(1–2):152–154.
Marlatt MW, Potter MC, Lucassen PJ, van Praag H. Running throughout middle-age improves memory function, hippocampal neurogenesis and BDNF levels in female C57Bl/6J mice. Dev Neurobiol. 2012.
Leasure JL, Jones M. Forced and voluntary exercise differentially affect brain and behavior. Neuroscience. 2008;156(3):456–465.
Li H, Liang A, Guan F, Fan R, Chi L, Yang B. Regular treadmill running improves spatial learning and memory performance in young mice through increased hippocampal neurogenesis and decreased stress. Brain Res. 2013;1531:1–8.
Uda M, Ishido M, Kami K, Masuhara M. Effects of chronic treadmill running on neurogenesis in the dentate gyrus of the hippocampus of adult rat. Brain Res. 2006;1104(1):64–72.
Stranahan AM, Khalil D, Gould E. Social isolation delays the positive effects of running on adult neurogenesis. Nat Neurosci. 2006;9(4):526–533.
Snyder JS, Glover LR, Sanzone KM, Kamhi JF, Cameron HA. The effects of exercise and stress on the survival and maturation of adult-generated granule cells. Hippocampus. 2009;19(10):898–906.
van Praag H, Schinder AF, Christie BR, Toni N, Palmer TD, Gage FH. Functional neurogenesis in the adult hippocampus. Nature. 2002;415(6875):1030–1034.
Yau SY, Li A, Hoo RL, Ching YP, Christie BR, Lee TM, et al. Physical exercise-induced hippocampal neurogenesis and antidepressant effects are mediated by the adipocyte hormone adiponectin. Proc Natl Acad Sci U S A. 2014;111(44):15810–15815.
Kronenberg G, Reuter K, Steiner B, Brandt MD, Jessberger S, Yamaguchi M, et al. Subpopulations of proliferating cells of the adult hippocampus respond differently to physiologic neurogenic stimuli. J Comparat Neurol. 2003;467(4):455–463.
Brandt MD, Maass A, Kempermann G, Storch A. Physical exercise increases Notch activity, proliferation and cell cycle exit of type-3 progenitor cells in adult hippocampal neurogenesis. Eur J Neurosci. 2010;32(8):1256–1264.
Schmidt-Hieber C, Jonas P, Bischofberger J. Enhanced synaptic plasticity in newly generated granule cells of the adult hippocampus. Nature. 2004;429(6988):184–187.
Patten AR, Sickmann H, Hryciw BN, Kucharsky T, Parton R, Kernick A, et al. Long-term exercise is needed to enhance synaptic plasticity in the hippocampus. Learning Memory (Cold Spring Harbor, NY). 2013;20(11):642–647.
O'Callaghan RM, Ohle R, Kelly AM. The effects of forced exercise on hippocampal plasticity in the rat: a comparison of LTP, spatial- and non-spatial learning. Behav Brain Res. 2007;176(2):362–366.
Zhao C, Teng EM, Summers RG, Jr., Ming GL, Gage FH. Distinct morphological stages of dentate granule neuron maturation in the adult mouse hippocampus. J Neurosci. 2006;26(1):3–11.
Redila VA, Christie BR. Exercise-induced changes in dendritic structure and complexity in the adult hippocampal dentate gyrus. Neuroscience. 2006;137(4):1299–1307.
Glasper ER, Llorens-Martin MV, Leuner B, Gould E, Trejo JL. Blockade of insulin-like growth factor-I has complex effects on structural plasticity in the hippocampus. Hippocampus. 2010;20(6):706–712.
Lin TW, Chen SJ, Huang TY, Chang CY, Chuang JI, Wu FS, et al. Different types of exercise induce differential effects on neuronal adaptations and memory performance. Neurobiol Learning Memory. 2012;97(1):140–147.
Neeper SA, Gomez-Pinilla F, Choi J, Cotman C. Exercise and brain neurotrophins. Nature. 1995;373(6510):109.
Vaynman S, Gomez-Pinilla F. License to run: exercise impacts functional plasticity in the intact and injured central nervous system by using neurotrophins. Neurorehabilitation Neural Repair. 2005;19(4):283–295.
Berchtold NC, Castello N, Cotman CW. Exercise and time-dependent benefits to learning and memory. Neuroscience. 2010;167(3):588–597.
Bekinschtein P, Oomen CA, Saksida LM, Bussey TJ. Effects of environmental enrichment and voluntary exercise on neurogenesis, learning and memory, and pattern separation: BDNF as a critical variable? Semin Cell Dev Biol. 2011.
Farmer J, Zhao X, van Praag H, Wodtke K, Gage FH, Christie BR. Effects of voluntary exercise on synaptic plasticity and gene expression in the dentate gyrus of adult male Sprague-Dawley rats in vivo. Neuroscience. 2004;124(1):71–79.
Taliaz D, Stall N, Dar DE, Zangen A. Knockdown of brain-derived neurotrophic factor in specific brain sites precipitates behaviors associated with depression and reduces neurogenesis. Mol Psychiat. 2010;15(1):80–92.
Scharfman H, Goodman J, Macleod A, Phani S, Antonelli C, Croll S. Increased neurogenesis and the ectopic granule cells after intrahippocampal BDNF infusion in adult rats. Exp Neurol. 2005;192(2):348–356.
Erickson KI, Voss MW, Prakash RS, Basak C, Szabo A, Chaddock L, et al. Exercise training increases size of hippocampus and improves memory. Proc Natl Acad Sci U S A. 2011;108(7):3017–3022.
Duman RS, Nakagawa S, Malberg J. Regulation of adult neurogenesis by antidepressant treatment. Neuropsychopharmacology. 2001;25(6):836–844.
Shimizu E, Hashimoto K, Okamura N, Koike K, Komatsu N, Kumakiri C, et al. Alterations of serum levels of brain-derived neurotrophic factor (BDNF) in depressed patients with or without antidepressants. Biol Psychiat. 2003;54(1):70–75.
Rachman IM, Unnerstall JR, Pfaff DW, Cohen RS. Estrogen alters behavior and forebrain c-fos expression in ovariectomized rats subjected to the forced swim test. Proc Natl Acad Sci U S A. 1998;95(23):13941–13946.
Yau SY, Lau BW, Zhang ED, Lee JC, Li A, Lee TM, et al. Effects of voluntary running on plasma levels of neurotrophins, hippocampal cell proliferation and learning and memory in stressed rats. Neuroscience. 2012;222:289–301.
Seifert T, Brassard P, Wissenberg M, Rasmussen P, Nordby P, Stallknecht B, et al. Endurance training enhances BDNF release from the human brain. Am J Physiol. 2010;298(2):R372-R377.
Knaepen K, Goekint M, Heyman EM, Meeusen R. Neuroplasticity - exercise-induced response of peripheral brain-derived neurotrophic factor: a systematic review of experimental studies in human subjects. Sports Med. 2010;40(9):765–801.
Lee TM, Wong ML, Lau BW, Lee JC, Yau SY, So KF. Aerobic exercise interacts with neurotrophic factors to predict cognitive functioning in adolescents. Psychoneuroendocrinology. 2014;39:214–224.
Carro E, Nunez A, Busiguina S, Torres-Aleman I. Circulating insulin-like growth factor I mediates effects of exercise on the brain. J Neurosci. 2000;20(8):2926–2933.
Butler AA, LeRoith D. Minireview: tissue-specific versus generalized gene targeting of the igf1 and igf1r genes and their roles in insulin-like growth factor physiology. Endocrinology. 2001;142(5):1685–1688.
Pulford BE, Ishii DN. Uptake of circulating insulin-like growth factors (IGFs) into cerebrospinal fluid appears to be independent of the IGF receptors as well as IGF-binding proteins. Endocrinology. 2001;142(1):213–220.
O'Kusky JR, Ye P, D'Ercole AJ. Insulin-like growth factor-I promotes neurogenesis and synaptogenesis in the hippocampal dentate gyrus during postnatal development. J Neurosci. 2000;20(22):8435–8442.
Aberg MA, Aberg ND, Hedbacker H, Oscarsson J, Eriksson PS. Peripheral infusion of IGF-I selectively induces neurogenesis in the adult rat hippocampus. J Neurosci. 2000;20(8):2896–2903.
Arwert LI, Deijen JB, Drent ML. The relation between insulin-like growth factor I levels and cognition in healthy elderly: a meta-analysis. Growth Hormone IGF Res. 2005;15(6):416–422.
Aleman A, de Vries WR, de Haan EH, Verhaar HJ, Samson MM, Koppeschaar HP. Age-sensitive cognitive function, growth hormone and insulin-like growth factor 1 plasma levels in healthy older men. Neuropsychobiology. 2000;41(2):73–78.
Aleman A, Verhaar HJ, De Haan EH, De Vries WR, Samson MM, Drent ML, et al. Insulin-like growth factor-I and cognitive function in healthy older men. J Clin Endocrinol Metabol. 1999;84(2):471–475.
Manetta J, Brun JF, Maimoun L, Fedou C, Prefaut C, Mercier J. The effects of intensive training on insulin-like growth factor I (IGF-I) and IGF binding proteins 1 and 3 in competitive cyclists: relationships with glucose disposal. J Sports Sci. 2003;21(3):147–154.
Zebrowska A, Gasior Z, Langfort J. Serum IGF-I and hormonal responses to incremental exercise in athletes with and without left ventricular hypertrophy. J Sports Sci Med. 2009;8(1):67–76.
Cearlock DM, Nuzzo NA. Effects of sustained moderate exercise on cholesterol, growth hormone and cortisol blood levels in three age groups of women. Clin Lab Sci. 2001;14(2):108–111.
Karatay S, Yildirim K, Melikoglu MA, Akcay F, Senel K. Effects of dynamic exercise on circulating IGF-1 and IGFBP-3 levels in patients with rheumatoid arthritis or ankylosing spondylitis. Clin Rheumatol. 2007;26(10):1635–1639.
Nishida Y, Matsubara T, Tobina T, Shindo M, Tokuyama K, Tanaka K, et al. Effect of low-intensity aerobic exercise on insulin-like growth factor-I and insulin-like growth factor-binding proteins in healthy men. Intl J Endocrinol. 2010.
Christie BR, Eadie BD, Kannangara TS, Robillard JM, Shin J, Titterness AK. Exercising our brains: how physical activity impacts synaptic plasticity in the dentate gyrus. Neuromolecular Med. 2008;10(2):47–58.
Spier SA, Delp MD, Meininger CJ, Donato AJ, Ramsey MW, Muller-Delp JM. Effects of ageing and exercise training on endothelium-dependent vasodilatation and structure of rat skeletal muscle arterioles. J Physiol. 2004;556(Pt 3):947–958.
Cao L, Jiao X, Zuzga DS, Liu Y, Fong DM, Young D, et al. VEGF links hippocampal activity with neurogenesis, learning and memory. Nat Genet. 2004;36(8):827–835.
Palmer TD, Willhoite AR, Gage FH. Vascular niche for adult hippocampal neurogenesis. J Comparat Neurol. 2000;425(4):479–494.
Gavin TP, Drew JL, Kubik CJ, Pofahl WE, Hickner RC. Acute resistance exercise increases skeletal muscle angiogenic growth factor expression. Acta Physiologica. 2007;191(2):139–146.
Gustafsson T, Knutsson A, Puntschart A, Kaijser L, Nordqvist AC, Sundberg CJ, et al. Increased expression of vascular endothelial growth factor in human skeletal muscle in response to short-term one-legged exercise training. Pflugers Archiv Eur J Physiol. 2002;444(6):752–759.
Hoffner L, Nielsen JJ, Langberg H, Hellsten Y. Exercise but not prostanoids enhance levels of vascular endothelial growth factor and other proliferative agents in human skeletal muscle interstitium. J Physiol. 2003;550(Pt 1):217–225.
Hiscock N, Fischer CP, Pilegaard H, Pedersen BK. Vascular endothelial growth factor mRNA expression and arteriovenous balance in response to prolonged, submaximal exercise in humans. Am J Physiol Heart Circulat Physiol. 2003;285(4):H1759-H1763.
Kraus RM, Stallings HW, 3rd, Yeager RC, Gavin TP. Circulating plasma VEGF response to exercise in sedentary and endurance-trained men. J Appl Physiol. 2004;96(4):1445–1450.
Voss MW, Erickson KI, Prakash RS, Chaddock L, Kim JS, Alves H, et al. Neurobiological markers of exercise-related brain plasticity in older adults. Brain Behav Immunity. 2013;28:90–99.
Pedersen BK, Akerstrom TC, Nielsen AR, Fischer CP. Role of myokines in exercise and metabolism. J Appl Physiol. 2007;103(3):1093–1098.
Scherer PE. Adipose tissue: from lipid storage compartment to endocrine organ. Diabetes. 2006;55(6):1537–1545.
Chandran M, Phillips SA, Ciaraldi T, Henry RR. Adiponectin: more than just another fat cell hormone? Diabetes Care. 2003;26(8):2442–2450.
Kawano J, Arora R. The role of adiponectin in obesity, diabetes, and cardiovascular disease. J Cardiometab Syndr. 2009;4(1):44–49.
Zhang D, Guo M, Zhang W, Lu XY. Adiponectin stimulates proliferation of adult hippocampal neural stem/progenitor cells through activation of p38 mitogen-activated protein kinase (p38MAPK)/glycogen synthase kinase 3beta (GSK-3beta)/beta-catenin signaling cascade. J Biol Chem. 2011;286(52):44913–44920.
Liu J, Guo M, Zhang D, Cheng SY, Liu M, Ding J, et al. Adiponectin is critical in determining susceptibility to depressive behaviors and has antidepressant-like activity. Proc Natl Acad Sci U S A. 2012;109(30):12248–12253.
Teixeira AL, Diniz BS, Campos AC, Miranda AS, Rocha NP, Talib LL, et al. Decreased levels of circulating adiponectin in mild cognitive impairment and Alzheimer's disease. Neuromol Med. 2013;15(1):115–121.
Ng R. Adiponectin deficiency induced cognitive impairment in aging mice through reductions in insulin sensitivity and AMPK activation (I12–4A). Neurology. 2015;84(14):I12–4A.
St-Pierre DH, Faraj M, Karelis AD, Conus F, Henry JF, St-Onge M, et al. Lifestyle behaviours and components of energy balance as independent predictors of ghrelin and adiponectin in young non-obese women. Diabetes Metab. 2006;32(2):131–139.
Matsuzawa Y. Adiponectin: identification, physiology and clinical relevance in metabolic and vascular disease. Atheroscler Suppl. 2005;6(2):7–14.
Jurimae J, Purge P, Jurimae T. Adiponectin and stress hormone responses to maximal sculling after volume-extended training season in elite rowers. Metabolism. 2006;55(1):13–19.
Kraemer RR, Aboudehen KS, Carruth AK, Durand RT, Acevedo EO, Hebert EP, et al. Adiponectin responses to continuous and progressively intense intermittent exercise. Med Sci Sports Exercise. 2003;35(8):1320–1325.
Jurimae J, Purge P, Jurimae T. Adiponectin is altered after maximal exercise in highly trained male rowers. Eur J Appl Physiol. 2005;93(4):502–505.
Ferguson MA, White LJ, McCoy S, Kim HW, Petty T, Wilsey J. Plasma adiponectin response to acute exercise in healthy subjects. Eur J Appl Physiol. 2004;91(2–3):324–329.
Jamurtas AZ, Theocharis V, Koukoulis G, Stakias N, Fatouros IG, Kouretas D, et al. The effects of acute exercise on serum adiponectin and resistin levels and their relation to insulin sensitivity in overweight males. Eur J Appl Physiol. 2006;97(1):122–126.
Punyadeera C, Zorenc AH, Koopman R, McAinch AJ, Smit E, Manders R, et al. The effects of exercise and adipose tissue lipolysis on plasma adiponectin concentration and adiponectin receptor expression in human skeletal muscle. Eur J Endocrinol. 2005;152(3):427–436.
Fatouros IG, Tournis S, Leontsini D, Jamurtas AZ, Sxina M, Thomakos P, et al. Leptin and adiponectin responses in overweight inactive elderly following resistance training and detraining are intensity related. J Clin Endocrinol Metab. 2005;90(11):5970–5977.
Bostrom P, Wu J, Jedrychowski MP, Korde A, Ye L, Lo JC, et al. A PGC1-alpha-dependent myokine that drives brown-fat-like development of white fat and thermogenesis. Nature. 2012;481(7382):463–468.
Huh JY, Mougios V, Kabasakalis A, Fatouros I, Siopi A, Douroudos, II, et al. Exercise-induced irisin secretion is independent of age or fitness level and increased irisin may directly modulate muscle metabolism through AMPK activation. J Clin Endocrinol Metab. 2014;99(11):E2154-E2161.
Kobilo T, Liu QR, Gandhi K, Mughal M, Shaham Y, van Praag H. Running is the neurogenic and neurotrophic stimulus in environmental enrichment. Learning Memory (Cold Spring Harbor, NY). 2011;18(9):605–609.
Moon HS, Dincer F, Mantzoros CS. Pharmacological concentrations of irisin increase cell proliferation without influencing markers of neurite outgrowth and synaptogenesis in mouse H19–7 hippocampal cell lines. Metabolism. 2013;62(8):1131–1136.
Brenmoehl J, Albrecht E, Komolka K, Schering L, Langhammer M, Hoeflich A, et al. Irisin is elevated in skeletal muscle and serum of mice immediately after acute exercise. Int J Biol Sci. 2014;10(3):338–349.
Wrann CD, White JP, Salogiannnis J, Laznik-Bogoslavski D, Wu J, Ma D, et al. Exercise induces hippocampal BDNF through a PGC-1alpha/FNDC5 pathway. Cell Metab. 2013;18(5):649–659.
Hashemi MS, Ghaedi K, Salamian A, Karbalaie K, Emadi-Baygi M, Tanhaei S, et al. Fndc5 knockdown significantly decreased neural differentiation rate of mouse embryonic stem cells. Neuroscience. 2013;231:296–304.
Moreno-Navarrete JM, Ortega F, Serrano M, Guerra E, Pardo G, Tinahones F, et al. Irisin is expressed and produced by human muscle and adipose tissue in association with obesity and insulin resistance. J Clin Endocrinol Metab. 2013;98(4):E769-E778.
Liu JJ, Wong MD, Toy WC, Tan CS, Liu S, Ng XW, et al. Lower circulating irisin is associated with type 2 diabetes mellitus. J Diabetes Complications. 2013;27(4):365–369.
Jedrychowski MP, Wrann CD, Paulo JA, Gerber KK, Szpyt J, Robinson MM, et al. Detection and quantitation of circulating human irisin by tandem mass spectrometry. Cell Metab. 2015;22(4):734–740.
Aydin S, Aydin S, Kuloglu T, Yilmaz M, Kalayci M, Sahin I, et al. Alterations of irisin concentrations in saliva and serum of obese and normal-weight subjects, before and after 45 min of a Turkish bath or running. Peptides. 2013;50:13–18.
Pan W, Hsuchou H, Yu C, Kastin AJ. Permeation of blood-borne IL15 across the blood-brain barrier and the effect of LPS. J Neurochem. 2008;106(1):313–319.
Beck RD, Jr., Wasserfall C, Ha GK, Cushman JD, Huang Z, Atkinson MA, et al. Changes in hippocampal IL-15, related cytokines, and neurogenesis in IL-2 deficient mice. Brain Res. 2005;1041(2):223–230.
Huang YS, Cheng SN, Chueh SH, Tsai YL, Liou NH, Guo YW, et al. Effects of interleukin-15 on neuronal differentiation of neural stem cells. Brain Res. 2009;1304:38–48.
Umehara T, Udagawa J, Takamura K, Kimura M, Ishimitsu R, Kiyono H, et al. Role of interleukin-15 in the development of mouse olfactory nerve. Congenital Anomalies. 2009;49(4):253–257.
Gomez-Nicola D, Valle-Argos B, Pallas-Bazarra N, Nieto-Sampedro M. Interleukin-15 regulates proliferation and self-renewal of adult neural stem cells. Mol Biol Cell. 2011;22(12):1960–1970.
Wu X, Hsuchou H, Kastin AJ, He Y, Khan RS, Stone KP, et al. Interleukin-15 affects serotonin system and exerts antidepressive effects through IL15Ralpha receptor. Psychoneuroendocrinology. 2011;36(2):266–278.
He Y, Hsuchou H, Wu X, Kastin AJ, Khan RS, Pistell PJ, et al. Interleukin-15 receptor is essential to facilitate GABA transmission and hippocampal-dependent memory. J Neurosci. 2010;30(13):4725–4734.
Wu X, He Y, Hsuchou H, Kastin AJ, Rood JC, Pan W. Essential role of interleukin-15 receptor in normal anxiety behavior. Brain Behav Immunity. 2010;24(8):1340–1346.
Rinnov A, Yfanti C, Nielsen S, Akerstrom TC, Peijs L, Zankari A, et al. Endurance training enhances skeletal muscle interleukin-15 in human male subjects. Endocrine. 2014;45(2):271–278.
Nielsen AR, Mounier R, Plomgaard P, Mortensen OH, Penkowa M, Speerschneider T, et al. Expression of interleukin-15 in human skeletal muscle effect of exercise and muscle fibre type composition. J Physiol. 2007;584(Pt 1):305–312.
Riechman SE, Balasekaran G, Roth SM, Ferrell RE. Association of interleukin-15 protein and interleukin-15 receptor genetic variation with resistance exercise training responses. J Appl Physiol (1985). 2004;97(6):2214–2219.
Prestes J, Shiguemoto G, Botero JP, Frollini A, Dias R, Leite R, et al. Effects of resistance training on resistin, leptin, cytokines, and muscle force in elderly post-menopausal women. J Sports Sci. 2009;27(14):1607–1615.