Irisin, Two Years Later

Abstract

In January 2012, Boström and colleagues identified a new muscle tissue secreted peptide, which they named irisin, to highlight its role as a messenger that comes from skeletal muscle to other parts of the body. Irisin is a cleaved and secreted fragment of FNDC5 (also known as FRCP2 and PeP), a member of fibronectin type III repeat containing gene family. Major interest in this protein arose because of its great therapeutic potential in diabetes and perhaps also therapy for obesity. Here we review the most important aspects of irisin’s action and discuss its involvement in energy and metabolic homeostasis and whether the beneficial effects of exercise in these disease states could be mediated by this protein. In addition the effects of irisin at the central nervous system (CNS) are highlighted. It is concluded that although current and upcoming research on irisin is very promising it is still necessary to deepen in several aspects in order to clarify its full potential as a meaningful drug target in human disease states.

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1. Introduction

Obesity is at present the most common nutritional disease in industrialized countries, constituting a priority health problem. It is associated with the development of cardiovascular disease, diabetes mellitus type II, increased incidence of certain forms of cancer, and respiratory complications from other diseases, which leads to higher rates of mortality and morbidity, reducing directly or indirectly the quality and life expectancy of sufferers [1, 2]. Lifestyle modification, specifically changes in diet, physical activity, and exercise, currently continues to be the best option for treatment of obesity. In this sense, the benefits of exercise have been extensively documented [3]. Moreover, it has recently been reported that especially during or immediately after physical activity, skeletal muscle releases into circulation several hormones. These hormones, named myokines, can influence metabolism and modify cytokine production in different tissues and organs. On the basis of this, the concept of skeletal muscle must be reconsidered and being truly considered as an endocrine organ [4, 5].

Since human brown adipose tissue (BAT), especially in adults, was rediscovered several years ago by using positron emission tomography (PET) [6–9], it has been postulated as a major candidate for the treatment of obesity. This is based on the fact that brown adipose cells can dissipate energy in the form of heat leading to weight loss. This process takes place through a specialized mitochondrial protein called uncoupling protein 1 (UCP1). The uncoupling activity of UCP1 is explained by its ability to transport protons across the inner mitochondrial membrane, avoiding ATP synthesis and dissipating energy as heat [10]. Regulation of UCP1 is mainly at transcriptional level, where peroxisome proliferator-activated receptor ϒ coactivator 1α (PGC1α) plays a key role [11].

Studies in immortal preadipocyte lines from the brown adipose tissue of mice lacking PGC1α corroborated their importance in thermogenesis [12]. Another important characteristic is its role in mitochondrial biogenesis; in fact the increased expression of PGC1α is parallel to increased mitochondrial DNA and gene expression of OXPHOS system (oxidative phosphorylation) in BAT [13, 14]. Although PGC1α is mainly expressed in BAT, it is also expressed at higher levels in red, oxidative muscle. In fact, its expression is increased by exercise in mice, in rats, and in human beings [15]. Exercise rapidly and robustly increases the expression of PGC1α, but this effect is transient as both mRNA and protein levels of PGC1α quickly revert to preexercise values [16]. Exercise also activates AMP-activated protein kinase (AMPK), a master regulator of cellular metabolism. AMPK directly phosphorylates PGC1α, which is required for PGC1α-dependent induction of the PGC1α promoter [17]. While brief training produces only a transient rise in PGC1α, endurance training results in persistent PGC1α elevation [18]. Moreover, mice with transgenically increased PGC-1α in muscle showed improved metabolic responses as age related obesity and insulin insensitivity [19]. When the adipose tissue of these transgenic mice was analysed, it was observed that subcutaneous fat inguinal had significantly increased thermogenic gene program. These “brite” (brown-in-white) adipocytes display several classical brown adipocyte characteristics, as elevated levels of UCP1 mRNA and protein [20]. Further, other reports showed that exercise also enhances certain brown adipocyte-specific gene expression in the BAT, as well as white adipose tissue (WAT), suggesting that exercise training may induce important alteration in BAT and/or BAT-like phenotypic changes in WAT [21]. In this context it has been proposed that irisin, a recently discovered myokine, may be the molecule that links exercise with increased thermogenesis. In fact, irisin is named for Iris, the Greek goddess who served as courier among the Gods [20].

2. Irisin, A Bridge between Exercise and Thermogenesis

2.1. First Experimental Studies

Recently, Spielgman’s group described that transgenic PGC-1α mice had greater levels of fibronectin type III domain containing (FNDC5) than wild-type mice [20]. FNDC5 (also known FRCP2 and PeP) is a type of transmembrane protein cloned by two groups in 2002. It has a signal peptide, two fibronectin domains and one hydrophobic domain inserted in the cell membrane [22, 23]. In fact, at present some authors question if FNDC5 might be a transmembrane receptor [24]. FNDC5 is proteolytically cleaved and secreted. Western blot of media fractions of cells overexpressing FNDC5 with antibodies against wild-type Fndc5 identified multiple bands; from 32 kDa to 20 kDa [20]. However, several aspects regarding proteolysis of this protein were not fully clarified yet. So, it seems that these possible discrepancies in molecular weight might be due to glycosylation in the culture media, while this is not observed in plasma mice. Moreover, the theoretically soluble secreted form, named irisin, would have a molecular weight of 12 kDa [20, 25] (Figure 1). A remarkable aspect about irisin is that the amino acid sequence is 100% identical among most mammalian species, which suggests a highly conserved function [20, 26].

[figure omitted; refer to PDF]

Boström and colleagues demonstrated that irisin has potent effects on the browning of certain white adipose tissues, both in culture and in vivo. So, when they applied FNDC5 to primary subcutaneous white adipocytes during differentiation a great increase in oxygen consumption was observed which suggests higher energy expenditure. Moreover, the increase in uncoupled respiration was accompanied by an important induction of UCP1 mRNA and other known brown fat genes. However, genes characteristic to WAT were downregulated. Surprisingly, FNDC5 showed almost no effects on the classical brown fat cells isolated from the interscapular depot [20].

This evidence opened up some questions about the physiological role of irisin. In the same study, in vivo, it was demonstrated that injection intravenously of adenoviral vectors expressing full-length Fndc5 resulted in Ucp1 mRNA increased in the subcutaneous depot. Moreover, a moderate increase irisin blood levels caused a significant improvement in energy expenditure, body weight, and insulin resistance in mice that were fed a high fat diet. Finally, it was demonstrated that irisin was required for the effect of exercise in the browning of subcutaneous white fat and concluded that the rise in irisin is mediated by augmented concentrations of PGC1α in muscle, while PPAR-α (peroxisome proliferator-activated receptor-α) acts as downstream target of this hormone [20].

2.2. Interplay with Other Myokines

There is an extensive literature about different exercise-related signals that can regulate the expression and/or secretion of the diverse myokines [4, 5, 27, 28]. In this context, it has recently been published that there is a close interaction between irisin and myostatin. Myostatin, besides being a critical autocrine/paracrine inhibitor of skeletal muscle growth, has been shown to play an important role in metabolism [29]. In fact, it has been described as myostatin-knockout mice (${\text{Mstn}}^{-/-}$) that show an increase muscle mass and a concomitant reduction of fat mass. Moreover, these mice show WAT with characteristics of BAT, an effect mediated by the AMPK-PGC1α-FNDC5 pathway in muscle [30].

Other studies have tried to elucidate the irisin role and other myokines in different physiological conditions. When male rats were subjected to calorie restriction (CR; $~$60% ad libitum) there were no significant diet-related differences in plasma levels of myonectin, myostatin, or irisin, although there were significant changes in fat and lean mass, and also in insulin resistance [31]. These results may indicate that alterations in plasma concentration of these proteins are not essential for the CR-related improvement in insulin sensitivity in rats; however, it does not rule out that these plasma proteins may be relevant for some of caloric restriction’s metabolic effects. On the other hand, Sánchez and collaborators have studied the possible effects of free fatty acids (FFA) alone and combined with adrenaline and AICAR (an activator of AMPK that acts as an exercise mimetic precursor) in the production of the myokines IL6, IL15, and irisin in mouse muscle cells in vitro [32]. They observed that FFA, adrenaline, and AICAR have a great influence in the IL6 expression and secretion, a little inhibitory effect on IL15 expression and almost no effect on the expression of FNDC5. In fact, the authors only found that FNDC5 had a tendency to be reduced with FFA and AICAR at isolated specific time points. Thus, it would be possible that more signals may be required in vivo for inducing FNDC5 expression. In this sense, recent evidence using human rhabdomyosarcoma cells showed that treatment for 24 and 48 hours with omega 3 fatty acids significantly induced irisin expression [33]. Finally, it has also been found that just as FNDC5, heart-derived natriuretic peptides activate white adipose thermogenic programs [34]. Taken together, these results may suggest that tissues such as skeletal and heart muscle, involved in high energy-expending activity, send signals to adipose tissue [35, 36].

2.3. Irisin Is Also an Adipokine

Current data by Roca-Rivada and coworkers proposed that irisin is not only secreted by muscle tissue. In fact, they demonstrated that irisin is a new adipokine with an important autocrine and endocrine function. Moreover, they showed that FNDC5/irisin has a different pattern of secretion depending on the anatomical location of adipose tissue. Thus, subcutaneous adipose tissue secretes more much FNDC5/irisin than visceral adipose tissue, reflecting one more time that visceral fat is more implicated in metabolic complications, while subcutaneous fat has a possible beneficial role. They also showed that short-term periods of exercise training induced FNDC5 secretion by WAT, that this secretion was significantly reduced in fasting animals, and that WAT of obese animals had an increase secretion of this hormone suggesting a type of resistance [25]. Another interesting feature, also reported by those authors, indicates that FNDC5/irisin has a secretion profile similar to other adipokines like leptin. Moreover, it is suggested that this hormone might be implicated in the regulation of circulating FNDC5/irisin levels. In fact, Zucker obese rats with no functional leptin receptor showed significantly diminished levels, while DIO (diet induce obesity) rats showed a significant increase. Ultimately, all these results suggest an interactions between muscle and adipose tissue interaction a regulatory feedback mechanism.

In this same context, Roberts et al. showed that obese/diabetic prone Otsuka Long-Evans Tokushima Fatty (OLETF) rats have more muscle expression FNDC5 than lean Long Evans Tokushima Otsuka (LETO); however, LETO rats have higher circulating irisin levels. The authors also observed that triceps FNDC5 mRNA expression was correlated with fat mass and with plasma leptin; however, in vitro leptin treatment had no effect on FNDC5 mRNA expression in myotubes [37]. Given that the effect of leptin treatment depends on endogenous levels of this hormone and on the physiological state [38], many studies are still needed to determinate a possible interaction between leptin and irisin in the so-called muscle-adipose tissue axis.

3. Irisin, Potential Roles in the Central Nervous System

Besides interaction between skeletal muscle and adipose tissue, it has been described that FNDC5/irisin might have a role in the central nervous system. In fact, it has already described previously that PGC1-α, an upstream of FNDC5, benefits tissues that do not have a primary metabolic function, such as the brain [39–41]. In this context, immunohistochemical studies have recently revealed that rat and mice cerebellar Purkinje cells expressed irisin and also FNDC5 [42]. Furthermore, the same authors hypothesize about a novel neural pathway, where irisin produced in cerebellum might regulate adipocyte metabolism via several intermediary synapses in the medulla and spinal cord, an interesting idea that still requires to be confirmed.

Supporting the role of FNDC5/irisin in the nervous system, it should be noted another study where it is demonstrated that FNDC5 is required for the adequate neural differentiation of mouse embryonic stem cells (mESCs) [43]. The authors observed that both Fndc5 knockdowns in mESCs during their differentiation after postneuronal progenitor formation and the neuronal differentiation were reduced. Finally, Moon et al. showed that hippocampal neurogenesis is regulated by irisin in a dose-dependent manner. So, while physiological concentrations of irisin (5–10 nmol/L) had no effect on mouse H19-7 hippocampal neuronal cells proliferation, pharmacological concentrations (50–100 nmol/L) increased proliferation when they were compared to control. This increase seems to occur trough signal transducer and activator of transcription (STAT)3 but not AMPK and/or extracellular signal-regulated kinase (ERK) signalling pathways [44].

Overall this evidence suggests a central role for irisin, In this regard, considering that the hippocampus is one of the principal regions affected by Alzheimer’s disease and that exercise causes neurogenesis in humans reducing risk of Alzheimer’s [45], Parkinson’s, and some other neurodegenerative diseases [26, 46], irisin might be the link between exercise and healthy brain. Another interesting question that needs to be addressed is whether irisin may be expressed and play a role in other brain areas involved in the regulation of energy balance, such as the hypothalamus and the brainstem.

4. Irisin, Studies in Humans

4.1. Human Exercise Gene

As stated above, irisin has a highly conserved function, and as in rodents, in humans this hormone is also predominantly expressed in muscle [47]. While, available data indicates that this is the main source of production, it was also found that both subcutaneous and visceral adipose tissue expressed and secreted FNDC5/irisin [25, 48]. On other hand, circulating irisin was detected in the serum or plasma of all subjects studied, whereas circulating FNDC5 was detected in only a minority of the subjects [47], which could be explained by a different processing in a minority group of humans.

Throughout the past two years, several studies in humans have tried to clarify the role of FNDC5/irisin in physiological conditions and in disease states. Spielgman’s group showed that endurance exercise training for 10 weeks in healthy adult humans increased plasma irisin levels compared to the baseline state [20]; however, there are some discrepancies about this. While Huh et al. also observed that circulating irisin levels were significantly upregulated 30 min after acute exercise [47], another study have questioned those results. So, other study has not been able to reproduce FNDC5 gene activation by aerobic exercise in younger subjects or in a resistance training study in 20–80 year olds [49]. These authors question therefore whether irisin is a human exercise gene. These discrepancies might be explained as that an increase in irisin levels occurs in states where more energy is needed, such as untrained individuals, while among trained individuals it is not necessary [47]. In the same direction, a recent study confirms that neither longer-term nor single exercise markedly increases skeletal muscle FNDC5 expression or serum irisin [50].

It seems, hence, that exercise might have an effect on irisin levels depending on physiological condition. In this sense, a new study describes that patients subjected to hemodialysis seem to have lower plasma irisin than healthy subjects and also show exercise training resistance; so despite increasing muscle mass, they not have higher irisin levels [51].

4.2. Metabolic Diseases

When analyzing the correlation between body max index (BMI) and irisin levels, differences were also found. Some studies observed a positive correlation with BMI [47, 52, 53], while other reported null [49] or even a negative correlation [48]. It would be necessary a deeper investigation in this field, and a possible resistance to this protein should be characterized, as animal studies suggest [25]. In addition, bariatric surgery-induced weight loss has been reported to decrease irisin levels, independently of BMI [47]. However the functional significance of this finding needs further exploring.

Similarly, it has been established by some groups a relation between diabetes mellitus type 2 (DMT2) and irisin levels, although it is also reported that irisin expression is not related to diabetes status in humans [49]. Most studies show lower irisin levels in patients with DMT2 [48, 54, 55]. Fernandez-Real’s group suggests that a lesser production of irisin in muscle/adipose tissue in obese and patients with DMT2 could be responsible of the obesity-associated lower brown or beige adipocytes in human adipose tissue. So, they consider increasing irisin levels and browning adipose tissue as a potential target for metabolic diseases’ treatment [48].

In this same context, another controversy has been reported. The study of single nucleotide polymorphisms (SNPs) in the human Fndc5 locus, encoding the irisin precursor, showed that a common genetic variation in this locus determines insulin sensitivity [56]. Moreover, data from human myotubes revealed a negative association between FNDC5 expression and in vivo measures of insulin sensitivity. This result appears conflicting with the mouse data from Boström et al. who reported reduced insulin resistance in high fat-fed mice after adenoviral Fndc5 overexpression [20]. Considering the association of DMT2 and cardiovascular disease, a role for irisin is also tempting to be speculated. In this sense the FNDC5 expression in a skeletal muscle biopsy from heart failure (HF) patients, it was observed that this expression relates to functional capacity in a human HF and that a decrease in FNDC5 expression might reduce aerobic performance in HF patients [57].

Circulating irisin has been also found to be directly associated with muscle mass and estradiol levels and inversely associated with age in middle-aged women. Also it is negatively correlated with age, insulin, cholesterol, and adiponectin levels [47, 52, 58], as well as intrahepatic triglyceride contents in obese adults [59]. While, another paper suggests that in a population of postmenopausal women with BMI between 24 and 45, irisin levels do not correlate with 24 h energy expenditure (EE); however, for a subpopulation with EE greater than predicted, irisin levels and EE are highly correlative [60].

Similar to physical activity, drugs might also increase irisin levels and thus affect lipid metabolism and improve risk among dyslipidemic and/or obesity individuals. Given recent data, everything seems to indicate that between these drugs, statins could have an important role in this sense [61]. In this context, recently, Gouni-Berthold and collaborators have described that simvastatin, a hypolipidemic drug member of the statins, increases irisin concentrations both in vivo as in vitro [62]. Although it could be postulated that this increase could be beneficial, for example, by influencing adipose tissue metabolism and insulin resistance, it will be necessary to determine if irisin levels are result of myocyte damage or/and a mechanism of statin-induced cellular stress protection [62].

Another disease with altered energy expenditure and with high prevalence of metabolic imbalance and abnormal energy homeostasis is also chronic kidney disease (CKD). It was observed that patients with CKD have lower irisin levels at rest, independently of high-density lipoprotein cholesterol levels. The mechanism underlying the decrease in irisin in CKD is unknown, even though it seems that indoxyl sulphate, which is a protein-bound uremic toxin, decreases FNDC5 expression in skeletal muscle cells and irisin level in the cell culture medium [58]. Authors consider that these results show good evidence on how uremia may affect irisin levels. Although this study has some limitations, it is suggested that irisin may be a novel therapeutic agent for treating metabolic diseases in CKD patients.

5. Future Prospects

When Böstrom and colleagues described irisin, rapidly, it was seen its great therapeutic potential. Irisin was seen as possible treatment for diabetes and perhaps also therapy for obesity. Moreover, it also was considered a possibility to treat patients with Alzheimer’s, Parkinson’s, and some other neurodegenerative diseases. However, new studies have started to question the initial expectations [24, 63]. So, while clear-cut data have been reported in rodents, the thermogenic effect of irisin in humans remains controversial, and it is not clear if exercise has an impact on irisin levels [49]. In fact, recently, Raschke and coworkers described that neither FNDC5 gene is activated by contraction in humans nor has effect on “brite” differentiation of human preadipocytes [63]; even they propose that irisin function for mice is lost in humans. Thus, it seems obvious that further studies are needed to elucidate, in depth, this field.

First more studies would be necessary to determinate what the precise role of different forms of FNDC5/irisin is and if there is a different mechanism of proteolysis as it already was suggested [47]. On the other hand, it is absolutely necessary to characterize the receptor and the signalling pathway, which will allow a better understanding of irisin function. Just as with other hormones it seems to be a tolerance or resistance mechanism to irisin [25, 60]. So, the factors that contribute to irisin tolerance and/or resistance also would be defined. Similarly more extensive studies, with different cohorts, assessing genetic variations in the irisin gene and its relationships to obesity and associated comorbidities across life span are eagerly awaited. Another important aspect that we need to consider is that human BAT is closely related to rodent beige fat, rather than classical BAT; so if we want to study the irisin effect in human BAT, a rodent model with beige fat would be necessary [26]. Intensive research efforts are needed to use BAT as a target organ for treatment of metabolic diseases.

In conclusion, although current and upcoming research on irisin is very promising and nowadays we already know so much about it (Figure 2), it is still necessary to deepen in several aspects in order to clarify its full potential as a meaningful drug target in human disease states.

[figure omitted; refer to PDF]

Acknowledgments

The research leading to these results has received funding from the European Community’s Seventh Framework Programme (FP7/2007–2013) under Grant agreement no. 281854—the ObERStress European Research Council Project(ML) and no. 245009—the Neurofast project (ML and CD), and Xunta de Galicia (ML: 10PXIB208164PR and 2012-CP070), Instituto de Salud Carlos III (ISCIII) (ML: PI12/01814), MINECO were co-funded by the FEDER Program of EU (CD:BFU2011-29102). CIBER de Fisiopatología de la Obesidad y Nutrición is an initiative of ISCIII. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the paper.

References

[1] P. G. Kopelman, "Obesity as a medical problem," Nature, vol. 404 no. 6778, pp. 635-643, 2000.

[2] N. S. Mitchell, V. A. Catenacci, H. R. Wyatt, J. O. Hill, "Obesity: overview of an epidemic," Psychiatric Clinics of North America, vol. 34 no. 4, pp. 717-732, DOI: 10.1016/j.psc.2011.08.005, 2011.

[3] B. Strasser, "Physical activity in obesity and metabolic syndrome," Annals of the New York Academy of Sciences, vol. 1281, pp. 141-159, DOI: 10.1111/j.1749-6632.2012.06785.x, 2013.

[4] B. K. Pedersen, T. C. A. Åkerström, A. R. Nielsen, C. P. Fischer, "Role of myokines in exercise and metabolism," Journal of Applied Physiology, vol. 103 no. 3, pp. 1093-1098, DOI: 10.1152/japplphysiol.00080.2007, 2007.

[5] B. K. Pedersen, M. A. Febbraio, "Muscles, exercise and obesity: skeletal muscle as a secretory organ," Nature Reviews Endocrinology, vol. 8, pp. 457-465, DOI: 10.1038/nrendo.2012.49, 2012.

[6] A. M. Cypess, S. Lehman, G. Williams, I. Tal, D. Rodman, A. B. Goldfine, F. C. Kuo, E. L. Palmer, Y. Tseng, A. Doria, G. M. Kolodny, C. R. Kahn, "Identification and importance of brown adipose tissue in adult humans," New England Journal of Medicine, vol. 360 no. 15, pp. 1509-1517, DOI: 10.1056/NEJMoa0810780, 2009.

[7] J. Nedergaard, T. Bengtsson, B. Cannon, "Unexpected evidence for active brown adipose tissue in adult humans," American Journal of Physiology, vol. 293 no. 2, pp. E444-E452, DOI: 10.1152/ajpendo.00691.2006, 2007.

[8] W. D. van Marken Lichtenbelt, J. W. Vanhommerig, N. M. Smulders, J. M. A. F. L. Drossaerts, G. J. Kemerink, N. D. Bouvy, P. Schrauwen, G. J. J. Teule, "Cold-activated brown adipose tissue in healthy men," New England Journal of Medicine, vol. 360 no. 15, pp. 1500-1508, DOI: 10.1056/NEJMoa0808718, 2009.

[9] K. A. Virtanen, M. E. Lidell, J. Orava, M. Heglind, R. Westergren, T. Niemi, M. Taittonen, J. Laine, N. Savisto, S. Enerbäck, P. Nuutila, "Functional brown adipose tissue in healthy adults," New England Journal of Medicine, vol. 360 no. 15, pp. 1518-1525, DOI: 10.1056/NEJMoa0808949, 2009.

[10] B. Cannon, J. Nedergaard, "Brown adipose tissue: function and physiological significance," Physiological Reviews, vol. 84 no. 1, pp. 277-359, DOI: 10.1152/physrev.00015.2003, 2004.

[11] P. Puigserver, Z. Wu, C. W. Park, R. Graves, M. Wright, B. M. Spiegelman, "A cold-inducible coactivator of nuclear receptors linked to adaptive thermogenesis," Cell, vol. 92 no. 6, pp. 829-839, DOI: 10.1016/S0092-8674(00)81410-5, 1998.

[12] M. Uldry, W. Yang, J. St-Pierre, J. Lin, P. Seale, B. M. Spiegelman, "Complementary action of the PGC-1 coactivators in mitochondrial biogenesis and brown fat differentiation," Cell Metabolism, vol. 3 no. 5, pp. 333-341, DOI: 10.1016/j.cmet.2006.04.002, 2006.

[13] J. A. Villena, M. C. Carmona, M. Rodriguez de la Concepción, M. Rossmeisl, O. Viñas, T. Mampel, R. Iglesias, M. Giralt, F. Villarroya, "Mitochondrial biogenesis in brown adipose tissue is associated with differential expression of transcription regulatory factors," Cellular and Molecular Life Sciences, vol. 59 no. 11, pp. 1934-1944, DOI: 10.1007/PL00012516, 2002.

[14] Z. Wu, P. Puigserver, U. Andersson, C. Zhang, G. Adelmant, V. Mootha, A. Troy, S. Cinti, B. Lowell, R. C. Scarpulla, B. M. Spiegelman, "Mechanisms controlling mitochondrial biogenesis and respiration through the thermogenic coactivator PGC-1," Cell, vol. 98 no. 1, pp. 115-124, DOI: 10.1016/S0092-8674(00)80611-X, 1999.

[15] K. Baar, A. R. Wende, T. E. Jones, M. Marison, L. A. Nolte, M. Chen, D. P. Kelly, J. O. Holloszy, "Adaptations of skeletal muscle to exercise: rapid increase in the transcriptional coactivator PGC-1," FASEB Journal, vol. 16 no. 14, pp. 1879-1886, DOI: 10.1096/fj.02-0367com, 2002.

[16] H. Pilegaard, B. Saltin, D. P. Neufer, "Exercise induces transient transcriptional activation of the PGC-1 α gene in human skeletal muscle," Journal of Physiology, vol. 546 no. 3, pp. 851-858, DOI: 10.1113/jphysiol.2002.034850, 2003.

[17] S. Jäer, C. Handschin, J. St-Pierre, B. M. Spiegelman, "AMP-activated protein kinase (AMPK) action in skeletal muscle via direct phosphorylation of PGC-1 α," Proceedings of the National Academy of Sciences of the United States of America, vol. 104 no. 29, pp. 12017-12022, DOI: 10.1073/pnas.0705070104, 2007.

[18] A. P. Russell, J. Feilchenfeldt, S. Schreiber, M. Praz, A. Crettenand, C. Gobelet, C. A. Meier, D. R. Bell, A. Kralli, J. Giacobino, O. Dériaz, "Endurance training in humans leads to fiber type-specific increases in levels of peroxisome proliferator-activated receptor- γ coactivator-1 and peroxisome proliferator-activated receptor- α in skeletal muscle," Diabetes, vol. 52 no. 12, pp. 2874-2881, DOI: 10.2337/diabetes.52.12.2874, 2003.

[19] T. Wenz, S. G. Rossi, R. L. Rotundo, B. M. Spiegelman, C. T. Moraes, "Increased muscle PGC-1 α expression protects from sarcopenia and metabolic disease during aging," Proceedings of the National Academy of Sciences of the United States of America, vol. 106 no. 48, pp. 20405-20410, DOI: 10.1073/pnas.0911570106, 2009.

[20] P. Boström, J. Wu, M. P. Jedrychowski, A. Korde, L. Ye, J. C. Lo, K. A. Rasbach, E. A. Boström, J. H. Choi, J. Z. Long, S. Kajimura, M. C. Zingaretti, B. F. Vind, H. Tu, S. Cinti, K. Højlund, S. P. Gygi, B. M. Spiegelman, "A PGC1- α -dependent myokine that drives brown-fat-like development of white fat and thermogenesis," Nature, vol. 481 no. 7382, pp. 463-468, DOI: 10.1038/nature10777, 2012.

[21] X. Xu, Z. Ying, M. Cai, Z. Xu, Y. Li, S. Y. Jiang, K. Tzan, A. Wang, S. Parthasarathy, G. He, S. Rajagopalan, Q. Sun, "Exercise ameliorates high-fat diet-induced metabolic and vascular dysfunction, and increases adipocyte progenitor cell population in brown adipose tissue," American Journal of Physiology, vol. 300 no. 5, pp. R1115-R1125, DOI: 10.1152/ajpregu.00806.2010, 2011.

[22] A. Ferrer-Martínez, P. Ruiz-Lozano, K. R. Chien, "Mouse PeP: a novel peroxisomal protein linked to myoblast differentiation and development," Developmental Dynamics, vol. 224 no. 2, pp. 154-167, DOI: 10.1002/dvdy.10099, 2002.

[23] A. Teufel, N. Malik, M. Mukhopadhyay, H. Westphal, "Frcp1 and Frcp2, two novel fibronectin type III repeat containing genes," Gene, vol. 297 no. 1-2, pp. 79-83, DOI: 10.1016/S0378-1119(02)00828-4, 2002.

[24] H. P. Erickson, "Irisin and FNDC5 in retrospect: an exercise hormone or a transmembrane receptor?," Adipocyte, vol. 2, pp. 289-293, DOI: 10.4161/adip.26082, 2013.

[25] A. Roca-Rivada, C. Castelao, L. L. Senin, M. O. Landrove, J. Baltar, C. A. Belen, L. M. Seoane, F. F. Casanueva, M. Pardo, "FNDC5/irisin is not only a myokine but also an adipokine," PLoS One, vol. 8, 2013.

[26] B. M. Spiegelman, "Banting lecture 2012: regulation of adipogenesis: toward new therapeutics for metabolic disease," Diabetes, vol. 62 no. 6, pp. 1774-1782, DOI: 10.2337/db12-1665, 2013.

[27] L. Pedersen, P. Hojman, "Muscle-to-organ cross talk mediated by myokines," Adipocyte, vol. 1 no. 3, pp. 164-167, DOI: 10.4161/adip.20344, 2012.

[28] S. Raschke, J. Eckel, "Adipo-myokines: two sides of the same coin—mediators of inflammation and mediators of exercise," Mediators of Inflammation, vol. 2013,DOI: 10.1155/2013/320724, 2013.

[29] Z. Huang, X. Chen, D. Chen, "Myostatin: a novel insight into its role in metabolism, signal pathways, and expression regulation," Cellular Signalling, vol. 23 no. 9, pp. 1441-1446, DOI: 10.1016/j.cellsig.2011.05.003, 2011.

[30] T. Shan, X. Liang, P. Bi, S. Kuang, "Myostatin knockout drives browning of white adipose tissue through activating the AMPK-PGC1alpha-Fndc5 pathway in muscle," The FASEB Journal, vol. 27 no. 5, pp. 1981-1989, DOI: 10.1096/fj.12-225755, 2013.

[31] N. Sharma, C. M. Castorena, G. D. Cartee, "Greater insulin sensitivity in calorie restricted rats occurs with unaltered circulating levels of several important myokines and cytokines," Nutrition & Metabolism, vol. 9,DOI: 10.1186/1743-7075-9-90, 2012.

[32] J. Sanchez, Y. Nozhenko, A. Palou, A. M. Rodriguez, "Free fatty acid effects on myokine production in combination with exercise mimetics," Molecular Nutrition & Food Research, vol. 57 no. 8, pp. 1456-1467, DOI: 10.1002/mnfr.201300126, 2013.

[33] R. A. Vaughan, R. Garcia-Smith, M. Bisoffi, C. A. Conn, K. A. Trujillo, "Conjugated linoleic acid or omega 3 fatty acids increase mitochondrial biosynthesis and metabolism in skeletal muscle cells," Lipids in Health and Disease, vol. 11,DOI: 10.1186/1476-511X-11-142, 2012.

[34] M. Bordicchia, D. Liu, E. Amri, G. Ailhaud, P. Dessì-Fulgheri, C. Zhang, N. Takahashi, R. Sarzani, S. Collins, "Cardiac natriuretic peptides act via p38 MAPK to induce the brown fat thermogenic program in mouse and human adipocytes," Journal of Clinical Investigation, vol. 122 no. 3, pp. 1022-1036, DOI: 10.1172/JCI59701, 2012.

[35] D. P. Kelly, "Medicine: Irisin, light my fire," Science, vol. 335 no. 6077, pp. 42-43, DOI: 10.1126/science.1221688, 2012.

[36] A. J. Whittle, A. Vidal-Puig, "NPs-heart hormones that regulate brown fat?," Journal of Clinical Investigation, vol. 122 no. 3, pp. 804-807, DOI: 10.1172/JCI62595, 2012.

[37] M. D. Roberts, D. S. Bayless, J. M. Company, N. T. Jenkins, J. Padilla, T. E. Childs, J. S. Martin, V. J. Dalbo, F. W. Booth, R. S. Rector, M. H. Laughlin, "Elevated skeletal muscle irisin precursor FNDC5 mRNA in obese OLETF rats," Metabolism, vol. 62 no. 8, pp. 1052-1056, DOI: 10.1016/j.metabol.2013.02.002, 2013.

[38] H. S. Moon, M. Dalamaga, S. Y. Kim, S. A. Polyzos, O. P. Hamnvik, F. Magkos, J. Paruthi, C. S. Mantzoros, "Leptin's role in lipodystrophic and nonlipodystrophic insulin-resistant and diabetic individuals," Endocrine Reviews, vol. 34 no. 3, pp. 377-412, DOI: 10.1210/er.2012-1053, 2013.

[39] J. I. Castillo-Quan, "Parkin' control: regulation of PGC-1 α through PARIS in Parkinson's disease," DMM Disease Models and Mechanisms, vol. 4 no. 4, pp. 427-429, DOI: 10.1242/dmm.008227, 2011.

[40] L. Cui, H. Jeong, F. Borovecki, C. N. Parkhurst, N. Tanese, D. Krainc, "Transcriptional repression of PGC-1 α by mutant huntingtin leads to mitochondrial dysfunction and neurodegeneration," Cell, vol. 127 no. 1, pp. 59-69, DOI: 10.1016/j.cell.2006.09.015, 2006.

[41] J. Lin, P. Wu, P. T. Tarr, K. S. Lindenberg, J. St-Pierre, C. Zhang, V. K. Mootha, S. Jäger, C. R. Vianna, R. M. Reznick, L. Cui, M. Manieri, M. X. Donovan, Z. Wu, M. P. Cooper, M. C. Fan, L. M. Rohas, A. M. Zavacki, S. Cinti, G. I. Shulman, B. B. Lowell, D. Krainc, B. M. Spiegelman, "Defects in adaptive energy metabolism with CNS-linked hyperactivity in PGC-1 α null mice," Cell, vol. 119 no. 1, pp. 121-135, DOI: 10.1016/j.cell.2004.09.013, 2004.

[42] S. L. Dun, R. M. Lyu, Y. H. Chen, J. K. Chang, J. J. Luo, N. J. Dun, "Irisin-immunoreactivity in neural and non-neural cells of the rodent," Neuroscience, vol. 240, pp. 155-162, DOI: 10.1016/j.neuroscience.2013.02.050, 2013.

[43] M. S. Hashemi, K. Ghaedi, A. Salamian, K. Karbalaie, M. Emadi-Baygi, S. Tanhaei, M. H. Nasr-Esfahani, H. Baharvand, "Fndc5 knockdown significantly decreased neural differentiation rate of mouse embryonic stem cells," Neuroscience, vol. 231, pp. 296-304, DOI: 10.1016/j.neuroscience.2012.11.041, 2013.

[44] H. S. Moon, F. Dincer, C. S. Mantzoros, "Pharmacological concentrations of irisin increase cell proliferation without influencing markers of neurite outgrowth and synaptogenesis in mouse H19-7 hippocampal cell lines," Metabolism, vol. 62 no. 8, pp. 1131-1136, 2013.

[45] K. I. Erickson, A. M. Weinstein, O. L. Lopez, "Physical activity, brain plasticity, and Alzheimer's disease," Archives of Medical Research, vol. 43 no. 8, pp. 615-621, DOI: 10.1016/j.arcmed.2012.09.008, 2012.

[46] M. P. Mattson, "Energy intake and exercise as determinants of brain health and vulnerability to injury and disease," Cell Metabolism, vol. 16 no. 6, pp. 706-722, 2012.

[47] J. Y. Huh, G. Panagiotou, V. Mougios, M. Brinkoetter, M. T. Vamvini, B. E. Schneider, C. S. Mantzoros, "FNDC5 and irisin in humans: I. Predictors of circulating concentrations in serum and plasma and II. mRNA expression and circulating concentrations in response to weight loss and exercise," Metabolism, vol. 61 no. 12, pp. 1725-1738, 2012.

[48] J. M. Moreno-Navarrete, F. Ortega, M. Serrano, E. Guerra, G. Pardo, F. Tinahones, W. Ricart, J. M. Fernandez-Real, "Irisin is expressed and produced by human muscle and adipose tissue in association with obesity and insulin resistance," Journal of Clinical Endocrinology & Metabolism, vol. 98 no. 4, pp. E769-E778, DOI: 10.1210/jc.2012-2749, 2013.

[49] J. A. Timmons, K. Baar, P. K. Davidsen, P. J. Atherton, "Is irisin a human exercise gene?," Nature, vol. 488, pp. E9-E10, 2012.

[50] S. Pekkala, P. Wiklund, J. J. Hulmi, J. P. Ahtiainen, M. Horttanainen, E. Pollanen, K. A. Makela, H. Kainulainen, K. Hakkinen, K. Nyman, M. Alen, K. H. Herzig, S. Cheng, "Are skeletal muscle FNDC5 gene expression and Irisin release regulated by exercise and related to health?," Journal of Physiology, 2013.

[51] C. Moraes, V. O. Leal, S. M. Marinho, S. G. Barroso, G. S. Rocha, G. T. Boaventura, D. Mafra, "Resistance exercise training does not affect plasma Irisin levels of hemodialysis patients," Hormone and Metabolic Research, 2013.

[52] K. H. Park, L. Zaichenko, M. Brinkoetter, B. Thakkar, A. Sahin-Efe, K. E. Joung, M. Tsoukas, E. V. Geladari, H. J. Young, F. Dincer, C. R. Davis, J. A. Crowell, C. S. Mantzoros, "Circulating Irisin in relation to insulin resistance and the metabolic syndrome," Journal of Clinical Endocrinology & Metabolism, 2013.

[53] A. Stengel, T. Hofmann, M. Goebel-Stengel, U. Elbelt, P. Kobelt, B. F. Klapp, "Circulating levels of irisin in patients with anorexia nervosa and different stages of obesity—correlation with body mass index," Peptides, vol. 39, pp. 125-130, DOI: 10.1016/j.peptides.2012.11.014, 2013.

[54] Y. K. Choi, M. K. Kim, K. H. Bae, H. A. Seo, J. Y. Jeong, W. K. Lee, J. G. Kim, I. K. Lee, K. G. Park, "Serum irisin levels in new-onset type 2 diabetes," Diabetes Research and Clinical Practice, vol. 100 no. 1, pp. 96-101, 2013.

[55] J. J. Liu, M. D. Wong, W. C. Toy, C. S. Tan, S. Liu, X. W. Ng, S. Tavintharan, C. F. Sum, S. C. Lim, "Lower circulating irisin is associated with type 2 diabetes mellitus," Journal of Diabetes and its Complications, vol. 27 no. 4, pp. 365-369, 2013.

[56] H. Staiger, A. Bohm, M. Scheler, L. Berti, J. Machann, F. Schick, F. Machicao, A. Fritsche, N. Stefan, C. Weigert, A. Krook, H. U. Haring, M. H. de Angelis, "Common genetic variation in the human FNDC5 locus, encoding the novel muscle-derived “Browning” factor Irisin, determines insulin sensitivity," PLoS One, vol. 8, 2013.

[57] S. H. Lecker, A. Zavin, P. Cao, R. Arena, K. Allsup, K. M. Daniels, J. Joseph, P. C. Schulze, D. E. Forman, "Expression of the irisin precursor FNDC5 in skeletal muscle correlates with aerobic exercise performance in patients with heart failure," Circulation, vol. 5, pp. 812-818, DOI: 10.1161/CIRCHEARTFAILURE.112.969543, 2012.

[58] M. S. Wen, C. Y. Wang, S. L. Lin, K. C. Hung, "Decrease in irisin in patients with chronic kidney disease," PLoS One, vol. 8, 2013.

[59] H. J. Zhang, X. F. Zhang, Z. M. Ma, L. L. Pan, Z. Chen, H. W. Han, C. K. Han, X. J. Zhuang, Y. Lu, X. J. Li, S. Y. Yang, X. Y. Li, "Irisin is inversely associated with intrahepatic triglyceride contents in obese adults," Journal of Hepatology, vol. 59 no. 3, pp. 557-562, DOI: 10.1016/j.jhep.2013.04.030, 2013.

[60] A. G. Swick, S. Orena, A. O'Connor, "Irisin levels correlate with energy expenditure in a subgroup of humans with energy expenditure greater than predicted by fat free mass," Metabolism, vol. 62 no. 8, pp. 1070-1073, 2013.

[61] P. F. Kokkinos, C. Faselis, J. Myers, D. Panagiotakos, M. Doumas, "Interactive effects of fitness and statin treatment on mortality risk in veterans with dyslipidaemia: a cohort study," The Lancet, vol. 381 no. 9864, pp. 394-399, DOI: 10.1016/S0140-6736(12)61426-3, 2013.

[62] I. Gouni-Berthold, H. K. Berthold, J. Y. Huh, R. Berman, N. Spenrath, W. Krone, C. S. Mantzoros, "Effects of lipid-lowering drugs on irisin in human subjects in vivo and in human skeletal muscle cells ex vivo," PLoS One, vol. 8, 2013.

[63] S. Raschke, M. Elsen, H. Gassenhuber, M. Sommerfeld, U. Schwahn, B. Brockmann, R. Jung, U. Wisloff, A. E. Tjonna, T. Raastad, J. Hallen, F. Norheim, C. A. Drevon, T. Romacho, K. Eckardt, J. Eckel, "Evidence against a beneficial effect of Irisin in humans," PLoS One, vol. 8, 2013.