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    Exercise,the endocannabinoid system and metabolic health

    2013-12-05 20:42:46PetriWiklundStuPekklSulinCheng
    Journal of Sport and Health Science 2013年1期

    Petri Wiklund,Stu Pekkl,Sulin Cheng,b,*

    aDepartment of Health Sciences,University of Jyva¨skyla¨,FI-40014 Jyva¨skyla¨,Finland

    bSchool of Kinesiology,Shanghai University of Sport,Shanghai 200438,China

    Exercise,the endocannabinoid system and metabolic health

    Petri Wiklunda,Satu Pekkalaa,Sulin Chenga,b,*

    aDepartment of Health Sciences,University of Jyva¨skyla¨,FI-40014 Jyva¨skyla¨,Finland

    bSchool of Kinesiology,Shanghai University of Sport,Shanghai 200438,China

    1.The endocannabinoid system in obesity and metabolic disorders

    As obesity and associated metabolic disorders,such as type 2 diabetes and dyslipidemia,are becoming one of the most serious health problems worldwide,development of effective therapies is a high priority.In the search for treatments,the recently discovered endocannabinoid system(ECS)has begun to garner attention,and a wealth of research is now focusing on this unique neuromodulatory system named after the plant that led to its discovery.1

    The ECS consists of G protein-coupled cannabinoid receptors(CB1 and CB2),their endogenous lipid-derived ligands (endocannabinoids, N-arachidonoylethanolamine, named anandamide(AEA)and 2-arachidonoylglycerol(2-AG)) and the enzymes for ligand synthesis and degradation.Endocannabinoids,the organic derivative of cannabis,produced naturally in the body,are well known to modulate many cognitive and emotional processes,through which they influence multiple behavioral responses.2However,a number of studies published in recentyears indicate that endocannabinoids are also key modulators of energy balance through central and peripheral mechanisms.1In the central nervous system,the activationofCB1receptorsbyendocannabinoidsincreasesfood intake,whereasintheperipheral organs,such asgastrointestinal tract,liver,adipose tissue,and skeletal muscle,endocannabinoids are involved in the regulation of nutrient absorption and glucose and lipid metabolism.3Considering the important regulatory role of the ECS in energy metabolism,it is not surprising to observe its dysregulation in obesity.

    Recent data suggest that ECS overactivity is associated with increased lipogenesis,insulin resistance,and dyslipidemia.4Hence,the ECS has become a promising pharmacological target in combating obesity and the associated metabolic disorders.5Although some clinical trials with specific CB1 receptor antagonists/inverse agonists have been successful in terms of reduction of body weight and amelioration of obesity-related metabolic abnormalities,the adverse central and peripheral side effects of these compounds have seriously limited their therapeutic potential.6However,recent findings show that combined calorie restriction and aerobic exercise can modulate endocannabinoid-related gene expression in adipose tissue of obese women during weight loss, suggesting that ECS may link exercise with metabolic adaptations and energy regulation.7

    2.Plausible metabolic implications of exercise-induced ECS activation

    Apart from the above cited study,the metabolic effects of ECS following exercise in humans have not been studied. Several lines of evidence indicate that the ECS may participate in the adaptive responses to exercise.A recent review by Heyman et al.8provides a comprehensive summary of the topic,and several possible mechanisms can be suggested. First,plasma AEA increases significantly following acute strenuous aerobic exercise in humans,while circulating levels of 2-AG appear not to be influenced by exercise.9—10Since AEA has vasodilatory11and bronchodilatory12effects, increase in circulating AEA may aid exercise performance by facilitating blood flow and breathing during exercise.AEA has also been shown to improve insulin sensitivity,glucose uptake and mitochondrial biogenesis in human skeletal muscle cells,13and inhibit fatty acid and cholesterol synthesis in hepatocytes.14These findingsindicate thatwhile CB1signaling negatively modulates insulin signaling and substrate oxidation in metabolically active tissues,15AEA has opposite effects,which appear to be mediated independently of the cannabinoid receptors.

    Second,exercise-induced elevation of plasma AEA is intensity-dependent.According to a recentstudy,only moderateexerciseintensities(~70%—85% age-adjusted maximum heart rate)significantly increase circulating levels of AEA.16This observation is consistent with findings that several cardio-metabolic risk factors are also most favorably affected by moderate-intensity exercise compared to lowintensity exercise.17

    Third,chronic aerobic exercise has been shown to attenuate CB1 mRNA over-expression in visceral and subcutaneous adipose tissues of obese rats fed with a high-fat diet.18Our unpublished data corroborate these findings by showing that chronic aerobic exercise decreases CB1 protein expression in skeletal muscle of mice fed with a high fat diet.Given the crucial role of skeletal muscle in whole body energy expenditure and substrate oxidation,especially during exercise,this observation may turn out to be of great importance for the treatment of obesity and the associated metabolic disorders.

    Finally,it has been demonstrated that glucocorticoids increase AEA in limbic structures,19indicating that endocannabinoid signaling is evoked by stress-induced activation of the hypothalamic-pituitary-adrenal axis,20which in turn,is inhibited by endocannabinoid signaling via non-genomic fastfeed mechanism.21The concurrent increase in AEA and cortisol observed during intense exercise10suggests that the increase in plasma AEA during exercise may be ascribed to the exercise-induced alterations in circulating cortisol.Thus,it seems that the ECS activation may be essential for the recovery from a transient stressful condition,such as intense physical exercise.

    3.Future challenges

    Accumulating evidence shows that the ECS is associated with physical activity,obesity and related metabolic disorders. However,to date,no data on the responses of the ECS to exercise in patients with metabolic diseases have been published.Whether acute or chronic exercise can attenuate ECS over-activity in humans remains to be confirmed.Both mechanistic and randomized controlled studies are needed to confirm whether the ECS is involved in the beneficial effects of exercise on metabolism and energy balance.Understanding the connection between exercise,ECS and metabolism deserves further investigation as exercise may represent a complementary approach to modulate ECS and treat and prevent obesity and metabolic disorders.

    Acknowledgments

    This study was supported by the Academy of Finland and Shanghai overseas visiting professor scholarship program.

    1.Andre A,Gonthier MP.The endocannabinoid system:its roles in energy balance and potential as a target for obesity treatment.Int J Biochem Cell Biol2010;42:1788—801.

    2.Zanettini C,Panlilio LV,Alicki M,Goldberg SR,Haller J,Yasar S.Effects of endocannabinoid system modulation on cognitive and emotional behavior.Front Behav Neurosci2011;5:57.

    3.Quarta C,Mazza R,Obici S,Pasquali R,Pagotto U.Energy balance regulation by endocannabinoids at central and peripheral levels.Trends Mol Med2011;17:518—26.

    4.Perkins JM,Davis SN.Endocannabinoid system overactivity and the metabolic syndrome:prospects for treatment.Curr Diab Rep2008;8:12—9.

    5.Di Marzo V.CB(1)receptor antagonism:biological basis for metabolic effects.Drug Discov Today2008;13:1026—41.

    6.Silvestri C,Di Marzo V.Second generation CB1 receptor blockers and other inhibitors of peripheral endocannabinoid overactivity and the rationale of their use against metabolic disorders.Expert Opin Investig Drugs2012;21:1309—22.

    7.You T,Disanzo BL,Wang X,Yang R,Gong D.Adipose tissue endocannabinoid system gene expression:depot differences and effects of diet and exercise.Lipids Health Dis2011;10:194.

    8.Heyman E,Gamelin FX,Aucouturier J,Di Marzo V.The role of the endocannabinoid system in skeletal muscle and metabolic adaptations to exercise:potential implications for the treatment of obesity.Obes Rev2012;13:1110—24.

    9.Feuerecker M,Hauer D,Toth R,Demetz F,Holzl J,Thiel M,et al.Effects of exercise stress on the endocannabinoid system in humans under field conditions.Eur J Appl Physiol2012;112:2777—81.

    10.Heyman E,Gamelin FX,Goekint M,Piscitelli F,Roelands B,Leclair E, et al.Intense exercise increases circulating endocannabinoid and BDNF levels in humans—possible implications for reward and depression.Psychoneuroendocrinology2012;37:844—51.

    11.Wagner JA,Jarai Z,Batkai S,Kunos G.Hemodynamic effects of cannabinoids:coronary and cerebral vasodilation mediated by cannabinoid CB(1)receptors.Eur J Pharmacol2001;423:203—10.

    12.Calignano A,Katona I,Desarnaud F,Giuffrida A,La Rana G,Mackie K, et al.Bidirectional control of airway responsiveness by endogenous cannabinoids.Nature2000;408:96—101.

    13.Eckardt K,Sell H,Taube A,Koenen M,Platzbecker B,Cramer A,et al. Cannabinoidtype1receptorsinhumanskeletalmusclecellsparticipateinthe negative crosstalk between fat and muscle.Diabetologia2009;52:664—74.

    14.Guzman M,Fernandez-Ruiz JJ,Sanchez C,Velasco G,Ramos JA.Effects of anandamide on hepatic fatty acid metabolism.Biochem Pharmacol1995;50:885—8.

    15.Ruby MA,Nomura DK,Hudak CS,Barber A,Casida JE,Krauss RM. Acute overactive endocannabinoid signaling induces glucose intolerance, hepatic steatosis,and novel cannabinoid receptor 1 responsive genes.PLoS One2011;6:e26415.

    16.Raichlen DA,Foster AD,Seillier A,Giuffrida A,Gerdeman GL.Exercise-induced endocannabinoid signaling is modulated by intensity.Eur J Appl Physiol2012.Sep 19.[Epub ahead of print].

    17.Slentz CA,Houmard JA,Kraus WE.Exercise,abdominal obesity,skeletal muscle,and metabolic risk:evidence for a dose response.Obes(Silver Spring)2009;17(Suppl.3):S27—33.

    18.Yan ZC,Liu DY,Zhang LL,Shen CY,Ma QL,Cao TB,et al.Exercise reduces adipose tissue via cannabinoid receptor type 1 which is regulated by peroxisome proliferator-activated receptor-delta.Biochem Biophys Res Commun2007;354:427—33.

    19.Hill MN,Karatsoreos IN,Hillard CJ,McEwen BS.Rapid elevations in limbic endocannabinoid content by glucocorticoid hormonesin vivo.Psychoneuroendocrinology2010;35:1333—8.

    20.Hill MN,Tasker JG.Endocannabinoid signaling,glucocorticoid-mediated negative feedback,and regulation of the hypothalamic-pituitary-adrenal axis.Neuroscience2012;204:5—16.

    21.Evanson NK,Tasker JG,Hill MN,Hillard CJ,Herman JP.Fast feedback inhibition of the HPA axis by glucocorticoids is mediated by endocannabinoid signaling.Endocrinology2010;151:4811—9.

    Received 18 January 2013;accepted 21 January 2013

    2095-2546/$-see front matter Copyright?2013,Shanghai University of Sport.Production and hosting by Elsevier B.V.All rights reserved. http://dx.doi.org/10.1016/j.jshs.2013.01.003

    *Corresponding author.School of Kinesiology,Shanghai University of Sport, Shanghai 200438,China.

    E-mail address:sulin.cheng@jyu.f i(S.Cheng)

    Peer review under responsibility of Shanghai University of Sport

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