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Animals : an open access journal from MDPI2025; 15(2); 215; doi: 10.3390/ani15020215

Methylsulfonylmethane (MSM) Supplementation in Adult Horses Supports Improved Skeletal Muscle Inflammatory Gene Expression Following Exercise.

Abstract: Methylsulfonylmethane (MSM) is a sulfur-containing molecule with reported anti-inflammatory and antioxidant activities. Exercise causes the formation of free radicals and stimulates inflammatory gene expression in leukocytes and skeletal muscle. The hypothesis that dietary supplementation with MSM alters the exercise-mediated inflammatory and oxidant response was assessed in unfit adult thoroughbred geldings. Ten geldings (6.7 ± 1.6 yr) were assigned to a diet supplemented without (CON, = 5) or with 21 g of MSM ( = 5) for 30 days. Following the supplementation period, horses performed a standardized exercise test (SET) with blood collections before (t = 0), 10 min, 1 h, 4 h, and 24 h post-SET. Skeletal muscle biopsies were retrieved from the middle gluteus before and 1 h post-SET for total RNA isolation. All horses were rested for 120 days before the experiment was repeated in a cross-over design. Plasma total antioxidant capacity was unaffected ( > 0.05) by either exercise or MSM. Plasma glutathione peroxidase activity was less ( 0.05) by either exercise or diet. Transcriptomic analysis of skeletal muscle revealed 35 genes were differentially expressed (DEG; 0.2; q < 0.05) by comparison to the CON (237), with many of these mapping to the immune response (71) and cytokine signal transduction (60) pathways. These results suggest supplementation of MSM as a dietary aid for improved anti-inflammatory responses in skeletal muscle following exercise.
Publication Date: 2025-01-14 PubMed ID: 39858215PubMed Central: PMC11758608DOI: 10.3390/ani15020215Google Scholar: Lookup
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  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research suggests that dietary supplementation with Methylsulfonylmethane (MSM) might enhance anti-inflammatory responses in skeletal muscle following exercise in adult horses.

Introduction and Methodology

  • This study tested the hypothesis that supplementing the diet with Methylsulfonylmethane (MSM), a sulfur-containing molecule known for its anti-inflammatory and antioxidant properties, could alter the inflammation and oxidant response typically initiated by exercise. The subjects of this study were unfit adult thoroughbred geldings (neturated male horses).
  • A total of 10 geldings were used in the experiment, with five assigned to a regular diet (the control group or CON) and five supplemented with 21 grams of MSM for 30 days.
  • The horses partook in a standardized exercise test (SET), with blood collections carried out at different intervals before and after the SET. Moreover, skeletal muscle biopsies were taken from the middle gluteus both before and one hour after the SET for total RNA isolation.
  • The experiment was conducted twice, with a rest period of 120 days in between, in a cross-over design. This means that the two groups switched diets in the second phase of the experiment.

Results and Findings

  • The outcome suggests that neither exercise nor MSM supplementation impacted plasma total antioxidant capacity (TAC). Compared to the CON group, the MSM-supplemented horses exhibited less plasma glutathione peroxidase activity, suggesting a lower production of free radicals or oxidative stress.
  • The levels of different inflammation markers (IL6, IL8, IL10, and TNFα) in plasma remained unaffected by exercise or diet, indicating that systemic inflammation was not induced.
  • Transcriptomic analysis of skeletal muscle revealed 35 genes showing some change in expression (2-fold or more) in response to exercise, although there were no noticeable changes caused directly by MSM. However, when the gene expression changes caused by exercise were compared between the diets, the MSM group showed a higher number (630) of exercise-responsive genes compared to the CON group (only 237).
  • Many of the exercise-responsive genes in the MSM-supplemented horses were mapped to the immune response and cytokine signal transduction pathways, suggesting a higher level of localized inflammation response.

Conclusion

  • The results indicate that MSM supplementation could enhance the anti-inflammatory response in skeletal muscle following physical exertion. This hints at MSM’s potential as a dietary aid for managing post-exercise inflammation in the skeletal muscles of horses, although further research is needed to ascertain these findings.

Cite This Article

APA
Barshick MR, Ely KM, Mogge KC, Chance LM, Johnson SE. (2025). Methylsulfonylmethane (MSM) Supplementation in Adult Horses Supports Improved Skeletal Muscle Inflammatory Gene Expression Following Exercise. Animals (Basel), 15(2), 215. https://doi.org/10.3390/ani15020215

Publication

ISSN: 2076-2615
NlmUniqueID: 101635614
Country: Switzerland
Language: English
Volume: 15
Issue: 2
PII: 215

Researcher Affiliations

Barshick, Madison R
  • School of Animal Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24060, USA.
Ely, Kristine M
  • School of Animal Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24060, USA.
Mogge, Keely C
  • School of Animal Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24060, USA.
Chance, Lara M
  • School of Animal Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24060, USA.
Johnson, Sally E
  • School of Animal Sciences, Virginia Polytechnic Institute and State University, Blacksburg, VA 24060, USA.

Grant Funding

  • G20 AI167200 / NIAID NIH HHS
  • UC6 AI058607 / NIAID NIH HHS
  • UC7 AI180254 / NIAID NIH HHS

Conflict of Interest Statement

The authors declare no conflicts of interest.

References

This article includes 60 references
  1. Chalchat E, Gaston A-F, Charlot K, Peñailillo L, Valdés O, Tardo-Dino P-E, Nosaka K, Martin V, Garcia-Vicencio S, Siracusa J. Appropriateness of Indirect Markers of Muscle Damage Following Lower Limbs Eccentric-Biased Exercises: A Systematic Review with Meta-Analysis. PLoS ONE 2022;17:e0271233.
  2. Morgan D.L, Allen D.G. Early Events in Stretch-Induced Muscle Damage. J. Appl. Physiol. 1999;87:2007–2015.
    doi: 10.1152/jappl.1999.87.6.2007pubmed: 10601142google scholar: lookup
  3. Tidball J.G, Villalta S.A. Regulatory Interactions between Muscle and the Immune System during Muscle Regeneration. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2010;298:R1173–R1187.
    doi: 10.1152/ajpregu.00735.2009pmc: PMC2867520pubmed: 20219869google scholar: lookup
  4. Chazaud B. Inflammation and Skeletal Muscle Regeneration: Leave It to the Macrophages!. Trends Immunol. 2020;41:481–492.
    doi: 10.1016/j.it.2020.04.006pubmed: 32362490google scholar: lookup
  5. Minari A.L.A, Thomatieli-Santos R.V. From Skeletal Muscle Damage and Regeneration to the Hypertrophy Induced by Exercise: What Is the Role of Different Macrophage Subsets?. Am. J. Physiol. Regul. Integr. Comp. Physiol. 2022;322:R41–R54.
    doi: 10.1152/ajpregu.00038.2021pubmed: 34786967google scholar: lookup
  6. Powers S.K, Radak Z, Ji L.L, Jackson M. Reactive Oxygen Species Promote Endurance Exercise-Induced Adaptations in Skeletal Muscles. J. Sport. Health Sci. 2024;13:780–792.
    doi: 10.1016/j.jshs.2024.05.001pmc: PMC11336304pubmed: 38719184google scholar: lookup
  7. Reid M.B. Reactive Oxygen Species as Agents of Fatigue. Med. Sci. Sports Exerc. 2016;48:2239–2246.
    doi: 10.1249/MSS.0000000000001006pubmed: 27285492google scholar: lookup
  8. Mrugala D, Leatherwood J.L, Morris E.F, Dickson E.C, Latham C.M, Owen R.N, Beverly M.M, Kelley S.F, White-Springer S.H. Dietary Conjugated Linoleic Acid Supplementation Alters Skeletal Muscle Mitochondria and Antioxidant Status in Young Horses. J. Anim. Sci. 2021;99:skab037.
    doi: 10.1093/jas/skab037pmc: PMC7918170pubmed: 33539534google scholar: lookup
  9. Latham C.M, Dickson E.C, Owen R.N, Larson C.K, White-Springer S.H. Complexed Trace Mineral Supplementation Alters Antioxidant Activities and Expression in Response to Trailer Stress in Yearling Horses in Training. Sci. Rep. 2021;11:7352.
    doi: 10.1038/s41598-021-86478-7pmc: PMC8016935pubmed: 33795725google scholar: lookup
  10. White S.H, Johnson S.E, Bobel J.M, Warren L.K. Dietary Selenium and Prolonged Exercise Alter Gene Expression and Activity of Antioxidant Enzymes in Equine Skeletal Muscle. J. Anim. Sci. 2016;94:2867–2878.
    doi: 10.2527/jas.2016-0348pubmed: 27482673google scholar: lookup
  11. Butawan M, Benjamin R.L, Bloomer R.J. Methylsulfonylmethane: Applications and Safety of a Novel Dietary Supplement. Nutrients 2017;9:290.
    doi: 10.3390/n逰290pmc: PMC5372953pubmed: 28300758google scholar: lookup
  12. Nakhostin-Roohi B, Barmaki S, Khoshkhahesh F, Bohlooli S. Effect of Chronic Supplementation with Methylsulfonylmethane on Oxidative Stress Following Acute Exercise in Untrained Healthy Men. J. Pharm. Pharmacol. 2011;63:1290–1294.
  13. van der Merwe M, Bloomer R.J. The Influence of Methylsulfonylmethane on Inflammation-Associated Cytokine Release before and Following Strenuous Exercise. J. Sports Med. 2016;2016:7498359.
    doi: 10.1155/2016/7498359pmc: PMC5097813pubmed: 27844051google scholar: lookup
  14. Toguchi A, Noguchi N, Kanno T, Yamada A. Methylsulfonylmethane Improves Knee Quality of Life in Participants with Mild Knee Pain: A Randomized, Double-Blind, Placebo-Controlled Trial. Nutrients 2023;15:2995.
    doi: 10.3390/nᔓ2995pmc: PMC10346176pubmed: 37447322google scholar: lookup
  15. Kalman D.S, Feldman S, Scheinberg A.R, Krieger D.R, Bloomer R.J. Influence of Methylsulfonylmethane on Markers of Exercise Recovery and Performance in Healthy Men: A Pilot Study. J. Int. Soc. Sports Nutr. 2012;9:46.
    doi: 10.1186/1550-2783-9-46pmc: PMC3507661pubmed: 23013531google scholar: lookup
  16. Withee E.D, Tippens K.M, Dehen R, Tibbitts D, Hanes D, Zwickey H. Effects of Methylsulfonylmethane (MSM) on Exercise-Induced Oxidative Stress, Muscle Damage, and Pain Following a Half-Marathon: A Double-Blind, Randomized, Placebo-Controlled Trial. J. Int. Soc. Sports Nutr. 2017;14:24.
    doi: 10.1186/s12970-017-0181-zpmc: PMC5521097pubmed: 28736511google scholar: lookup
  17. Marañón G, Muñoz-Escassi B, Manley W, García C, Cayado P, de la Muela M.S, Olábarri B, León R, Vara E. The Effect of Methyl Sulphonyl Methane Supplementation on Biomarkers of Oxidative Stress in Sport Horses Following Jumping Exercise. Acta Vet. Scand. 2008;50:45.
    doi: 10.1186/1751-0147-50-45pmc: PMC2586020pubmed: 18992134google scholar: lookup
  18. Henneke D.R, Potter G.D, Kreider J.L, Yeates B.F. Relationship between Condition Score, Physical Measurements and Body Fat Percentage in Mares. Equine Vet. J. 1983;15:371–372.
  19. Gregg S.R, Barshick M.R, Johnson S.E. Intravenous Injection of Sodium Hyaluronate Diminishes Basal Inflammatory Gene Expression in Equine Skeletal Muscle. Animals 2023;13:3030.
    doi: 10.3390/ani13193030pmc: PMC10571686pubmed: 37835636google scholar: lookup
  20. Busse N.I, Gonzalez M.L, Krason M.L, Johnson S.E. β-Hydroxy β-Methylbutyrate Supplementation to Adult Thoroughbred Geldings Increases Type IIA Fiber Content in the Gluteus Medius. J. Anim. Sci. 2021;99:skab264.
    doi: 10.1093/jas/skab264pmc: PMC8493890pubmed: 34516615google scholar: lookup
  21. Akhmedov M, Martinelli A, Geiger R, Kwee I. Omics Playground: A Comprehensive Self-Service Platform for Visualization, Analytics and Exploration of Big Omics Data. NAR Genom. Bioinform. 2020;2:lqz019.
    doi: 10.1093/nargab/lqz019pmc: PMC7671354pubmed: 33575569google scholar: lookup
  22. Milacic M, Beavers D, Conley P, Gong C, Gillespie M, Griss J, Haw R, Jassal B, Matthews L, May B. The Reactome Pathway Knowledgebase 2024. Nucleic Acids Res. 2024;52:D672–D678.
    doi: 10.1093/nar/gkad1025pmc: PMC10767911pubmed: 37941124google scholar: lookup
  23. Fabregat A, Sidiropoulos K, Viteri G, Forner O, Marin-Garcia P, Arnau V, D’Eustachio P, Stein L, Hermjakob H. Reactome Pathway Analysis: A High-Performance in-Memory Approach. BMC Bioinform. 2017;18:142.
    doi: 10.1186/s12859-017-1559-2pmc: PMC5333408pubmed: 28249561google scholar: lookup
  24. Leguillette R, Bond S.L, Lawlor K, de Haan T, Weber L.M. Comparison of Physiological Demands in Warmblood Show Jumping Horses over a Standardized 1.10 m Jumping Course versus a Standardized Exercise Test on a Track. BMC Vet. Res. 2020;16:182–189.
    doi: 10.1186/s12917-020-02400-9pmc: PMC7282170pubmed: 32513241google scholar: lookup
  25. Riley J.W, Chance L.M, Barshick M.R, Johnson S.E. Administration of Sodium Hyaluronate to Adult Horses Prior to and Immediately after Exercise Does Not Alter the Range of Motion in Either the Tarsus or Metacarpophalangeal Joints. Transl. Anim. Sci. 2024;8:txae153.
    doi: 10.1093/tas/txae153pmc: PMC11568345pubmed: 39554613google scholar: lookup
  26. Powers S.K, Goldstein E, Schrager M, Ji L.L. Exercise Training and Skeletal Muscle Antioxidant Enzymes: An Update. Antioxidants 2022;12:39.
    doi: 10.3390/antiox12010039pmc: PMC9854578pubmed: 36670901google scholar: lookup
  27. White S.H, Warren L.K. Submaximal Exercise Training, More than Dietary Selenium Supplementation, Improves Antioxidant Status and Ameliorates Exercise-Induced Oxidative Damage to Skeletal Muscle in Young Equine Athletes. J. Anim. Sci. 2017;95:657–670.
    doi: 10.2527/jas.2016.1130pubmed: 29432539google scholar: lookup
  28. Williams C.A, Gordon M.E, Betros C.L, McKeever K.H. Apoptosis and Antioxidant Status Are Influenced by Age and Exercise Training in Horses. J. Anim. Sci. 2008;86:576–583.
    doi: 10.2527/jas.2007-0585pubmed: 18156356google scholar: lookup
  29. Ott E.C, Cavinder C.A, Wang S, Smith T, Lemley C.O, Dinh T.T.N. Oxidative Stress Biomarkers and Free Amino Acid Concentrations in the Blood Plasma of Moderately Exercised Horses Indicate Adaptive Response to Prolonged Exercise Training. J. Anim. Sci. 2022;100:skac086.
    doi: 10.1093/jas/skac086pmc: PMC9030216pubmed: 35298640google scholar: lookup
  30. Peake J.M, Neubauer O, Della Gatta P.A, Nosaka K. Muscle Damage and Inflammation during Recovery from Exercise. J. Appl. Physiol. 2017;122:559–570.
  31. Niemelä M, Niemelä O, Bloigu R, Bloigu A, Kangastupa P, Juvonen T. Serum Calprotectin, a Marker of Neutrophil Activation, and Other Mediators of Inflammation in Response to Various Types of Extreme Physical Exertion in Healthy Volunteers. J. Inflamm. Res. 2020;13:223–231.
    doi: 10.2147/JIR.S250675pmc: PMC7250293pubmed: 32547154google scholar: lookup
  32. Gökbel H, Okudan N, Gül I, Belviranli M, Gergerlioğlu H.S, Başaral M.K. Effects of Repeated Bouts of Supramaximal Exercise on Plasma Adiponectin, Interleukin-6, and Tumor Necrosis Factor-α Levels in Sedentary Men. J. Strength Cond. Res. 2012;26:1675–1679.
    doi: 10.1519/JSC.0b013e318231ac1cpubmed: 22614149google scholar: lookup
  33. Zabriskie H.A, Blumkaitis J.C, Moon J.M, Currier B.S, Stefan R, Ratliff K, Harty P.S, Stecker R.A, Rudnicka K, Jäger R. Yeast Beta-Glucan Supplementation Downregulates Markers of Systemic Inflammation after Heated Treadmill Exercise. Nutrients 2020;12:1144.
    doi: 10.3390/nሄ1144pmc: PMC7230631pubmed: 32325856google scholar: lookup
  34. Suagee-Bedore J.K, Shen Y, Porr S, Girard I.D, Bennett-Wimbush K, Wagner A.L. Impacts of DigestaWell NRG Supplementation on Post Exercise Muscle Soreness in Unconditioned Horses, a Pilot Study. J. Equine Vet. Sci. 2021;101:103455.
    doi: 10.1016/j.jevs.2021.103455pubmed: 33993938google scholar: lookup
  35. Filho H.C.M, Trindade K.L.G, Silva C.J.F.L, Cruz R.K.S, Vilela C.F, Coelho C.S, Filho J.D.R, Manso H.E.C.C.C. The Welfare of Horses Competing in Three-Barrel Race Events Is Shown to Be Not Inhibited by Short Intervals between Starts. Animals 2024;14:583.
    doi: 10.3390/ani14040583pmc: PMC10886278pubmed: 38396551google scholar: lookup
  36. Valigura H.C, Leatherwood J.L, Martinez R.E, Norton S.A, White-Springer S.H. Dietary Supplementation of a Saccharomyces Cerevisiae Fermentation Product Attenuates Exercise-Induced Stress Markers in Young Horses. J. Anim. Sci. 2021;99:skab199.
    doi: 10.1093/jas/skab199pmc: PMC8521742pubmed: 34181712google scholar: lookup
  37. Hale J.N, Hughes K.J, Hall S, Labens R. The Effect of Exercise on Cytokine Concentration in Equine Autologous Conditioned Serum. Equine Vet. J. 2023;55:551–556.
    doi: 10.1111/evj.13586pubmed: 35569120google scholar: lookup
  38. Moellerberndt J, Hagen A, Niebert S, Büttner K, Burk J. Cytokines in Equine Platelet Lysate and Related Blood Products. Front. Vet. Sci. 2023;10:1117829.
    doi: 10.3389/fvets.2023.1117829pmc: PMC10033973pubmed: 36968472google scholar: lookup
  39. Colahan P.T, Kollias-Bakert C, Leutenegger C.M, Jones J.H. Does Training Affect mRNA Transciption for Cytokine Production in Circulating Leucocytes?. Equine Vet. J. Suppl. 2002;34:154–158.
  40. Donovan D.C, Jackson C.A, Colahan P.T, Norton N, Hurley D.J. Exercise-Induced Alterations in pro-Inflammatory Cytokines and Prostaglandin F2alpha in Horses. Vet. Immunol. Immunopathol. 2007;118:263–269.
    doi: 10.1016/j.vetimm.2007.05.015pubmed: 17617470google scholar: lookup
  41. Eivers S.S, McGivney B.A, Fonseca R.G, MacHugh D.E, Menson K, Park S.D, Rivero J-L.L, Taylor C.T, Katz L.M, Hill E.W. Alterations in Oxidative Gene Expression in Equine Skeletal Muscle Following Exercise and Training. Physiol. Genom. 2010;40:83–93.
  42. Hill E.W, Eivers S.S, McGivney B.A, Fonseca R.G, Gu J, Smith N.A, Browne J.A, MacHugh D.E, Katz L.M. Moderate and High Intensity Sprint Exercise Induce Differential Responses in COX4I2 and PDK4 Gene Expression in Thoroughbred Horse Skeletal Muscle. Equine Vet. J. Suppl. 2010;42:576–581.
  43. Kinnunen S, Hyyppä S, Lappalainen J, Oksala N, Venojärvi M, Nakao C, Hänninen O, Sen C.K, Atalay M. Exercise-Induced Oxidative Stress and Muscle Stress Protein Responses in Trotters. Eur. J. Appl. Physiol. 2005;93:496–501.
    doi: 10.1007/s00421-004-1162-xpubmed: 15221402google scholar: lookup
  44. Ebisuda Y, Mukai K, Takahashi Y, Yoshida T, Kawano A, Matsuhashi T, Miyata H, Kuwahara M, Ohmura H. Acute Exercise in a Hot Environment Increases Heat Shock Protein 70 and Peroxisome Proliferator-Activated Receptor γ Coactivator 1α mRNA in Thoroughbred Horse Skeletal Muscle. Front. Vet. Sci. 2023;10:1230212.
    doi: 10.3389/fvets.2023.1230212pmc: PMC10475567pubmed: 37671280google scholar: lookup
  45. Bending D, Zikherman J. Nr4a Nuclear Receptors: Markers and Modulators of Antigen Receptor Signaling. Curr. Opin. Immunol. 2023;81:102285.
    doi: 10.1016/j.coi.2023.102285pubmed: 36764055google scholar: lookup
  46. De Paoli F, Eeckhoute J, Copin C, Vanhoutte J, Duhem C, Derudas B, Dubois-Chevalier J, Colin S, Zawadzki C, Jude B. The Neuron-Derived Orphan Receptor 1 (NOR1) Is Induced upon Human Alternative Macrophage Polarization and Stimulates the Expression of Markers of the M2 Phenotype. Atherosclerosis 2015;241:18–26.
  47. Pillon N.J, Gabriel B.M, Dollet L, Smith J.A.B, Sardón Puig L, Botella J, Bishop D.J, Krook A, Zierath J.R. Transcriptomic Profiling of Skeletal Muscle Adaptations to Exercise and Inactivity. Nat. Commun. 2020;11:470.
    doi: 10.1038/s41467-019-13869-wpmc: PMC6981202pubmed: 31980607google scholar: lookup
  48. Pearen M.A, Eriksson N.A, Fitzsimmons R.L, Goode J.M, Martel N, Andrikopoulos S, Muscat G.E.O. The Nuclear Receptor, Nor-1, Markedly Increases Type II Oxidative Muscle Fibers and Resistance to Fatigue. Mol. Endocrinol. 2012;26:372–384.
    doi: 10.1210/me.2011-1274pmc: PMC5417129pubmed: 22282471google scholar: lookup
  49. Paez H.G, Ferrandi P.J, Pitzer C.R, Mohamed J.S, Alway S.E. Loss of NOR-1 Represses Muscle Metabolism through mTORC1-Mediated Signaling and Mitochondrial Gene Expression in C2C12 Myotubes. FASEB J. 2023;37:e23050.
    doi: 10.1096/fj.202202029Rpubmed: 37389860google scholar: lookup
  50. Perkins R.K, Lavin K.M, Raue U, Jemiolo B, Trappe S.W, Trappe T.A. Effects of Aging and Lifelong Aerobic Exercise on Expression of Innate Immune Components in Skeletal Muscle of Women. J. Appl. Physiol. 2024;136:482–491.
  51. Perkins R.K, Lavin K.M, Raue U, Jemiolo B, Trappe S.W, Trappe T.A. Effects of Aging and Lifelong Aerobic Exercise on Expression of Innate Immune Components in Human Skeletal Muscle. J. Appl. Physiol. 2020;129:1483–1492.
  52. McFarlin B.K, Hill D.W, Vingren J.L, Curtis J.H, Tanner E.A. Dietary Polyphenol and Methylsulfonylmethane Supplementation Improves Immune, DAMP Signaling, and Inflammatory Responses During Recovery From All-Out Running Efforts. Front. Physiol. 2021;12:712731.
    doi: 10.3389/fphys.2021.712731pmc: PMC8438219pubmed: 34531760google scholar: lookup
  53. Tingstad R.H, Norheim F, Haugen F, Feng Y.Z, Tunsjø H.S, Thoresen G.H, Rustan A.C, Charnock C, Aas V. The Effect of Toll-like Receptor Ligands on Energy Metabolism and Myokine Expression and Secretion in Cultured Human Skeletal Muscle Cells. Sci. Rep. 2021;11:24219.
    doi: 10.1038/s41598-021-03730-wpmc: PMC8688447pubmed: 34930972google scholar: lookup
  54. Tonkin J, Temmerman L, Sampson R.D, Gallego-Colon E, Barberi L, Bilbao D, Schneider M.D, Musarò A, Rosenthal N. Monocyte/Macrophage-Derived IGF-1 Orchestrates Murine Skeletal Muscle Regeneration and Modulates Autocrine Polarization. Mol. Ther. 2015;23:1189–1200.
    doi: 10.1038/mt.2015.66pmc: PMC4817788pubmed: 25896247google scholar: lookup
  55. Welc S.S, Wehling-Henricks M, Antoun J, Ha T.T, Tous I, Tidball J.G. Differential Effects of Myeloid Cell PPARδ and IL-10 in Regulating Macrophage Recruitment, Phenotype, and Regeneration Following Acute Muscle Injury. J. Immunol. 2020;205:1664–1677.
    doi: 10.4049/jimmunol.2000247pmc: PMC7484367pubmed: 32817369google scholar: lookup
  56. Wang L, He C. Nrf2-Mediated Anti-Inflammatory Polarization of Macrophages as Therapeutic Targets for Osteoarthritis. Front. Immunol. 2022;13:967193.
    doi: 10.3389/fimmu.2022.967193pmc: PMC9411667pubmed: 36032081google scholar: lookup
  57. Ma W, Ao S, Zhou J, Li J, Liang X, Yang X, Zhang H, Liu B, Tang W, Liu H. Methylsulfonylmethane Protects against Lethal Dose MRSA-Induced Sepsis through Promoting M2 Macrophage Polarization. Mol. Immunol. 2022;146:69–77.
    doi: 10.1016/j.molimm.2022.04.001pubmed: 35461144google scholar: lookup
  58. Roman W, Muñoz-Cánoves P. Muscle Is a Stage, and Cells and Factors Are Merely Players. Trends Cell. Biol. 2022;32:835–840.
    doi: 10.1016/j.tcb.2022.03.001pubmed: 35370056google scholar: lookup
  59. Hayashiji N, Yuasa S, Miyagoe-Suzuki Y, Hara M, Ito N, Hashimoto H, Kusumoto D, Seki T, Tohyama S, Kodaira M. G-CSF Supports Long-Term Muscle Regeneration in Mouse Models of Muscular Dystrophy. Nat. Commun. 2015;6:6745.
    doi: 10.1038/ncomms7745pubmed: 25865621google scholar: lookup
  60. Li H, Chen Q, Li C, Zhong R, Zhao Y, Zhang Q, Tong W, Zhu D, Zhang Y. Muscle-Secreted Granulocyte Colony-Stimulating Factor Functions as Metabolic Niche Factor Ameliorating Loss of Muscle Stem Cells in Aged Mice. EMBO J. 2019;38:e102154.
    doi: 10.15252/embj.2019102154pmc: PMC6912059pubmed: 31736098google scholar: lookup

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