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Lactobacillus rhamnosus JY02 Ameliorates Sarcopenia by Anti-Atrophic Effects in a Dexamethasone-Induced Cellular and Murine Model

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Sarcopenia is defined as loss of muscle mass and strength due to aging. Recent studies show that sarcopenia may improve via the gut–muscle axis, suggesting that gut health may affect muscle phenotypes. In this study, we aimed to investigate the ability of Lactobacillus rhamnosus JY02 as a probiotic strain isolated from kimchi to alleviate sarcopenia. L. rhamnosus JY02-conditioned medium (CM) reduced dexamethasone (DEX)-induced myotube diameter atrophy and expression of muscle degradation markers (MuRF1 and atrogin-1) in C2C12 cells. The amelioration of sarcopenia was investigated by measuring body composition (lean mass), hand grip strength, myofibril size (using histological analysis), and mRNA and protein expression of muscle-related factors in a DEX-induced mouse model. The results of these analyses showed that L. rhamnosus JY02 supplementation promoted the production of muscle-enhancement markers (MHC Iβ, MHC IIα, and Myo-D) and reduced both the production of muscle degradation markers and the symptoms of muscle atrophy (loss of lean mass and muscle strength). We also found decreased levels of pro-inflammatory cytokines (IL-6, IFN- γ) and increased levels of anti-inflammatory cytokines (IL-10) in the serum of DEX+JY02-administered mice compared to those in DEX-treated mice. Overall, these results suggest that L. rhamnosus JY02 is a potent probiotic supplement that prevents sarcopenia by suppressing muscle atrophy.

Abstract

Sarcopenia is defined as loss of muscle mass and strength due to aging. Recent studies show that sarcopenia may improve via the gut–muscle axis, suggesting that gut health may affect muscle phenotypes. In this study, we aimed to investigate the ability of Lactobacillus rhamnosus JY02 as a probiotic strain isolated from kimchi to alleviate sarcopenia. L. rhamnosus JY02-conditioned medium (CM) reduced dexamethasone (DEX)-induced myotube diameter atrophy and expression of muscle degradation markers (MuRF1 and atrogin-1) in C2C12 cells. The amelioration of sarcopenia was investigated by measuring body composition (lean mass), hand grip strength, myofibril size (using histological analysis), and mRNA and protein expression of muscle-related factors in a DEX-induced mouse model. The results of these analyses showed that L. rhamnosus JY02 supplementation promoted the production of muscle-enhancement markers (MHC Iβ, MHC IIα, and Myo-D) and reduced both the production of muscle degradation markers and the symptoms of muscle atrophy (loss of lean mass and muscle strength). We also found decreased levels of pro-inflammatory cytokines (IL-6, IFN- γ) and increased levels of anti-inflammatory cytokines (IL-10) in the serum of DEX+JY02-administered mice compared to those in DEX-treated mice. Overall, these results suggest that L. rhamnosus JY02 is a potent probiotic supplement that prevents sarcopenia by suppressing muscle atrophy.

참고문헌 (70)

  1. Ali S, "Sarcopenia, cachexia and aging: diagnosis, mechanisms and therapeutic options - a mini-review", Gerontology, 60, pp.294~305 (2014)
  2. Wiedmer P, "Sarcopenia - molecular mechanisms and open questions", Ageing Res. Rev, 65, pp.101200~ (2021)
  3. Xie WQ, "Mouse models of sarcopenia: classification and evaluation", J. Cachexia Sarcopenia Muscle, 12, pp.538~554 (2021)
  4. Giron M, "Gut microbes and muscle function: can probiotics make our muscles stronger?", J. Cachexia Sarcopenia Muscle, 13, pp.1460~1476 (2022)
  5. Jimenez-Gutierrez GE, "Molecular mechanisms of inflammation in sarcopenia: Diagnosis and therapeutic update", Cells, 11, pp.2359~ (2022)
  6. Nardone OM, "Inflammatory bowel diseases and sarcopenia: The role of inflammation and gut microbiota in the development of muscle failure", Front. Immunol, 12, pp.694217~ (2021)
  7. Li HY, "Effects and mechanisms of probiotics, prebiotics, synbiotics, and postbiotics on metabolic diseases targeting gut microbiota: A narrative review", Nutrients, 13, pp.3211~ (2021)
  8. Strasser B, "The effects of lifestyle and diet on gut microbiota composition, inflammation and muscle performance in our aging society", Nutrients, 13, pp.2045~ (2021)
  9. van Krimpen SJ, "The effects of Pro-, Pre-, and synbiotics on muscle wasting, a systematic review-gut permeability as potential treatment target", Nutrients, 13, pp.1115~ (2021)
  10. de Vrese M, "Probiotics, prebiotics, and synbiotics", Adv. Biochem. Eng. Biotechnol, 111, pp.1~66 (2008)
  11. Jäger R, "Probiotic administration increases amino acid absorption from plant protein: a placebo-controlled, randomized, double-blind, multicenter, crossover study", Probiotics Antimicrob. Proteins, 12, pp.1330~1339 (2020)
  12. Gamallat Y, "Lactobacillus rhamnosus induced epithelial cell apoptosis, ameliorates inflammation and prevents colon cancer development in an animal model", Biomed. Pharmacother, 83, pp.536~541 (2016)
  13. Azad MAK, "Probiotic species in the modulation of gut microbiota: an overview", BioMed Res. Int, 2018, pp.9478630~ (2018)
  14. Pagnini C, "Mucosal adhesion and anti-inflammatory effects of Lactobacillus rhamnosus GG in the human colonic mucosa: A proof-of-concept study", World J. Gastroenterol, 24, pp.4652~4662 (2018)
  15. Slover CM, "Lactobacillus: a review", Clin. Microbiol. Newslett, 30, pp.23~27 (2008)
  16. Li B, "Lactobacillus helveticus KLDS1. 8701 alleviates d-galactose-induced aging by regulating Nrf-2 and gut microbiota in mice", 9, pp.6586~6598 (2018)
  17. Lee CC, "Lactobacillus plantarum TWK10 attenuates aging-associated muscle weakness, bone loss, and cognitive impairment by modulating the gut microbiome in mice", Front. Nutr, 8, pp.708096~ (2021)
  18. 김선균, "Role of Probiotics in Human Gut Microbiome-Associated Diseases", Journal of Microbiology and Biotechnology, 29(9), pp.1335~1340 (2019), 한국미생물·생명공학회[DOI]
  19. Markowiak P, "Effects of probiotics, prebiotics, and synbiotics on human health", Nutrients, 9, pp.1021~ (2017)
  20. Prokopidis K, "Impact of probiotics on muscle mass, muscle strength, and lean body mass: a systematic review and meta-analysis Jof randomized controlled trials", J. Cachexia Sarcopenia Muscle, 14, pp.30~44 (2022)
  21. Lee K, "Lactobacillus plantarum HY7715 ameliorates sarcopenia by improving skeletal muscle mass and function in aged Balb", c mice, 2021, pp.22, 10023~
  22. Chen LH, "Probiotic supplementation attenuates age-related sarcopenia via the gut-muscle axis in SAMP8 mice", J. Cachexia Sarcopenia Muscle, 13, pp.515~531 (2022)
  23. Bindels LB, "Restoring specific lactobacilli levels decreases inflammation and muscle atrophy markers in an acute leukemia mouse model", PLoS One, 7, pp.e37971~ (2012)
  24. Mehta J, "Role of dexamethasone and methylprednisolone corticosteroids in Coronavirus disease 2019 hospitalized patients: a review", Front. Microbiol, 13, pp.813358~ (2022)
  25. Noreen S, "Dexamethasone: Therapeutic potential, risks, and future projection during COVID-19pandemic", Eur. J. Pharmacol, 894, pp.173854~ (2021)
  26. Jiang R, "Panax ginseng total protein facilitates recovery from dexamethasoneinduced muscle atrophy through the activation of glucose consumption in C2C12 myotubes", BioMed Res. Int, 2019, pp.3719643~ (2019)
  27. Jia H, "Laurel attenuates dexamethasone-induced skeletal muscle atrophy in vitro and in a rat model", Nutrients, 14, pp.2029~ (2022)
  28. Baehr LM, "Muscle sparing in muscle RING finger 1 null mice: response to synthetic glucocorticoids", J. Physiol, 589, pp.4759~4776 (2011)
  29. Seo E, "Psoralea corylifolia L. seed extract attenuates dexamethasone-induced muscle atrophy in mice by inhibition of oxidative stress and inflammation", J. Ethnopharmacol, 296, pp.115490~ (2022)
  30. Wang BYH, "Is dexamethasone-induced muscle atrophy an alternative model for naturally aged sarcopenia model?", J. Orthop. Translat, 39, pp.12~20 (2023)
  31. Otsuka Y, "Quercetin glycosides prevent dexamethasone-induced muscle atrophy in mice", Biochem. Biophys. Rep, 18, pp.100618~ (2019)
  32. Massaccesi L, "Dexamethasone-induced skeletal muscle atrophy increases O-GlcNAcylation in C2C12 cells", J. Cell Biochem, 117, pp.1833~1842 (2016)
  33. Ticinesi A, "Aging gut microbiota at the cross-road between nutrition, physical frailty, and sarcopenia: is there a gut-muscle axis?", Nutrients, 9, pp.1303~ (2017)
  34. Przewłócka K, "Gut-muscle axis exists and may affect skeletal muscle adaptation to training", Nutrients, 12, pp.1451~ (2020)
  35. Chen LH, "Probiotic supplementation attenuates age-related sarcopenia via the gut–muscle axis in SAMP8 mice", J. Cachexia Sarcopenia Muscle, 13, pp.515~531 (2022)
  36. Markowiak-Kopeć P, "The Effect of Probiotics on the production of short-chain fatty acids by human intestinal microbiome", Nutrients, 12, pp.1107~ (2020)
  37. Zhao J, "A narrative review of gut-muscle axis and sarcopenia: the potential role of gut microbiota", Int. J. Gen. Med, 14, pp.1263~1273 (2021)
  38. Gou HZ, "How do intestinal probiotics restore the intestinal barrier?", Front. Microbiol, 13, pp.929346~ (2022)
  39. Liu Q, "Surface components and metabolites of probiotics for regulation of intestinal epithelial barrier", Microb. Cell Fact, 19, pp.23~ (2020)
  40. Indira M, "Bioactive molecules of probiotic bacteria and their mechanism of action: a review", 3 Biotech, 9, pp.306~ (2019)
  41. Park YS, "Quantitative analysis of myosin heavy chain (MHC) mRNA expression in thyropharyngeus muscle and cricopharyngeus muscle in rats", Korean J. Otorhinolaryngol-Head Neck Surg, 43, pp.300~305 (2000)
  42. Konopka AR, "Myosin heavy chain plasticity in aging skeletal muscle with aerobic exercise training", J. Gerontol. Series A, 66A, pp.835~841 (2011)
  43. Chen L, "Matrine improves skeletal muscle atrophy by inhibiting E3 ubiquitin ligases and activating the Akt", mTOR, Oncol. Rep, pp.2019, 42[DOI]
  44. Wijaya YT, "Amelioration of muscle wasting by gintonin in cancer cachexia", Neoplasia (New York, N.Y.), 23, pp.1307~1317 (2021)
  45. Parry T, "Muscle-specific ubiquitin ligase MuRF1 regulates myocardial autophagic flux in vivo", 29, pp.148~ (2015)
  46. Kitajima Y, "The ubiquitin–proteasome system in regulation of the skeletal muscle homeostasis and atrophy: from basic science to disorders", J. Physiol. Sci, 70, pp.40~ (2020)
  47. Bindels LB, "Restoring specific lactobacilli levels decreases inflammation and muscle atrophy markers in an acute leukemia mouse model", PLoS One, 7, pp.e37971~ (2012)
  48. Bodine SC, "Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx", atrogin-1, 2014, pp.307, E469~E484
  49. Gumucio JP, "Atrogin-1, MuRF-1, and sarcopenia", Endocrine, 43, pp.12~21 (2013)
  50. 송영준, "Setdb1 Is Required for Myogenic Differentiation of C2C12 Myoblast Cells via Maintenance of MyoD Expression", Molecules and Cells, 38(4), pp.362~372 (2015), 한국분자세포생물학회
  51. Lin M, "Alpha mangostin promotes myogenic differentiation of C2C12 mouse myoblast cells", Biochem. Biophys. Res. Commun, 528, pp.193~198 (2020)
  52. Liu XH, "Nandrolone-induced nuclear accumulation of MyoD protein is mediated by Numb, a Notch inhibitor, in C2C12 myoblasts", Physiol. Rep, 6, pp.e13520~ (2018)
  53. Luo W, "Myomaker, regulated by MYOD, MYOG and miR-140-3p, promotes chicken myoblast fusion", Int. J. Mol. Sci, 16, pp.26186~26201 (2015)
  54. Hong Y, "Amelioration of muscle wasting by glucagon-like peptide-1 receptor agonist in muscle atrophy", J. Cachexia Sarcopenia Muscle, 10, pp.903~918 (2019)
  55. Lee MC, "Effectiveness of human-origin Lactobacillus plantarum PL-02 in improving muscle mass, exercise performance and anti-fatigue", 11, pp.19469~ (2021)
  56. Chen L, "Probiotic Lactobacillus rhamnosus GG reduces mortality of septic mice by modulating gut microbiota composition and metabolic profiles", 78, pp.110863~ (2020)
  57. Pomeroy E, "Relationship between body mass, lean mass, fat mass, and limb bone cross-sectional geometry: implications for estimating body mass and physique from the skeleton", Am. J. Phys. Anthr, 166, pp.56~69 (2018)
  58. Klover P, "Skeletal muscle growth and fiber composition in mice are regulated through the transcription factors STAT5a", b: linking growth hormone to the androgen receptor, 2009, pp.23, 3140~3148
  59. Kim S, "Curcuma longa L. Water extract improves dexamethasone-induced sarcopenia by modulating the muscle-related gene and oxidative stress in mice", Antioxidants, 10, pp.1000~ (2021)
  60. Sang Yoon Lee, "Handgrip Strength: An Irreplaceable Indicator of Muscle Function", Annals of Rehabilitation Medicine, 45(3), pp.167~169 (2021), 대한재활의학회[DOI]
  61. Savary I, "Effect of glucocorticoid excess on skeletal muscle and heart protein synthesis in adult and old rats", Br. J. Nutr, 79, pp.297~304 (1998)
  62. Wells L, "Myosin heavy chain isoforms regulate muscle function but not myofibril assembly", Embo J, 15, pp.4454~4459 (1996)
  63. Lee H, "Chrysanthemum zawadskil herbich attenuates dexamethasoneinduced muscle atrophy through the regulation of proteostasis and mitochondrial function", Biomed. Pharmacother, 136, pp.111226~ (2021)
  64. Hata J, "Noninvasive technique to evaluate the muscle fiber characteristics using q-space imaging", PLoS One, 14, pp.e0214805~ (2019)
  65. Ramón Ríos, "Myostatin is an inhibitor of myogenic differentiation", Am. J. Physiol. Cell Physiol, 282, pp.C993~C999 (2002)
  66. White TA, "Myostatin and Sarcopenia: opportunities and challenges - a mini-review", Gerontology, 60, pp.289~293 (2014)
  67. Dong Y, "Myostatin suppression of akirin1 mediates glucocorticoid-induced satellite cell dysfunction", PLoS One, 8, pp.e58554~ (2013)
  68. Pedersen M, "Circulating levels of TNF-alpha and IL-6-relation to truncal fat mass and muscle mass in healthy elderly individuals and in patients with type-2 diabetes", Mech. Ageing. Dev, 124, pp.495~502 (2003)
  69. Rong YD, "Study on relationship between elderly sarcopenia and inflammatory cytokine IL-6, anti-inflammatory cytokine IL-10", BMC Geriatr, 18, pp.308~ (2018)
  70. Visser M, "Relationship of interleukin-6 and tumor necrosis factor-alpha with muscle mass and muscle strength in elderly men and women: the Health ABC Study", J. Gerontol. A Biol. Sci. Med. Sci, 57, pp.M326~M332 (2002)

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