DOI QR코드

DOI QR Code

Effect of water extract Phellinus linteus-discard Schisandra chinensis solid fermented extracts in an Animal Model of Dexamethasone-Induced Muscle Loss

Dexamethasone으로 유도한 근감소 동물모델에서 상황버섯-오미자박 고상발효 열수추출물의 근감소 개선에 대한 효과

  • Su-Jin, Hwang (Department of Physiology, College of Korean Medicine Dongguk University) ;
  • Young-Suk, Kim (Glucan Co. Ltd.) ;
  • Tae Woo, Oh (Korean Medicine (KM)-Application Center, Korea Institute of Oriental Medicine (KIOM))
  • 황수진 (동국대학교 한의과대학, 한방생리학교실) ;
  • 김영숙 ((주)글루칸) ;
  • 오태우 (한국한의학연구원 한의기술응용센터)
  • Received : 2022.11.06
  • Accepted : 2022.11.13
  • Published : 2022.11.30

Abstract

Objectives : In this study, it was investigated the effects of solid-phase fermentation extraction with Phellinus linteus of discarded Schisandra chinensis extract (PS) and its action mechanism on dexamethasone-induced muscle atrophy in mice. Methods : In mice, muscle atrophy model was induced by dexamethasone (5 mg/kg, I.p) once daily for 2 weeks and with PS extract administration (100 and 300 mg/kg, p.o.) as treatment groups. The changes in body weights, grip strength, Treadmill test, muscle weights, and the expression of atrophy-related genes were measured in muscle atrophy mice. The histological changes of gastrocnemius tissues were also observed by H&E staining with measurement of myofiber size. Results : The administration of PS extract increased significantly body weights, grip strength, treadmill test and muscle weights in muscle atrophy mice. PS extract administration increased significantly the area of myofibers and inhibited structural damages of muscle and increased significantly the expression of myogenin and decreased significantly the expression of MuRF1, Atrogin1 and phosphorylation of AMPK and PGC1α in muscle tissues of muscle atrophy mice. Conclusions : These results indicate that PS extract has a improvement effects on muscle atrophy with stimulation of myogenic differentiation and inhibition of mRNA degradation that could be related with the activation of AMPK and PGC1α signaling pathways in muscle. This suggests that PS extract can apply to treat muscle atrophy in clinics.

Keywords

Acknowledgement

본 연구는 환경부의 재원으로 한국환경산업기술원의 야생생물 유래 친환경 신소재 및 공정기술개발사업의 지원을 받아 연구되었습니다. (RE202101318, 한국한의학연구원 ERTERT2112080).

References

  1. Dimon T., "Anatomy of the moving body: a basic course in bones, muscles, and joints", North Atlantic Books, 2001. 
  2. Seldin, Marcus M., et al., "Myonectin (CTRP15), a novel myokine that links skeletal muscle to systemic lipid homeostasis", Journal of Biological Chemistry, Vol. 287(15), 2012. 
  3. Rooyackers O E, Nair K S., "Hormonal regulation of human muscle protein metabolism", Annual review of nutrition, Vol. 17, 1997. 
  4. Melby J C., "Clinical pharmacology of systemic corticosteroids", Annual review of pharmacology and toxicology, Vol. 17(1), 1977. 
  5. Weinstein S P, Paquin T, Pritsker A, et al., "Glucocorticoid-induced insulin resistance: dexamethasone inhibits the activation of glucose transport in rat skeletal muscle by both insulin-and non-insulin-related stimuli", Diabetes, Vol. 44(4), 1995. 
  6. Kim H, Jang M, Park R, et al., "Conessine treatment reduces dexamethasone-induced muscle atrophy by regulating MuRF1 and atrogin-1 expression", Journal of Microbiology and Biotechnology, Vol. 28(4), 2018. 
  7. Habukuihakwon. youngchu-kyungkyosuk. Beijing: Inminwisheng publisher; 1982:161.24 
  8. Liu H B., "Literature research on clinical treatment of Withering disease", China Academic Journal Electronic Publishing House, 2011. 
  9. Yin L, Li N, Jia W, et al., "Skeletal muscle atrophy: From mechanisms to treatments", Pharmacological Research, Vol. 172, 2021. 
  10. Quittan M., "Aspects of physical medicine and rehabilitation in the treatment of deconditioned patients in the acute care setting: the role of skeletal muscle", Wiener Medizinische Wochenschrift, Vol. 166(1), 2016. 
  11. YS Kim, SJ Hwang, KI Park, Jet al., Protective Effect of water extract Phellinus linteus-discard Schisandra chinensis solid fermented extracts on improvement of sarcopenia by Atorvastatin-induced muscle atrophy cell model. Herbal Formula Science. 2021;29(4):239-252.  https://doi.org/10.14374/HFS.2021.29.4.239
  12. Fried LP, Xue QL, Cappola AR, Ferrucci L, Chaves P, Varadhan R, et al. Nonlinear multisystem physiological dysregulation associated with frailty in older women: implications for etiology and treatment. J Gerontol A Biol Sci Med Sci. 2009;64:1049-1057. 
  13. Cebron Lipovec N, Schols AMWJ, van den Borst B, Beijers RJHCG, Kosten T, Omersa D, Lainscak M. Sarcopenia in advanced COPD affects cardiometabolic risk reduction by shortterm high-intensity pulmonary rehabilitation. J Am Med Dir Assoc. 2016;17(9):814-820  https://doi.org/10.1016/j.jamda.2016.05.002
  14. Park SH, Park JH, Song PS, Kim DK, Kim KH, Seol SH, Kim HK, Jang HJ, Lee JG, Park HY, Park JS, Shin KJ, Kim DI, Moon YS. Sarcopenic obesity as an independent risk factor of hypertension. J Am Soc Hypertens. 2013;7(6):420-425  https://doi.org/10.1016/j.jash.2013.06.002
  15. China Traditional Chinese Medicine Press. Chinese Internal Medicine,2007. 
  16. Kim Y I, Lee H, Nirmala F S, et al., "Antioxidant Activity of Valeriana fauriei Protects against Dexamethasone-Induced Muscle Atrophy", Oxidative Medicine and Cellular Longevity, Vol. 2022, 2022. 
  17. Otsuka Y, Egawa K, Kanzaki N, et al., "Quercetin glycosides prevent dexamethasone-induced muscle atrophy in mice", Biochemistry and biophysics reports, Vol. 18, 2019. 
  18. Zammit P S., "Function of the myogenic regulatory factors Myf5, MyoD, Myogenin and MRF4 in skeletal muscle, satellite cells and regenerative myogenesis[C]//Seminars in cell & developmental biology", Academic Press, Vol. 72, 2017. 
  19. Bandman E., "Functional properties of myosin isoforms in avian muscle", Poultry science, Vol. 78(5), 1999. 
  20. Gomes MD, Lecker SH, Jagoe RT, Navon A, Goldberg AL. Atrogin-1, a muscle-specific F-box protein highly expressed during muscle atrophy. Proc Natl Acad Sci USA 2001;98:14440-14445.  https://doi.org/10.1073/pnas.251541198
  21. Foletta V C, White L J, Larsen A E, et al., "The role and regulation of MAFbx/atrogin-1 and MuRF1 in skeletal muscle atrophy", Pflugers Archiv-European Journal of Physiology, Vol. 461(3), 2011. 
  22. Zheng B, Ohkawa S, Li H, et al., "FOXO3a mediates signaling crosstalk that coordinates ubiquitin and atrogin-1/MAFbx expression during glucocorticoid-induced skeletal muscle atrophy", The FASEB Journal, Vol. 24(8), 2010. 
  23. Bodine SC, Latres E, Baumhueter S, et al. Identification of ubiquitin ligases required for skeletal muscle atrophy. Science 2001;294:1704-1708.  https://doi.org/10.1126/science.1065874
  24. Thomson D M., "The role of AMPK in the regulation of skeletal muscle size, hypertrophy, and regeneration", International journal of molecular sciences, Vol. 19(10), 2018.