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Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy in vitro through improving mitochondrial biogenesis and myotube growth

  • Authors:
    • Ryuni Kim
    • Jee Won Kim
    • Sang-Jin Lee
    • Gyu-Un Bae
  • View Affiliations / Copyright

    Affiliations: Drug Information Research Institute, College of Pharmacy, Sookmyung Women's University, Seoul 04310, Republic of Korea, Research Institute of Aging Related Disease, AniMusCure Inc., Suwon 16419, Republic of Korea
    Copyright: © Kim et al. This is an open access article distributed under the terms of Creative Commons Attribution License.
  • Article Number: 94
    |
    Published online on: January 20, 2022
       https://doi.org/10.3892/mmr.2022.12610
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Abstract

Ginsenoside Rg3 (Rg3), amplified by iterative heating processing with fresh ginseng, has a broad range of pharmacological activities and improves mitochondrial biogenesis in skeletal muscle. However, thus far no study has examined how Rg3 affects myotube growth or muscle atrophy, to the best of the authors' knowledge. The present study was conducted to examine the myogenic effect of Rg3 on dexamethasone (DEX)‑induced myotube atrophy and the underlying molecular mechanisms. Rg3 activated Akt/mammalian target of rapamycin signaling to prevent DEX‑induced myotube atrophy thereby stimulating the expression of muscle‑specific genes, including myosin heavy chain and myogenin, and suppressing muscle‑specific ubiquitin ligases as demonstrated by immunoblotting and immunostaining assays. Furthermore, Rg3 efficiently prevented DEX‑triggered mitochondrial dysfunction of myotubes through peroxisome proliferator‑activated receptor‑γ coactivator1α activities and its mitochondrial biogenetic transcription factors, nuclear respiratory factor‑1 and mitochondrial transcription factor A. These were confirmed by immunoblotting, luciferase assays, RT‑qPCR and mitochondrial analysis measuring the levels of ROS, ATP and membrane potential. By providing a mechanistic insight into the effect of Rg3 on myotube atrophy, the present study suggested that Rg3 has potential as a therapeutic or nutraceutical remedy to intervene in muscle aging or diseases including cancer cachexia.
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Copy and paste a formatted citation
Spandidos Publications style
Kim R, Kim JW, Lee S and Bae G: Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth. Mol Med Rep 25: 94, 2022.
APA
Kim, R., Kim, J.W., Lee, S., & Bae, G. (2022). Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth. Molecular Medicine Reports, 25, 94. https://doi.org/10.3892/mmr.2022.12610
MLA
Kim, R., Kim, J. W., Lee, S., Bae, G."Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth". Molecular Medicine Reports 25.3 (2022): 94.
Chicago
Kim, R., Kim, J. W., Lee, S., Bae, G."Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth". Molecular Medicine Reports 25, no. 3 (2022): 94. https://doi.org/10.3892/mmr.2022.12610
Copy and paste a formatted citation
x
Spandidos Publications style
Kim R, Kim JW, Lee S and Bae G: Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth. Mol Med Rep 25: 94, 2022.
APA
Kim, R., Kim, J.W., Lee, S., & Bae, G. (2022). Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth. Molecular Medicine Reports, 25, 94. https://doi.org/10.3892/mmr.2022.12610
MLA
Kim, R., Kim, J. W., Lee, S., Bae, G."Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth". Molecular Medicine Reports 25.3 (2022): 94.
Chicago
Kim, R., Kim, J. W., Lee, S., Bae, G."Ginsenoside Rg3 protects glucocorticoid‑induced muscle atrophy <em>in vitro</em> through improving mitochondrial biogenesis and myotube growth". Molecular Medicine Reports 25, no. 3 (2022): 94. https://doi.org/10.3892/mmr.2022.12610
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