Effects of American wild ginseng and Korean cultivated wild ginseng pharmacopuncture extracts on the regulation of C2C12 myoblasts differentiation through AMPK and PI3K/Akt/mTOR signaling pathway

Mol Med Rep. 2022 Jun;25(6):192. doi: 10.3892/mmr.2022.12708. Epub 2022 Apr 8.

Abstract

Targeting impaired myogenesis and mitochondrial biogenesis offers a potential alternative strategy for balancing energy to fight muscle disorders such as sarcopenia. In traditional Korean medicine, it is believed that the herb wild ginseng can help restore energy to the elderly. The present study investigated whether American wild ginseng pharmacopuncture (AWGP) and Korean cultivated wild ginseng pharmacopuncture (KCWGP) regulate energy metabolism in skeletal muscle cells. C2C12 mouse myoblasts were differentiated into myotubes using horse serum for 5 days. An MTT colorimetric assay verified cell viability. AWGP, KCWGP (0.5, 1, or 2 mg/ml), or metformin (2.5 mM) for reference were used to treat the C2C12 myotubes. The expressions of differentiation and mitochondrial biogenetic factors were measured by western blotting in C2C12 myotubes. Treatment of C2C12 cells stimulated with AWGP and KCWGP at a concentration of 10 mg/ml did not affect cell viability. AWGP and KCWGP treatments resulted in significant increases in the myogenesis proteins, myosin heavy chain, myostatin, myoblast determination protein 1 and myogenin, as well as increases to the biogenic regulatory factors, peroxisome proliferator‑activated receptor‑γ coactivator‑1‑α, nuclear respiratory factor 1, mitochondrial transcription factor A and Sirtuin 1, in the myotubes through AMPK and PI3K/AKT/mTOR signaling pathway activation. These results suggest that AWGP and KCWGP may be beneficial to muscle function by improving muscle differentiation and energy metabolism.

Keywords: C2C12 myotubes; biogenesis; myoblast differentiation; pharmacopuncture; wild ginseng.

MeSH terms

  • AMP-Activated Protein Kinases / metabolism
  • Acupuncture*
  • Animals
  • Cell Differentiation
  • Mice
  • Muscle Fibers, Skeletal / metabolism
  • Myoblasts / metabolism
  • Panax* / metabolism
  • Phosphatidylinositol 3-Kinases / metabolism
  • Plant Extracts / metabolism
  • Plant Extracts / pharmacology
  • Proto-Oncogene Proteins c-akt / metabolism
  • Republic of Korea
  • Signal Transduction
  • TOR Serine-Threonine Kinases / metabolism

Substances

  • Plant Extracts
  • Proto-Oncogene Proteins c-akt
  • TOR Serine-Threonine Kinases
  • AMP-Activated Protein Kinases

Grants and funding

The present study was funded by the National Research Foundation of Korea (NRF; grant nos. 2020R1A6A3A01099936 and 2021R1A2C1012267).