The Effects of Marine Algal Polyphenols, Phlorotannins, on Skeletal Muscle Growth in C2C12 Muscle Cells via Smad and IGF-1 Signaling Pathways

Mar Drugs. 2021 May 10;19(5):266. doi: 10.3390/md19050266.

Abstract

Skeletal muscle is an important tissue in energy metabolism and athletic performance. The use of effective synthetic supplements and drugs to promote muscle growth is limited by various side effects. Moreover, their use is prohibited by anti-doping agencies; hence, natural alternatives are needed. Therefore, we evaluated the muscle growth effect of substances that can act like synthetic supplements from edible marine algae. First, we isolated six marine algal polyphenols belonging to the phlorotannin class, namely dieckol (DK), 2,7″-phloroglucinol-6,6'-bieckol (PHB), phlorofucofuroeckol A (PFFA), 6,6'-bieckol (6,6-BK), pyrogallol-phloroglucinol-6,6'-bieckol (PPB), and phloroglucinol (PG) from an edible brown alga, Ecklonia cava and evaluated their effects on C2C12 myoblasts proliferation and differentiation. Of the six phlorotannin isolates evaluated, DK and PHB induced the highest degree of C2C12 myoblast proliferation. In addition, DK and PHB regulates myogenesis by down-regulating the Smad signaling, a negative regulator, and up-regulating the insulin-like growth factor-1 (IGF-1) signaling, a positive regulator. Interestingly, DK and PHB bind strongly to myostatin, which is an inhibitor of myoblast proliferation, while also binding to IGF-1 receptors. Moreover, they bind to IGF-1 receptor. These results suggest that DK and PHB are potential natural muscle building supplements and could be a safer alternative to synthetic drugs.

Keywords: Ecklnoia cava; marine algae; marine algal polyphenols; muscle growth; myogenesis; phlorotannins.

MeSH terms

  • Animals
  • Aquatic Organisms / chemistry*
  • Cell Line
  • Cell Proliferation / drug effects
  • Cell Survival / drug effects
  • Creatine Kinase, MM Form / metabolism
  • Cyanobacteria / chemistry*
  • Insulin-Like Growth Factor I / metabolism*
  • Mice
  • Molecular Docking Simulation
  • Muscle Cells / drug effects
  • Muscle Development / drug effects
  • Muscle, Skeletal / drug effects
  • Muscle, Skeletal / growth & development*
  • Myostatin / chemistry
  • Myostatin / metabolism
  • Polyphenols / pharmacology*
  • Prohibitins
  • Receptor, IGF Type 1 / chemistry
  • Receptor, IGF Type 1 / metabolism
  • Signal Transduction / drug effects*
  • Smad Proteins / metabolism*

Substances

  • IGF1R protein, human
  • Myostatin
  • PHB protein, human
  • Polyphenols
  • Prohibitins
  • Smad Proteins
  • insulin-like growth factor-1, mouse
  • Insulin-Like Growth Factor I
  • Receptor, IGF Type 1
  • Creatine Kinase, MM Form