Syringaresinol induces mitochondrial biogenesis through activation of PPARβ pathway in skeletal muscle cells

Bioorg Med Chem Lett. 2016 Aug 15;26(16):3978-83. doi: 10.1016/j.bmcl.2016.07.001. Epub 2016 Jul 1.

Abstract

Activation of peroxisome proliferator-activated receptors (PPARs) plays a crucial role in cellular energy metabolism that directly impacts mitochondrial biogenesis. In this study, we demonstrate that syringaresinol, a pharmacological lignan extracted from Panax ginseng berry, moderately binds to and activates PPARβ with KD and EC50 values of 27.62±15.76μM and 18.11±4.77μM, respectively. Subsequently, the expression of peroxisome proliferator-activated receptor γ coactivator-1α together with PPARβ transcriptional targets, mitochondrial carnitine palmitoyltransferase 1 and uncoupling protein 2, was also enhanced in terms of both mRNA and protein levels. The activation of these proteins induced mitochondrial biogenesis by enrichment of mitochondrial replication and density within C2C12 myotubes. Importantly, knockdown of PPARβ reduced the syringaresinol-induced protein expression followed by the significant reduction of mitochondrial biogenesis. Taken together, our results indicate that syringaresinol induces mitochondrial biogenesis by activating PPARβ pathway.

Keywords: Mitochondrial biogenesis; PPARβ; Skeletal muscle; Syringaresinol.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Carnitine O-Palmitoyltransferase / genetics
  • Carnitine O-Palmitoyltransferase / metabolism
  • Cell Line
  • Furans / chemistry*
  • Furans / isolation & purification
  • Furans / pharmacology
  • Gene Expression / drug effects
  • Lignans / chemistry*
  • Lignans / isolation & purification
  • Lignans / pharmacology
  • Mice
  • Mitochondria / drug effects*
  • Mitochondria / metabolism
  • Myoblasts / cytology
  • Myoblasts / metabolism
  • PPAR-beta / antagonists & inhibitors
  • PPAR-beta / genetics
  • PPAR-beta / metabolism*
  • Panax / chemistry
  • Panax / metabolism
  • RNA Interference
  • RNA, Messenger / metabolism
  • RNA, Small Interfering / metabolism
  • Uncoupling Protein 2 / genetics
  • Uncoupling Protein 2 / metabolism

Substances

  • Furans
  • Lignans
  • PPAR-beta
  • RNA, Messenger
  • RNA, Small Interfering
  • Uncoupling Protein 2
  • syringaresinol
  • Carnitine O-Palmitoyltransferase