Inhibitory effects of herbal decoction Ojeoksan on proliferation and migration in vascular smooth muscle cells

B H Han1,2, J J Yoon1,2, H Y Kim1,2

  • 1Hanbang Cardio-Renal Syndrome Research Center, Wonkwang University, Iksan, Republic of Korea.

Insights

Ojeoksan (OJS) significantly inhibits human aortic smooth muscle cell proliferation and migration induced by tumor necrosis factor-alpha (TNF-α). This herbal treatment downregulates reactive oxygen species (ROS) and nuclear factor-kappa B (NF-κB) signaling pathways, offering potential for cardiovascular disease therapy.

Area of Science:

  • Cardiovascular Biology
  • Pharmacology
  • Cell Biology

Background:

  • Vascular smooth muscle cell proliferation is a key factor in cardiovascular disease development.
  • Tumor necrosis factor-alpha (TNF-α) is a pro-inflammatory cytokine that stimulates HASMC proliferation.

Purpose of the Study:

  • To investigate the inhibitory effects of Ojeoksan (OJS) on TNF-α-induced human aortic smooth muscle cell (HASMC) proliferation and migration.
  • To elucidate the underlying molecular mechanisms of OJS action.

Main Methods:

  • Assessed thymidine incorporation and live cell imaging for HASMC proliferation and migration.
  • Analyzed cell-cycle regulatory proteins (cyclins, CDKs, p21, p27) using Western blot.
  • Quantified matrix metalloproteinase (MMP-2/-9) mRNA expression via RT-PCR.
  • Measured hydrogen peroxide (H₂O₂) and reactive oxygen species (ROS) production.
  • Investigated nuclear factor-kappa B (NF-κB) signaling pathway activation (IκB-α phosphorylation and translocation).

Main Results:

  • OJS significantly inhibited TNF-α-induced thymidine incorporation, proliferation, and migration in HASMCs.
  • OJS attenuated the expression of TNF-α-induced cyclins/CDKs and modulated p21/p27 levels.
  • OJS suppressed TNF-α-induced mRNA expression of MMP-2/-9, ROS production, and NF-κB pathway activation.
  • OJS inhibited the phosphorylation and nuclear translocation of IκB-α.

Conclusions:

  • OJS demonstrates significant inhibitory effects on TNF-α-induced HASMC proliferation and migration.
  • The mechanisms involve the downregulation of MMP-2/-9 expression and the ROS/NF-κB signaling pathway.
  • OJS presents a potential therapeutic strategy for cardiovascular diseases like atherosclerosis.

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