Role of Carvedilol in Inhibiting the Proliferation and Migration of Vascular Smooth Muscle Cells by Upregulating

G Yang1, Z Zhang, X Ma

  • 1The First School of Clinical Medicine, Shanxi Medical University, Taiyuan, China, qinghuahanhqh@126.com.

Physiological Research
|August 31, 2025
PubMed

Insights

Carvedilol inhibits vascular smooth muscle cell proliferation and migration by increasing microRNA-145 (miR-145) levels. This study reveals miR-145 as a key mediator in carvedilol

Area of Science:

  • Cardiovascular Biology
  • Molecular Medicine
  • Cell Biology

Background:

  • Vascular smooth muscle cell (VSMC) proliferation and migration are key drivers of restenosis after percutaneous coronary intervention (PCI).
  • MicroRNA-145 (miR-145) is implicated in VSMC pathobiology.
  • The precise mechanism by which carvedilol inhibits VSMC activity remains incompletely understood.

Purpose of the Study:

  • To investigate if carvedilol modulates miR-145 expression.
  • To determine if miR-145 mediates carvedilol's inhibitory effects on VSMC proliferation and migration.

Main Methods:

  • VSMCs were treated with miR-145 mimics or inhibitors.
  • Cell proliferation was assessed using CCK-8 and EdU assays.
  • Cell migration was evaluated via wound healing and Transwell assays.
  • Protein expression and miR-145 targets were analyzed using Western blot and luciferase reporter assays.

Main Results:

  • Carvedilol treatment upregulated miR-145 expression and downregulated Krüppel-like factor 4 (KLF4).
  • Overexpression of miR-145 inhibited VSMC proliferation and migration.
  • KLF4 was confirmed as a direct target of miR-145.
  • Inhibition of miR-145 diminished the anti-proliferative and anti-migratory effects of carvedilol.

Conclusions:

  • Carvedilol inhibits VSMC proliferation and migration, partly by upregulating miR-145.
  • miR-145 acts as a crucial mediator in the therapeutic action of carvedilol on VSMCs.
  • These findings highlight miR-145 as a potential therapeutic target for preventing restenosis.

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