Atheroprotective Effects and Molecular Mechanism of Berberine

Lu Xing1, Xin Zhou1, Ai-Hong Li2

  • 1Shaanxi Key Laboratory of Ischemic Cardiovascular Disease, Institute of Basic and Translational Medicine, Xi'an Medical University, Xi'an, China.

Insights

Berberine (BBR) effectively combats atherosclerosis by addressing multiple factors like dyslipidemia and inflammation. This natural compound offers a promising therapeutic avenue for cardiovascular disease management.

Area of Science:

  • Cardiovascular medicine
  • Pharmacology
  • Natural product research

Background:

  • Cardiovascular diseases (CVDs) are a leading global cause of death.
  • Atherosclerosis, the primary pathology of CVDs, involves hyperlipidemia, endothelial injury, foam cell formation, VSMC proliferation, platelet aggregation, and gut microbiota changes.
  • Current atherosclerosis treatments have limitations, including long-term administration and adverse effects.

Purpose of the Study:

  • To review the anti-atherosclerosis mechanisms of Berberine (BBR).
  • To highlight recent advances in understanding BBR's therapeutic effects on atherosclerosis.
  • To provide a scientific perspective on BBR for atherosclerosis management.

Main Methods:

  • Literature review of recent advances in BBR's anti-atherosclerosis mechanisms.
  • Analysis of BBR's effects on key pathological aspects of atherosclerosis.
  • Synthesis of current scientific understanding of BBR's molecular mechanisms.

Main Results:

  • Berberine (BBR) attenuates dyslipidemia and corrects endothelial dysfunction.
  • BBR inhibits macrophage inflammation and foam cell formation while activating autophagy.
  • BBR regulates vascular smooth muscle cell (VSMC) proliferation and migration and reduces platelet aggregation.
  • BBR modulates gut microbiota composition, impacting atherosclerosis progression.

Conclusions:

  • Berberine (BBR) demonstrates multifaceted anti-atherosclerosis effects.
  • BBR offers a promising natural compound for managing atherosclerosis and associated cardiovascular diseases.
  • Further research into BBR's molecular mechanisms can inform novel therapeutic strategies.