Functional roles and mechanisms of ginsenosides from Panax ginseng in atherosclerosis

Qianqian Xue1,2, Ningning He3, Zhibin Wang4

  • 1Department of Pharmacology, School of Pharmacy, Qingdao University, China.

Insights

Ginsenosides from ginseng show potential in treating atherosclerosis, a major cause of cardiovascular disease. This review explores their mechanisms for developing new anti-cardiovascular drugs.

Area of Science:

  • Pharmacology
  • Cardiovascular Medicine
  • Natural Products

Background:

  • Atherosclerosis (AS) is a primary driver of cardiovascular diseases (CVDs), characterized by inflammation, lipid accumulation, and plaque formation.
  • Despite therapeutic advances, AS prevalence increases with age, necessitating novel treatments.
  • Ginsenosides, derived from ginseng, exhibit diverse pharmacological activities, including anti-inflammatory and cardiovascular benefits.

Purpose of the Study:

  • To review the pharmacological functions of specific ginsenosides (Rb1, Rd, F, Rg1, Rg2, Rg3, and compound K) in the context of atherosclerosis.
  • To elucidate the underlying mechanisms by which these ginsenosides exert their effects on AS.
  • To provide insights for the development of novel anti-atherosclerosis therapies.

Main Methods:

  • Literature review of studies on ginsenosides and atherosclerosis.
  • Analysis of pharmacological activities and mechanisms of action.
  • Focus on key ginsenosides including Rb1, Rd, F, Rg1, Rg2, Rg3, and compound K.

Main Results:

  • Ginsenosides demonstrate significant anti-atherosclerotic properties.
  • Mechanisms include anti-inflammatory effects, lipid metabolism regulation, and plaque stabilization.
  • Specific ginsenosides show distinct therapeutic potentials against AS progression.

Conclusions:

  • Active ginsenosides possess promising therapeutic potential for atherosclerosis.
  • Understanding their mechanisms can guide the development of effective anti-cardiovascular drugs.
  • Ginseng-derived compounds offer a natural avenue for managing cardiovascular disease burden.

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