Abstract
The hepatoprotective effect of majonoside R2 (MR2), the major saponin constituent from Vietnamese ginseng (Panax vietnamensis, Araliaceae), was evaluated in vivo on D-galactosamine (D-GalN)/lipopolysaccharide (LPS)-induced hepatic apoptosis and subsequent liver failure in mice. Pretreatment of mice with MR2 (50 or 10 mg/kg, intraperitoneal) at 12 and 1 h before D-GalN/LPS injection significantly inhibited apoptosis and suppressed following hepatic necrosis. Importantly, the elevation of serum tumor necrosis factor-alpha (TNF-α) level, an important mediator for apoptosis in this model, was significantly inhibited by MR2 at a dose of 50 mg/kg. On the other hand, MR2 was found to protect primary cultured mouse hepatocytes from cell death by inhibiting apoptosis induced by D-GalN/TNF-α in vitro, as evidenced by DNA fragmentation analysis. These findings suggested that MR2 may have protected the hepatocytes from apoptosis via an inhibition of TNF-α production by activated macrophages and a direct inhibition of apoptosis induced by TNF-α.
Key words
Panax vietnamensis
- Araliaceae - hepatoprotective effect - apoptosis - Vietnamese ginseng - majonoside R2
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Prof. Dr. Shigetoshi Kadota
Department of Natural Products Chemistry
Institute of Natural Medicine
Toyama Medical and Pharmaceutical University
2630 Sugitani
Toyama 930-0194
Japan
Phone: +81-76-434-7625
Fax: +81-76-434-5059
Email: kadota@ms.toyama-mpu.ac.jp