Enhancement of anti-inflammatory and antinociceptive actions of red ginseng extract by fermentation

• Published in: Journal of pharmacy and pharmacology 2012-05, Vol.64 (5), p.756-762
• Main Authors: Jung, Hyun-Joo, Choi, Hojin, Lim, Hye-Won, Shin, Daehyun, Kim, Hacksoo, Kwon, Bin, Lee, Jong Eun, Park, Eun-Hee, Lim, Chang-Jin
• Format: Article
• Language: English
• Subjects: Abdominal Pain - chemically induced; Abdominal Pain - drug therapy; Acetic Acid; Analgesics - pharmacology; Analgesics - therapeutic use; Angiogenesis Inhibitors - pharmacology; Angiogenesis Inhibitors - therapeutic use; Animals; anti-inflammatory; Anti-Inflammatory Agents - pharmacology; Anti-Inflammatory Agents - therapeutic use; antinociceptive; Bifidobacterium; Carrageenan; Chick Embryo; Chorioallantoic Membrane - drug effects; Fermentation; Inflammation - chemically induced; Inflammation - drug therapy; Inflammation - metabolism; Lipopolysaccharides; Macrophages - drug effects; Male; Mice; Mice, Inbred ICR; Nitrites - metabolism; Panax; Permeability; Phytotherapy; Plant Preparations - pharmacology; Plant Preparations - therapeutic use; red ginseng
• ISSN: 0022-3573; 2042-7158
• DOI: 10.1111/j.2042-7158.2012.01460.x

Objectives  This work aimed to compare some pharmacological properties of red ginseng extract (RG) and fermented red ginseng extract (FRG). Methods  Antinociceptive activity was analysed using the acetic acid‐induced abdominal constriction response. Anti‐inflammatory activity was evaluated using acetic acid‐induced vascular permeability and carrageenan‐induced inflammation in the air pouch, and analysed through the measurement of nitrite content in the lipopolysaccharide (LPS)‐stimulated macrophage cells. Anti‐angiogenic activity was determined using the chick chorioallantoic membrane assay. Key findings  In‐vivo anti‐inflammatory activity of FRG was stronger than that of RG in two animal models, vascular permeability and air‐pouch models. In the vascular permeability model, the doses of RG and FRG required for half‐maximal inhibition (IC50) were 181 and 59 mg/kg, respectively. FRG exhibited significantly stronger antinociceptive activity than RG. In the acetic acid‐induced abdominal constriction response, the IC50 values of RG and FRG were 153 and 27 mg/kg, respectively. Although both RG and FRG were able to suppress production of nitric oxide in the LPS‐stimulated RAW264.7 macrophage cells, the suppressive activity of FRG appeared to be stronger than that of RG. However, RG and FRG showed similar anti‐angiogenic activity. Conclusions  FRG possesses enhanced anti‐inflammatory and antinociceptive activity but similar anti‐angiogenic activity than RG.