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 59mg/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 27mg/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.
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 59mg/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 27mg/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.
Authors: Hyun Ah Lee; Bo Ram Song; Hye Ryeong Kim; Ji Eun Kim; Woo Bin Yun; Jin Ju Park; Mi Lim Lee; Jun Young Choi; Hee Seob Lee; Dae Youn Hwang Journal: Exp Ther Med Date: 2017-09-25 Impact factor: 2.447
Authors: Nam-Hoon Kim; Murukarthick Jayakodi; Sang-Choon Lee; Beom-Soon Choi; Woojong Jang; Junki Lee; Hyun Hee Kim; Nomar E Waminal; Meiyappan Lakshmanan; Binh van Nguyen; Yun Sun Lee; Hyun-Seung Park; Hyun Jo Koo; Jee Young Park; Sampath Perumal; Ho Jun Joh; Hana Lee; Jinkyung Kim; In Seo Kim; Kyunghee Kim; Lokanand Koduru; Kyo Bin Kang; Sang Hyun Sung; Yeisoo Yu; Daniel S Park; Doil Choi; Eunyoung Seo; Seungill Kim; Young-Chang Kim; Dong Yun Hyun; Youn-Il Park; Changsoo Kim; Tae-Ho Lee; Hyun Uk Kim; Moon Soo Soh; Yi Lee; Jun Gyo In; Heui-Soo Kim; Yong-Min Kim; Deok-Chun Yang; Rod A Wing; Dong-Yup Lee; Andrew H Paterson; Tae-Jin Yang Journal: Plant Biotechnol J Date: 2018-05-25 Impact factor: 9.803