2011
DOI: 10.5142/jgr.2011.35.3.325
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Red Ginseng Saponin Fraction A Isolated from Korean Red Ginseng by Ultrafiltration on the Porcine Coronary Artery

Abstract: Red ginseng saponin fraction-A (RGSF-A) contains a high percentage of panaxadiol saponins that were isolated from Korean red ginseng by ultrafiltration. The aim of this study was to elucidate the effects of RGSF-A on the porcine distal left anterior descending (LAD) coronary artery. The relaxant responses to RGSF-A were examined during contractions induced by 100 nM U46619 (9,11-dideoxy-9a,11a-methanoepoxy-prostaglandin F2a), a stable analogue of thromboxane A2. RGSF-A dose-dependently induced biphasic (fast- … Show more

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Cited by 9 publications
(8 citation statements)
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“…RGSF-A contains a high percentage of panaxadiol saponins, and Rg3 is one of the characteristic panaxadiol saponin constituents of RGSF-A [18]. Therefore, to gain more insight into the inhibitory effects of RGSF-A on Brucella infection, we hypothesized that the Rg3 component of RGSF-A possesses the ability to control Brucella infection.…”
Section: Discussionmentioning
confidence: 99%
“…RGSF-A contains a high percentage of panaxadiol saponins, and Rg3 is one of the characteristic panaxadiol saponin constituents of RGSF-A [18]. Therefore, to gain more insight into the inhibitory effects of RGSF-A on Brucella infection, we hypothesized that the Rg3 component of RGSF-A possesses the ability to control Brucella infection.…”
Section: Discussionmentioning
confidence: 99%
“…RGSF extraction was performed as described previously [12,13] . Korean red ginseng was extracted with ethanol and the extract was air dried at 60°C for 2 d. The powder was then subjected to aqueous extraction three times at 95–100°C.…”
Section: Methodsmentioning
confidence: 99%
“…NO, PGE 2 , and TNF-α production After the preincubation of RAW264.7 cells or peritoneal macrophages (1×10 6 cells/mL) for 18 h, the cells were pre-treated with test compounds 1 through 7 for 30 min and were then incubated with LPS (1 µg/mL) for 24 h. The inhibitory effects of the test compounds on NO, PGE 2 , and TNF-α production were determined by analyzing the NO, PGE 2 , and TNF-α levels with the Griess reagent and enzyme-linked immunosorbent assay (ELISA) kits, as described previously [16][17][18] .…”
Section: Cell Culturementioning
confidence: 99%