1%

DMSO were added to each well to make a final concentration of VG corresponding to 0.5 mg, 1 mg, and 3 mg of dried VG/mL of medium. After incubation for 24 h, the supernatant was removed and 50 μL of 4 mg/mL MTT in PBS was added to each well, and then incubated for 60 min. The supernatant was removed and 100 μL DMSO was added into each well, and then incubated for 30 min to dissolve the purple formazan crystal formed. The absorbance of each well was measured at 570 nm. The free radical scavenging activity was determined by measuring the reducing power of the stable radical DPPH PLX3397 cell line [17]. The MeOH extract of VG was mixed with DPPH solution (0.25 mg/mL in MeOH). The amount of remaining DPPH was measured at 520 nm. Inhibition of DPPH in percent (%) was calculated by: I (%) = [1– (Si – Bi) / (C – Bi)] × 100, where Si, Bi, and Selleck Dasatinib C are the absorbance of sample with DPPH, of sample with MeOH, and of

DPPH with MeOH, respectively. The data are presented as the mean ± standard deviation. Data were analyzed by Student t test for comparing two groups using SPSS version 21.0. A p-value of <0.05 was considered statistically significant. It has been reported that the steaming process modifies the chemical composition of ginseng, in particular of ginsenosides. Reported chemical modification of ginsenosides includes an elimination of sugar at the C-20 position and further dehydration to form a new double bond (Fig. 2). Some acetylated ginsenosides were also reported. As a result, the contents of polar ginsenosides were decreased whereas those of less polar ginsenosides were increased

[12], [14], [15], [18], [19], [20] and [21]. This phenomenon was also observed in this study as demonstrated in the HPLC chromatogram (Fig. 3). Peak intensities of polar ginsenosides, which appeared prior to 45 min, were decreased, whereas those of less polar ginsenosides, Aldehyde dehydrogenase which appeared after 45 min, were increased. In our HPLC condition, ginsenoside Rg1 and Re, as well as vina-ginsenoside R1 and R2 were not separated. Therefore, the total amount of ginsenoside Re and Rg1 was calculated as ginsenoside Rg1, and that of vina-ginsenoside R1 and R2 was calculated as vina-ginsenoside R2. The contents of polar ginsenosides, such as Rb1, Rb2, Rc, Rd, Re, and Rg1, were rapidly decreased during steaming process (Fig. 4). The sum of the contents of these ginsenosides was 85.4 mg/g in dried VG, which decreased to 44.2 mg/g and 12.5 mg/g after 2 h and 4 h steaming, respectively. In particular, PPT ginsenosides, namely Rg1 and Re, were shown to be less stable than PPD ginsenosides. Only 39% and 4% of PPT ginsenosides remained after 2 h and 4 h steaming, respectively, whereas 59% and 20% of PPD ginsenosides remained after the same steaming condition. However, ocotillol saponins including majonoside R1 and R2, and vina-ginsenoside R1 and R2 were stable until 20 h. This can be explained by the fact that ocotillol saponins have no heat-labile C-20 glycoside.