TY - JOUR
T1 - Effects of steaming the root of Panax notoginseng on chemical composition and anticancer activities
AU - Sun, Shi
AU - Wang, Chong Zhi
AU - Tong, Robin
AU - Li, Xiao Li
AU - Fishbein, Anna
AU - Wang, Qi
AU - He, Tong Chuan
AU - Du, Wei
AU - Yuan, Chun Su
N1 - Funding Information:
This work was supported in part by Grants from the NIH/NCCAM AT003255 and AT004418 (to C.S.Y.), from the NIH/NCI CA106569 and American Cancer Society RSG-05-254-01DDC (to T.C.H.), and from the NIH GM074197 and the American Cancer Society RSG-05-230-01DDC (to W.D.).
PY - 2010/1/15
Y1 - 2010/1/15
N2 - The root of Panax notoginseng has been shown to change its saponin composition upon steaming. This study examines the effects of different steaming times and temperature on notoginseng root for saponin composition and anticancer activities. Steaming decreased the content of notoginsenoside R1, ginsenosides Rg1, Re, Rb1, Rc, R2, Rb3 and Rd, but increased the content of Rh1, Rg2, 20R-Rg2, Rg3 and Rh2. Steaming significantly influenced the transformation of Rg3. The amount of ginsenoside Rg3, an anticancer compound, was 5.23-fold greater in root steamed for 2 h at 120 °C than at 100 °C, and 3.22-fold greater when steamed for 4 h than for 1 h at 120 °C. For anticancer effects, the extract of steamed root significantly inhibited proliferation of SW-480 human colorectal cancer cells. The IC50 of the steamed extract for 1, 2, 4 and 6 h at 120 °C was 259.2, 131.4, 123.7 and 127.1 μg/mL, respectively; the effect of unsteamed extract was low. Flow cytometric analysis demonstrated that the apoptotic cell induction rates of SW-480 cells were 56.3% and 64.4% with 150.0 and 200.0 μg/mL extract steamed for 6 h. Compared with Rg1 and Rb1, only Rg3 had a significant antiproliferative effect.
AB - The root of Panax notoginseng has been shown to change its saponin composition upon steaming. This study examines the effects of different steaming times and temperature on notoginseng root for saponin composition and anticancer activities. Steaming decreased the content of notoginsenoside R1, ginsenosides Rg1, Re, Rb1, Rc, R2, Rb3 and Rd, but increased the content of Rh1, Rg2, 20R-Rg2, Rg3 and Rh2. Steaming significantly influenced the transformation of Rg3. The amount of ginsenoside Rg3, an anticancer compound, was 5.23-fold greater in root steamed for 2 h at 120 °C than at 100 °C, and 3.22-fold greater when steamed for 4 h than for 1 h at 120 °C. For anticancer effects, the extract of steamed root significantly inhibited proliferation of SW-480 human colorectal cancer cells. The IC50 of the steamed extract for 1, 2, 4 and 6 h at 120 °C was 259.2, 131.4, 123.7 and 127.1 μg/mL, respectively; the effect of unsteamed extract was low. Flow cytometric analysis demonstrated that the apoptotic cell induction rates of SW-480 cells were 56.3% and 64.4% with 150.0 and 200.0 μg/mL extract steamed for 6 h. Compared with Rg1 and Rb1, only Rg3 had a significant antiproliferative effect.
KW - Antiproliferation
KW - Apoptosis
KW - Ginsenoside
KW - High performance liquid chromatography (HPLC)
KW - Panax notoginseng
KW - SW-480 human colorectal cancer cells
KW - Saponin
KW - Steaming
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U2 - 10.1016/j.foodchem.2009.04.122
DO - 10.1016/j.foodchem.2009.04.122
M3 - Article
AN - SCOPUS:69049084468
SN - 0308-8146
VL - 118
SP - 307
EP - 314
JO - Food Chemistry
JF - Food Chemistry
IS - 2
ER -