目的探究水杨梅根乙酸乙酯提取物(Ethyl acetate extraction from the root of Adina rubella Hance,EARH)对人肝癌Bel7402细胞凋亡及增殖的作用。方法将细胞随机分为4组:对照组、1mg/mL EARH组、2mg/mL EARH组、4mg/mL EARH组。MTT法观...目的探究水杨梅根乙酸乙酯提取物(Ethyl acetate extraction from the root of Adina rubella Hance,EARH)对人肝癌Bel7402细胞凋亡及增殖的作用。方法将细胞随机分为4组:对照组、1mg/mL EARH组、2mg/mL EARH组、4mg/mL EARH组。MTT法观察EARH对Bel7402的增殖影响;Hoechst33258染色法检测细胞凋亡率;RT-PCR法检测凋亡相关因子p53、survivin基因表达量。结果 EARH体外能抑制Bel7402细胞增殖,诱导细胞凋亡,并且上调p53和降低survivin表达。结论 EARH可能通过上调p53基因、下调survivin表达,促进Bel7402细胞凋亡,从而体外抑制Bel7402细胞增殖。展开更多
Four new triterpenoid saponins were isolated from the roots of Adina rubella Hance. They were characterized as adinaic acid 3 beta-O-[alpha-L-rhamnopyranosyl(1-->2)-beta-D-glucopyranosyl(1-->2)-beta-D-glucurono-...Four new triterpenoid saponins were isolated from the roots of Adina rubella Hance. They were characterized as adinaic acid 3 beta-O-[alpha-L-rhamnopyranosyl(1-->2)-beta-D-glucopyranosyl(1-->2)-beta-D-glucurono-pyranoside-6-O-methyl ester]-28-O-beta-D-glucopyranoside, adinaic acid 3 beta-O-[alpha-L-rhamnopyranosyl(1-->2)-beta-D-glucopyranosyl(1-->2)-beta-D-glucuronopyranoside-6-O-butyl ester]-28-O-beta-D-glucopyranoside, adinaic acid 3 beta-O-[beta-D-glucopyranosyl(1-->2)-beta-D-glucopyrnaosyl]-(28-->1)-beta-D-glucopyranosyl(1-->6)-beta-D-glucopyranosyl ester, 27-hydroxyursolic acid 3 beta-O-[alpha-L-rhamnopyranosyl (1-->2)-beta-D-glucopyranosyl(1-->2)-beta-D-glucuronopyranoside-6-O-methyl ester]-28-O-beta-D-glycopyranoside. Their structures were elucidated by spectral methods, especially with the aid of 2D NMR techniques. Their complete assignments of the H-1 and C-13 NMR signals were carried out.展开更多
文摘目的探究水杨梅根乙酸乙酯提取物(Ethyl acetate extraction from the root of Adina rubella Hance,EARH)对人肝癌Bel7402细胞凋亡及增殖的作用。方法将细胞随机分为4组:对照组、1mg/mL EARH组、2mg/mL EARH组、4mg/mL EARH组。MTT法观察EARH对Bel7402的增殖影响;Hoechst33258染色法检测细胞凋亡率;RT-PCR法检测凋亡相关因子p53、survivin基因表达量。结果 EARH体外能抑制Bel7402细胞增殖,诱导细胞凋亡,并且上调p53和降低survivin表达。结论 EARH可能通过上调p53基因、下调survivin表达,促进Bel7402细胞凋亡,从而体外抑制Bel7402细胞增殖。
文摘Four new triterpenoid saponins were isolated from the roots of Adina rubella Hance. They were characterized as adinaic acid 3 beta-O-[alpha-L-rhamnopyranosyl(1-->2)-beta-D-glucopyranosyl(1-->2)-beta-D-glucurono-pyranoside-6-O-methyl ester]-28-O-beta-D-glucopyranoside, adinaic acid 3 beta-O-[alpha-L-rhamnopyranosyl(1-->2)-beta-D-glucopyranosyl(1-->2)-beta-D-glucuronopyranoside-6-O-butyl ester]-28-O-beta-D-glucopyranoside, adinaic acid 3 beta-O-[beta-D-glucopyranosyl(1-->2)-beta-D-glucopyrnaosyl]-(28-->1)-beta-D-glucopyranosyl(1-->6)-beta-D-glucopyranosyl ester, 27-hydroxyursolic acid 3 beta-O-[alpha-L-rhamnopyranosyl (1-->2)-beta-D-glucopyranosyl(1-->2)-beta-D-glucuronopyranoside-6-O-methyl ester]-28-O-beta-D-glycopyranoside. Their structures were elucidated by spectral methods, especially with the aid of 2D NMR techniques. Their complete assignments of the H-1 and C-13 NMR signals were carried out.