Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Pharmaceutical Research and Technology Institute, Kinki University, 3-4-1 Kowakae, Higashi-osaka, Osaka 577-8502, Japan.
Phytochemistry. 2014 Jun;102:169-81. doi: 10.1016/j.phytochem.2014.03.002. Epub 2014 Mar 31.
A methanol extract from the tuberous roots of Potentilla anserina (Rosaceae) exhibited hepatoprotective effects against d-galactosamine (d-GalN)/lipopolysaccharide-induced liver injuries in mice. Six triterpene 28-O-monoglucopyranosyl esters, potentillanosides A-F, were isolated from the extract along with 32 known compounds, including 15 triterpenes. The structures of potentillanosides A-F were determined on the basis of spectroscopic properties and chemical evidence. Four ursane-type triterpene 28-O-monoglycosyl esters, potentillanoside A (IC50=46.7μM), 28-O-β-d-glucopyranosyl pomolic acid (IC50=9.5μM), rosamutin (IC50=35.5μM), and kaji-ichigoside F1 (IC50=14.1μM), inhibited d-GalN-induced cytotoxicity in primary cultured mouse hepatocytes. Among these four triterpenes, potentillanoside A, rosamutin, and kaji-ichigoside F1 exhibited in vivo hepatoprotective effects at doses of 50-100mg/kg, p.o. The mode of action was ascribable to the reduction in cytotoxicity caused by d-GalN.
从委陵菜(蔷薇科)块根的甲醇提取物中分离得到了六种三萜 28-O-单葡萄糖苷酯,即 potentillanosides A-F,以及 32 种已知化合物,包括 15 种三萜。根据光谱性质和化学证据确定了 potentillanosides A-F 的结构。四种 Ursane 型三萜 28-O-单糖苷酯,包括 potentillanoside A(IC50=46.7μM)、28-O-β-d-吡喃葡萄糖基齐墩果酸(IC50=9.5μM)、rosamutin(IC50=35.5μM)和虎杖苷 F1(IC50=14.1μM),抑制原代培养的小鼠肝细胞中 d-GalN 诱导的细胞毒性。在这四种三萜中,potentillanoside A、rosamutin 和虎杖苷 F1 在 50-100mg/kg,po 剂量下具有体内保肝作用。作用模式归因于降低 d-GalN 引起的细胞毒性。