Sophora

Abstract: A methanol extract of Sophora japonica was subjected to anti-platelet activity guided fractionation affording the isolation of four flavonoids and six flavonoid-glycosides: biochanin A (1), irisolidone (2), genistein (3), sissotrin (4), sophorabioside (5), genistin (6), tectoridin (7), apigenin (8), quercitrin (9), and rutin (10). The structure of each compound was determined by a variety of spectroscopic methods. Among the compounds, 1, 3, and 7 showed ∼2.5–6.5 fold greater inhibitory effects on arachidonic acid (AA) and U46619 induced platelet aggregation (IC50: 19.9 and 99.8 μM; 20.3 and 53.8 μM; 25.9 and 123.4 μM, respectively) than acetylsalicylic acid (ASA, IC50: 63.0 and 350.0 μM). Compound 2 was an ∼22–40 fold stronger inhibitor than ASA on AA and U46619 induced aggregation (IC50: 1.6 and 15.6 μM, respectively).

Abstract: Previously, it was reported that some prenylated flavonoids contained in the dichloromethane fraction of the ethanolic extract of Sophora flavescens, such as kuraridin, sophoraflavanone G, kurarinone, and kushenol F, are tyrosinase inhibitors; however, based on the level of these inhibitors in the extract, its inhibitory effect on tyrosinase activity was higher than expected. This has led us to further investigate other possible constituents that may contribute to the extract's strong inhibitory activity. The results of this study indicate that kurarinol (1), kuraridinol (2), and trifolirhizin (3), from the ethyl acetate fraction of Sophora extract, can inhibit tyrosinase activity. Compared with kojic acid (16.22+/-1.71 microM), compounds 1-3 possessed potent tyrosinase inhibitory activity with IC(50) values of 8.60+/-0.51, 0.88+/-0.06, and 506.77+/-4.94 microM, respectively. These three compounds were further tested for their inhibitory effects on melanogenesis. In cultured B16 melanoma cells, 1-3 markedly inhibited (>50%) melanin synthesis at 50 microM. This is the first study indicating that 1-3 exert varying degrees of inhibition on tyrosinase-dependent melanin biosynthesis, and therefore, are candidates as skin-whitening agents.

Abstract: Summary Aim The aim is to use DNA sequence data to test between vicariance and long range dispersal (by floating seed-pods) explanations for the origin and range of the Edwardsia species of Sophora (Sophoreae: Papilionoideae: Leguminosae). Location This group is widely distributed around the South Pacific and into the South Atlantic on both continental fragments and oceanic islands. Methods DNA sequences from an intergene region (atpB-rbcL) of the chloroplast were determined for twelve taxa (including outgroups) and used to test these hypotheses. Sophora fossils were used to calibrate the evolutionary tree. Results The Edwardsia group of Sophora appears monophyletic and is well differentiated from other Sophora. However, the genetic difference between species within the South Pacific and to the South Atlantic is very low. Main conclusionsThe results eliminate vicariance explanations for this section of Sophora and strongly support an origin from other (non-Edwardsia) Sophora in the north-west Pacific. Dispersal appears initially to be to Tuvalu, Lord Howe Island, New Zealand, and subsequently across the South Pacific, probably within the last 2–5 million years. Dispersal of buoyant Sophora seeds to oceanic islands is the most likely explanation of its distributions. Fossil pollen dates in New Zealand are consistent with the conclusion.

Abstract: The dry root of Sophora flavescens Ait. (SF) has long been used in a variety of Chinese herbal formulations to treat patients with cancer. Alkaloids are commonly known to present in SF as main active constituents. Here, we report that among the six characterized SF-derived quinolizidine alkaloids including sophoridine, aloperine, sophocarpine, matrine, oxymatrine and cytisine, aloperine exerted the most potent in vitro cytotoxic activity against the human cancer cell lines and oxymatrine exhibited selective anti-cancer activity against hepatocellular carcinoma HepG2 cells. Analysis of DNA fragmentation and PARP cleavage revealed that aloperine treatment for 48 hr induced apoptosis in HL-60 cells. In addition, autophagic formation of acidic vacuole was also observed in HL-60 cells exposed to aloperine. These results suggest that aloperine may be a novel contributor to the anti-cancer properties of SF.