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Cell cytotoxity and anti-glycation activity of taxifolin-rich extract from Japanese larch Larix kaempferi

机译:日本落叶松落叶松富含紫杉醇提取物的细胞毒性和抗糖化活性

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摘要

The larches, the Larix genus of plants are known as a natural source of taxifolin (dihydroquercetin), and extracts of its taxifolin rich xylem are used in dietary supplements to maintain health. In the present study, to assess biological activities of a methanol extract of the Japanese larch, Larix kaempferi (LK-ME), the effects of LK-ME on cell viability, inflammatory cytokine expression, and glycation were investigated. The effects of taxifolin which is known to be a main compound of LK-ME, and its related flavonoids, quercetin and luteolin were also examined. The results show that taxifolin exhibits lower growth inhibition activity and lesser induction activity of inflammatory cytokines in a human monocyte derived cell line, THP-1 cells, while in vitro anti-glycation activities of taxifolin were inhibiting at comparable levels to those of quercetin and luteolin. The growth inhibition and the cytokine induction activities, and the anti-glycation effects of LK-ME are assumed to have properties similar to taxifolin. The results of high performance liquid chromatography (HPLC) analysis indicated that taxifolin was detected as the main peak of LK-ME at the absorbance of 280 nm, and the concentration of taxifolin was measured as 3.12 mg/ml. The actual concentration of taxifolin in LK-ME is lower than the concentration estimated from the IC50 values calculated by the results of glycation assays, suggesting that other compounds contained in LK-ME are involved in the anti-glycation activity.
机译:落叶松是植物的落叶松属,被称为滑石粉(二氢槲皮素)的天然来源,富含滑石粉的木质部提取物被用于膳食补充剂中以保持健康。在本研究中,为了评估日本落叶松落叶松(Larix kaempferi,LK-ME)的甲醇提取物的生物活性,研究了LK-ME对细胞活力,炎性细胞因子表达和糖基化的影响。还研究了作为LK-ME主要化合物的滑石粉及其相关类黄酮,槲皮素和木犀草素的作用。结果表明,滑石粉在人单核细胞衍生的THP-1细胞系中表现出较低的生长抑制活性和较低的炎症细胞因子诱导活性,而滑石粉的体外抗糖化活性抑制能力与槲皮素和木犀草素相当。 。 LK-ME的生长抑制和细胞因子诱导活性以及抗糖基化作用被认为具有与滑石粉相似的性质。高效液相色谱(HPLC)分析的结果表明,在280nm的吸光度下检测到滑石粉是LK-ME的主峰,测得的滑石粉浓度为3.12mg / ml。 LK-ME中的滑石粉的实际浓度低于根据糖化测定结果计算的IC50值估算的浓度,这表明LK-ME中包含的其他化合物也参与了抗糖化活性。

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