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Inhibitory Activities of Daidzein Derivatives Against Human Vascular Smooth Muscle Cells Proliferation and Migration

机译:大豆苷元衍生物对人血管平滑肌细胞增殖和迁移的抑制作用

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In order to explore the application possibility of daidzein derivatives(DDs), 3-(4'-phenylsulphonylphenyl)-7-phenylswlphonyl-4H-chromen-4-one (DDl) and 3-(4'-hydroxyphenyl)-7-phenylsulphonyl-4H-chromen-4-one (DD2), their absorption inhibitory activities against human vascular smooth muscle cells (VSMCs) proliferation and migration were investigated in present study. Results showed that the partition coefficients of DDl and DD2 were much better than that of daidzein in octanol-water solvent. Final absorptions of DDl, DD2 and daidzein by human umbilical vascular smooth muscle cells were 71.67,61.44 and 54.58 %. respectively. The inhibitory rate of DD1, DD2 and daidzein of 100 μM measured against vascular smooth muscle ceils proliferation were 84.47,68.53 and 66.35 %, respectively. Human umbilical vascular smooth muscle cells migration ability was dose-dependently inhibited by daidzein derivatives and daidzein. At the concentration of 100 μM, the inhibitory effect of migrated cell number which cells were treated with DDl, DD2 and daidzein were respectively at 85.00,73.75 and 67.50 % compared with untreated control. Meanwhile, the cell migration distance of them were significantly inhibited as 81.17, 71.43 and 63.64 % of untreated control, respectively (p < 0.05). AH those results from the experiment suggested that these derivatives of daidzein as functional food ingredients might contribute to the prevention of cardiovascular diseases via inhibiting vascular smooth muscle cells proliferation and migration.
机译:为了探索黄豆苷元衍生物(DDs)的应用可能性,3-(4'-苯基磺酰基苯基)-7-苯基swlphonyl-4H-chromen-4-one(DDl)和3-(4'-羟基苯基)-7-苯基磺酰基-4H-chromen-4-one(DD2),其对人血管平滑肌细胞(VSMCs)增殖和迁移的吸收抑制活性进行了研究。结果表明,在辛醇-水溶剂中,DD1和DD2的分配系数比黄豆苷元好得多。人脐带血管平滑肌细胞对DD1,DD2和黄豆苷元的最终吸收分别为71.67、61.44和54.58%。分别。测得的100μMDD1,DD2和黄豆苷元对血管平滑肌细胞增殖的抑制率分别为84.47、68.53和66.35%。大豆苷元衍生物和大豆苷元抑制人脐血管平滑肌细胞的迁移能力。在100μM的浓度下,与未处理的对照相比,用DD1,DD2和黄豆苷元处理的细胞的迁移细胞数的抑制作用分别为85.00、73.75和67.50%。同时,它们的细胞迁移距离被显着抑制,分别为未处理对照的81.17%,71.43%和63.64%(p <0.05)。所有来自实验的结果表明,大豆苷元的这些衍生物作为功能性食品成分可能通过抑制血管平滑肌细胞的增殖和迁移而有助于预防心血管疾病。

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