首页> 外文期刊>BMC Complementary and Alternative Medicine >Phenolic compounds isolated from fermented blueberry juice decrease hepatocellular glucose output and enhance muscle glucose uptake in cultured murine and human cells
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Phenolic compounds isolated from fermented blueberry juice decrease hepatocellular glucose output and enhance muscle glucose uptake in cultured murine and human cells

机译:从发酵蓝莓汁中分离出的酚类化合物会降低培养的鼠类和人类细胞的肝细胞葡萄糖输出并增强肌肉葡萄糖的摄取

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Background We recently reported that blueberry juice fermented (FJ) with Serratia vaccinii bacterium has antidiabetic activities both in vivo and in vitro. The purpose of this project was to elucidate the effect of FJ on glucose homeostasis in liver and skeletal muscle cells and to identify active fractions/compounds responsible for this effect. Methods FJ was fractionated using standard chromatography procedures. Hepatic (H4IIE, HepG2) and skeletal muscle cells (C2C12) were treated with maximum non-toxic concentrations of FJ, fractions and isolated compounds thereof. Glucose-6-phosphatase (G6Pase) activity was measured using glucose oxidase method. To measure glucose uptake and glycogen synthase (GS) activity, radioactive assays were used. Results Fractionation of FJ yielded seven fractions. FJ and its phenolic fractions F2, F3-1 and F3-2 respectively inhibited G-6Pase by 31, 45, 51 and 26%; activated GS by 2.3-, 2.3-, 2.2- and 2-fold; and stimulated glucose uptake by 19, 25, 18 and 15%, as compared to DMSO vehicle control. Subfractionation of the active fractions yielded 4 compounds (catechol, chlorogenic, gallic and protocatechuic acid). Catechol, yielding the greatest bioactivity in G6Pase and glucose uptake assays, decreased G6Pase activity by 54%, increased GS by 2-fold and stimulated glucose uptake by 44% at 45.5 μ M. Conclusions This study identifies novel potential antidiabetic compounds that can help standardize FJ.
机译:背景技术我们最近报道,用沙雷氏菌(Serratia vaccinii)细菌发酵的蓝莓汁(FJ)在体内和体外均具有抗糖尿病活性。该项目的目的是阐明FJ对肝脏和骨骼肌细胞中葡萄糖稳态的影响,并确定引起这种作用的活性成分/化合物。方法使用标准色谱法对FJ进行分级分离。肝(H4IIE,HepG2)和骨骼肌细胞(C2C12)用最大无毒浓度的FJ,其馏分和分离的化合物处理。使用葡萄糖氧化酶方法测量6-葡萄糖磷酸酶(G6Pase)的活性。为了测量葡萄糖摄取和糖原合酶(GS)活性,使用了放射性测定法。结果FJ的分馏产生七个馏分。 FJ及其酚类组分F2,F3-1和F3-2分别抑制G-6Pase 31、45、51和26%。激活GS 2.3倍,2.3倍,2.2倍和2倍;与DMSO媒介物对照相比,葡萄糖吸收率提高了19%,25%,18%和15%。细分活性成分可得到4种化合物(邻苯二酚,绿原酸,没食子酸和原儿茶酸)。儿茶酚在G6Pase和葡萄糖吸收测定中具有最大的生物活性,在45.5μM时,G6Pase活性降低54%,GS增加2倍,刺激葡萄糖吸收增加44%。结论本研究发现了可以帮助标准化的新型潜在抗糖尿病化合物缩略词。

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