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首页> 外文期刊>Oxidative Medicine and Cellular Longevity >Biotransformation of Cranberry Proanthocyanidins to Probiotic Metabolites by Lactobacillus rhamnosus Enhances Their Anticancer Activity in HepG2 Cells In Vitro
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Biotransformation of Cranberry Proanthocyanidins to Probiotic Metabolites by Lactobacillus rhamnosus Enhances Their Anticancer Activity in HepG2 Cells In Vitro

机译:乳酸乳杆菌的生物转化丁香丁香霉素对益生菌代谢物的益生菌代谢物在体外增强它们的HepG2细胞中的抗癌活性

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This study was designed to unravel the role of Lactobacillus rhamnosus in the bioconversion of cranberry proanthocyanidins and cytotoxicity of resulting metabolites to hepatocellular carcinoma HepG2 cells. Crude (CR) and flavonol+dihydrochalcone- (FL+DHC-), anthocyanin- (AN-), proanthocyanidin- (PR-), and phenolic acid+catechin- (PA+C-) rich fractions were subjected to fermentation with L. rhamnosus at 37°C for 12, 24, and 48 h under anaerobic conditions. The major metabolites produced by bioconversion of polyphenols were 4-hydroxyphenylacetic acid, 3-(4-hydroxyphenyl)propionic acid, hydrocinnamic acid, catechol, and pyrogallol. Furthermore, cytotoxicity of the biotransformed extracts was compared to their parent extracts using human hepatocellular carcinoma HepG2 cells. The results showed that PR-biotransformed extract completely inhibited HepG2 cell proliferation in a dose- and time-dependent manner with IC50 values of 47.8 and 20.1 μg/mL at 24 and 48 h, respectively. An insight into the molecular mechanisms involved revealed that the cytotoxic effects of PR at 24 h incubation were mitochondria-controlled and not by proapoptotic caspase-3/7 dependent. The present findings suggest that the application of a bioconversion process using probiotic bacteria can enhance the pharmacological activities of cranberry proanthocyanidins by generating additional biologically active metabolites.
机译:本研究旨在揭开乳酸乳杆菌在蔓越莓原花青素的生物转化中的作用和将代谢物与肝细胞癌Hepg2细胞的代谢物的细胞毒性。粗(Cr)和黄酮醇+二羟基葡聚糖(FL + DHC-),花青素 - (AN-),原花青素 - (PR-)和酚醛酸+儿茶素 - (PA + C-)富分数与L发酵。在厌氧条件下37℃,24和48小时的rhamnosus。通过聚酚生物转化产生的主要代谢物是4-羟基苯基乙酸,3-(4-羟基苯基)丙酸,升级酸,儿茶酚和吡替金属。此外,使用人肝细胞癌HepG2细胞将生物转化提取物的细胞毒性与其亲本提取物进行比较。结果表明,PR-生物转化提取物分别在24和48小时的IC 50值以47.8和20.1μg/ ml的IC 50值完全抑制Hepg2细胞增殖。探讨所涉及的分子机制揭示了PR在24小时孵育时的细胞毒性效应是线粒体控制的,而不是由凋亡的Caspase-3/7受依赖性。本研究结果表明,使用益生菌的生物转化过程的应用可以通过产生额外的生物活性代谢物来增强酸丁香花青霉素的药理活性。

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