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首页> 外文期刊>World journal of gastroenterology : >Biotransformation of aesculin by human gut bacteria and identification of its metabolites in rat urine.
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Biotransformation of aesculin by human gut bacteria and identification of its metabolites in rat urine.

机译:人肠细菌对七叶皂苷的生物转化及其在大鼠尿液中的代谢产物鉴定。

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AIM: To observe the biotransformation process of a Chinese compound, aesculin, by human gut bacteria, and to identify its metabolites in rat urine. METHODS: Representative human gut bacteria were collected from 20 healthy volunteers, and then utilized in vitro to biotransform aesculin under anaerobic conditions. At 0, 2, 4, 8, 12, 16, 24, 48 and 72 h post-incubation, 10 mL of culture medium was collected. Metabolites of aesculin were extracted 3 x from rat urine with methanol and analyzed by HPLC. For in vivo metabolite analysis, aesculetin (100 mg/kg) was administered to rats via stomach gavage, rat urine was collected from 6 to 48 h post-administration, and metabolite analysis was performed by LC/ESI-MS and MS/MS in the positive and negative modes. RESULTS: Human gut bacteria could completely convert aesculin into aesculetin in vitro. The biotransformation process occurred from 8 to 24 h post-incubation, with its highest activity was seen from 8 to 12 h. The in vitro process was much slower than the in vivo process. In contrast to the in vitro model, six aesculetin metabolites were identified in rat urine, including 6-hydroxy-7-gluco-coumarin (M1), 6-hydroxy-7-sulf-coumarin (M2), 6, 7-di-gluco-coumarin (M3), 6-glc-7-gluco-coumarin (M4), 6-O-methyl-7-gluco-coumarin (M5) and 6-O-methyl-7-sulf-coumarin (M6). Of which, M2 and M6 were novel metabolites. CONCLUSION: Aesculin can be transferred into aesculetin by human gut bacteria and is further modified by the host in vivo. The diverse metabolites of aesculin may explain its pleiotropic pharmaceutical effects.
机译:目的:观察人类肠道细菌对七叶皂甙化合物的生物转化过程,并鉴定其在大鼠尿液中的代谢产物。方法:从20名健康志愿者中收集有代表性的人体肠道细菌,然后在厌氧条件下体外用于转化七叶皂甙。孵育后0、2、4、8、12、16、24、48和72 h,收集到10 mL培养基。用甲醇从大鼠尿液中提取3次七叶皂苷的代谢物,并用HPLC分析。为了进行体内代谢物分析,通过胃管给大鼠注射七叶皂苷(100 mg / kg),给药后6至48小时收集大鼠尿液,并通过LC / ESI-MS和MS / MS进行代谢物分析。正负模式。结果:人肠道细菌可以在体外完全将七叶皂甙转化为七叶皂素。生物转化过程在孵育后8至24 h发生,在8至12 h观察到其最高活性。体外过程比体内过程慢得多。与体外模型相反,在大鼠尿液中鉴定出六种七叶皂苷代谢物,包括6-羟基-7-葡萄糖香豆素(M1),6-羟基-7-硫代香豆素(M2),6、7-二-葡萄糖-香豆素(M3),6-glc-7-葡萄糖-香豆素(M4),6-O-甲基-7-葡萄糖-香豆素(M5)和6-O-甲基-7-硫代香豆素(M6)。其中,M2和M6是新型代谢产物。结论:七叶皂苷可以被人的肠道细菌转移到七叶皂苷中,并且可以在宿主体内进行进一步修饰。七叶苷的多种代谢产物可以解释其多效性药物作用。

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