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Biotransformation of aesculin by human gut bacteria and identification of its metabolites in rat urine 被引量:5
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作者 Wei-Jun Ding Yun Deng +5 位作者 Hao Feng Wei-Wei Liu Rong Hu Xiang Li Zhe-Ming Gu Xiao-Ping Dong 《World Journal of Gastroenterology》 SCIE CAS CSCD 2009年第12期1518-1523,共6页
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 he... 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 postincubation, 10 mL of culture medium was collected. Metabolites of aesculin were extracted 3 × 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-glucocoumarin(M1), 6-hydroxy-7-sulf-coumarin (M2), 6, 7-digluco-coumarin (M3), 6-glc-7-gluco-coumarin (M4), 6-O-methyl-7-gluco-coumarin (MS) 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. 展开更多
关键词 Aesculin BIOTRANSFORMATION Human gutbacteria Rat urine Sulfated derivatives LC/ESI-MS aseculetin
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秦皮乙素对人肝癌BEL-7402细胞体外增殖的影响 被引量:11
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作者 姬剑 伟忠民 《中药药理与临床》 CAS CSCD 北大核心 2015年第3期38-41,共4页
目的:探讨秦皮乙素对人肝癌BEL-7402细胞体外增殖的影响,并探讨其可能的作用机制。方法:MTT法观察药物对细胞的抑制率;流式细胞仪分析细胞凋亡率和周期;JC-1染色法检测线粒体膜电位;酶标仪检测Caspase-3、Caspase-8、Caspase-9的活性;... 目的:探讨秦皮乙素对人肝癌BEL-7402细胞体外增殖的影响,并探讨其可能的作用机制。方法:MTT法观察药物对细胞的抑制率;流式细胞仪分析细胞凋亡率和周期;JC-1染色法检测线粒体膜电位;酶标仪检测Caspase-3、Caspase-8、Caspase-9的活性;免疫印迹法检测Bax、Bcl-2蛋白表达。结果:秦皮乙素能显著的抑制人肝癌BEL-7402细胞的体外增殖,随着秦皮乙素浓度增加(0.025、0.05、0.1、0.2、0.4、0.8μg/ml),抑制率分别为15.74%、28.25%、41.81%、51.01%、58.13%、71.51%。随秦皮乙素浓度上升(0.2、0.4、0.8μg/ml)细胞凋亡率为11.50%、20.96%、58.60%,并使细胞阻滞于S期,线粒体膜电位下降,Caspase-3、Caspase-9的活性上升,均呈剂量依赖性;而Caspase-8的活性没明显变化。Bax蛋白表达上调,Bcl-2蛋白表达下降,均呈剂量依赖性。结论:秦皮乙素能抑制人肝癌BEL-7402细胞的体外增殖,可能通过线粒体途径诱导细胞的凋亡。 展开更多
关键词 秦皮乙素 人肝癌BEL-7402细胞 细胞周期 凋亡 线粒体膜电位 CASPASE
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秦皮乙素对人肺癌H460细胞体外增殖与凋亡的影响 被引量:8
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作者 万新立 朱红军 马莲年 《癌症进展》 2017年第9期1023-1025,共3页
目的探讨秦皮乙素对人肺癌H460细胞体外增殖与凋亡的影响。方法将体外培养人肺癌H460细胞分为4组:空白对照组、秦皮乙素0.2 mg/ml组、秦皮乙素0.4 mg/ml组、秦皮乙素0.8 mg/ml组。给药干预48 h后,MTT法观察细胞增殖抑制率;流式细胞仪分... 目的探讨秦皮乙素对人肺癌H460细胞体外增殖与凋亡的影响。方法将体外培养人肺癌H460细胞分为4组:空白对照组、秦皮乙素0.2 mg/ml组、秦皮乙素0.4 mg/ml组、秦皮乙素0.8 mg/ml组。给药干预48 h后,MTT法观察细胞增殖抑制率;流式细胞仪分析细胞凋亡率和周期;比色法检测Caspase-3的活性。结果不同浓度的秦皮乙素均能抑制人肺癌细胞H460的体外增殖,并使细胞阻滞于S期,Caspase-3的活性上升,上述结果均呈剂量依赖性。结论秦皮乙素能抑制人肺癌H460细胞的体外增殖,并能诱导H460细胞的凋亡,具有良好的抗肿瘤作用。 展开更多
关键词 秦皮乙素 人肺癌H460细胞 增殖 凋亡
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